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Article

Dissemination of OXA-48- and NDM-1-Producing Enterobacterales Isolates in an Algerian Hospital

by
Amel Abderrahim
1,
Nassima Djahmi
2,
Lotfi Loucif
3,
Sabrina Nedjai
2,
Widad Chelaghma
4,
Djamila Gameci-Kirane
1,
Mazouz Dekhil
2,
Jean-Philippe Lavigne
5,* and
Alix Pantel
5
1
Département de Biochimie, Faculté des Sciences, Université Badji Mokhtar Annaba, Annaba 23000, Algeria
2
Laboratoire de Microbiologie, CHU Ibn Rochd, Annaba 23000, Algeria
3
Laboratoire de Biotechnologie des Molécules Bioactives et de la Physiopathologie Cellulaire (LBMBPC), Faculté des Sciences de la Nature et de la Vie, Université de Batna 2, Batna 05000, Algeria
4
Laboratoire de Microbiologie Appliquée à l’Agroalimentaire au Biomédical et à l’Environnement, Département de Biologie, Faculté des Sciences de la Nature et de la Vie et Sciences de la Terre et de l’Univers, Université Abou Bekr Belkaid, Tlemcen 13000, Algeria
5
Virulence Bactérienne et Infections Chroniques, INSERM U1047, Université Montpellier, Service de Microbiologie et Hygiène Hospitalière, CHU Nîmes, 30900 Nîmes, France
*
Author to whom correspondence should be addressed.
Antibiotics 2022, 11(6), 750; https://doi.org/10.3390/antibiotics11060750
Submission received: 1 May 2022 / Revised: 27 May 2022 / Accepted: 27 May 2022 / Published: 31 May 2022
(This article belongs to the Special Issue Diversity of Antimicrobial Resistance Genes in Clinical Settings)
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Abstract

:
Multidrug-resistant (MDR) Enterobacterales remain an increasing problem in Algeria, notably due to the emergence of carbapenemase producers. We investigated the molecular characteristics of carbapenem-resistant Enterobacterales isolates recovered from outpatients and inpatients in Eastern Algeria. Non-repetitive Enterobacterales with reduced susceptibility to carbapenems were consecutively collected from clinical specimens in Annaba University Hospital (Algeria) between April 2016 and December 2018. Isolates were characterized with regard to antibiotic resistance, resistome and virulome content, clonality, and plasmid support. Of the 168 isolates analyzed, 29 (17.3%) were carbapenemase producers and identified as K. pneumoniae (n = 23), E. coli (n = 5), and E. cloacae (n = 1). blaOXA-48 was the most prevalent carbapenemase-encoding gene (n = 26/29), followed by blaNDM-1 gene (n = 3/29). K. pneumoniae isolates harbored some virulence traits (entB, ugeF, ureA, mrkD, fimH), whereas E. coli had a commensal origin (E, A, and B1). Clonality analysis revealed clonal expansions of ST101 K. pneumoniae and ST758 E. coli. Plasmid analysis showed a large diversity of incompatibility groups, with a predominance of IncM (n = 26, 89.7%). A global dissemination of OXA-48-producing Enterobacterales in the Algerian hospital but also the detection of NDM-1-producing E. coli in community settings were observed. The importance of this diffusion must be absolutely investigated and controlled.

1. Introduction

Antimicrobial resistance has become a major threat for public health worldwide. Currently, the emergence of carbapenem resistance is gaining considerable attention because these drugs were considered for a long time as the last-line agents for the treatment of critical infections caused by multidrug-resistant Enterobacterales [1]. Their use has significantly increased since the 1980s, due to the rapid spread of extended-spectrum β-lactamases (ESBL) producers worldwide [2], which led to the emergence of carbapenem-resistant Enterobacterales. The first detected carbapenemase type, NmcA, was described in 1993 among Enterobacter cloacae isolates [3]. Since then, increasing studies on carbapenem resistance in Enterobacterales species have been reported in many countries, which are mainly caused by the spread of carbapenemase producers [4]. Three carbapenemase classes have been identified in Enterobacterales. These classes include class A serine enzymes (KPC), class B metallo-β-lactamases (VIM, IMP, NDM), and class D enzymes (OXA-48-like) [5]. The OXA-48 carbapenemase was first identified in Klebsiella pneumoniae in 2001 in Turkey. The OXA-48-like β-lactamase has spread in several regions, gradually becoming endemic in North Africa and Turkey while emerging in several other parts of the world, including Europe and other African countries [5]. The New Delhi metallo-β-lactamase (NDM) enzyme group is among the recent described MBLs, and is responsible for major health concerns due to its rapid propagation in all continents and its severe clinical impact [6].
Carbapenemase-producing Enterobacterales (CPE) strains are often multidrug- or pan-drug-resistant, leaving only very few therapeutic options for treating serious infections. In addition, the co-occurrence of carbapenemase with other resistant determinants such as aminoglycosides and quinolones resistance is a cause for global health concern. In Algeria, data concerning the emergence and diffusion of the CPE strains are available [5,7]. OXA-48-like enzymes have been extensively reported [5], notably, in different ecological niches (human, livestock, wild animals, and wildlife), and are thought to be endemic in Algeria. However, KPC- and NDM-producing Enterobacterales have also been observed in humans and the environment [8,9,10,11,12].
Thus, the aim of the present study was to describe the molecular epidemiology (resistance and virulence determinants, clonality) of Enterobacterales isolates with reduced susceptibility to carbapenems recovered from outpatients and inpatients in Annaba University Hospital, in Algeria.

2. Results

2.1. Phenotypic Characterization and Antibiotic Susceptibility

During the studied period, 168 non-repetitive Enterobacterales isolates with reduced susceptibility to carbapenems were included in our study. Using a KPC, MBL, and OXA-48 Confirm kit [12], 29 of these 168 isolates (17.3%) were suspected to produce a carbapenemase, with 26 belonging to class D and 3 to class B. The other isolates (n = 139) were non-carbapenemase-producing Enterobacterales with an impermeability of the outer membrane. The bacterial isolates were identified as K. pneumoniae (n = 23), Escherichia coli (n = 5), and E. cloacae (n = 1). All the isolates were resistant to ertapenem, 86.2% (n = 25) to imipenem, and 69.0% (n = 20) to meropenem. Variable rates of resistance were noted for the other antibiotics, with 82.8% (n = 24) to fluoroquinolones (ofloxacin and ciprofloxacin) and cefoxitin, 79.3% (n = 23) to cefotaxime, ceftazidime, and tobramycin, 75.9% (n = 22) to cefepime, 72.4% (n = 21) to aztreonam and gentamicin, and 37.9% (n = 11) to amikacin. All isolates were susceptible to colistin (Supplementary Materials Tables S1 and S2).

