Candida sp. Infections in Patients with Diabetes Mellitus

Abstract

Candidiasis has increased substantially worldwide over recent decades and is a significant cause of morbidity and mortality, especially among critically ill patients. Diabetes mellitus (DM) is a metabolic disorder that predisposes individuals to fungal infections, including those related to Candida sp., due to a immunosuppressive effect on the patient. This review aims to discuss the latest studies regarding the occurrence of candidiasis on DM patients and the pathophysiology and etiology associated with these co-morbidities. A comprehensive review of the literature was undertaken. PubMed, Scopus, Elsevier’s ScienceDirect, and Springer’s SpringerLink databases were searched using well-defined search terms. Predefined inclusion and exclusion criteria were applied to classify relevant manuscripts. Results of the review show that DM patients have an increased susceptibility to Candida sp. infections which aggravates in the cases of uncontrolled hyperglycemia. The conclusion is that, for these patients, the hospitalization periods have increased and are commonly associated with the prolonged use of indwelling medical devices, which also increase the costs associated with disease management.

1. Introduction

Diabetes mellitus (DM) is a chronic metabolic and degenerative disorder that is characterized by chronic hyperglycemia and causes long-term complications like retinopathy, neuropathy, and nephropathy, generally accelerating macro- and micro-vascular changes. It is becoming one of the largest emerging threats to public health in the 21st century [1,2]. Several immune alterations have been described in diabetes with cellular immunity being more compromised and with changes in polymorphonuclear cells, monocytes, and lymphocytes [3]. DM individuals have higher glucose serum concentrations than healthy individuals (between 4.0 to 5.4 mmol/L or 72 to 99 mg/dL when fasting and up to 7.8 mmol/L or 140 mg/dL two hours after eating [4]; hemoglobin A1c (glycohemoglobin) ≤5.7%). In type 1 DM, the pathogenesis is multifactorial because of antibody-mediated autoimmunity, environmental toxins exposure, and major histocompatibility complex (MHC) Class II histocompatibility complex HLA-DR/DQ genetic polymorphisms. These features create an increased susceptibility to disease onset due to a continuous loss of insulin-producing β-cells in the pancreas, which is due to the T-cells’ infiltration through mitochondrial-driven apoptosis [5]. On the other hand, in type 2 DM, there is an insulin resistance that is associated with changes in the mitochondrial metabolism with reduced mitochondrial density, ATP production, and mitochondrial RNA (mtRNA) levels, as well as increased markers for oxidative stress. The chronic exposure of the circular mtDNA to these effects might trigger significant tissue modifications found in the pancreas and endothelial cells, leading to secondary vascular disease and causing cardiac, renal, ophthalmic, and neurological complications [5,6,7] (Figure 1).

In 2017, the worldwide prevalence of adult-onset diabetes (20–79 years) was nearly 425 million, and the World Health Organization and the International Diabetes Federation predicted that the number of adults in the world with diabetes will rise near 629 million by the year 2045 [8,9] (Figure 2). A higher prevalence of DM, cardiac, and pulmonary diseases can be found in senior patients with candidemia [10,11,12,13]. The relationship between diabetes and candidiasis has been widely studied [13,14,15,16], particularly due to the increased susceptibility of diabetic patients to fungal infections compared to those without DM [14,15,17,18].

Several mechanisms are attributed to higher Candida sp. predisposition among DM patients depending on the local or systemic infection. Among the recognized host conditions for candidal colonization and subsequent infection are yeast adhesion to epithelial cell surfaces [19], higher salivary glucose levels [15,20], reduced salivary flow [21], microvascular degeneration, and impaired candidacidal activity of neutrophils. These conditions are particularly serious in the presence of glucose [22,23], secretion of several degradative enzymes [24,25,26], or even a generalized immunosuppression state of the patient [8,27,28,29,30,31]. These factors have a major influence on the balance between host and yeasts, favoring the transition of Candida sp. from commensal to pathogen and causing infection. In fact, in a very recent study, Gürsoy et al. [32] suggested that there is a higher presence of intestinal Candida albicans colonization in diabetic patients. In fact, there may be a tendency of type 1 DM in patients with a high prevalence of intestinal C. albicans. C. albicans is also known to wait for a change in some aspect of the host physiology that normally suppress growth and invasiveness through a phenomenon called phenotypic switch system or white-opaque transition, described in 1987.

This involves reversible and heritable switching between alternative cellular phenotypes. It occurs at sites of infection and recurrently in episodes of infection in certain cases in diabetic patients [33].

Yeasts are part of the normal gut microflora, but cell counts do not normally surpass 10 colony forming units (CFU)/g feces [34,35]. Nevertheless, it has been described that Candida sp. is more widespread in the feces of patients with type 1 and type 2 DM with poor glycemic control as opposed to healthy subjects [36]. The main reasons for this colonization seem to be altered functions of the immune system in diabetic patients with poor glycemic control or a direct effect of elevated blood glucose levels, creating specific conditions for intensive fungal colonization [36]. In fact, another report [37] showed that in patients with type 1 DM, the total gut CFUs significantly rise up to 40% in C. albicans colonization compared to 14.3% in healthy individuals. This may be related to the decrease in commensal bacteria-probably the result of yeast-bacterial competition. Also, this higher growth may disrupt the ecological balance of intestinal flora, which occurs in type 1 DM [37]. Regarding the gastrointestinal colonization, Kowalewska et al. [38] studied the serum levels of interleukin-12 (IL12) in relation to the percentage of yeast-like fungi colonies residing in the gastrointestinal tract in children and adolescents with DM type 1. Results showed that high IL12 levels can inhibit infection with yeast-like fungal colonizing the gastrointestinal tract in children and adolescents with type 1 DM. However, further studies are needed to confirm the antifungal activity of IL12 [38].

The development of drug resistance among Candida sp. isolates allied to epidemiologic variations in Candida sp. natural flora has significant implications for morbidity and mortality [39,40,41,42]. The extensive use of medications, especially azoles, has promoted the selection of resistant species by shifting colonization to more naturally resistant Candida sp., such as C. glabrata, C. dubliniensis, and C. krusei [43,44,45,46]. Presently, the world distribution of Candida sp. is a feature of the epidemiology in the area, but it indicates a predominance of C. albicans, C. glabrata, C. tropicalis, C. parapsilosis, and C. krusei [45,47]. It has been confirmed that 90% of fungemia cases are attributed to Candida sp. [39,40], and the mortality has ranged from 40% to 80% in immunocompromised hosts [39,40,48]. Furthermore, a high mortality rate was also detected among non-immunocompromised patients (60%) [49] and those with diabetes (67%) [41].

The main pathophysiologic and nutritionally relevant sugars in diabetic patients are glucose and fructose, but other simple carbon sources also play an important part in the growth of Candida sp. in DM patients. Man et al. [50] evaluated the growth rate of C. albicans in the presence of different concentrations of glucose and fructose to obtain a better understanding of the nutrient acquisition strategy and its possible relation to the hyperglycemic status of diabetic patients. The authors determined that the glucose concentration is directly related to C. albicans growth, which may be linked to the frequent yeast infections that occur in non-controlled diabetic patients. Interestingly, fructose showed C. albicans inhibition capacities. This implies fructose-containing food may prevent the development of candidiasis. This is an important outcome in oral Candida sp. biofilms, especially for patients who use prosthesis [50]. In fact, other carbon compounds such as sucrose, maltose, and lactose increase the fungal population density [43,51,52] and decrease the activity of antifungal agents. A recent report explored the effects of glucose in diabetic mice on the susceptibility of Candida sp. to antifungal agents [53]. In that work, Mandal et al. [53] revealed that voriconazole (Vcz) has the greatest reduction in antifungal drug efficacy followed by amphotericin B (AmB). Glucose displayed a higher affinity to bind to Vcz through hydrogen bonding, decreasing the susceptibility of antifungal agents during chemotherapy. Additionally, Mandal et al. [53] confirmed that Vcz presented three important hydrogen bonds and AmB presented two hydrogen bonds that stabilized the glucose. In vivo results of the same study proposed that the physiologically relevant higher glucose level in the bloodstream of mice with DM might interact with the available selective agents during antifungal therapy, decreasing glucose activity by complex formation. Vcz-glucose and AmB-glucose complexes seem to present less effectiveness as their pure molecule. Accordingly, a proper selection of drugs for DM patients is important if we are to control infectious diseases [53]. Similarly, Rodaki et al. [54] studied the impact of glucose on C. albicans transcriptome for the modulation of carbon assimilatory pathways during pathogenesis. The elevated resistance to oxidative and cationic stresses and resistance to miconazole uncovered that glucose concentrations in the bloodstream have a significant impact upon C. albicans gene regulation. No significant susceptibility level was perceived for anidulafungin, while Vcz and AmB became less effective [54]. In another study, Rodrigues et al. [52] demonstrated that C. glabrata decreases its susceptibility to fluconazole when cultured in a medium enriched with glucose [52].

