Next Article in Journal
Chromatic Acclimation Processes and Their Relationships with Phycobiliprotein Complexes
Next Article in Special Issue
Molecular Epidemiology of Multidrug-Resistant Pseudomonas aeruginosa Acquired in a Spanish Intensive Care Unit: Using Diverse Typing Methods to Identify Clonal Types
Previous Article in Journal
Parasitic Protists: Diversity of Adaptations to a Parasitic Lifestyle
Previous Article in Special Issue
Screening and Characterization of Multidrug-Resistant Enterobacterales among Hospitalized Patients in the African Archipelago of Cape Verde
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Microorganisms
Volume 10
Issue 8
10.3390/microorganisms10081561
microorganisms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Whole Genome Sequencing and Molecular Analysis of Carbapenemase-Producing Escherichia coli from Intestinal Carriage in Elderly Inpatients

by
Maria Giufrè
1,*,
Giulia Errico
1,
Monica Monaco
1,
Maria Del Grosso
1,
Michela Sabbatucci
1,2,
Annalisa Pantosti
1,
Marina Cerquetti
1,
Michela Pagnotta
1,
Manuela Marra
3,
Maria Carollo
3,
Angelo Rossini
4,
Elena Fogato
5,
Elisabetta Cesana
6,
Flaminia Gentiloni Silverj
7,
Dorjan Zabzuni
6 and
Marco Tinelli
6,8
1
Department of Infectious Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy
2
Ministry of Health, Directorate General Health Prevention, Communicable Diseases and International Prophylaxis, 00144 Rome, Italy
3
Core Facilities Technical-Scientific Service (FAST), Istituto Superiore di Sanità, 00161 Rome, Italy
4
IRCCS Fondazione Santa Lucia, 00179 Rome, Italy
5
Golgi-Redaelli Geriatric Institute, 20146 Milan, Italy
6
IRCCS Istituto Auxologico Italiano, San Luca Hospital, 20149 Milan, Italy
7
IRCCS Fondazione Ca’ Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy
8
Italian Society of Infectious and Tropical Diseases (SIMIT), 59100 Prato, Italy
*
Author to whom correspondence should be addressed.
Microorganisms 2022, 10(8), 1561; https://doi.org/10.3390/microorganisms10081561
Submission received: 4 July 2022 / Revised: 25 July 2022 / Accepted: 30 July 2022 / Published: 3 August 2022
(This article belongs to the Special Issue ß-Lactamases 2.0)
Browse Figures
Versions Notes

Abstract

:
The spread of carbapenemase-producing (CP) Enterobacterales is currently a worldwide concern, especially in the elderly. Twelve CP-E. coli isolated from rectal swabs of colonized inpatients aged ≥65 years from four hospitals in two Italian cities (Milan and Rome) were analyzed by whole genome sequencing (WGS) to obtain multi-locus sequence typing (MLST), identification of carbapenemase-encoding genes, resistome, plasmid content, and virulence genes. MLST analysis showed the presence of 10 unrelated lineages: ST410 (three isolates from three different hospitals in two cities) and ST12, ST38, ST69, ST95, ST131, ST189, ST648, ST1288, and ST1598 (one isolate each). Most isolates (9/12, 75%) contained a serine-β-lactamase gene (5 blaKPC-3, 2 blaKPC-2, and 2 blaOXA-181), while three isolates harbored a metallo-β-lactamase gene (two blaNDM-5 and one blaVIM-1). In most CP-E. coli, the presence of more than one plasmid was observed, with the predominance of IncF. Several virulence genes were detected. All isolates contained genes enhancing the bacterial fitness, such as gad and terC, and all isolates but one, fimH, encoding type 1 fimbriae. In conclusion, CP-E. coli clones colonizing elderly patients showed heterogeneous genetic backgrounds. We recommend strict surveillance to monitor and prevent the spread of successful, high-risk clones in healthcare settings.

1. Introduction

Antimicrobial resistance is currently one of the most worrying global public health problems. The European Centre for Disease Prevention and Control (ECDC) estimated the occurrence of almost 700,000 infections with antibiotic-resistant bacteria that accounted for nearly 33,000 attributable deaths each year in the EU/EAA countries [1]. The emergence and spread of carbapenem-resistant Enterobacterales (CRE) represents a major threat worldwide, especially in the most vulnerable patients, the elderly [2,3]. CRE infections, in particular those caused by carbapenemase-producing Enterobacterales (CPE), are associated with high mortality rates [4]. In Europe, CRE have been reported in most countries, although with very different prevalence. Most countries have a low overall prevalence, while few countries (such as Italy and Greece) report a high level of CRE endemicity [5]. Although the prevalence of invasive carbapenem resistant (CR)-E. coli is currently much lower than that of CR-Klebsiella pneumoniae, a small but significant increase in CR-E. coli in the EU/EEA population-weighted mean was reported between 2016 and 2020 (from 0.1% to 0.2%, with a 2020 country range of 0.0–0.8%) [5]. In Italy, an endemic country for CR-K. pneumoniae, the percentage of CR-E. coli has slightly increased from 0.3% in 2016 to 0.5% in 2020, in line with the European trend [5]. The principal resistance mechanism to carbapenems is the production of the carbapenemase enzymes in CPE isolates. Genes coding for carbapenemases are frequently located on plasmids, which can enhance the transfer of resistance determinants between bacteria and also spread the resistance to other species [6]. To date, few antibiotics are active against CPE, including the new β-lactam/β-lactamase inhibitor combinations such as ceftazidime–avibactam, meropenem–vaborbactam, and imipenem–relebactam [7,8]. However, resistance to these new molecules is already being reported [9].
Several virulence factors (VFs) have been identified in E. coli. VFs are proteins encoded by genes located either on the chromosome or on plasmids, and are classified in four main classes, based on their function: colonization (adhesion and invasion), fitness (iron acquisition and motility), toxins, and effectors [10]. The presence of VFs in colonizing isolates is concerning, since they can make E. coli capable of causing extraintestinal diseases in humans.
Asymptomatic colonization in the intestinal tract with carbapenemase-producing (CP)-E. coli, especially in the elderly, can lead to infections that are difficult to treat [11,12]. The potential spread of CP-E. coli among elderly patients or among people living in long-term care facilities (LTCF) is a matter of concern, since these infections are characterized by increased morbidity and mortality. Therefore, infection control measures are needed to prevent them [13]. In a previous longitudinal study aimed at evaluating the persistence of CPE colonization in elderly patients discharged from hospitals, our group found that out of 137 patients with CPE colonization, 91% carried CP-K. pneumoniae and 8.8% CP-E. coli. Notably, 43.1% of the available patients were still colonized after 4 months, representing a serious threat for the possibility of spreading such pathogens in the community or in healthcare settings [14]. Since little is known about colonizing CP-E. coli clones, the present study aims to describe the microbiologic and genomic features of isolates collected in the framework of a wider Italian research project on CPE colonization and persistence in the elderly [14].