2.2. Molecular Detection of Resistant Determinants

Using molecular tools, we definitively confirmed 29 carbapanemase producers, of which 26 isolates (89.7% of the carbapenemase producers) harbored the blaOXA-48 gene, including twenty-one K. pneumoniae, four E. coli, and one E. cloacae. The blaNDM-1 gene was detected in the three remaining isolates, with two K. pneumoniae isolates and one E. coli isolate (Table 1).
In addition, 22 CPE isolates (75.9%) also contained a blaCTX-M gene, of which 21 (95.5%) blaCTX-M-15 and 1 (4.5%) blaCTX-M-9.
Interestingly, these isolates co-harbored different PMQR and aminoglycoside-modifying enzyme-encoding genes: oqxAB (n = 23, 79.3%), aac6′-Ib-cr (n = 22, 75.9%), aac3-II (n = 19, 65.5%), qnrB (n = 15, 51.7%), qnrS (n = 12, 41.4%), qnrA (n = 10, 34.5%), and ant2″ (n = 1, 3.4%). The methylase-encoding gene rmtB was detected in two isolates (6.8%): one NDM-1-producing E. coli and one OXA-48-producing K. pneumoniae isolate (Table 1). Finally, we noted association between qnrB and aac(6′)-Ib-cr in twelve isolates (41.4%) and qnrB and aac(6′)-Ib-cr in the two NDM-1-producing K. pneumoniae, and in twelve OXA-48-producing isolates (57.1%).

2.3. Virulence Profiles of the Carbapanemase-Producing Enterobacterales

The evaluation of the virulence of the carbapenemase-producing K. pneumoniae isolates by specific PCR detection of the main virulence factors (VF) genes showed that no hypervirulent strain has been identified. However, the distribution of the 18 virulence-associated genes indicated that the isolates harbored between six and eight genes per isolate (Table 1). All isolates harbored entB, ugeF, ureA, mrkD, and fimH genes. ybtS gene was detected in 95.7% of isolates (n = 22), and wabG in 91.3% of isolates (n = 21). kfu was observed in 73.9% of the isolates (n = 17). iutA was only detected in one isolate. Neither capsular serotype genes nor hypermucoviscous phenotype were noted (Table 1).
The E. coli isolates belonged to the phylogroup E (n = 3/5), the B1 phylogroup (n = 1), or the A phylotype (n = 1). These isolates presented a low content of VF genes with only traT and fimH detected in all the isolates (n = 5), hlyA in three, iutA in two, and the other genes in one isolate (irp2, malX, papAH, papC, papG2, and kpsMT2), suggesting that E. coli had a commensal origin, except the Z27 isolate, which could be considered as an Extraintestinal pathogenic E. coli (ExPEC).

2.4. Clonal Relationships among Species

MLST analysis revealed that ST101 was the most common ST (n = 16, 69.6%) for K. pneumoniae. All these isolates harbored the blaOXA-48 gene. The other ST types identified were ST147 (n = 4), ST48 (n = 1), ST113 (n = 1), and ST405 (n = 1). Among the four ST147, two K. pneumoniae isolates carried the blaNDM-1 gene. The Rep-PCR results showed a large diversity of the isolates. Among K. pneumoniae, 11 clusters were observed (Figure 1), with a main cluster (pattern V) including 11 isolates (47.8%): Z6, Z11, Z12, Z13, Z14, Z16, Z21, Z23, Z27, Z33, and 859.
The four OXA-48-positive E. coli strains were totally diverse, belonging to ST44, 758, 759, and 834 (Figure 2). The last E. coli isolate (56) harboring blaNDM-1 belonged to ST759 and was clonal to the 58B isolate.
Finally, the OXA-48-producing E. cloacae belonged to ST68.

2.5. Plasmid Typing of the Carbapanemase-Producing Enterobacterales

The PBRT showed a large diversity of plasmids identified as follows: IncL, Mobc11, IncR, MobQU, colE NT2, FIIK, FV, IncAC, X3, colE NT1, and colE NT2 plasmid type. The different plasmids identified in the CPE isolates are summarized in Table 1.
IncM was the most prevalent (n = 26/29, 89.7%), notably, in OXA-48 producers (n = 26/26 isolates, 100%). IncFV was the most frequent plasmid detected in E. coli (n = 5/6 isolates, 83.3%). Finally, IncR and IncFV groups (n = 2 and n = 1, respectively) were detected in NDM-1-producers.