Accordingly, the aim of this review is to analyze the literature related to the occurrence of candidiasis in diabetic patients by discussing specific features of Candida sp. that relate directly to the occurrence of candidiasis in DM patients and related diseases, as well as by reviewing recent and relevant studies on the topic.

2. Particular Features of Candida sp. that Increase the Incidence of Candidiasis in Diabetic Patients

2.1. Enzymatic Activity

Several studies have established an association between hydrolytic enzymes activity and an increase in the pathogenic ability of Candida sp. [55,56].

It has been demonstrated that, due to higher blood glucose concentration, diabetic Candida sp. isolates present significantly higher hemolytic and esterase enzymatic activity, which may contribute to increased enzyme activity among diabetic patients [57,58,59,60]. The same authors also hypothesized that these species are more pathogenic under abnormal conditions such as DM [61,62]. Secreted aspartyl proteinases (SAP) capable of degrading numerous substrates that constitute host proteins in the oral cavity have also been studied. These enzymes are thought to help Candida sp. to acquire essential nitrogen for growth, to attach to and penetrate oral mucosa, or both [63,64]. They can also cause amplified vascular permeability, leading to inflammatory reactions [65] and clinical symptoms, which may disturb the humoral host defense [66]. Similarly, phospholipase (PL) targets the membrane phospholipids and digests these components, initiating cell lysis and facilitating the penetration of the infecting fungi [67]. This enzyme induces the accumulation of inflammatory cells and plasma proteins, releasing several inflammatory mediators in vivo [67].

Very recently, it was revealed that C. albicans hyphae induce both epithelial damage and innate immunity through the secretion of a cytolytic peptide toxin called candidalysin [68,69]. This enzyme is encoded by the hypha-associated ECE1 gene and is the first peptide toxin to be identified in any human fungal pathogen. Candidalysin induces calcium ion influx and lactate dehydrogenase (LDH) release in oral epithelial cells, which are features of cell damage and membrane destabilization. Importantly, the study also reported that C. albicans mutants where the entire ECE1 gene or the candidalysin-encoding region had been deleted have full invasive potential in vitro but are incapable of inducing tissue damage or cytokine release and are highly weakened in a mouse model of oropharyngeal candidiasis and a zebrafish swim bladder mucosal model [68].

2.2. Biofilm Formation

Biofilms are communities of microorganisms embedded in an extracellular matrix [70,71], which confer substantial resistance to antifungal therapy and increased host immune responses [72,73]. These communities can be formed in both biotic (e.g., mouth mucosae) or abiotic (e.g., catheters) surfaces [74,75]. In fact, candidemia are the most prevalent invasive mycoses worldwide with mortality rates close to 40% [76]. Candida sp. are often recognized as the origin of candidemia, urinary tract infections, and hospital pneumonia. In practically all of these cases, the infections are related with the use of a medical device and biofilm formation on its surface [20]. The most frequently colonized medical device is the central venous catheter used for administration of fluids, nutrients, and medicines [77]. The contamination of the catheter or the infusion fluid can arise from the skin of the patient, the hands of health professionals [77], or by migration into the catheter from a pre-existing lesion. Less commonly, if Candida sp. that colonize the gastrointestinal tract as a commensal start to develop a pathogenic behavior, they are able to infiltrate the intestinal mucosa and diffuse through the bloodstream. Consequently, circulating yeast may colonize the catheter endogenously. This is more common in cancer patients, as chemotherapy leads to damage to the intestinal mucosa [78]. In the other patients, infected catheters are the most significant source of bloodstream infections, followed by widespread invasive candidiasis. The catheter removal is recommended in patients with disseminated Candida sp. infection to enable disinfection of the blood and to increase prognosis [79,80].

Biofilm development of Candida sp. (Figure 3) can be explained in four chronological steps: adherence-initial phase in which the yeast in suspension and planktonic cells adhere to the surface (first 1–3 h); intermediate phase-development of biofilm (11–14 h); maturation phase-the polymeric matrix (PEM) completely penetrates all layers of the cells adhered to the surface in a three-dimensional structure (20–48 h); dispersion-the most superficial cells leave the biofilm and colonize areas surrounding the surface (after 24 h) [81]. Hence, a mature biofilm comprises of a dense network of cells in the form of yeasts, hyphae, or pseudohyphae (or not, depending on the Candida sp.) involved by PEM and with water channels between the cells. These help in the diffusion of nutrients from the environment through the biomass to the lower layers and also allow the removal of waste [81,82]. Formed using in vivo models, Candida sp. biofilms seem to follow the same sequence of in vitro formation [83]. Nonetheless, the maturation step happens more quickly, and the thickness is increased. The final architecture of the biofilm is variable and depends, in part, on the Candida sp. involved, the growing conditions, and the substrate on which it is formed [81,84].

High levels of glucose are thought to serve as the carbohydrate energy source necessitated by Candida sp. for the biofilm formation and are probably required to produce the polysaccharide matrix [85], which is secreted by sessile cells, providing protection against environmental challenges [86]. Biofilm formation has been shown to be dependent on the Candida sp. and its clinical origin. Biofilms are refractory to antifungal drugs and more difficult to treat than infections with planktonic cells [44]. Moreover, it has been verified that Candida sp. isolated from patients with DM have a higher pathogenic potential for biofilm-forming [87]. The communities are extremely common on medical devices.

2.3. Hydrophobicity

In Candida sp., the adhesion phenomenon is mediated by agglutinin-like (Als) sequence proteins [88], which are glycosylphosphatidylinositol (GPI)-linked to β-1-6 glucans in the fungal cell wall. Als-dependent cellular adhesion is connected with increases in cell surface hydrophobicity (CSH) [89]. The CSH of Candida sp. enhances virulence by promoting adhesion to host tissues [89,90]. C. albicans Als3p (hypha-associated) is a major epithelial adhesin that is strongly upregulated during epithelial infection in vitro [90], and the disruption of the ALS3 gene reduces epithelial adhesion in vitro. Likewise, decreasing the expression of the ALS2 gene also reduces adhesion [91,92]. On the other side, deletion of the ALS5, ALS6, or ALS7 genes increased adhesion [93], demonstrating that the Als proteins can have opposing roles in fungal attachment to surfaces. Putative homologues of Als proteins have also been identified in NCAC [94]. In C. glabrata, for example, epithelial adhesins (Epa) have a comparable structure to the Als proteins [95,96].

Together with adhesion ability, hydrophobicity is a virulent factor that is gene-regulated and usually positively correlated with biofilm metabolic activity [97,98] since hydrophobic interactions seem to be crucial in promoting tissue invasion by the mycelial phase of Candida sp. It is presumed that Candida sp. can grow under anaerobic conditions, although in these conditions fermentation is the dominant pathway for ATP production [99]. The results of Sardi et al. [100] indicated that 51.97% of diabetic patients’ isolates were highly hydrophobic under anaerobic conditions when compared to 21.90% under the aerobic atmosphere [100]. It is recognized that the germ tubes are able to adhere to fibronectin, fibrinogen, and complement via cell surface receptors [101], helping the attachment of filament yeasts to extracellular matrix components (ECM) [102] and producing impairment of phagocytosis, consequently increasing the resistance to blood clearance and the virulence of Candida sp. [103].

3. Candidiasis and DM

3.1. Oral Diseases

3.1.1. Oral Candidiasis

The prevalence of oral candidiasis is increasing, as it is one of the most common fungal infections [104]. Oral candidiasis can be diagnosed by the differential patterns of mucosal changes like erythematous, pseudomembranous, and curd-like plaques (biofilms) [105,106]. Higher Candida sp. colonization rates were reported in patients with DM type 1 when compared to DM type 2 patients (84% vs. 68%, respectively), while the percentage in nondiabetic subjects was around 27% [18]. The studies also describe how this colonization does not always lead to infection. Nonetheless, it is a prelude to infection when host immunity is compromised and the risk of a disseminated infection is high [107]. Such infections continue to be a major healthcare challenge [108].

The risk factors for oral candidal infection are complex, but it is known that tongue lesions, tobacco smoking, denture wearing, and immunosuppression (e.g., diabetes mellitus) clearly influence oral Candida sp. carriage and the upsurge of oral candidiasis [30,109,110,111,112,113,114]. The causes influencing the higher incidence of oral candidiasis in diabetic patients are presented in

Table 1. Physiopathology and etiology related to the occurrence of oral candidiasis in diabetics.