2. Materials and Methods

2.1. Bacterial Strain Identification and Antimicrobial Susceptibility Testing (AST)

CP-E. coli isolates were collected during the period January 2018 January 2020 from intestinal samples of hospitalized patients aged ≥65 years, within 3 days from hospital discharge in 4 hospitals located in two Italian cities (Milan and Rome, Italy), and during a 12-month follow-up, as described previously [14].
Samples processing, microbial identification, and antibiotic susceptibility testing were performed by the microbiology laboratories of the 4 hospitals, according to a shared protocol. Briefly, rectal swabs were collected in Amies medium (Copan, Brescia, Italy), refrigerated at 4 °C, and analyzed within 18 h. To detect CP-E. coli, swabs were streaked onto chromID CARBA SMART agar plates (bioMerieux, Marcy l’Etoile, France), and incubated at 35 °C for 48 h. Identification to species level was performed by a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS) using a Microflex Biotyper® LT (Bruker Daltonik GmbH, Bremen, Germany). Carbapenemase production was investigated using the agar tablet/disc diffusion method (KPC/MBL and OXA-48 Confirm Kit; ROSCO Diagnostica A/S, Taastrup, Denmark). Twelve confirmed CP-E. coli isolates were sent to the reference laboratory at Istituto Superiore di Sanità where further phenotypic and molecular characterizations were carried out. Antibiotic susceptibility testing (AST) was carried out by the reference broth microdilution method using lyophilized, custom microtitration plates (Merlin Diagnostika, Berlin, Germany), and by reference agar dilution for fosfomycin using an AD Fosfomycin panel (Liofilchem, Roseto degli Abruzzi, Italy). E. coli ATCC25922 was used as the control strain for AST. The interpretative breakpoints were based on EUCAST, version 11.0 [15].

2.2. Whole Genome Sequencing and In Silico Analysis

Genomic DNAs were extracted from an overnight culture using the NucleoSpin DNA extract kit (Macherey-Nagel, Duren, Germany). Whole-genome sequencing (WGS) was performed using Ion Torrent technologies (Life Technologies, Thermo Fisher Scientific, Waltham, MA, USA), according to the manufacturers’ instructions. De novo assembly of sequence reads was performed using SPAdes 3.9 software through the ARIES Galaxy server (https://w3.iss.it/site/aries/, accessed on 4 May 2022). MLST analysis was carried out according to the E. coli MLST website scheme (https://enterobase.warwick.ac.uk/species/index/ecoli, accessed on 4 May 2022). A core genome single-nucleotide polymorphism (SNPs) phylogeny was generated by CSI Phylogeny at the Center for Genomic Epidemiology (https://cge.cbs.dtu.dk/services/, accessed on 4 May 2022) using the complete genome of E. coli strain K12 (accession no. NC_000913.2) as a reference. The resulting maximum likelihood phylogenetic tree was visualized by uploading the Newick file to the Interactive Tree of Life platform, iTOL (http://itol.embl.de/upload.cgi, accessed on 4 May 2022) [16]. In silico analysis of the assembled contigs were performed using tools available at the CGE server SeroTypeFinder and FimTyper were used to predict serotype and Fim type isolates, respectively. Contigs were also screened for plasmid and resistance gene content using PlasmidFinder and ResFinder tools, respectively, at the CGE server. Plasmids of the IncF, IncH1, IncH2, IncI1, IncN, or IncA/C types were subtyped by assigning a replicon allele at the plasmid MLST site (https://pubmlst.org/plasmid/, accessed on 4 May 2022). Identification of virulence genes related to CP-E. coli was performed by VirulenceFinder at CGE.

3. Results

3.1. Antimicrobial Susceptibility Testing and Characterization of Resistance Genes

Between 2018 and 2020, 12 CP-E. coli isolates were recovered from elderly inpatients and were available for antibiotic susceptibility testing and WGS.
Antibiotic susceptibility profiles of CP-E. coli isolates are shown in Figure 1. All isolates were resistant to at least one of the tested carbapenem (meropenem or ertapenem). The resistance rates to meropenem or ertapenem were 16.7% (2/12) and 91.7% (11/12), respectively. Seven isolates (58.3%) were resistant to trimethoprim/sulfamethoxazole, six (50.0%) to ciprofloxacin, and five (41.7%) to gentamicin. Three isolates (25.0%) were resistant to ceftazidime/avibactam and one (8.3%) to amikacin. All isolates were susceptible to colistin, fosfomycin, and tigecycline.