3. Discussion

The emergence and spread of carbapenemase-producing Gram-negative bacteria has become a major public health problem worldwide including North African countries. In developing countries, such as Algeria, several studies on carbapenemase producers have been reported [13,14,15,16,17,18,19]. This study demonstrated that OXA-48 enzyme is the most prevalent carbapenemase among patients admitted in our hospital, supporting the previous finding that OXA-48 is endemic in Algeria and is commonly disseminated in the Mediterranean region [5]. These results are in accordance with various reports from Algeria reporting the isolation of OXA-48-producing enterobacterial isolates, specifically, K. pneumoniae, E. coli, and E. cloacae from various ecological niches [5,20,21]. In this investigation, we also reported the isolation of NDM-1-producing Enterobacterales isolates. The first identification of a blaNDM gene in a clinical strain was described in 2009 in a Swedish patient of Indian origin, hospitalized in Sweden [22]. Following this report, NDM producers have been shown to be globally distributed, with virtually all countries, where the Asian continent, particularly India, the Middle East, and Balkan states serve as a reservoir of blaNDM genes [6,23]. In Algeria, the blaNDM-1 gene was detected mostly in A. baumannii isolates [19]. However, the first case of NDM-1-producing K. pneumoniae was identified in Annaba University Hospital from a patient with a urinary tract infection in 2017 [14]. Initially, CPE appeared to cause hospital-acquired infections, but more recently it has spread to the community setting [17,24]. To the best of our knowledge, here we report for the first time the detection of blaNDM-1 gene in E. coli isolate causing community-acquired infection in Algeria. This later co-harbored also the blaCTX-M-1, aac6′-Ib-cr, and rmtB genes. In Algeria, the first detection of CPE from a community setting through the isolation of OXA-48-producing K. pneumoniae isolate in community-acquired urinary tract infection was described in Batna city [24]. Since then, only one study has described the isolation of OXA-48-producing E. coli and K. pneumoniae in Annaba University Hospital [17]. Different carbapenemase producers were described from community-acquired infection worldwide. In India, blaNDM-5 has previously been reported in E. coli strains co-harboring extended-spectrum β-lactamases genes in community-acquired urinary tract infection [25]. In addition, blaNDM-1, blaNDM-5, and blaOXA-181 genes were also reported in E. coli isolates co-harboring the blaCTX-M-15 ESBL gene in Riyadh, Saudi Arabia, and in Czech Republic [26,27]. CPE commonly exhibit multidrug-resistant or extensively drug-resistant phenotypes, limiting treatment options. This was also observed in our strain collection due to the association of a wide variety of other acquired resistance genes, including those conferring resistance, with aminoglycosides and quinolones.
MLST analysis of K. pneumoniae, E. coli, and E. cloacae isolates showed the occurrence of several clones, with the ST101 in K. pneumoniae isolates being the most frequent. Indeed, in Algeria, the international high-risk resistant lineages ST101 carrying K. pneumoniae harboring the blaOXA-48 gene had accounted for an outbreak in Batna University Hospital, Algeria [4]. Interestingly, this epidemic clone has been involved in several outbreaks in Spain [28,29]. Therefore, ST101 was reported as a predominant OXA-48-producing K. pneumoniae clone in various Mediterranean countries. In addition, the ST101 is also reported as multidrug-resistant clones present in several African, American, and European countries [30]. ST147, the second most common clone in this study, has been found among three OXA-48-producing strains and two isolates harboring blaNDM-1 genes. This other international high-risk resistant lineage has recently been reported to be the main clone of K. pneumoniae strains carrying the blaNDM-1 gene in Annaba University Hospital [2]. Another report in the same city isolated OXA-48-producing K. pneumoniae ST147 isolates in 2018 [17]. These two sequence types, ST101 and ST147, are known to have strong epidemic potential and have been associated with various carbapenemases such as NDM-1 with ST147 in Yemen [31], VIM with ST147 in Greece [32], and ST101 with OXA-48 in Tunisia and Germany [33,34]. Furthermore, ST405 was associated in this work with one K. pneumoniae strain co-harboring the blaOXA-48, blaCTX-M-15, aac6′-1b-cr, aac3-II, oqxAB, and qnrB genes. The sequence type ST405 is also described as a multidrug-resistant clone present in Algeria from inanimate surfaces in hospital environments [35], from ready-to-eat sandwiches [36], and also in various European countries including Italy [37] and Spain [30]. Finally, our study reports for the first time the detection of OXA-48-producing E. cloacae ST68 as well as the first K. pneumoniae ST113, and E. coli ST758, ST44, and ST834 in Algeria. ST44 has been reported in household cockroaches in Ghana [38], in Ecuador from fresh vegetables samples [39], and in Chile from migratory Franklin’s Gulls (Leucophaeus pipixcan) [40]. In our study, the association of multidrug-resistant phenotypes with the detection of multiple VFs notably in K. pneumoniae isolates poses a serious global health risk, which increases the mortality rates. The diversity of the virulence genes within clones from the same hospital suggests that they were mostly acquired horizontally rather than vertically and could be associated with mobile genetic elements integrated into the chromosome. Further investigations must be performed to corroborate this result.

4. Materials and Methods

4.1. Bacterial Collection

From April 2016 to December 2018, all non-repetitive Enterobacterales isolates with reduced susceptibility to carbapenems (intermediately or resistant to at least one carbapenem molecule) were consecutively collected from different clinical specimens of both inpatients and outpatients in Annaba University Hospital (Algeria). The isolates were identified using the Vitek® MS system (bioMérieux, Marcy l’Etoile, France).

4.2. Antibiotic Susceptibility Testing

Susceptibility to antimicrobial agents was tested by the disk diffusion method (Bio-Rad, Marnes La Coquette, France) on Mueller–Hinton agar according to EUCAST recommendations (www.eucast.org, accessed on 20 January 2022). The following antibiotics were tested: amoxicillin (20 μg), cefoxitin (30 μg), cefotaxime (30 μg), ceftazidime (30 μg), cefepime (30 μg), aztreonam (30 μg), amoxicillin–clavulanic acid (20–10 μg), ertapenem (10 μg), meropenem (10 μg), imipenem (10 μg), gentamicin (10 μg), amikacin (30 μg), tobramycin (10 μg), ofloxacin (5 μg), and ciprofloxacin (5 μg). The minimal inhibition concentrations (MIC) of colistin and carbapenems (ertapenem, imipenem, and meropenem) were measured, respectively, by broth microdilution (UMIC®, Biocentric, Bandol, France) and E-test strips (bioMérieux), and interpreted following the EUCAST Breakpoints (v1.0, 2021). The non-susceptibility to the carbapenems and colistin was assessed on the MICs cut-offs: ertapenem: >0.5 mg/L, imipenem and meropenem: >2 mg/L, and colistin: >2 mg/L.

4.3. Phenotypic Characterization of Carbapenemase Production

Detection of carbapenemase producers was investigated using the KPC, MBL, and OXA-48 Confirm kit (Rosco Diagnostica A/S, Taastrup, Denmark) following the manufacturer’s recommendations [12].

4.4. Molecular Characterization of Antibiotic Resistance Genes

Total DNA was extracted using the EZ1 DNA Tissue kit on the BioRobot EZ1 extraction platform (Qiagen, Courtaboeuf, France). Carbapenemase-encoding genes (blaKPC, blaVIM, blaIMP, blaNDM-1, blaOXA-48-like) and extended-spectrum β-lactamases (ESBLs) determinants (blaTEM, blaSHV, and blaCTX-M) were screened by multiplex PCR using specific primers and confirmed by sequencing, as previously described [41,42]. Simplex or multiplex PCR for detecting aminoglycoside-modifying enzymes (aac(3)-I, aac(3)-II, aac(3)-IV, aac(6′)-Ib, ant(2″), aph(3′)-Ia, aph(3′)-VI), and the 16S rRNA methyltranferases genes (armA, rmtA, rmtB, rmtC, rmtD, rmtE, rmtF, npmA) was carried out [43,44,45]. In addition, plasmid-mediated quinolone resistance genes (qnrA, qnrB, qnrS, oqxA, oqxB, qepA, and aac(6′)-Ib/Ib-cr) were also investigated by multiplex PCR as described previously [46,47,48,49,50]. All PCR products were sequenced and analyzed using BLAST search.