	Physiopathology	Reference (s)
Uncontrolled hyperglycemia (high HbA1c) and high glucose levels in saliva	-Uncontrolled hyperglycemia may cause intensification in salivary glucose levels because in diabetics the basement membrane of the parotid salivary gland is more permeable -High glucose levels allow Candida sp. to multiply, even in the presence of normal bacterial flora -During hyperglycemic episodes, the chemically reversible glycosylation products with proteins in tissues and the accumulation of glycosylation products on buccal epithelial cells may sequentially increase the number of available receptors for Candida sp. -Glucose suppression of the killing capacity of neutrophils, emphasizing colonization (immunosuppression) -Glucose, maltose, and sucrose boost the adhesion of Candida to buccal epithelial cells	[15,29,31,52,134,140,141,142,143,144,145,146,147]
Lower salivary pH	-The growth of Candida in saliva is accompanied by a rapid decline in pH, which favors their growth and triggers the extracellular phospholipase (PL) and acid proteases, increasing the yeast adhesion to oral mucosal surfaces	[31,128,148]
Tissue response to injury is diminished	-Diabetes mellitus (DM) is known to diminish the host resistance and modify the tissue response to injury. This can result in severe colonization, even in the absence of any clinically evident oral candidiasis and possibly with further dissemination via the blood.	[130,149]
Oral epithelium	-It is most probable that the host oral epithelium of patients with diabetes favors the adhesion of colonization and subsequent infection.	[150,151]
Poor oral hygiene	The lack of control of the oral environment, especially concerning the prevention of dental caries (coronary, root, and periodontal), leads to a higher rate of oral candidiasis, especially in DM older patients	[152,153,154]
Aging	Diabetic women, orally colonized with Candida sp. have higher oral glucose levels than diabetics without oral Candida sp.	[134]
Gender
Prostheses	Inadequate use of prostheses, together with inadequate hygienization, favours the growth of Candida sp.	[155,156,157]
Drugs	Xerostomia (abnomal lack if saliva): Candida sp. stagnation and growth on oral tissues	[30,109,110,111,136,158,159]

.

Higher expressions in enzymatic activity and the biofilm forming capacity of Candida sp. are two of the most important features in oral candidiasis. In a study by Sanitá et al. [115], the virulence of 148 clinical isolates of C. albicans from oral candidiasis was characterized by measuring the expression of PL and SAP in healthy subjects (HS), diabetics with oral candidiasis (DOC), and non-diabetics with oral candidiasis (NDOC). For PL, C. albicans from NDOC and DOC had the highest enzymatic activity (76.6%); for SAP, C. albicans from NDOC exhibited lower enzymatic activity (48.9%). Similar results have been reported in the past [59,87], with percentages greater than 90% for both PL and SAP activity among clinical isolates of C. albicans [26,116,117] found. Arlsan and colleagues found 12 different genotypes and compared the virulence factors of several Candida sp. isolated from the oral cavities of 142 healthy and diabetic individuals, with and without caries. Although the most isolated species was also C. albicans, there were statistical differences in terms of isolated Candida frequency between healthy subjects and diabetic patients. DM showed no effect on the activities of virulence factors (biofilm production, proteinase, and phospholipase activity) of Candida sp. Yet, different genotypes of C. albicans exhibited different virulence activities [118]. Other authors showed that the activity of SAPs suggestively rises in denture wearers with signs of candidiasis compared to denture wearers with a normal palatal mucosa [119]. The inconsistency of results of these reports can be explained by the large variation of intra-and interspecies of Candida and deviations in the methodology in most reports [24,26,59,87,116,117,119,120,121,122,123]. A longitudinal study by Sanchés-Vargas et al. [124] quantified biofilms in oral clinical isolates of Candida sp. from adults with local and systemic predisposing factors for candidiasis. Between the isolates, authors found C. albicans, C. tropicalis, C. glabrata, C. krusei, C. lusitaniae, C. kefyr, C. guilliermondii, and C. pulcherrima from the oral mucosa of totally and partially edentulous patients (62.3%) and the oral mucosa of diabetics (37.7%). On average, the oral isolates of C. glabrata were considered strong biofilm producers, whereas C. albicans (the most common species) and C. tropicalis were moderate producers. This might be because C. glabrata has been shown to have a higher aggressiveness, producing a great quantity of biofilm matrices yet also increasing chitin concentrations in the cell walls [125,126,127].

Additional important features are the oral pH and the glycemic control. A study performed by Samaranayake et al. [128] demonstrated that pyruvates and acetates are the major ionic species, generating a quick decrease in pH with Candida sp., as found in batch cultures of mixed saliva supplemented with glucose [128].

Other authors indicated that yeasts have a superior ability to adhere to epithelia and denture acrylic surfaces at a low pH of approximately 2–4.14 [31,129]. Balan and colleagues stated that during hyperglycemic episodes, the environmental alteration in the oral cavity increased salivary glucose and acid production, which favored the transition of Candida sp. from commensal to pathogen [31]. In another report, while comparing diabetics and non-diabetics, Pallavan et al. [130] verified that 70% of the healthy individuals had lower colonization and 43.3% of the diabetic patients had severe colonization by Candida sp., which was also observed in other studies [14,18,21,131]. Prediabetes is a condition where there is an elevation of plasma glucose above the normal range but below that of clinical diabetes [132]. Javed and their colleagues isolated oral Candida sp. from 100% of patients with prediabetes and from 65.7% of the controls, observing that the carriage of C. albicans was greater among patients with prediabetes (48.7%) than with controls (25.7%) [133]. They also observed that the colonization with Candida sp. reduced the salivary flow rate and was independent of glycemic status in patients with prediabetes [132].

In fact, while some studies found a direct significant association between glycosylated hemoglobin and oral Candida colonization [134,135], other authors found no relationship between glycosylated hemoglobin and high Candida-burden in patients with DM [14,18,136,137]. Furthermore, studies indicate that the concentration of glucose present in the gingival crevicular fluid is related to the blood glucose level [138]. The quality of glycemic control can also partially explain the presence of a significant relationship between subgingival plaque candidal colonization and higher concentrations of glucose [138].

Although most of the scientific community believes that diabetes is a risk factor associated with oral yeast infections, in a recent paper, Costa and colleagues [139] reported that the presence of yeasts in the oral cavity of patients with type 1 DM (60% of total) was not affected by diabetes, metabolic control, duration of the disease, salivary flow rate, or saliva buffer capacity by age, sex, place of residence, number of daily meals, consumption of sweets, or frequency of tooth brushing. Candida albicans was the most prevalent yeast species, but a higher number of yeast species was isolated in nondiabetics [139]. The fact that this study was developed exclusively in children may be related to this conclusion.

3.1.2. Antifungal Treatment of Oral Candidiasis

Importantly, several reports have stated the importance of the evaluation of the susceptibility of the oral isolates to the antifungal drugs in order to choose proper therapy in diabetic patients to control the fungal diseases. Aitken-Saavedra et al. [160] revealed that 66% of the yeasts isolated in diabetic patients were C. albicans, followed by C. glabrata (20.7%). In patients with decompensated type 2 DM, higher levels of salivary acidification and a greater diversity and quantity of yeasts of the genus Candida were observed. When nystatin was administered in these patients, higher inhibition was observed at a lower pH [160]. The study presented by Lydia Rajakumari and Saravana Kumari [161] showed a lower glycemic control leads to a higher candidal colonization in diabetic patients. The predominant species was C. albicans, but among denture wearers, C. glabrata was predominant. More importantly, ketoconazole, fluconazole, and itraconazole were effective against the isolated Candida sp. [161].

Similarly, Premkumar et al. [162] stated that, although C. albicans was the most predominantly isolated species, C. dubliniensis, C. tropicalis, and C. parapsilosis were also observed. The authors showed variable resistance toward amphotericin B, and fluconazole was observed in clinical isolates from diabetics but not from healthy patients. Again, a positive correlation was observed between glycemic control and candidal colonization [162]. In 2011, Bremenkamp et al. [163] found no significant differences in antifungal susceptibility to the tested agents between Candida sp. isolates from diabetic and non-diabetic subjects, which was consistent with the study by Manfredi et al. [164]. Furthermore, a high prevalence of C. dubliniensis in diabetic patients was found, which may suggest a potential misdiagnosis of its morphologically-related species, C. albicans. Other authors found the same two species in DM patients [1,16,57,135]. In yet another study, Sanitá and their colleagues [165] investigated the susceptibility of 198 oral clinical isolates of Candida sp. against caspofungin, amphotericin B, itraconazole, and fluconazole. Their findings confirmed the resistant profile of C. glabrata isolates against azole antifungals—especially itraconazole—in individuals with diabetes and denture stomatitis. The clinical sources of the isolates were shown to have no effect on the mininum inhibitory concentration (MIC) values obtained for all antifungals tested, which was in accordance with previous reports [26,119]. Additionally, Candida sp. isolates with higher rates of resistance to flucytosine, ketoconazole, miconazole, and econazole were confirmed in patients with diabetes when compared to healthy controls [163,166]. The increase in the environment glucose concentration may trigger the expression of several genes responsible for several carbohydrate cell wall and biofilm matrices components, consequently leading to resistant strains. This has been demonstrated before in gene and drug studies [126]. The variability in the susceptibility results may be related to the different antifungal drugs tested in those works.

Using a different approach, Mantri et al. [149] evaluated Candida sp. colonization in dentures with a silicone soft liner in diabetic and non-diabetic patients, assessing the antifungal efficacy of chlorhexidine gluconate [149]. The results showed normal oral flora in diabetics and non-diabetics and no difference between groups. They also showed a significant reduction of the colonization after cleaning the dentures with 4% chlorhexidine gluconate. This suggests that this drug has a good antiseptic effect on Candida sp. by killing it and preventing new adhesion. In 2015, Indira et al. [167] conducted a study that compared the common opportunistic infections (OIs) between 37 people living with HIV with DM (PLHIV-DM) and 37 people living with HIV without DM (PLHIV). Both of the groups were treated with anti-retroviral therapy (ART) [167]. The most common Ois included oral candidiasis (49% of PLHIV-DM and 35% of PLHIV) and C. krusei was the most common Candida sp. isolated (50%). No significant difference in the profile of Ois was found between PLHIV with and without DM.