3.2. WGS Analysis of CP-E. coli

Whole-genome sequencing and in silico analysis was carried out on all the CP-E. coli isolates. Serotype O8:H9 was relatively the most frequent (3/12) and found in the isolates belonging to the same ST410; the remaining nine isolates were classified into nine different serotypes (Table 1). MLST analysis showed the presence of 10 CP-E. coli lineages: ST410 (3 isolates), ST12, ST38, ST69, ST95, ST131, ST189, ST648, ST1288, and ST1598 (one isolate each) (Table 1). Six different fimH types were detected; fimH24 was relatively the most frequent (3/12) and found in isolates belonging to two different STs (ST410 and ST38).
A core genome SNP Tree showed that the isolates were not closely related, as no major clades were present (Figure 2), except the branch including the three ST410 isolates. No single-locus variants were detected, and all STs belonged to different Clonal Complexes (CCs), except ST1288 and ST1598, which did not cluster in any established CC. The three isolates belonging to ST410 did not represent an epidemic cluster, since they originated from three different hospitals in the two cities: two isolates from the same city differed by 21 SNPs, while the third isolate differed by 59 and 60 SNPs from the other two, respectively (Supplementary Table S1).

3.3. Plasmid Content of CP-E. coli

Plasmid content was determined by PlasmidFinder and is summarized in Table 1. All CP-E. coli isolates harbored plasmids, and in all but one, the simultaneous presence of more than one plasmid was detected. Overall, IncF was the predominant plasmid found in most of the CP-E. coli (10/12, 83.3%), followed by Col (6/12, 50%). Ten isolates carried IncFIB and IncFII plasmids; IncFIA was present in five isolates. Besides IncF, several plasmid classes (IncA, IncB/O/K/Z, IncI-1, IncQ, IncR, IncX1, IncX3, and IncY), were found among the isolates in different combinations. Isolates belonging to ST410 shared the same pMLST for IncF [F1;A1;B49]. The remaining isolates had different pMLST.
Plasmid location of carbapenemase-encoding genes was identified in seven cases due to the short read technology used. blaKPC genes were located on an IncFII(K) plasmid in four cases and on an IncX3 in one case, while blaOXA-181 were on a ColKP3 plasmid in two cases.

3.4. Resistome of CP-E. coli

The resistome of the isolates is shown in Table 1. Characterization of the genes responsible for carbapenemase production showed that most isolates (7/12, 58.3%) harbored blaKPC genes (five isolates blaKPC-3 and two blaKPC-2) (Table 1). Among the remaining isolates, two (16.7%) were positive for blaNDM-5, two (16.7%) for blaOXA-181, and one (8.3%) for blaVIM-1. No isolate co-harbored different carbapenemase-encoding genes.
Extended-spectrum β-lactamase (ESBL) genes were found in nearly all isolates (10/12 CP-E. coli, 83.3%). In particular, blaCTX-M-15 was found in six isolates, blaCMY-2 in three isolates, and blaSHV-12 in one isolate. ESBL genes were associated with different carbapenemase genes (Table 1). Aminoglycoside-modifying enzymes were identified in 10/12 isolates (83.3%): five isolates carried aac(6′)-Ib-cr, associated with aadA5, aadA2, or aadA1. Plasmid-mediated resistance to fluoroquinolones was found in six isolates, five carrying aac(6′)-Ib-cr, alone or in combination to qnrS1, and one carrying only qnrS1. Sulfamethoxazole/trimethoprim resistance genes dfrA12, dfrA14, and/or dfrA17 were found in eight isolates. The macrolide resistance mph(A) gene was found in six isolates; sulphonamide resistance sul1 and sul2 genes were detected in six and seven isolates, respectively. Tetracycline resistance genes tet(A), tet(B), and tet(D) were detected in seven isolates. Chloramphenicol resistance genes catB2 and catB3 were found in three isolates. No streptomycin, colistin, or fosfomycin acquired resistance genes were found. Notably, the three ST410 isolates carried blaNDM-5 or blaOXA-181 genes, with different combinations of resistance genes and plasmids.

3.5. Virulence Genes of CP-E. coli

The virulence genes identified in CP-E. coli are summarized in Table 2.
Virulence genes were detected in each isolate with a variable distribution. Several virulence genes coding for virulence factors (VFs) involved in adhesion (83% of the isolates), capsule formation (50%), iron acquisition (67%), serum resistance (67%), and toxicity (25%) were detected. All isolates possessed the glutamate decarboxylase gene gad, essential in maintaining the bacterial physiological pH in acidic conditions, and terC, a metal sensing stress response system. The sequences encoding adhesion proteins (adhesins, fimbriae, pilin, and outer membrane proteins) were found in most strains: the fimH gene, coding for the type 1 fimbria, was found in eleven isolates; lpfA, encoding fimbriae, was found in six isolates; and yfcV, associated with papA/C and coding for pilin, was found in four isolates. Kps genes, encoding the group two capsule, were detected in six isolates. Several siderophores for iron acquisition were detected: sitA, coding for an iron transport protein, in seven isolates, and chuA and/or fyuA plus irp2, coding for iron receptors, in six and five isolates, respectively. Regarding serum resistance, the traT gene, coding for an outer membrane protein for complement resistance, was found in eight isolates. iss, for increased serum survival, and ompT, an outer membrane protease, were found in five isolates. Virulence genes coding for VFs related to toxicity were only found in 25% of isolates: usp, an uropathogenic specific protein, and vat, a vacuolating autotransporter toxin, were found in three and two isolates, respectively.