4.5. Clonal Relationships

The genetic relationship between CPE isolates was evaluated using repetitive sequence-based PCR (rep-PCR), using the DiversiLab™ strain typing system (bioMérieux, Marcy l’Etoile, France). Results were interpreted with DiversiLab web-based software. This software calculated a dendrogram based on the Pearson correlation and the modified Kullback–Leibler method and created a scatter plot and a virtual gel image. The relatedness was determined by cluster analysis according to guidelines provided by the manufacturer. Isolates with identical strain patterns were considered indistinguishable if the similarity percentage was ≥ 95%. Multilocus sequence typing (MLST) analysis was also performed using the PubMLST scheme (https://pubmlst.org/, accessed on 20 January 2022).

4.6. Phylogenetic Grouping and Screening for Virulence Determinants

For carbapenemase-producing K. pneumoniae isolates, multiplex PCR was used to detect VF-associated genes including: (i) fimbriae and/or adhesins: fimH (type 1 fimbriae), mrkD (adhesion type 3 fimbriae), and cf29a (adhesion CF29K); (ii): toxins: ureA (urease synthesis); (iii) iron uptake: entB (siderophore), ybtS (yersiniabactin), kfu (iron transport and phosphotransferase function), and iutA (hydroxamate siderophore); (iv) protectins: magA (capsular serotype K1 and hypermucoviscosity phenotype), rmpA (regulator of mucoid phenotype A), kpsMII (group2 capsule), and the genes of capsular serotypes K5, K57, K54, and K20; and (v) others: allS (associated with allantoin metabolism), uge (uridine diphosphate galacturonate 4-epimerase), and wabG (core LPS biosynthesis) [51,52].
All carbapenemase-producing E. coli isolates were assigned to the phylogenetic groups (A, B1, B2, C, D, E, and F) by using multiplex PCR based on the method described by Clermont et al. [53]. E. coli isolates were also examined for the presence of genes encoding certain putative virulence determinants including papAH, papC, papEF, papG alleles I, II, III (encoding P fimbriae), sfaS/focG (S fimbriae and FIC fimbrae), afa/draBC (Dr family adhesin), fimH (mannose-specific adhesin subunit of type 1 fimbriae), hlyA (hemolysin), cnf1 (cytotoxic necrotizing factor-1), iutA (aerobactin siderophore receptor), kpsMTII and kpsMKI (capsule synthesis), traT (serum resistance-associated factor), malX (pathogenicity island marker from strain CFT073), iroN (iron siderophore receptor), and irp2 (yersiniabactin). ExPEC status (i.e., exhibition of ≥ 2 VF genes among the following VFs: pap, sfa/focDE, afa/draBC, iutA, and kpsMT2) was determined as previously described [54].

4.7. Plasmid Typing

Plasmid incompatibility groups were determined using Plasmid Relaxase gene Typing (PRaseT) [55]. This latter includes six different multiplex PCRs using primers targeting the most frequently encountered Relaxase genes in Enterobacterales. A simplex PCR was performed to target IncR [56].

5. Conclusions

In conclusion, this study highlighted the emergence of pan-drug-resistant Enterobacterales in Annaba University Hospital mainly mediated by blaOXA-48 and blaNDM-1 genes. It also described the first report of E. coli-producing blaNDM-1 genes in community-acquired infection in Algeria. These results corroborate the importance of the commitment of a multidisciplinary team and raise the urgency of the implementation of a nationwide surveillance program combating nosocomial and community infections caused by such multidrug-resistant bacteria and limiting their spread.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/antibiotics11060750/s1, Table S1: Antibiotic resistance profiles and phenotypic characteristics of carbapenemase-producing Enterobacterales isolates recovered in out- and in-patients at Annaba University Hospital, Algeria. Table S2: MICs values of carbapenems and colistin for the carbapenemase-producing Enterobacterales.