3.1.3. Periodontal Diseases

Periodontal diseases of fungal origin are relatively unusual in healthy individuals but arise more often in immunocompromised people or in cases when normal oral flora has been distressed (e.g., the use of broad-spectrum antibiotics) [168,169]. Diabetes is a stated risk factor for periodontitis, which is the sixth-leading complication of diabetes [170,171]. Alterations in host response, collagen metabolism, vascularity, gingival crevicular fluid, heredity patterns, and immunosuppressive treatment (drugs, dosage, and treatment duration) are known factors that promote periodontitis in diabetes [172,173]. The etiology and pathogenesis of periodontitis is still imprecise, but it is recognized that Candida sp. is part of the oral and subgingival microbiota of individuals who suffer from severe periodontal inflammation [174]. The virulence factors of Candida sp. simplify the colonization and the proliferation in the periodontal pockets by co-aggregating with bacteria in dental biofilms and adhering to epithelial cells [30], which are essential in the microbial colonization, thereby contributing to the evolution of oral diseases [175,176]. As much as 20% of patients with chronic periodontitis have been shown to have periodontal pockets that are colonized by several species of Candida sp., predominantly C. albicans [177,178], but C. dubliniensis [174], C. glabrata, and C. tropicalis have been reported too [176,179]. Furthermore, C. albicans strains isolated from subgingival sites of diabetic and periodontal patients showed high PL in cases of chronic periodontitis. Environmental oxygen concentration demonstrated influence on the virulence factors [100,180,181]. Sardi et al. [100], in a study using PCR experiments, demonstrated that the quantities of several Candida sp. were higher in diabetic patients with a chronic periodontal disease than in patients without diabetes. C. albicans, C. dubliniensis, C. tropicalis, and C. glabrata were detected in 57%, 75%, 16%, and 5% of the periodontal pockets, respectively. In non-diabetic patients, C. albicans and C. dubliniensis were present in 20% and 14%, respectively. Periodontal inflammation has been described to be worse in prediabetics when compared to healthy controls [182,183,184,185], assuming that the oxidative stress induced by chronic hyperglycemia with a reduced unstimulated whole salivary flow rate (UWSFR) in these patients may contribute to deteriorating periodontal status [133]. Thus, it has been suggested that glycemic control enhances healing and reduces periodontal inflammation in patients with DM and prediabetes [134,182,185,186,187,188,189,190,191]. As a result, some authors believe that it may reduce oral Candida sp. carriage in patients with prediabetes [133]. The HbA1c concentration is an important diagnostic tool for monitoring long-term glycemic control [192]. Also, in these cases, higher Candida sp. infection levels have also been associated with low diabetic control (HbA1c > 9), occurring less frequently in subjects with well-controlled blood sugar levels (HbA1c < 6).

3.1.4. Denture Prosthetics and Candidiasis

Since the oral cavity is highly populated with several polymicrobial communities, each one occupies very precise niches that diverge in both anatomical location and as well as nutrient availability [193]. A consequence of strong commensal bacteria/yeast colonization is the inhibition of pathogenic microorganism colonization through resistance. The vital function of commensal yeast and bacteria and the harmful effects of commensal depletion through the use of broad spectrum antibiotics [194,195] are well recognized. Recent studies disclosed that commensal microorganisms not only protect the host by niche occupation, but also interact with host tissue, promoting the development of proper tissue structure and function [196,197].

Dentures represent a protective reservoir for oral microorganisms, mostly in biofilm form, favoring yeast proliferation, improving their infective potential, and protecting fungal cells against several medications [198,199,200,201,202]. Elderly edentulous denture wearers, patients with debilitating diseases, and users of acrylic prosthetics have a significant risk of virulent oral yeast infections [124]. Furthermore, elderly patients with diabetes have a 4.4 times higher estimated risk of developing oral candidiasis when compared with individuals without this disease. No statistically significant relation was determined between xerostomia, the use of prosthesis, and oral candidiasis [154], as suggested by some studies [203,204]. Sanitá et al. [199] studied the prevalence of Candida sp. in diabetics and non-diabetics with and without denture stomatitis (DS) and found that C. albicans was the predominant species isolated in the three groups (81.9%). They also detected C. tropicalis (15.71%) and C. glabrata (15.24%), as found in previous studies [10,14,15,21,24,57,136,144,173,205,206,207,208,209,210]. Interestingly, and contrary to other reports, the authors did not detect C. dubliniensis among any Candida sp. isolates. Even though these results confirm previous findings [10,14,16,21,24,26,136,144,173,207,209,210], this species has been isolated in both diabetic [12,57,206] and non-diabetic [208] patients. This discrepancy among studies may be related to problems with identification techniques, since C. dubliniensis and C. albicans have similar phenotypic characteristics. The same authors also found that the prevalence of C. tropicalis significantly increased, showing the highest degree of inflammation in DS, as observed in previous studies [12,16,24,136,144,173,208,209,210].

3.1.5. Co-Occurrence of Dental Plaque, Periodontitis, and Gingivitis

The existence of numerous different oral diseases in a single patient is frequent in diabetics. Hammad et al. [29] studied the relationship between the tongue and subgingival plaque Candida sp. colonization, as well as its relationship with the quality of glycemic control in type 2 diabetics with periodontitis. The results showed that Candida sp. colonized 59% and 48.7% of the patients’ tongues and subgingival plaque, respectively. In this cross-sectional study, the authors concluded that poorly controlled type 2 diabetics and female patients with periodontitis showed a higher prevalence of subgingival plaque Candida sp. colonization than men, regardless of oral hygiene, tobacco smoking, age, or duration of DM [29]. The authors could not correlate oral candidal colonization and the amount of dental plaque, a patient’s gingival status, or oral hygiene, as in other studies [211], but noticed Candida sp. present in the dental plaque in the form of biofilm. Remarkably, and compared with the control group, they found that C. albicans cells isolated from the subgingival plaque of patients with periodontitis adhered more to epithelial cells [212], suggesting that the oxygen concentration in the periodontal pockets affects the virulence of C. albicans [213]. A study that evaluated the effect of Candida sp. and general disease- or treatment-related factors on plaque-related gingivitis severity in children and adolescents with Nephrotic syndrome (NS, a clinical condition with a proteinuria level exceeding the body’s compensating abilities) and diabetes concluded that poor hygiene control was the main cause of gingivitis. Olczak-Kowalczyk and colleagues [172] showed in their work that Candida sp. often occurred in healthy patients, but oral candidiasis was found only in the NS and diabetes groups (9.37% and 11.43%). Their work also showed that gingivitis occurred more frequently in patients with NS/diabetes. Moreover, gingivitis severity was most likely correlated to age, lipid disorders, and an increase in body mass and Candida sp. In uncompensated diabetes and in those patients using immunosuppressive treatment, it was assumed that NS would increase the plaque-related gingivitis.

3.1.6. Esophagitis and Oropharyngeal Candidiasis

Candida sp. esophagitis and oropharyngeal are also oral complications found to moderately affect DM patients. Recently, Takahashi et al. [214] determined long-term trends in Candida sp. esophagitis (CE) prevalence and associated risk factors for patients with or without HIV infections. A risk analysis revealed that, among other factors, DM is associated with CE. Also, Mojazi and their colleagues [215] identified risk factors for oropharyngeal Candida sp. colonization in critically ill patients, with the results confirming DM as a risk factor [215]. Likewise, Owotade and colleagues [216] investigated the role of anti-retroviral (ARV) therapy and other factors related to oral candidiasis. Results demonstrated that 59.4% of the individuals were colonized by yeasts. C. albicans was the most common species (71%) and C. dubliniensis was the most frequent non-Candida albicans Candida species (NCAC). The probabilities of colonization were five times greater in patients with diabetes [216], confirming previous findings [16].

Oral and esophageal candidiasis sometimes leads to mucosal hyperplasia and progresses to carcinoma. There are many reports of the antibacterial effects of probiotics, but consensus about their antifungal effect has not been reached. In order to find alternative therapies, Terayama et al. [217] investigated whether probiotic (yogurt) containing Lactobacillus gasseri OLL2716 (LG21 yogurt) could prevent proliferative and inflammatory changes caused by C. albicans in a mucosal candidiasis animal model. Diabetes was induced in eight-week-old WBN/Kob rats by the intravenous administration of alloxan. The results suggested that probiotic (yogurt) containing L. gasseri OLL2716 can suppress squamous hyperplastic change and inflammation associated with C. albicans infection in the forestomach [217].