4. Discussion

The prevalence of multidrug-resistant (MDR) E. coli strains is increasing worldwide, mainly due to the spread of mobile genetic elements carrying resistance determinants such as ESBLs and carbapenemase-encoding genes. According to a recent survey on CPE in Europe (EuSCAPE), resistance to carbapenems in E. coli is uncommon, and only a small proportion of CP-E. coli isolates (0.2–0.5%) is present among European and Italian isolates [17,18]. In our previous studies, few E. coli isolates from infection cases were found to be resistant to carbapenems; some did not produce any carbapenemase, and others carried a blaNDM-5 or blaVIM-1 gene [19,20,21]. In a carriage study in the elderly, our group observed a 1% prevalence of intestinal CP-E. coli colonization [22]. CP-E. coli infections are difficult to treat because isolates are frequently resistant to several different antibiotic classes, and the therapeutic options are scarce.
In this study, we confirmed CP-E. coli to be resistant to several antibiotics besides carbapenems: the most frequent resistance phenotype was resistance to amoxicillin/clavulanic acid, trimethoprim-sulfamethoxazole, ciprofloxacin, and/or gentamicin, in line with data from the European Antimicrobial Resistance Surveillance Network [5,17]. However, all isolates maintained susceptibility to colistin, fosfomycin, and tigecycline. The most common mechanism of carbapenem resistance was KPC production that represents the main cause of the endemic CPE situation in Italy [18]. We also found that three isolates, all harboring a carbapenemase gene of the metallo β-lactamase, were resistant to ceftazidime/avibactam, as already reported [23].
As reported in the literature [24,25], a high genetic diversity was observed: by MLST genotyping, no specific clone was associated with the presence of a carbapenemase, as we found 10 different lineages in the 12 isolates tested. Specifically, we found clones that are frequently associated with urinary tract infections or bloodstream infections, such as ST131, ST69, ST410, and ST95. ST131 is the most frequent E. coli clone associated with fluoroquinolone resistance and ESBL production, predominating globally and causing most human infections [19,26]. Carbapenem-resistant ST131 isolates are not common, but few cases have been previously reported worldwide [27]. The finding of this pandemic and diffusible clone carrying a carbapenemase-encoding gene is particularly worrisome due to its high potential to cause severe infections. ST410 and ST648 are now emerging as other globally disseminated E. coli clones that can carry carbapenemases [28,29]. ST410 was the relatively more frequent strain detected in our study, confirming the emergence of such a strain as one of the main drivers of carbapenem resistance in E. coli that needs to be monitored [24,25,28]. The ST410 isolates were associated with different combinations of plasmid/resistance genes, even if their virulence gene content was similar, confirming that they are not part of an epidemic cluster. ST69 strains are often multidrug-resistant [30]; ST95 are characterized by a relatively low frequency of multidrug resistance but sometimes associated with blaKPC [31].
Plasmid analysis showed that the IncF plasmid is present in several different STs examined in this study, as already reported [32]. Besides IncF, we found several plasmid classes, carrying several resistance genes belonging to different antimicrobial classes, reflecting the MDR genotypes of the CP-E. coli isolates [32]. Serine-β-lactamase genes were more frequently detected than metallo-β-lactamase genes (75% vs. 25%), reflecting the Italian epidemiology [18]. Acquired resistance genes were observed in all strains of the different STs. The majority of isolates carried carbapenemase in association with different ESBL and/or AmpC β-lactamase genes; blaCTX-M-15 and blaOXA-9 were the most frequent ESBL. blaCTX-M-15 has been reported as the most prevalent ESBL enzymes in our country in the last decade and has usually been associate with ExPEC E. coli isolates [19,22].
In this study, virulence genes coding for VFs such as adhesins and siderophores were present in almost all isolates, with an overall heterogeneity in their distribution, as being reported by other authors in pathogenic E.coli [33]. The presence of virulence genes is worrying because it enhances the ability of the microorganisms to survive in the colonized host and eventually cause disease. The majority of isolates contained genes for VFs involved in adhesion (mostly the fimbrial fimH gene), regarded as the first step in pathogenesis, enabling close contact of the bacteria with the host cell wall, which is essential for colonizing specific niches [34]. VFs of the siderophore systems related to iron acquisition and essential for bacterial growth, especially during bacterial infection [35], were found in 67% of the isolates.
Such a wide distribution of clones and resistance genes and/or virulence genes confirms that no particular CP-E. coli clone has emerged until now in colonization/infection, as found in other studies [36,37,38,39].

5. Conclusions

In conclusion, by analyzing genome sequences of CP-E. coli isolates from intestinal colonization of the elderly, we found several different clones carrying a multitude of resistance and virulence genes. The combination of multiple resistance and virulence genes may play a fundamental role in increasing the fitness and the potential to cause disease of CP-E. coli. This is concerning, since it could result in the spreading of these MDR strains in hospital settings or the community and in the development of difficult to treat infections. Continued monitoring of CP-E. coli will be critical to prevent the expansion of high-risk clones as well as to limit the dissemination of antimicrobial-resistance genes to fight the burden of AMR.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/microorganisms10081561/s1, Table S1: Matrix of core genome single nucleotide polymorphisms (SNPs) between E. coli isolates from the elderly.

Author Contributions

Conceptualization, M.G., M.D.G. and M.M. (Monica Monaco); methodology, G.E., M.P., M.M. (Manuela Marra) and M.C. (Maria Carollo); software, M.G., G.E. and M.D.G.; validation, M.G., G.E. and M.D.G.; formal analysis, M.G. and M.D.G.; investigation, A.R., E.F., E.C., F.G.S. and D.Z.; resources, M.T.; data curation, D.Z.; writing—original draft preparation, M.G.; writing—review and editing, M.G., A.P., G.E., M.S., M.D.G., M.C. (Marina Cerquetti) and M.M. (Monica Monaco); visualization, M.G.; supervision, M.T.; project administration, M.T.; funding acquisition, M.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Italian Society of Infectious and Tropical Diseases (SIMIT), funding number 1000/6791.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Ethics Committee of Sacco Hospital (protocol code 4990/2018, date of approval 8 February 2018).

Informed Consent Statement

All subjects or their legal guardians gave their informed consent for inclusion in the study.