Author Contributions

Conceptualization, A.A., J.-P.L., and A.P.; methodology, A.A., N.D., J.-P.L. and A.P.; software, A.A. and A.P.; validation, J.-P.L. and A.P.; formal analysis, A.A. and N.D.; investigation, A.A., N.D. and A.P.; resources, A.A., N.D., L.L., S.N., W.C., D.G.-K. and M.D.; data curation, A.A., N.D. and A.P.; writing—original draft preparation, A.A., J.-P.L., and A.P.; writing—review and editing, N.D., L.L., S.N., W.C., D.G.-K. and M.D.; supervision, J.-P.L.; project administration, A.A. and A.P.; funding acquisition, J.-P.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We thank the Nîmes University Hospital for its structural, human, and financial support through the award obtained by our team during the internal call for tenders “Thématiques phares”.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Potter, R.F.; D’Souza, A.W.; Dantas, G. The rapid spread of carbapenem-resistant Enterobacteriaceae. Drug Resist. Updates 2016, 29, 30–46. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Bush, K.; Bradford, P.A. Epidemiology of β-lactamase-producing pathogens. Clin. Microbiol. Rev. 2020, 33, e00047-19. [Google Scholar] [CrossRef] [PubMed]
  3. Naas, T.; Vandel, L.; Sougakoff, W.; Livermore, D.M.; Nordmann, P. Cloning and sequence analysis of the gene for a carbapenem-hydrolyzing class A beta-lactamase, Sme-1, from Serratia marcescens S6. Antimicrob. Agents Chemother. 1994, 38, 1262–1270. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Iovleva, A.; Doi, Y. Carbapenem-Resistant Enterobacteriaceae. Clin. Lab. Med. 2017, 37, 303–315. [Google Scholar] [CrossRef]
  5. Mairi, A.; Pantel, A.; Sotto, A.; Lavigne, J.P.; Touati, A. OXA-48-like carbapenemases producing Enterobacteriaceae in different niches. Eur. J. Clin. Microbiol. Infect. Dis. 2018, 37, 587–604. [Google Scholar] [CrossRef]
  6. Wu, W.; Feng, Y.; Tang, G.; Qiao, F.; McNally, A.; Zong, Z. NDM metallo-beta-lactamases and their bacterial producers in health care settings. Clin. Microbiol. Rev. 2019, 32, e00115-18. [Google Scholar] [CrossRef] [Green Version]
  7. Touati, A.; Mairi, A. Carbapenemase-Producing Enterobacterales in Algeria: A Systematic Review. Microb. Drug Resist. 2020, 26, 475–482. [Google Scholar] [CrossRef]
  8. Cherak, Z.; Loucif, L.; Moussi, A.; Rolain, J.M. Carbapenemase-producing Gram-negative bacteria in aquatic environments: A review. J. Glob. Antimicrob. Resist. 2021, 25, 287–309. [Google Scholar] [CrossRef]
  9. Loucif, L.; Chelaghma, W.; Cherak, Z.; Bendjama, E.; Beroual, F.; Rolain, J.M. Detection of NDM-5 and MCR-1 antibiotic resistance encoding genes in Enterobacterales in long-distance migratory bird species Ciconia ciconia, Algeria. Sci. Total Environ. 2022, 814, 152861. [Google Scholar] [CrossRef]
  10. Brahmia, S.; Lalaoui, R.; Nedjai, S.; Djahmi, N.; Chettibi, S.; Rolain, J.M.; Bakour, S. First Clinical Cases of KPC-2-Producing Klebsiella pneumoniae ST258 in Algeria and Outbreak of Klebsiella pneumoniae ST101 Harboring blaOXA-48 Gene in the Urology Department of Annaba Hospital. Microb. Drug Resist. 2021, 27, 652–659. [Google Scholar] [CrossRef]
  11. Chaalal, N.; Touati, A.; Bakour, S.; Aissa, M.A.; Sotto, A.; Lavigne, J.P.; Pantel, A. Spread of OXA-48 and NDM-1-Producing Klebsiella pneumoniae ST48 and ST101 in Chicken Meat in Western Algeria. Microb. Drug Resist. 2021, 27, 492–500. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Abderrahim, A.; Djahmi, N.; Pujol, C.; Nedjai, S.; Bentakouk, M.C.; Kirane-Gacemi, D.; Dekhil, M.; Sotto, A.; Lavigne, J.P.; Pantel, A. First case of NDM-1-producing Klebsiella pneumoniae in Annaba University Hospital, Algeria. Microb. Drug Resist. 2017, 23, 895–900. [Google Scholar] [CrossRef] [PubMed]
  13. Yanat, B.; Rodriguez-Martinez, J.M.; Touati, A. Plasmid-mediated quinolone resistance in Enterobacteriaceae: A systematic review with a focus on Mediterranean countries. Eur. J. Clin. Microbiol. Infect. Dis. 2017, 36, 421–435. [Google Scholar] [CrossRef] [PubMed]
  14. Agabou, A.; Pantel, A.; Ouchenane, Z.; Lezzar, N.; Khemissi, S.; Satta, D.; Sotto, A.; Lavigne, J.P. First description of OXA-48-producing Escherichia coli and the pandemic clone ST131 from patients hospitalised at a military hospital in Algeria. Eur. J. Clin. Microbiol. Infect. Dis. 2014, 33, 1641–1646. [Google Scholar] [CrossRef] [PubMed]
  15. Belbel, Z.; Lalaoui, R.; Bakour, S.; Nedjai, S.; Djahmi, N.; Rolain, J.M. First report of colistin resistance in an OXA-48- and a CTX-M-15 producing Klebsiella pneumoniae clinical isolate in Algeria due to PmrB protein modification and mgrB inactivation. J. Glob. Antimicrob. Resist. 2018, 14, 158–160. [Google Scholar] [CrossRef]
  16. Bouguenoun, W.; Bakour, S.; Bentorki, A.A.; Al Bayssari, C.; Merad, T.; Rolain, J.M. Molecular epidemiology of environmental and clinical carbapenemase-producing Gram-negative bacilli from hospitals in Guelma, Algeria: Multiple genetic lineages and first report of OXA-48 in Enterobacter cloacae. J. Glob. Antimicrob. Resist. 2016, 7, 135–140. [Google Scholar] [CrossRef]
  17. Bourafa, N.; Chaalal, W.; Bakour, S.; Lalaoui, R.; Boutefnouchet, N.; Diene, S.M.; Rolain, J.M. Molecular characterization of carbapenem-resistant Gram-negative bacilli clinical isolates in Algeria. Infect. Drug Resist. 2018, 11, 735–742. [Google Scholar] [CrossRef] [Green Version]
  18. Cuzon, G.; Bentchouala, C.; Vogel, A.; Hery, M.; Lezzar, A.; Smati, F.; Dortet, L.; Naas, T. First outbreak of OXA-48-positive carbapenem-resistant Klebsiella pneumoniae isolates in Constantine, Algeria. Int. J. Antimicrob. Agents 2015, 46, 725–727. [Google Scholar] [CrossRef] [PubMed]
  19. Djahmi, N.; Dunyach-Remy, C.; Pantel, A.; Dekhil, M.; Sotto, A.; Lavigne, J.P. Epidemiology of carbapenemase-producing Enterobacteriaceae and Acinetobacter baumannii in Mediterranean countries. BioMed Res. Int. 2014, 2014, 305784. [Google Scholar] [CrossRef] [Green Version]
  20. Bachiri, T.; Bakour, S.; Lalaoui, R.; Belkebla, N.; Allouache, M.; Rolain, J.M.; Touati, A. Occurrence of carbapenemase-producing Enterobacteriaceae isolates in the wildlife: First report of OXA-48 in wild boars in Algeria. Microb. Drug Resist. 2018, 24, 337–345. [Google Scholar] [CrossRef]
  21. Bouaziz, A.; Loucif, L.; Ayachi, A.; Guehaz, K.; Bendjama, E.; Rolain, J.M. Migratory white stork (Ciconia ciconia): A potential vector of the OXA-48-producing Escherichia coli ST38 clone in Algeria. Microb. Drug Resist. 2018, 24, 461–468. [Google Scholar] [CrossRef]
  22. Yong, D.; Toleman, M.A.; Giske, C.G.; Cho, H.S.; Sundman, K.; Lee, K.; Walsh, T.R. Characterization of a new metallo-beta-lactamase gene, bla(NDM-1), and a novel erythromycin esterase gene carried on a unique genetic structure in Klebsiella pneumoniae sequence type 14 from India. Antimicrob. Agents Chemother. 2009, 53, 5046–5054. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Dortet, L.; Poirel, L.; Nordmann, P. Worldwide dissemination of the NDM-type carbapenemases in Gram-negative bacteria. BioMed Res. Int. 2014, 2014, 249856. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Loucif, L.; Kassah-Laouar, A.; Saidi, M.; Messala, A.; Chelaghma, W.; Rolain, J.M. Outbreak of OXA-48-producing Klebsiella pneumoniae involving a Sequence Type 101 clone in Batna University Hospital, Algeria. Antimicrob. Agents Chemother. 2016, 60, 7494–7497. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Gajamer, V.R.; Bhattacharjee, A.; Paul, D.; Deshamukhya, C.; Singh, A.K.; Pradhan, N.; Tiwari, H.K. Escherichia coli encoding bla(NDM-5) associated with community-acquired urinary tract infections with unusual MIC creep-like phenomenon against imipenem. J. Glob. Antimicrob. Resist. 2018, 14, 228–232. [Google Scholar] [CrossRef] [PubMed]