3.2. Vulvovaginal Candidiasis

The exact association between DM and vulvovaginal candidiasis (VVC) remains to be clarified, but some investigations propose that the general reduced immune response associated with DM is the main cause of recurrent VVC [218,219,220,221]. Additionally, diabetes type, severity, and degree of glucose control are probable risk factors associated with VVC prevalence, and it is acknowledged that the metabolic disorders that predispose to clinical vaginitis can be reduced by performing an appropriate diabetic control [222,223]. C. albicans is the most common species isolated, followed by C. glabrata in patients both with and without diabetes [219,224,225]. Studies have been reporting an increased frequency of infection by NCAC over time [226,227], especially C. glabrata, which is more recurrently associated with VVC in African and Asian countries [228,229,230,231].

Table 2. Physiopathology and etiology related to the occurrence of vulvovaginitis in diabetics.

Condition	Physiopathology	Reference (s)
Uncontrolled hyperglycemia (high HbA1c) and high glucose levels in vaginal mucosae	- The increased serum glucose level is thought to lead to impaired monocyte, granulocyte, and neutrophil adherence, as well as reduced chemotaxis, phagocytosis, and pathogen killing - Diabetics secretions contain glucose, which can be used as a nutrient by yeasts - pH, nutritional substance, temperature, and adherence capacity in the vulvovaginal tissue may induce Candida sp. virulence. The vaginal epithelial cell receptor of fucose supports the adhesion of Candida sp. to vaginal epithelial cells -The rise in vaginal glucose and secretions and activities of hydrolytic enzymes [e.g., secreted aspartyl proteinases (SAPs), PL] increases the pathogenicity of Candida sp. -Increased levels of glycogen increase colonization and infection by Candida sp. by lowering the vaginal pH, facilitating the development of vulvovaginal candidiasis (VVC)	[55,56,59,219,222,224,225,231,238,239,240,241,242,243,244,245,246,247,248,249,250,251,252,253]
Pregnancy	-The increased circulation of estrogen levels and the deposition of glycogen and other substrates in the vagina leads to a 10–50% higher incidence of vaginal colonization by Candida sp. -Variability of constitutive defensins (e.g., lactoferrins, peptides) and lysozyme, leading to a poor innate immune response -Hyperglycemia can rise the anaerobic glycolysis in vaginal epithelial cells, increasing lactic acid and acetone production, decreasing the vaginal pH, thus enabling fungal colonization and proliferation	[241,254,255,256,257,258,259,260]
Diabetes type	- The incidence of VVC related to the type 1 DM or type 2 DM and is variable among studies	[218,221,222,223]
Aging	- The older one is, the higher VVC prevalence is	[222,223]

summarizes the metabolic disorders that can predispose one to VVC and those that can be decreased with proper diabetic control.

Several studies explored the association between VVC and DM. Gunther et al. [232] investigated the frequency of total isolation of vaginal Candida sp. and its different clinical profiles in women with type 2 DM compared to non-diabetic women in Brazil [232]. Vaginal yeast isolation occurred in 18.8% in the diabetic group and in 11.8% of women in the control group. The diabetic group was shown to be more symptomatic (VVC + recurrent VVC (RVVC) = 66.66%) than colonized women (33.33%), and indicated more colonization, VVC, and RVVC than the controls. Sherry et al. [233] studied the epidemiology of VVC in a cohort in order to find the causative organisms associated with VVC. The authors noticed a shifting prevalence of Candida sp. with C. albicans as the most common yeast but an increase of NCAC. A heterogeneous biofilm-forming capacity associated with lower antifungal drug sensitivity was also reported.

On the contrary, Ray et al. [234] stated that out of 11 diabetic patients, C. glabrata was isolated in 61.3% and C. albicans in 28.8% of VVC cases [234]. Other studies have shown similar results in diabetic women [221,235,236]. Results showed a persistent vaginal colonization with C. glabrata in estrogenized streptozotocin-induced type 1 diabetic mice, and vaginal polymorphonuclear (PMN) infiltration (constantly low) was found in a murine model study by Nash and colleagues [237]. Contrary to what happens in women and in other in vivo studies, in this case, curiously, biofilm formation was not detected, and co-infection of C. glabrata with C. albicans did not induce synergistic immunopathogenic effects [237].

In a different study, Nyirjesy and colleagues evaluated the effects of sodium glucose co-transporter 2 inhibitors (e.g., canagliflozin, dapagliflozin, sitagliptin) used for the treatment of type 2 DM. These drugs improve glycemic control by increasing urinary glucose excretion and are related to increased vaginal colonization with Candida sp. and in VVC adverse events in women with type 2 DM [252]. Of the nine subjects with VVC with a positive vaginal culture at the time of the adverse event, six cultures were positive for C. albicans, only one was positive for C. glabrata, and one was positive for C. tropicalis. These findings confirm previous suggestions that C. glabrata is less pathogenic than C. albicans and more often associated with asymptomatic colonization in VVC [261]. The investigation theorized that urinary glucose excretion and the subsequent deposition of urine on the vulvovaginal tissues with voiding are more significant factors in increasing the risk of VVC in diabetic women than overall glycemic control. In this study, women showed improved glycemic control due to the administration of canagliflozin [262,263] with a higher prevalence of Candida sp. colonization and symptomatic infection, which was also detected with dapaglifozin [264]. Also related to SGLT2 inhibitors, the prevalence and risk of VVC before SGLT2 inhibitors was carefully evaluated in real-world practice by Yokoyama and colleagues [265]. They reported that before starting SGLT2 inhibitors, 14.9% of the participants had positive vaginal Candida sp. colonization. Younger age and the presence of microangiopathy were significantly associated with the colonization. Moreover, of the 65 participants who were negative for Candida sp., 24 participants (36.9%) converted to a positive culture, and 18 participants (15.8%) developed symptomatic vaginitis. The authors concluded that the rates of developing positive colonization and symptomatic vaginitis after starting SGLT2 inhibitors appear to be higher in real-world practice than the rates of 31% and 5–10% in clinical trials, respectively. Risk factors of vaginal Candida colonization might be different before and after taking SGLT2 inhibitors [265].

The colonization of the vagina in prepubertal girls with Candida sp. is rare, as the low estrogen levels during childhood result in a rich anaerobic vaginal flora which inhibits Candida sp. Growth [266,267]. In a recent report, Atabek et al. [219] isolated Candida sp. in 39% of children with type 1 DM between 8–16 years in age. The subjects who had Candida sp. colonization and candidiasis were considered all acute. C. albicans was found in 50% of all cases, followed by C. glabrata (36.6%), C. krusei (3.3%), and C. dubliniensis (3.3%). Patients with VVC had a greater mean HbA1c when compared to those without such infections, and the authors thus suggested that patients with DM should undergo periodic screening for genital candidiasis [219]. Similarly, Sonck et al. [268] studied the anogenital yeast flora of 166 diabetic girls of less than 15 years of age with vulvitis, revealing that 55% were colonized, mostly by C. albicans.

Numerous studies have described the higher prevalence of asymptomatic vaginal colonization and symptomatic infection with Candida sp. in diabetic women, and some studies suggest pregnancy as an additional risk factor [254,255,256], although results are inconsistent [28,226].

Several studies have also shown that pregnancy and uncontrolled diabetes increase the infection risk. It is likely that reproductive hormone fluctuations during pregnancy and elevated glucose levels characteristic of diabetes provide the carbon needed for Candida overgrowth and infection. However, Sopian IL et al. [269] showed no relationship between diabetes and the occurrence of vaginal yeast infection in pregnant women, showing that there was no significant association between infection and age group, race, or education level [269]. In another report, Zheng et al. [254] studied the diversity of the vaginal fungal flora in healthy non-pregnant women, healthy pregnant women, women with gestational DM, and pregnant women with DM type 1 through an 18S rRNA gene clone library method [254]. Results showed that the most predominant vaginal fungal species belonged to the Candida and Saccharomyces genera. In a study of 251 women, Nowakowska et al. [270] demonstrated that the probability of vaginal mycosis was 4-fold greater in type 1 DM patients and nearly 2-fold greater in those with gestational DM when compared to healthy pregnant women. The report also highlighted the predominant role of poor glycemic control in the increased prevalence of vaginal candidiasis in pregnant women with type 1 DM [270]. In 2011, Masri et al. [271] determined the prevalence of Candida sp. in vaginal swabs of pregnant women from Serdang Hospital, Selangor, Malaysia, and their antifungal susceptibility. Results showed that 17.2% of the specimens were Candida sp., with C. albicans being the most common species detected (83.5%), followed by C. glabrata (16%) and C. famata (0.05%). All C. albicans and C. famata isolates were susceptible to fluconazole, whereas C. glabrata isolates had a dose-dependent susceptibility. The authors concluded that the first trimester, the second trimester, and DM were significant risk factors in patients for the vaginal candidiasis (p < 0.001). However, other studies noted that DM or impaired glucose tolerance during pregnancy was not connected with vaginal candidiasis [256]. Bassyouni et al. [242] explored the prevalence of VVC in diabetic women versus non-diabetic women and compared the ability of identified Candida sp. isolates to secrete PL and SAPs with the characterization of their genetic profile. The study involved 80 females with type 2 DM and 100 non-diabetics within the child-bearing period. Results revealed that VVC was significantly higher among the diabetic group (50%) versus the non-diabetic group (20%), and C. albicans was the predominant species in both groups (75% in non-diabetics and 50% in diabetics), followed by C. glabrata (20% in non-diabetics and 42.5% in diabetics). They also found that Candida sp. isolated from diabetics secreted higher quantities of proteinase than non-diabetics (87.7% and 65%, respectively), especially for C. albicans and C. glabrata, but non-significant associations between any of the tested proteinase or PL genes and DM were detected. These results were—by some means—in agreement with the ones from other reports [243,244] that also detected C. parapsilosis and C. tropicalis in a group of diabetic women. Kumari et al. [248] detected poor PL production in the isolated Candida sp. (causing vulvovaginitis), of which 81.25% were C. parapsilosis, 30.43% C. albicans, and 18.75% C. glabrata. Moreover, insignificant differences in the expression of Candida sp. PLB1-2 genes and SAP1–SAP8 genes between diabetic and non-diabetic women were reported by Bassyouni and colleagues [242]. Still, they concluded that the higher prevalence of VVC among diabetics could be directly correlated to increased SAPs production. The discrepancies between the results of different reports may be due to changes in growth conditions and host factors that alter the gene expression qualitatively and quantitatively [59,247], although findings suggest that the expression of hydrolytic enzymes by Candida sp. is a multifactorial process in patients with DM and the hyperglycemia level is thus not the only implicated factor.