Data Availability Statement

Sequence data were submitted to GenBank at NCBI under the BioProject PRJNA789446.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Cassini, A.; Högberg, L.D.; Plachouras, D.; Quattrocchi, A.; Hoxha, A.; Simonsen, G.S.; Colomb-Cotinat, M.; Kretzschmar, M.E.; Devleesschauwer, B.; Cecchini, M.; et al. Attributable deaths and disability-adjusted life-years caused by infections with antibiotic-resistant bacteria in the EU and the European Economic Area in 2015: A population-level modelling analysis. Lancet Infect. Dis. 2019, 19, 56–66. [Google Scholar] [CrossRef] [Green Version]
  2. Latour, K.; Huang, T.D.; Jans, B.; Berhin, C.; Bogaerts, P.; Noel, A.; Nonhoff, C.; Dodémont, M.; Denis, O.; Ieven, M.; et al. Prevalence of multidrug-resistant organisms in nursing homes in Belgium in 2015. PLoS ONE 2019, 14, e0214327. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Gorrie, C.L.; Mirceta, M.; Wick, R.R.; Judd, L.M.; Wyres, K.L.; Thomson, N.R.; Strugnell, R.A.; Pratt, N.F.; Garlick, J.S.; Watson, K.M.; et al. Antimicrobial-Resistant Klebsiella pneumoniae Carriage and Infection in Specialized Geriatric Care Wards Linked to Acquisition in the Referring Hospital. Clin. Infect. Dis. 2018, 67, 161–170. [Google Scholar] [CrossRef] [Green Version]
  4. Tumbarello, M.; Viale, P.; Viscoli, C.; Trecarichi, E.M.; Tumietto, F.; Marchese, A.; Spanu, T.; Ambretti, S.; Ginocchio, F.; Cristini, F.; et al. Predictors of mortality in bloodstream infections caused by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae: Importance of combination therapy. Clin. Infect. Dis. 2012, 55, 943–950. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. WHO Regional Office for Europe/European Centre for Disease Prevention and Control. Antimicrobial Resistance Surveillance in Europe 2022—2020 Data; WHO Regional Office for Europe: Copenhagen, Denmark, 2022. [Google Scholar]
  6. Jiang, Y.; Wang, Y.; Hua, X.; Qu, Y.; Peleg, A.Y.; Yu, Y. Pooled plasmid sequencing reveals the relationship between mobile genetic elements and antimicrobial resistance genes in clinically isolated Klebsiella pneumoniae. Genom. Proteom. Bioinform. 2020, 18, 539–548. [Google Scholar] [CrossRef]
  7. Kiratisin, P.; Kazmierczak, K.; Stone, G.G. In vitro activity of ceftazidime/avibactam and comparators against carbapenemase-producing Enterobacterales and Pseudomonas aeruginosa isolates collected globally between 2016 and 2018. J. Glob. Antimicrob. Resist. 2021, 27, 132–141. [Google Scholar] [CrossRef]
  8. Yu, W.; Xiong, L.; Luo, Q.; Chen, Y.; Ji, J.; Ying, C.; Liu, Z.; Xiao, Y. In Vitro Activity Comparison of Ceftazidime-Avibactam and Aztreonam-Avibactam against Bloodstream Infections with Carbapenem-Resistant Organisms in China. Front. Cell Infect. Microbiol. 2021, 11, 780365. [Google Scholar] [CrossRef] [PubMed]
  9. Di Bella, S.; Giacobbe, D.R.; Maraolo, A.E.; Viaggi, V.; Luzzati, R.; Bassetti, M.; Luzzaro, F.; Principe, L. Resistance to ceftazidime/avibactam in infections and colonisations by KPC-producing Enterobacterales: A systematic review of observational clinical studies. J. Glob. Antimicrob. Resist. 2021, 25, 268–281. [Google Scholar] [CrossRef]
  10. Pakbin, B.; Brück, W.M.; Rossen, J.W.A. Virulence Factors of Enteric Pathogenic Escherichia coli: A Review. Int. J. Mol. Sci. 2021, 22, 9922. [Google Scholar] [CrossRef] [PubMed]
  11. Gruber, I.; Heudorf, U.; Werner, G.; Pfeifer, Y.; Imirzalioglu, C.; Ackermann, H.; Brandt, C.; Besier, S.; Wichelhaus, T.A. Multidrug-resistant bacteria in geriatric clinics, nursing homes, and ambulant cared prevalence and risk factors. Int. J. Med. Microbiol. 2013, 303, 405.e9. [Google Scholar] [CrossRef]
  12. Lim, C.J.; Cheng, A.C.; Kennon, J.; Spelman, D.; Hale, D.; Melican, G.; Sidjabat, H.E.; Paterson, D.L.; Kong, D.C.M.; Peleg, A.Y. Prevalence of multidrug-resistant organisms and risk factors for carriage in long-term care facilities: A nested caseecontrol study. J. Antimicrob. Chemother. 2014, 69, 1972–1980. [Google Scholar] [CrossRef] [PubMed]
  13. Aschbacher, R.; Pagani, E.; Confalonieri, M.; Farina, C.; Fazii, P.; Luzzaro, F.; Montanera, P.G.; Piazza, A.; Pagani, L. Review on colonization of residents and staff in Italian long-term care facilities by multidrug-resistant bacteria compared with other European countries. Antimicrob. Resist. Infect. Control 2016, 5, 33. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Tinelli, M.; Rossini, A.; Scudeller, L.; Zabzuni, D.; Errico, G.; Fogato, E.; D’Angelo, R.; Gentiloni Silverj, F.; Cesana, E.; Bergamaschini, L.C. Dynamics of carbapenemase-producing Enterobacterales intestinal colonization in the elderly population after hospital discharge, Italy, 2018–2020. Int. J. Antimicrob. Agents 2022, 59, 106594. [Google Scholar] [CrossRef] [PubMed]
  15. EUCAST. Breakpoint Tables for Interpretation of MICs and Zone Diameters, Version 12.0; 2022. Available online: http://www.eucast.org (accessed on 8 April 2022).
  16. Letunic, I.; Bork, P. Interactive tree of life (iTOL) v3: An online tool for the display and annotation of phylogenetic and other trees. Nucleic Acids Res. 2016, 44, W242–W245. [Google Scholar] [CrossRef]
  17. Grundmann, H.; Glasner, C.; Albiger, B.; Aanensen, D.M.; Tomlinson, C.T.; Andrasević, A.T.; Cantón, R.; Carmeli, Y.; Friedrich, A.W.; Giske, C.G. Occurrence of carbapenemase-producing Klebsiella pneumoniae and Escherichia coli in the European survey of carbapenemase-producing Enterobacteriaceae (EuSCAPE): A prospective, multinational study. Lancet Infect. Dis. 2017, 17, 153–163. [Google Scholar] [CrossRef] [Green Version]