  26. Abd El Ghany, M.; Sharaf, H.; Al-Agamy, M.H.; Shibl, A.; Hill-Cawthorne, G.A.; Hong, P.Y. Genomic characterization of NDM-1 and 5, and OXA-181 carbapenemases in uropathogenic Escherichia coli isolates from Riyadh, Saudi Arabia. PLoS ONE 2018, 13, e0201613. [Google Scholar] [CrossRef]
  27. Paskova, V.; Medvecky, M.; Skalova, A.; Chudejova, K.; Bitar, I.; Jakubu, V.; Bergerova, T.; Zemlickova, H.; Papagiannitsis, C.C.; Hrabak, J. Characterization of NDM-encoding plasmids from Enterobacteriaceae recovered from Czech hospitals. Front. Microbiol. 2018, 9, 1549. [Google Scholar] [CrossRef]
  28. Cubero, M.; Cuervo, G.; Dominguez, M.A.; Tubau, F.; Marti, S.; Sevillano, E.; Gallego, L.; Ayats, J.; Pena, C.; Pujol, M.; et al. Carbapenem-resistant and carbapenem-susceptible isogenic isolates of Klebsiella pneumoniae ST101 causing infection in a tertiary hospital. BMC Microbiol. 2015, 15, 177. [Google Scholar] [CrossRef] [Green Version]
  29. Pitart, C.; Solé, M.; Roca, I.; Fàbrega, A.; Vila, J.; Marco, F. First outbreak of a plasmid-mediated carbapenem-hydrolyzing OXA-48 beta-lactamase in Klebsiella pneumoniae in Spain. Antimicrob. Agents Chemother. 2011, 55, 4398–4401. [Google Scholar] [CrossRef] [Green Version]
  30. Argente, M.; Miro, E.; Marti, C.; Vilamala, A.; Alonso-Tarres, C.; Ballester, F.; Calderon, A.; Galles, C.; Gasos, A.; Mirelis, B.; et al. Molecular characterization of OXA-48 carbapenemase-producing Klebsiella pneumoniae strains after a carbapenem resistance increase in Catalonia. Enferm. Infecc. Microbiol. Clin. 2019, 37, 82–88. [Google Scholar] [CrossRef]
  31. Gharout-Sait, A.; Alsharapy, S.A.; Brasme, L.; Touati, A.; Kermas, R.; Bakour, S.; Guillard, T.; de Champs, C. Enterobacteriaceae isolates carrying the New Delhi metallo-beta-lactamase gene in Yemen. J. Med. Microbiol. 2014, 63, 1316–1323. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Papagiannitsis, C.C.; Miriagou, V.; Giakkoupi, P.; Tzouvelekis, L.S.; Vatopoulos, A.C. Characterization of pKP1780, a novel IncR plasmid from the emerging Klebsiella pneumoniae ST147, encoding the VIM-1 metallo-β-lactamase. J. Antimicrob. Chemother. 2013, 68, 2259–2262. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Kaase, M.; Schimanski, S.; Schiller, R.; Beyreiss, B.; Thürmer, A.; Steinmann, J.; Kempf, V.A.; Hess, C.; Sobottka, I.; Fenner, I.; et al. Multicentre investigation of carbapenemase-producing Escherichia coli and Klebsiella pneumoniae in German hospitals. Int. J. Med. Microbiol. 2016, 306, 415–420. [Google Scholar] [CrossRef] [PubMed]
  34. Lahlaoui, H.; Poirel, L.; Barguellil, F.; Moussa, M.B.; Nordmann, P. Carbapenem-hydrolyzing class D beta-lactamase OXA-48 in Klebsiella pneumoniae isolates from Tunisia. Eur. J. Clin. Microbiol. Infect. Dis. 2012, 31, 937–939. [Google Scholar] [CrossRef] [PubMed]
  35. Zenati, K.; Sahli, F.; Garcia, V.; Bakour, S.; Belhadi, D.; Rolain, J.M.; Touati, A. Occurrence and clonal diversity of multidrug-resistant Klebsiella pneumoniae recovered from inanimate surfaces in Algerian hospital environment: First report of armA, qnrB and aac(6’)-Ib-cr genes. J. Glob. Antimicrob. Resist. 2017, 10, 148–153. [Google Scholar] [CrossRef]
  36. Yaici, L.; Haenni, M.; Métayer, V.; Saras, E.; Mesbah, Z.F.; Ayad, M.; Touati, A.; Madec, J.Y. Spread of ESBL/AmpC-producing Escherichia coli and Klebsiella pneumoniae in the community through ready-to-eat sandwiches in Algeria. Int. J. Food Microbiol. 2017, 245, 66–72. [Google Scholar] [CrossRef] [PubMed]
  37. Fasciana, T.; Gentile, B.; Aquilina, M.; Ciammaruconi, A.; Mascarella, C.; Anselmo, A.; Fortunato, A.; Fillo, S.; Petralito, G.; Lista, F.; et al. Co-existence of virulence factors and antibiotic resistance in new Klebsiella pneumoniae clones emerging in south of Italy. BMC Infect. Dis. 2019, 19, 928. [Google Scholar] [CrossRef] [Green Version]
  38. Obeng-Nkrumah, N.; Labi, A.K.; Blankson, H.; Awuah-Mensah, G.; Oduro-Mensah, D.; Anum, J.; Teye, J.; Kwashie, S.D.; Bako, E.; Ayeh-Kumi, P.F.; et al. Household cockroaches carry CTX-M-15-, OXA-48- and NDM-1-producing enterobacteria, and share beta-lactam resistance determinants with humans. BMC Microbiol. 2019, 19, 272. [Google Scholar] [CrossRef]
  39. Ortega-Paredes, D.; Barba, P.; Mena-López, S.; Espinel, N.; Zurita, J. Escherichia coli hyperepidemic clone ST410-A harboring bla(CTX-M-15) isolated from fresh vegetables in a municipal market in Quito-Ecuador. Int. J. Food Microbiol. 2018, 280, 41–45. [Google Scholar] [CrossRef]
  40. Báez, J.; Hernández-García, M.; Guamparito, C.; Díaz, S.; Olave, A.; Guerrero, K.; Cantón, R.; Baquero, F.; Gahona, J.; Valenzuela, N.; et al. Molecular characterization and genetic diversity of ESBL-producing Escherichia coli colonizing the migratory Franklin’s gulls (Leucophaeus pipixcan) in Antofagasta, North of Chile. Microb. Drug Resist. 2015, 21, 111–116. [Google Scholar] [CrossRef]
  41. Pitout, J.D.; Hanson, N.D.; Church, D.L.; Laupland, K.B. Population-based laboratory surveillance for Escherichia coli-producing extended-spectrum beta-lactamases: Importance of community isolates with blaCTX-M genes. Clin. Infect. Dis. 2004, 38, 1736–1741. [Google Scholar] [CrossRef] [Green Version]
  42. Poirel, L.; Walsh, T.R.; Cuvillier, V.; Nordmann, P. Multiplex PCR for detection of acquired carbapenemase genes. Diagn Microbiol. Infect. Dis. 2011, 70, 119–123. [Google Scholar] [CrossRef] [PubMed]
  43. Hidalgo, L.; Hopkins, K.L.; Gutierrez, B.; Ovejero, C.M.; Shukla, S.; Douthwaite, S.; Prasad, K.N.; Woodford, N.; Gonzalez-Zorn, B. Association of the novel aminoglycoside resistance determinant RmtF with NDM carbapenemase in Enterobacteriaceae isolated in India and the UK. J. Antimicrob. Chemother. 2013, 68, 1543–1550. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Huang, J.; Ye, M.; Jia, X.; Yu, F.; Wang, M. Coexistence of armA and genes encoding aminoglycoside-modifying enzymes in Acinetobacter baumannii. Afr. J. Microbiol. Res. 2012, 6, 5325–5330. [Google Scholar]
  45. Jakobsen, L.; Sandvang, D.; Hansen, L.H.; Bagger-Skjot, L.; Westh, H.; Jorgensen, C.; Hansen, D.S.; Pedersen, B.M.; Monnet, D.L.; Frimodt-Moller, N.; et al. Characterisation, dissemination and persistence of gentamicin resistant Escherichia coli from a Danish university hospital to the waste water environment. Environ. Int. 2008, 34, 108–115. [Google Scholar] [CrossRef]
  46. Noppe-Leclercq, I.; Wallet, F.; Haentjens, S.; Courcol, R.; Simonet, M. PCR detection of aminoglycoside resistance genes: A rapid molecular typing method for Acinetobacter baumannii. Res. Microbiol. 1999, 150, 317–322. [Google Scholar] [CrossRef]