Lastly, VVC is intimately related to vaginal mucosae biofilms. Mikamo and colleagues studied the involvement of Candida’s complement receptor (ICAM-1) in the adhesion of C. albicans or C. glabrata to the genitourinary epithelial cells in high glucose states. Their results demonstrated that, while the adhesion of C. albicans to human vaginal epithelial cells VK2/E6E7 significantly increased in the high glucose, human vulvovaginal epidermal cells A431 did not. ICAM-1 expression was increased in VK2/E6E7 cultured in the high glucose, but the expression level in A431 was not elevated. These data suggested that ICAM-1 is a ligand in the adhesion of C. albicans to the vaginal epithelial cells in an environment with high glucose concentration. Moreover, both host immune dysfunction and the adjustment in epithelial cells were considered responsible for VVC in diabetic patients [272].

3.3. Urinary Tract Candidiasis

Around 10% to 15% of in-hospital urinary tract infections (UTIs) are related to Candida sp. and the prevalence is still increasing [273]. Some predisposing factors such as DM, urinary retention, urinary stasis, renal transplantation, and hospitalization can increase the risk of candiduria. Specifically, DM has been known to cause severe complicated UTIs as a result of its various changes in the genitourinary system [274]. Since the 1980s, there has been a marked increase in opportunistic fungal infections involving the urinary tract, of which C. albicans is the most commonly isolated species, but NCAC sp. is now the majority in many countries worldwide [275,276]. Candiduria (presence of Candida sp. in urine) is an increasingly common finding in hospitalized patients [14], and subjects with DM are at a higher risk of developing fungal UTIs. Thus, reducing risk factors such as increasing glycemic control and the removal of urinary catheters can result in the remission of candiduria [273]. Physiopathology and etiology related to the occurrence of UTIs related to Candida sp. and DM are presented in

Table 3. Physiopathology and etiology related to the occurrence of urinary tract infections and systemic candidiasis in diabetics.

Condition	Physiopathology	Reference (s)
Uncontrolled hyperglycemia (high HbA1c) and high glucose levels in urinary tract (UT) mucosae or blood	- Favorable microenvironment for the gas-forming organisms, such as Candida sp., to grow	[282,283]
Gender	-An association between candiduria and being female	[27,273,279]
Drugs	-SGLT2 inhibitors (e.g., dapagliflozin, canagliflozin, tofogliflozin) administration leads to a greater susceptibility to urinary tract infection (UTI) -Association with a persistent increase in urine glucose concentration	[287]

.

According to the results of the Falahati et al. [277] study, there were significant associations between candiduria and the female gender, high fasting blood sugar and urine glucose, uncontrolled diabetes (HbA1c ≥ 8), and acidic urine pH (p < 0.05). Causative agents were identified as C. glabrata (n = 19, 50%), C. albicans (n = 12, 31.6%), C. krusei (n = 4, 10.5%), C. tropicalis (n = 2, 5.3%), and C. kefyr (n = 1, 2.6%). The study concluded that when considering the high incidence rate of candiduria in diabetic patients, the control of diabetes, predisposing factors, and causal relationships between diabetes and candiduria should be highlighted [277]. In a 2018 study, Esmailzadeh et al. [276] evaluated candiduria among type 2 diabetic patients. Indeed, the results showed that the rate of candiduria was relatively high in type 2 diabetic patients and they were also suffering from a lack of proper blood glucose control. Although the frequency of NCAC sp. was not significantly higher than C. albicans, they obtained more from those with symptomatic candiduria [276]. In a cross-sectional study, Yismaw et al. [273] determined the fungal causative agents of UTIs in asymptomatic and symptomatic diabetic patients and associated risk factors. Significant candiduria was detected in 7.5% and 17.1% of asymptomatic and symptomatic type 2 diabetic patients, respectively. Among the isolated Candida sp., 84.2% was observed in the asymptomatic diabetic patients and the remaining 15.8% in symptomatic patients. Rizzi and Trevisan studied the prevalence and significance of UTIs and genital infections (GI) in diabetes and the effects of sodium glucose cotransporter 2 (SGLT-2) inhibitors on these complications. Results presented that diabetic patients are at high risk of UTIs and of GIs. The authors concluded that only GIs were associated with poor glycemic control. Although patients treated with SGLT-2 inhibitors have an increased 3–5 fold risk of GIs, proper medical education may reduce this risk [278].

Diabetes mellitus, indwelling bladder catheter, sex (female), and the use of antibacterial agents have been found as the risk factors identified for both C. glabrata and C. albicans candiduria [275], as previously reported [27,279]. Emphysematous cystitis, which almost exclusively occurs in diabetic patients, is rare and is seldom the result of a fungal infection [280,281]. This condition is associated with a gas formation that may present itself as cystitis, pyelitis, or pyelonephritis. Uncontrolled DM is a major risk factor for this type of infection, as it provides a favorable microenvironment in which the gas-forming organisms can grow [282,283]. Alansari et al. [284] reported a case in which a patient with uncontrolled DM was diagnosed with emphysematous pyelitis by C. tropicalis, while Wang et al. [285] also reported the case of a 53-year-old male patient with fungus ball and emphysematous cystitis caused concurrently by C. tropicalis. The predisposing factors were DM and usage of broad-spectrum antibiotics. Garg et al. [286], in a one-year prospective single center study at Dayanand Medical College and Hospital, observed 151 diabetic and non-diabetic female patients diagnosed with UTIs. Uncontrolled diabetes was more commonly associated with severe UTIs like pyelonephritis and emphysematous pyelonephritis.

Escherichia coli was the most frequently isolated species in both groups, followed by Klebsiella, Pseudomonas, and Candida sp., and the latter was only isolated from the diabetic population. Tumbarello et al. [288] identified DM and urinary catheterization as features that are specifically associated with biofilm-forming Candida sp. bloodstream infections. Later, Vaidyanathan et al. [281] related a case of a 58-year-old diabetic paraplegic male with a long-term indwelling urethral catheter that developed a catheter block. Results showed an E. coli and C. albicans co-infection and HbA1c (glycosylated haemoglobin) was 111 mmol/mol, which is associated with uncontrolled DM. C. albicans later disseminated into the bloodstream through the damaged bladder and the urethral mucosa. Moreover, those isolates formed consistently high levels of biofilm formation in vitro and a resistance to voriconazole was also detected [281]. In another report, Suzuki et al. [287] investigated the relationship between UTIs and glucosuria, observing the effect of glucosuria induced by sodium-glucose cotransporter 2 (SGLT2) inhibitors on the progression of UTIs in mice. The results showed that in mice treated with dapagliflozin and canagliflozin (not tofogliflozin), the amount of C. albicans colony forming units (CFU) in kidneys increased in accordance with both treatment duration and dosage. The urine glucose concentration (UGC) significantly increased up to 12 (tofogliflozin) to 24 h (dapagliflozin and canagliflozin) after SGLT2 administration, indicating that a greater susceptibility to UTIs is associated with a persistent increase in UGC [287].