  18. Viale, P.; Tumietto, F.; Giannella, M.; Bartoletti, M.; Tedeschi, S.; Ambretti, S.; Cristini, F.; Gibertoni, C.; Venturi, S.; Cavalli, M.; et al. Impact of a hospital–wide multifaceted programme for reducing carbapenem-resistant Enterobacteriaceae infections in a large teaching hospital in northern Italy. Clin. Microbiol. Infect. 2015, 21, 242–247. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Giufrè, M.; Mazzolini, E.; Cerquetti, M.; Brusaferro, S. CCM2015 One-Health ESBL-producing Escherichia coli Study Group. Extended-spectrum β-lactamase-producing Escherichia coli from extraintestinal infections in humans and from food-producing animals in Italy: A ‘One Health’ study. Int. J. Antimicrob. Agents 2021, 58, 106433. [Google Scholar] [CrossRef]
  20. Giufrè, M.; Errico, G.; Accogli, M.; Monaco, M.; Villa, L.; Distasi, M.A.; Del Gaudio, T.; Pantosti, A.; Carattoli, A.; Cerquetti, M. Emergence of NDM-5 producing Escherichia coli sequence type 167 clone in Italy. Int. J. Antimicrob. Agents 2018, 52, 76–81. [Google Scholar] [CrossRef] [Green Version]
  21. Giufrè, M.; Accogli, M.; Ricchizzi, E.; Barbanti, F.; Farina, C.; Fazii, P.; Mattei, R.; Sarti, M.; Barozzi, A.; Buttazzi, R.; et al. Multidrug-resistant infections in long-term care facilities: Extended-spectrum β-lactamase-producing Enterobacteriaceae and hypervirulent antibiotic resistant Clostridium difficile. Diagn. Microbiol. Infect. Dis. 2018, 91, 275–281. [Google Scholar] [CrossRef]
  22. Giufrè, M.; Ricchizzi, E.; Accogli, M.; Barbanti, F.; Monaco, M.; Pimentel de Araujo, F.; Farina, C.; Fazii, P.; Mattei, R.; Sarti, M.; et al. Colonization by multidrug-resistant organisms in long-term care facilities in Italy: A point-prevalence study. Clin. Microbiol. Infect. 2017, 23, 961–967. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Thaden, J.T.; Pogue, J.M.; Kaye, K.S. Role of newer and re-emerging older agents in the treatment of infections caused by carbapenem-resistant Enterobacteriaceae. Virulence 2017, 8, 403–416. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Karlsson, M.; Lutgring, J.D.; Ansari, U.; Lawsin, A.; Albrecht, V.; McAllister, G.; Daniels, J.; Lonsway, D.; McKay, S.; Beldavs, Z.; et al. Molecular Characterization of Carbapenem-Resistant Enterobacterales Collected in the United States. Microb. Drug Resist. 2022, 28, 389–397. [Google Scholar] [CrossRef] [PubMed]
  25. Hopkins, K.L.; Ellaby, N.; Ellington, M.J.; Doumith, M.; Mustafa, N.; Meunier, D.; Woodford, N. Diversity of carbapenemase-producing Enterobacterales in England as revealed by whole-genome sequencing of isolates referred to a national reference laboratory over a 30-month period. J. Med. Microbiol. 2022, 71, 001518. [Google Scholar] [CrossRef] [PubMed]
  26. Nicolas-Chanoine, M.H.; Bertrand, X.; Madec, J.Y. Escherichia coli ST131, an intriguing clonal group. Clin. Microbiol. Rev. 2014, 27, 543–574. [Google Scholar] [CrossRef] [Green Version]
  27. Peirano, G.; Bradford, P.A.; Kazmierczak, K.M.; Badal, R.E.; Hackel, M.; Hoban, D.J.; Pitout, J.D. Global incidence of carbapenemase-producing Escherichia coli ST131. Emerg. Infect. Dis. 2014, 20, 1928–1931. [Google Scholar] [CrossRef] [PubMed]
  28. Roer, L.; Overballe-Petersen, S.; Hansen, F.; Hansen, F.; Schønning, K.; Wang, M.; Hansen, D.S.; Justesen, U.S.; Andersen, L.P.; Fulgsang-Damgaard, D.; et al. Escherichia coli Sequence Type 410 is causing new international high-risk clones. mSphere 2018, 3, e00337-18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Manges, A.R.; Geum, H.M.; Guo, A.; Edens, T.J.; Fibke, C.D.; Pitout, J.D.D. Global extraintestinal pathogenic Escherichia coli (ExPEC) lineages. Clin. Microbiol. Rev. 2019, 32, e00135-18. [Google Scholar] [CrossRef]
  30. Adams-Sapper, S.; Diep, B.A.; Perdreau-Remington, F.; Riley, L.W. Clonal composition and community clustering of drug-susceptible and resistant Escherichia coli isolates from blood stream infections. Antimicrob. Agents Chemother. 2013, 57, 490–497. [Google Scholar] [CrossRef] [Green Version]
  31. Mitra, S.D.; Irshad, P.; Anusree, M.; Rekha, I.; Shailaja, S.; Suresh, J.; Aishwarya, G.; Shrestha, S.; Shome, B.R. Whole genome global insight of antibiotic resistance gene repertoire and virulome of high-risk multidrug-resistant Uropathogenic Escherichia coli. Microb. Pathog. 2021, 161, 105256. [Google Scholar] [CrossRef] [PubMed]
  32. Kopotsa, K.; Osei Sekyere, J.; Mbelle, N.M. Plasmid evolution in carbapenemase-producing Enterobacteriaceae: A review. Ann. N. Y. Acad. Sci. 2019, 1457, 61–91. [Google Scholar] [CrossRef]
  33. Sora, V.M.; Meroni, G.; Martino, P.A.; Soggiu, A.; Bonizzi, L.; Zecconi, A. Extraintestinal Pathogenic Escherichia coli: Virulence Factors and Antibiotic Resistance. Pathogens 2021, 10, 1355. [Google Scholar] [CrossRef] [PubMed]
  34. Lindberg, S.; Xia, Y.; Sondén, B.; Göransson, M.; Hacker, J.; Uhlin, B.E. Regulatory Interactions among adhesin gene systems of uropathogenic Escherichia coli. Infect. Immun. 2008, 76, 771–780. [Google Scholar] [CrossRef] [Green Version]
  35. Chu, B.C.; Garcia-Herrero, A.; Johanson, T.H.; Krewulak, K.D.; Lau, C.K.; Peacock, R.S.; Slavinskaya, Z.; Vogel, H.J. Siderophore uptake in bacteria and the battle for iron with the host; a bird’s eye view. Biometals 2010, 23, 601–611. [Google Scholar] [CrossRef]
  36. Chen, B.; Berglund, B.; Wang, S.; Börjesson, S.; Bi, Z.; Nilsson, M.; Yin, H.; Zheng, B.; Xiao, Y.; Bi, Z.; et al. Rapid increase in occurrence of carbapenem-resistant Enterobacteriaceae in healthy rural residents in Shandong Province, China, from 2015 to 2017. J. Glob. Antimicrob. Resist. 2022, 28, 38–42. [Google Scholar] [CrossRef]
  37. Liu, X.; Li, X.; Yang, A.W.; Tang, B.; Jian, Z.J.; Zhong, Y.M.; Li, H.L.; Li, Y.M.; Yan, Q.; Liang, X.H.; et al. Community Fecal Carriage and Molecular Epidemiology of Extended-Spectrum β-Lactamase- and Carbapenemase-Producing Escherichia coli from Healthy Children in the Central South China. Infect. Drug Resist. 2022, 15, 1601–1611. [Google Scholar] [CrossRef] [PubMed]