  47. Cattoir, V.; Poirel, L.; Rotimi, V.; Soussy, C.J.; Nordmann, P. Multiplex PCR for detection of plasmid-mediated quinolone resistance qnr genes in ESBL-producing enterobacterial isolates. J. Antimicrob. Chemother. 2007, 60, 394–397. [Google Scholar] [CrossRef] [Green Version]
  48. Kim, H.B.; Wang, M.; Park, C.H.; Kim, E.C.; Jacoby, G.A.; Hooper, D.C. oqxAB encoding a multidrug efflux pump in human clinical isolates of Enterobacteriaceae. Antimicrob. Agents Chemother. 2009, 53, 3582–3584. [Google Scholar] [CrossRef] [Green Version]
  49. Park, C.H.; Robicsek, A.; Jacoby, G.A.; Sahm, D.; Hooper, D.C. Prevalence in the United States of aac(6′)-Ib-cr encoding a ciprofloxacin-modifying enzyme. Antimicrob. Agents Chemother. 2006, 50, 3953–3955. [Google Scholar] [CrossRef] [Green Version]
  50. Yamane, K.; Wachino, J.; Suzuki, S.; Arakawa, Y. Plasmid-mediated qepA gene among Escherichia coli clinical isolates from Japan. Antimicrob. Agents Chemother. 2008, 52, 1564–1566. [Google Scholar] [CrossRef] [Green Version]
  51. Compain, F.; Babosan, A.; Brisse, S.; Genel, N.; Audo, J.; Ailloud, F.; Kassis-Chikhani, N.; Arlet, G.; Decre, D. Multiplex PCR for detection of seven virulence factors and K1/K2 capsular serotypes of Klebsiella pneumoniae. J. Clin. Microbiol. 2014, 52, 4377–4380. [Google Scholar] [CrossRef] [Green Version]
  52. Turton, J.F.; Perry, C.; Elgohari, S.; Hampton, C.V. PCR characterization and typing of Klebsiella pneumoniae using capsular type-specific, variable number tandem repeat and virulence gene targets. J. Med. Microbiol. 2010, 59, 541–547. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Clermont, O.; Christenson, J.K.; Denamur, E.; Gordon, D.M. The Clermont Escherichia coli phylo-typing method revisited: Improvement of specificity and detection of new phylo-groups. Environ. Microbiol. Rep. 2013, 5, 58–65. [Google Scholar] [CrossRef] [PubMed]
  54. Johnson, J.R.; Stell, A.L. Extended virulence genotypes of Escherichia coli strains from patients with urosepsis in relation to phylogeny and host compromise. J. Infect. Dis. 2000, 181, 261–272. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Compain, F.; Poisson, A.; Le Hello, S.; Branger, C.; Weill, F.X.; Arlet, G.; Decre, D. Targeting relaxase genes for classification of the predominant plasmids in Enterobacteriaceae. Int. J. Med. Microbiol. 2014, 304, 236–242. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Garcia-Fernandez, A.; Fortini, D.; Veldman, K.; Mevius, D.; Carattoli, A. Characterization of plasmids harbouring qnrS1, qnrB2 and qnrB19 genes in Salmonella. J. Antimicrob. Chemother. 2009, 63, 274–281. [Google Scholar] [CrossRef]
Antibiotics 11 00750 g001 550
Figure 1. Dendrogram of NDM-1- and OXA-48-producing Klebsiella pneumoniae isolates. Red line corresponds to the limit of the clonality recommended by the manufacturer.
Figure 1. Dendrogram of NDM-1- and OXA-48-producing Klebsiella pneumoniae isolates. Red line corresponds to the limit of the clonality recommended by the manufacturer.
Antibiotics 11 00750 g001
Antibiotics 11 00750 g002 550
Figure 2. Dendrogram of NDM-1- and OXA-48-producing Escherichia coli isolates. Red line corresponds to the limit of the clonality recommended by the manufacturer.
Figure 2. Dendrogram of NDM-1- and OXA-48-producing Escherichia coli isolates. Red line corresponds to the limit of the clonality recommended by the manufacturer.
Antibiotics 11 00750 g002
Table
Table 1. Clinical features of carbapenemase-producing isolates obtained in this study.
Table 1. Clinical features of carbapenemase-producing isolates obtained in this study.
IsolatesSpeciesCarbapenemase GenesAdditional Antibiotic
Resistance Genes		Sequence TypeVirulence GenesPhylogenetic Groups
(E. coli)		Plasmid Type
2490K. pneumoniaeblaOXA-48qnrB, qnrS, oqxABST48ybtS, mrkD, entB, ugeF, wabG, ureA, fimHNA *IncM, IncR, MobC11
859K. pneumoniaeblaOXA-48blaCTX-M-15, qnrB, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, ugeF, wabG, ureA, fimH, kfuNAIncM, MobQu
2578BK. pneumoniaeblaOXA-48qnrB, oqxABST113mrkD, entB, ugeF, wabG, ureA, fimHNAIncM
19M3K. pneumoniaeblaNDM-1qnrB, aac(6′)-Ib-cr, oqxAB, aac(3)-IIST147ybtS, mrkD, entB, ugeF, wabG, ureA, fimHNAIncR
19VK. pneumoniaeblaNDM-1blaCTX-M-15, qnrB, oqxABaac(6′)-Ib-cr, aac(3)-IIST147ybtS, mrkD, entB, ugeF, wabG, ureA, fimHNAIncR
27K. pneumoniaeblaOXA-48blaCTX-M-15, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, colE NT2
57K. pneumoniaeblaOXA-48blaCTX-M-15, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST147ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, IncR FIIK
51AK. pneumoniaeblaOXA-48blaCTX-M-15, oqxAB, aac(6′)-Ib-cr, rmtBST147ybtS, mrkD, entB, iutA, ugeF, wabG, ureA, fimHNAIncM, FIIK, FV, IncAC, X3
51BK. pneumoniaeblaOXA-48blaCTX-M-15, qnrB, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST405ybtS, mrkD, entB, ugeF, ureA, fimHNAIncM, FIIK
58AK. pneumoniaeblaOXA-48blaCTX-M-15, oqxAB, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, colE NT1, colE NT2
6K. pneumoniaeblaOXA-48blaCTX-M-15, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, ureA, fimHNAIncM, IncR, colE NT2
Z6K. pneumoniaeblaOXA-48qnrS, oqxABST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z7K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-II, ant(2″)ST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z9K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z11K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z12K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-crST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z13K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z14K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z15K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z16K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrB, qnrS, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, colE NT2
Z21K. pneumoniaeblaOXA-48blaCTX-M-15, qnrA, qnrS, oqxAB, aac(6′)-Ib-crST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, MobQu
Z23K. pneumoniaeblaOXA-48blaCTX-M-15, oqxAB, aac(6′)-Ib-cr, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, MobQu
Z33K. pneumoniaeblaOXA-48qnrA, qnrS, oqxAB, aac(3)-IIST101ybtS, mrkD, entB, kfu, ugeF, wabG, ureA, fimHNAIncM, FIIK, MobQu
2578AE. cloacaeblaOXA-48blaCTX-M-9, qnrBST68NANAIncM, colE NT2
30E. coliblaOXA-48aac(6′)-Ib-crST758traT, fimHB1IncM, AC, FV, colE NT1
58BE. coliblaOXA-48blaCTX-M-15, aac(6′)-Ib-crST759traT, fimH, iutAEIncM, colE NT1, colE NT2, IncAC, FV, X3
56E. coliblaNDM-1blaCTX-M-15, aac(6′)-Ib-cr, rmtBST759traT, fimH, hlyAEcolE NT2, FV, X3
Z18E. coliblaOXA-48aac(3)-IIST834traT, fimH, hlyAAIncM, FV, X3
Z27E. coliblaOXA-48blaCTX-M-15, aac(6′)-Ib-cr, aac(3)-IIST44traT, fimH, hlyA, irp2, malX, papAH, papC, iutA, papG2, kpsMT2EIncM, FV
* NA, not applicable.
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Abderrahim, A.; Djahmi, N.; Loucif, L.; Nedjai, S.; Chelaghma, W.; Gameci-Kirane, D.; Dekhil, M.; Lavigne, J.-P.; Pantel, A. Dissemination of OXA-48- and NDM-1-Producing Enterobacterales Isolates in an Algerian Hospital. Antibiotics 2022, 11, 750. https://doi.org/10.3390/antibiotics11060750