3.4. Systemic Candidiasis

It is recognized that DM predisposes one to systemic candidiasis for several factors [289]. Among these factors, the most important are the microvascular disease progression, the low host defense mechanisms, and the diabetic vasculopathy, which exacerbates hypoperfusion and hyperglycemia and may lead to neutrophil and lymphocyte dysfunction with impaired opsonization [11,42,290,291,292,293,294,295,296,297,298,299,300,301,302,303,304,305,306,307,308,309,310,311,312,313,314,315,316,317,318,319,320,321,322]. Catheter-associated candiduria is a common clinical finding in hospitalized patients, especially in intensive care units [295], and is intimately related to biofilms. Padawer et al. [295] studied demographic and clinical data at an Israeli hospital between 2011 and 2013 on the prevalence of Candida sp. in catheterized in-patients and the medical interventions provided to these patients. Their results showed that candiduria was observed in 146 catheterized in-patients out of the 1408 evaluated and was directly associated with DM. C. albicans was present in 69.1% of the subjects, followed by C. parapsilosis (9.58%), C. krusei (7.53%), C. tropicalis (6.16%), C. glabrata (4.79%), and other species (2.73%). DM was found to be a significant risk factor of infection by Candida sp. In another report, Padawer et al. [295] concluded that Candida sp. was the second leading pathogen causing catheter-associated urinary tract infections or asymptomatic colonization. Previously, Tambyah et al. [296], Makin and Tambyah [297], and Sievert et al. [298] found similar results.

Muskett et al. [299] performed a systematic review to identify the most prevalent risk factors, looking at published analyses, risk prediction models, and clinical decision rules for invasive fungal disease (IFD) in critically ill adult patients. The authors found studies that had a significant association of DM and IFD on both univariable and multivariable analyses. Paphitou and colleagues [300] established that patients with any combination of DM, new onset hemodialysis, use of total parenteral nutrition, or receipt of broad-spectrum antibiotics had an invasive candidiasis rate of 16.6% compared to a 5.1% rate in patients lacking these characteristics (p = 0.001). Also, Michalopuolos et al. [301], in a univariate regression analysis study between 1997 and 2002, confirmed that DM is a significant candidemia-associated factor and an independent candidemia predictor. C. albicans (70%), C. parapsilosis (10%), C. glabrata (6.7%), C. tropicalis (6.7%), and C. krusei (6.7%) were isolated in patients with candidemia. C. albicans was simultaneously isolated from blood (89.5%) and the central venous catheter tip. Among other factors, the authors found that DM was associated with a high 30-day mortality in candidemia. Candidemia due to C. parapsilosis was associated with high rates of survival [11], probably due to the fact that adherence and protein secretion do not correlate with strain pathogenicity in this species as opposed to the other Candida sp., as had been discussed [323]. Another retrospective study from 2007 to 2015 of candidemia in hospitalized adults was performed by Khatib et al. Most of the isolates (97.5%) were C. albicans. C. glabrata was more common in diabetics (52.9% vs. 32.0% in non-diabetics; p = 0.004) and in abdominal sources. The findings suggested possible species-related differences in colonization dynamics or pathogenicity [324].

Abad et al. [304] carried out a different study to investigate the susceptibilities of clinical fluconazole-resistant and fluconazole-susceptible dose-dependent to caspofungin of 207 Candida sp. in Iranian patients. Results showed that only 9.7% of the isolates were non-sensitive to caspofungin and that these isolates were observed in cancer, DM, and AIDS patients [304]. Wu et al. [305] investigated 238 candidemia hospitalized patients between 2009 and 2011 so as to study the incidence rates of candidemia and identify the differences in risk factors of patients with C. albicans and NCACs and with C. guilliermondii and non-C. guilliermondii candidemia. DM was identified as a significant risk factor in patients with candidemia due to C. albicans (35.2%) compared to candidemia related to NCACs (13.2%). Although C. guilliermondii is an uncommon cause of candidemia, even in immunocompromised hosts [306,307,308,309,310,311], it was also found to occur in a significant amount of the hospitalized patients. Over the three year period, the percentage of candidemia due to C. albicans decreased, while the percentage of candidemia due to C. parapsilosis and C. guilliermondii increased in more than 80% of all candidemia cases in 2011 [305].

Candida sp. bloodstream infections (CBSI) are the fourth leading cause of nosocomial bloodstream infections in the United States [316,318,325]. CBSIs occur in up to 10% of all bloodstream infections in hospitalized patients [313,314,315], and the mortality rate is about 40% [316,317]. Normally, this mortality is higher than in bloodstream infections involving bacteria [326,327]. Risk factors for CBSIs include critically ill patients in intensive care units, DM, immunosuppressive states, mechanical ventilation, neutropenia, recent surgical procedures, and prematurity [315,318,319]. In a study by Tumbarello and colleagues [328], it was found that DM is an independent predictor of biofilm-forming Candida sp. CBSIs. The use of total parenteral nutrition, hospital mortality, post-CBSI hospital length of stay (LOS), and the costs of antifungal therapy were all significantly greater among patients infected by biofilm-forming isolates when compared to those infected by non-biofilm-forming isolates. It was concluded that biofilm-forming CBSI was significantly related with a high risk of death compared to non-biofilm forming CBSI [328]. Corzo-Leon and colleagues [320] investigated the clinical and epidemiologic characteristics of patients with CBSI in two tertiary care reference medical institutions in Mexico City. Their results showed that CBSIs represented 3.8% of nosocomial bloodstream infections and C. albicans was the predominant species (46%), followed by C. tropicalis (26%). C. glabrata was isolated from 50% of patients with diabetes and elderly patients. Nucci et al. [321] published a paper reporting an incidence of 1.18 episodes of candidemia per 1000 admissions. C. albicans, C. tropicalis, and C. parapsilosis were isolated in 80% of cases and DM was also found in 11% of the total cases. Gupta et al. [322] reviewed the influence of C. glabrata candidemia in intensive care unit (ICU) patients between 2006 and 2010. Results showed that this species was the third most isolated, and DM was a risk factor among 50% of the total cases. Also, urine was the most common source of C. glabrata candidemia, while the overall mortality rate was 53.8% [322]. In another report, Wang et al. [42] observed no differences in the distribution of Candida sp. between elderly and young patients in China, but the resistance to fluconazole and voriconazole for NCAC in the first group was double the amount of the latter. Host-related risk factors included DM, mechanical ventilation, central vascular and urethral catheter placement, and were more common in elderly patients [42].

3.5. Other Candidiasis

Diabetic patients are highly predisposed to cutaneous fungal infections due to the higher blood sugar levels. These infections are frequently characterized by thick biofilms, and sometimes the use of medical devices to drain these lesions is mandatory. Foot infection (tinea pedis and toenail onychomycosis) is particularly important to diabetic individuals due to the high incidence of diabetic foot in these patients [329,330]. The most significant Candida sp. causing onychomycosis are C. albicans and C. parapsilosis and it is known that DM patients have a high rate of tinea pedis and onychomycosis. Thus, this infection is now considered to be a predictor of diabetic foot syndrome [331]. The predisposing factors for tinea pedis et unguium are presented in

Table 4. Physiopathology and etiology related to the occurrence of nail fungal diseases linked to Candida sp. in diabetics.

Condition	Physiopathology	Reference (s)
Uncontrolled hyperglycemia (high HbA1c) and high glucose levels in vaginal mucosae	-Circulatory disorders affecting the lower extremities (peripheral circulation), peripheral neuropathy, and retinopathy - Nail thickness is associated with an elevated HbA1c value - Diabetics using hemodialysis exhibit a higher probability of onychomycosis	[329,330,334,335,336,337,338]
Duration of DM	-More time leads to a higher probability of onychomycosis	[336]
Gender Aging	-Being male and being older are directly associated with onychomycosis in diabetics	[331,336]

.

Diabetic foot ulcers are a serious cause of diagnostic and therapeutic concern, and Non-albicans Candida spp. with potential biofilm forming abilities are emerging as a predominant cause of this problematic condition. Indeed, in a recent study, the prevalence of different Candida sp. was identified as C. tropicalis (34.6%), C. albicans (29.3%), C. krusei (16.0%), C. parapsilosis (10.6%), and C. glabrata (9.33%) [332]. In order to find the frequency of fungal infections among cutaneous lesions of diabetic patients and to investigate azole antifungal agent susceptibility of the isolates, Raiesi et al. [333] studied type 1 and type 2 DM patients with foot ulcers (38.5%) and with skin and nail lesions (61.5%). Results showed that 24.5% had fungal infections and were at a higher frequency in patients with skin and nail lesions (28%) than in foot ulcers (19.1%). C. albicans and Aspergillus flavus were the most common species isolated, and a high prevalence of fluconazole-resistant Candida sp., particularly in diabetic foot ulcers, was determined [333].