  38. Yen, N.T.P.; Nhung, N.T.; Phu, D.H.; Dung, N.T.T.; Van, N.T.B.; Kiet, B.T.; Hien, V.B.; Larsson, M.; Olson, L.; Campbell, J.; et al. Prevalence of carbapenem resistance and its potential association with antimicrobial use in humans and animals in rural communities in Vietnam. JAC Antimicrob. Resist. 2022, 4, dlac038. [Google Scholar] [CrossRef] [PubMed]
  39. Hernández-García, M.; Pérez-Viso, B.; Carmen Turrientes, M.; Díaz-Agero, C.; López-Fresneña, N.; Bonten, M.; Malhotra-Kumar, S.; Ruiz-Garbajosa, P.; Cantón, R. Characterization of carbapenemase-producing Enterobacteriaceae from colonized patients in a university hospital in Madrid, Spain, during the R-GNOSIS project depicts increased clonal diversity over time with maintenance of high-risk clones. J. Antimicrob. Chemother. 2018, 73, 3039–3043. [Google Scholar] [CrossRef]
Microorganisms 10 01561 g001 550
Figure 1. Antimicrobial susceptibility profiles of 12 CP-E. coli isolates from intestinal carriage in elderly patients. Red/orange/grey color in each column indicates percentage of resistant/susceptible, increased exposure/susceptible isolates, respectively.
Figure 1. Antimicrobial susceptibility profiles of 12 CP-E. coli isolates from intestinal carriage in elderly patients. Red/orange/grey color in each column indicates percentage of resistant/susceptible, increased exposure/susceptible isolates, respectively.
Microorganisms 10 01561 g001
Microorganisms 10 01561 g002 550
Figure 2. SNP-based phylogeny of CP-E. coli isolates from intestinal carriage in elderly patients. The maximum likelihood tree was rooted in a reference isolate E. coli strain K12 (accession no. NC_000913.2). Sequence type (ST) is shown for each isolate.
Figure 2. SNP-based phylogeny of CP-E. coli isolates from intestinal carriage in elderly patients. The maximum likelihood tree was rooted in a reference isolate E. coli strain K12 (accession no. NC_000913.2). Sequence type (ST) is shown for each isolate.
Microorganisms 10 01561 g002
Table
Table 1. Molecular and resistome analysis of 12 CP-Escherichia coli isolates from carriage in elderly patients.
Table 1. Molecular and resistome analysis of 12 CP-Escherichia coli isolates from carriage in elderly patients.
IsolateSerotypeSTCCfimHPlasmid ContentpMLST *β-LactamasesAminoglycoside Modifying EnzimesFQsMLSPhenicolSulphonamideTETTrimethoprim
MI3.2.1O8:H9410ST2324IncFIA, IncFIB, IncFII, IncQ1IncF[F1:A1:B49]NDM-5, CTX-M-15, CMY-2, OXA-1, TEM-1Baac(6′)-Ib-cr, aadA2, aadA5, aph(6)-Id, aph(3″)-Ib, aac(3)-IIdaac(6′)-Ib-crmph(A)catB3sul1, sul2tet(B)dfrA12,
dfrA17
MI4.1.1O8:H9410ST2324IncFIA, IncFIB, IncFII, Col (BS512)IncF[F1:A1:B49]NDM-5, CTX-M-15, CMY-2aac(6′)-Ib-cr, aadA2, aph(6)-Id, aph(3″)-Ib, aac(3)-IIdaac(6′)-Ib-crmph(A) sul1, sul2 dfrA12
RM32.1O8:H9410ST2321IncFIA, IncFIB, IncFII, IncQ1, IncX3, IncY, Col (BS512), ColKP3IncF[F1:A1:B49]OXA-181, CTX-M-15CMY-2, OXA-1, TEM-1Baac(6′)-Ib-cr, aadA5, aph(6)-Id, aph(3″)-Ib, aac(3)-IIdaac(6′)-Ib-cr, qnrS1mph(A)catB3sul1, sul2tet(B)dfrA17
MI4.14.1-:H512ST125IncFIA, IncFIB, IncFII, IncX1, IncB/O/K/Z, Col156, ColKP3IncF[F1:A6:B20]OXA-181, TEM-1BaadA5, aph(6)-Id, aph(3″)-Ib, aac(3)-IId mph(A) sul1, sul2tet(A), tet(C)dfrA17
MI4.15.1O188:H21189ST16554IncX3 KPC-3, SHV-182aadA5 sul2tet(A)dfrA17
MI5.4.1O9:H91288-54IncFIB, IncFII, ColpVCIncF[K2:A-:B-]KPC-2aph(3″)-Ib, aph(6)-Id tet(B)
MI5.8.1O15:H1869ST6927IncA, IncB/O/K/ZIncA/C [12]VIM-1, SHV-12aac(6′)-Ib-cr, aadA1, aph(6)-Id, aph(3″)-Ib, aac(6′)-Ib3aac(6′)-Ib-cr, qnrS1mph(A)catB2sul1, sul2 dfrA14
MI5.18.1-:H6648ST64827IncFIB, IncFIIIncF[K2:A-:B-]KPC-2, CTX-M-15, OXA-9
RM18.1O9:H41598--IncFIB, IncFII, IncI1-I, IncR, IncX3, Col (BS512)IncF[K2:A-:B53], IncI1[154]KPC-3, CTX-M-15, OXA-9, SHV-182, TEM-1Baph(3″)-Ib, aph(6)-IdqnrS1 sul2tet(A)dfrA14
RM38.1O1:H795ST9530IncFIB, IncFIIIncF[F2:A-:B1]KPC-3, OXA-9, TEM-1A
RM52.1O25:H4131ST13130IncFIA, IncFIB, IncFIIIncF[K2:A4:B1]KPC-3, CTX-M-15, OXA-1, OXA-9, TEM-1A aac(6′)-Ib-cr, aadA5, aac(3)-IIaaac(6′)-Ib-crmph(A)catB3sul1tet(A)dfrA17
RM70.1-:H938ST3824IncFIB, IncFIIIncF[K2:A-:B-]KPC-3, OXA-9, TEM-1A
* Allele numbers assigned by pMLST are in bracket; ST-sequence type; CC-Clonal Complex; MLS- Macrolide, lincosamide, and streptogramin; FQs- Fluoroquinolones; TET-tetracycline.
Table
Table 2. Virulence gene content, according to their functions, of 12 CP-Escherichia coli isolates from carriage in elderly patients.
Table 2. Virulence gene content, according to their functions, of 12 CP-Escherichia coli isolates from carriage in elderly patients.
IsolateAdhesinsCapsuleSiderophoresSerum ResistanceToxinsOther
MI3.2.1fimH, lpfA gad, terC
MI4.1.1fimH, lpfA gad, terC
RM32.1fimH, lpfA gad, terC
MI4.14.1fimH, focC, papA/C, sfaD, yfcVkpsE/MIIchuA, fyuA, iroN, irp2, sitAiss, ompT, traTcea, senB, usp, vatgad, terC
MI4.15.1fimH, lpfA gad, terC
MI5.4.1fimH sitAtraT gad, terC
MI5.8.1fimH, lpfAkpsE/MIIchuA, fyuA, irp2, sitAiss, ompT, traT gad, terC
MI5.18.1fimH, lpfA, papA/C, yfcVkpsE/MII, neuCchuA, fyuA, irp2ompT, traT gad, terC
RM18.1 sitAiss, traT gad, terC
RM38.1fimH, papA/C, yfcVkpsE/MII, neuCchuA, fyuA, ireA, iroN, irp2, iucC, sitAiss, ompT, traTcia, hlyF, usp, vatgad, terC
RM52.1afaA/C/D, fimH, hra, iha, nfaE, papA/C, yfcVkpsE/MIIchuA, fyuA, irp2, iucC, sitAiss, ompT, traTcnf1, sat, uspgad, terC
RM70.1fimH, hrakpsE/MIIchuA, sitAtraT gad, terC
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Giufrè, M.; Errico, G.; Monaco, M.; Del Grosso, M.; Sabbatucci, M.; Pantosti, A.; Cerquetti, M.; Pagnotta, M.; Marra, M.; Carollo, M.; et al. Whole Genome Sequencing and Molecular Analysis of Carbapenemase-Producing Escherichia coli from Intestinal Carriage in Elderly Inpatients. Microorganisms 2022, 10, 1561. https://doi.org/10.3390/microorganisms10081561