AMA Style

Abderrahim A, Djahmi N, Loucif L, Nedjai S, Chelaghma W, Gameci-Kirane D, Dekhil M, Lavigne J-P, Pantel A. Dissemination of OXA-48- and NDM-1-Producing Enterobacterales Isolates in an Algerian Hospital. Antibiotics. 2022; 11(6):750. https://doi.org/10.3390/antibiotics11060750

Chicago/Turabian Style

Abderrahim, Amel, Nassima Djahmi, Lotfi Loucif, Sabrina Nedjai, Widad Chelaghma, Djamila Gameci-Kirane, Mazouz Dekhil, Jean-Philippe Lavigne, and Alix Pantel. 2022. "Dissemination of OXA-48- and NDM-1-Producing Enterobacterales Isolates in an Algerian Hospital" Antibiotics 11, no. 6: 750. https://doi.org/10.3390/antibiotics11060750

APA Style

Abderrahim, A., Djahmi, N., Loucif, L., Nedjai, S., Chelaghma, W., Gameci-Kirane, D., Dekhil, M., Lavigne, J. -P., & Pantel, A. (2022). Dissemination of OXA-48- and NDM-1-Producing Enterobacterales Isolates in an Algerian Hospital. Antibiotics, 11(6), 750. https://doi.org/10.3390/antibiotics11060750

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