Diabetics with onychomycosis have a greater risk of having a diabetic foot ulcer [336,337,339,340], as confirmed by numerous studies. In Germany, Eckhard and colleagues [337] found that out of 95 patients with type 1 DM, 84.6% had a fungal infection. The most frequent Candida sp. found were C. albicans, C. parapsilosis, and C. guilliermondii, followed by C. lipolytica, C. catenulate, and C. famata. In another study conducted at the Umm Al-Qura University, Makkah, Saudi Arabia from June 2011 to June 2012, the antimicrobial susceptibility of the most common bacterial and fungal infections among infected diabetic patients (foot infections) was determined. All Candida sp. showed susceptibility to amphotericin B, econazole, fluconazole, ketoconazole, and nystatin (100% each) [340]. Cases with Candida sp. co-infection were also observed in patients with fungal nail infections—both cutaneous and nail infections [337]. Lugo-Somolinos et al. [334] performed a cross-sectional study in Japan and revealed that 51.3% of patients with DM had onychomycosis of the toenails. In this particular case, C. albicans was more prevalent in the control group (24% vs. 15% in the DM patients) and nail thickness was significantly associated with an elevated HbA1c value [334]. Gupta et al. [341] reported that there was a 2.77-fold greater risk for diabetic subjects than for healthy individuals to have toenail onychomycosis. In the same year, a previous study in Taiwan reported that 60.5% of onychomycosis was caused by dermatophytes, 31.5% by Candida sp., and 8% by non-dermatophyte molds [342]. A total of 20 patients with onychomycosis had concomitant DM. Regarding gender, in diabetic males, the most common pathogens were dermatophytes (58.3%), while in diabetic females, Candida sp. was more prevalent (87.5%) [342]. However, on the contrary, Dogra and colleagues found that in Indian diabetics, yeasts were the most common isolate (48.1%), followed by dermatophytes (37%) and non-dermatophyte molds (14.8%) [336]. The authors concluded that diabetics had a 2.5 times greater probability of having onychomycosis when compared to the controls [336]. Chang et al. [331] studied 1245 Taiwanese patients with DM. Among them, 30.76% were reported to suffer from onychomycosis. In this investigation, the diagnosis of onychomycosis was limited to a general histopathologic examination (KOH stain) of the toenails. Therefore, the patients may have been affected by Candida sp. and by other fungi. Another study performed by Pierard et al. [335] investigated onychomycosis in 100 DM patients on chronic hemodialysis, showing that 39% of participants had a nail disease. Candida sp. was the second most prevalent pathogen (15%), and the authors concluded that diabetics on hemodialysis had about an 88% greater probability of acquiring onychomycosis than non-diabetics [335]. Another report by Wijesuriya and colleagues [338] described the etiological agents causing superficial fungal foot infections (SFFI) in patients with type 2 DM for one year. Their results demonstrated that 295 patients had SFFI and that, among patients with diabetes, more than 10 showed a prevalence of SFFI of 98%. Aspergillus niger was the most common pathogen, followed by C. albicans. Aging, gender, the duration of diabetes, and less-controlled glycemic levels were significantly associated with SFFIs [338].

A 2018 study explored the differential expression of toll-like receptor 2 (TLR2) and interleukin (IL)-8 secretion by keratinocytes in diabetic patients when challenged with C. albicans. Wang et al. [343] determined that the expression levels of both TLR2 and IL-8 increased and then decreased in the control and the diabetic groups, but in different dynamics. The observations revealed that TLR2 and IL-8 act on the keratinocytes interacting with C. albicans, and high glucose status can distress the function of HaCaT cells by reducing the secretion of IL-8 and TLR2. The study clearly supports the immunosuppression state that diabetic patients live in [343].

Adherence to the vascular endothelium, neutrophil chemotaxis, phagocytosis and opsonization, intracellular bactericidal activity, and cell-mediated immunity are all decreased in DM patients with hyperglycemia [344,345]. Regarding this matter, Souza et al. [346] treated diabetic rats with aminoguanidine (AMG, an inhibitor of protein glycation) and evaluated neutrophil reactive oxygen species (ROS) generation and C. albicans killing ability in order to evaluate the effects of hyperglycemia and the glycation of proteins on the NOX2 (phagocyte NADPH oxidase) activity of neutrophils and its implications for cellular physiology. The authors indicated that AMG increased the NOX2 response and microbicidal activity by neutrophils of the diabetic status. AMG seems to be a promising therapeutic answer for these patients [346].

In another interesting recent in vivo report, the interference of diabetic conditions in diabetic mice and the relation to the progress of C. albicans infection and anti-inflammatory response was evaluated. Compared to non-diabetic mice, diabetic mice indicated a significantly lower density of F4/80 and M2 macrophages, higher fungal burden, and deficiency in cytokine responses. C. albicans also increased tissue injury, highlighting significant deviations in diabetic animal responses to C. albicans infection that may be critical to the pathophysiological processes supporting cutaneous candidiasis in diabetic patients [347].

Several other pathologies related to Candida sp. have also been linked to a DM predisposition. Researchers often recognize the importance of DM in the development of the pathology due to immunosuppression issues [348]. The reports are summarized in

Table 5. Physiopathology and etiology related to the occurrence of other diseases linked to Candida sp. in diabetics.

Condition	Physiopathology	Candida sp. Found in the Study	Reference (s)
Arterial infection	-Direct invasion or haematogenous spread of Candida sp. to the vessels wall (less common): a. infection of a pre-existing aneurysm (most possible from atherosclerotic) with fungi after an episode of candidemia b. contained fungal infection of the arterial wall (linked mostly to intravenous drug abuse).	C. albicans C. tropicalis C. parapsilosis Other Candida sp. (not specified)	[348,349,350,351,352,353,354,355,356,357]
Endophthalmitis	- Uncontrolled DM concomitant with other co-morbidities	C. albicans	[358]
Cholecystitis	- Uncontrolled DM concomitant with other co-morbidities	C. famata	[359]
Skin abscesses	- Uncontrolled DM concomitant with other co-morbidities	C. albicans	[360,361]
Brain abscesses	-Immunocompromised states and poorly-controlled diabetes (the role of DM as an immunosuppressive condition in this particular case is uncertain)	C. albicans C. parapsilosis C. tropicalis C. guilliermondi Other Candida sp. (not specified)	[362,363,364]
Fungal infections after liver transplantation	- Chronically high blood sugar may be a predisposing factor (among other factors)	C. albicans	[365]
Peritonitis	- Uncontrolled DM concomitant with other co-morbidities	C. haemulonii C. glabrata Other Candida sp. (not specified)	[366,367,368]
Penile prosthesis Infections		Other Candida sp. (not specified)	[369,370,371,372]
Balanitis		C. albicans	[373]
Fournier’s gangrene		Candida sp. (not specified)	[374]
Chronic obstructive pulmonary disease		C. ciferrii	[375]

.

4. Diabetes Mellitus In Vivo Models

Diabetes mellitus is a serious epidemic disease, and the research for new therapies is becoming critical. Thus, the correct choice of the animal models is of vital importance for the validity of the reported studies.

In DM type 1, the choices range from chemical ablation of the pancreatic β-cells to animals with spontaneously developing autoimmune diabetes. In DM type 2, the animal models can be both obese and non-obese animals with varying degrees of insulin resistance and beta cell failure [376]. The animal models (e.g., species, strain, gender, genetic) of DM type 1 and type 2 have diverse purposes, and the choice of a model depends on the purpose of the study (e.g., applied for pharmacological or genetics studies and understanding disease mechanisms) [376,377,378,379,380,381].

Table 6. Main animal models used in diabetes mellitus studies [376].

Diabetes Mellitus	Model/Induction	Studies	Features
Type 1	Chemical induction
	High dose streptozotocin	New formulations of insulin	Hyperglicaemia model
	Alloxan	Transplantation	Induced insulitis
	Multiple low dose streptozotocin	Treatment to prevent β-cell death
	Spontaneous autoimmune
	NOD mice	Understanding genetic mechanisms	Autoimmune β-cell destruction
	BB rats
	LEW.1AR1/-iddm rats	Treatment to prevent β-cell death or to manipulate autoimmune processes
	Genetically Induced
	AKITA rats*	New formulations of insulin Transplantation Treatment to prevent ER stress	β-cell destruction due to ER + Insulin dependent
	Virally induction
	Coxsackie B virus	Study of potencial role of viruses in DM type 1	Viral β-cell destruction
	Encephalomyocarditis virus
	Kilham rat virus
	Lymphocytic choriomeningitis virus (LCMV) under insulin promoter
Type 2	Monogenic—obese models
		Obese-induced hyperglycemia
	Lepob/ob mice	Treatment to improve insulin resistance
	Leprdb/db mice	Treatment to improve β-cell resistance
	KDF rats
	Polygenic—obese models
	KK mice	Treatment to insulin resistance
	OLEFT rat	Treatment to improve β-cell function
	NZO mice	Some models show diabetic complications
	TallyHO/Jng mice
	NoncNZO10/|LtJ mice
	Induced obesity
	High fat feeding (mice or rats)	Treatment to insulin resistance
	Nile grass rat	Treatment to prevent diet-induced obesity
	Desert gerbil	Treatment to improve β-cell function

* can be also used as a DM type 2 model.

summarizes the main animal models used in diabetes mellitus in vivo studies.

5. Conclusions

Diabetes mellitus is a severe metabolic chronic disease that is most prevalent in developed countries. The general immunocompromised state with an often-poor glucose control often leads to secondary diseases in DM individuals. The biofilm fungal infections in diabetic patients are recognized to be more complicated to treat than they are in healthy patients, especially if related to medical devices. Among the candidiasis, oral diseases are the most frequent infections that occur in DM patients, as well as VVC and, more seriously, systemic candidiasis. The reports of these cases and the results of the elected therapeutic are extremely important if we are to continue to treat these patients in the most effective manner.