AMA Style

Giufrè M, Errico G, Monaco M, Del Grosso M, Sabbatucci M, Pantosti A, Cerquetti M, Pagnotta M, Marra M, Carollo M, et al. Whole Genome Sequencing and Molecular Analysis of Carbapenemase-Producing Escherichia coli from Intestinal Carriage in Elderly Inpatients. Microorganisms. 2022; 10(8):1561. https://doi.org/10.3390/microorganisms10081561

Chicago/Turabian Style

Giufrè, Maria, Giulia Errico, Monica Monaco, Maria Del Grosso, Michela Sabbatucci, Annalisa Pantosti, Marina Cerquetti, Michela Pagnotta, Manuela Marra, Maria Carollo, and et al. 2022. "Whole Genome Sequencing and Molecular Analysis of Carbapenemase-Producing Escherichia coli from Intestinal Carriage in Elderly Inpatients" Microorganisms 10, no. 8: 1561. https://doi.org/10.3390/microorganisms10081561

APA Style

Giufrè, M., Errico, G., Monaco, M., Del Grosso, M., Sabbatucci, M., Pantosti, A., Cerquetti, M., Pagnotta, M., Marra, M., Carollo, M., Rossini, A., Fogato, E., Cesana, E., Gentiloni Silverj, F., Zabzuni, D., & Tinelli, M. (2022). Whole Genome Sequencing and Molecular Analysis of Carbapenemase-Producing Escherichia coli from Intestinal Carriage in Elderly Inpatients. Microorganisms, 10(8), 1561. https://doi.org/10.3390/microorganisms10081561

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop