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The emergence of a novel sequence type of MDR Acinetobacter baumannii from the intensive care unit of an Egyptian tertiary care hospital
https://doi.org/10.1186/s12941-017-0208-y
© The Author(s) 2017
- Received: 14 December 2016
- Accepted: 12 April 2017
- Published: 10 May 2017
Abstract
Background and aim of work
Acinetobacter baumannii is known for nosocomial outbreaks worldwide. In this study, we aimed to investigate the antibiotic susceptibility patterns and the clonal relationship of A. baumannii isolates from the intensive care unit (ICU) of an Egyptian hospital.
Methods
In the present study, 50 clinical isolates of multidrug resistant (MDR)-A. baumannii were obtained from patients admitted into the ICU from June to December 2015. All isolates were analyzed for antimicrobial susceptibilities. Multiplex PCR was performed to detect genes encoding oxacillinase genes (bla OXA-51-like, bla OXA-23-like, bla OXA-24-like, and bla OXA-58-like). Multilocus sequence typing (MLST) based on the seven-gene scheme (gltA, gyrB, gdhB, recA, cpn60, gpi, rpoD) was used to examine these isolates.
Results
All A. baumannii clinical isolates showed the same resistance pattern, characterized by resistance to most common antibiotics including imipenem (MIC ≥ 8μ/mL), with the only exception being colistin. Most isolates were positive for bla OXA-51-like and bla OXA-23-like (100 and 96%, respectively); however, bla OXA-24-like and bla OXA-58-like were not detected. MLST analysis identified different sequence types (ST195, ST208, ST231, ST441, ST499, and ST723) and a new sequence type (ST13929) with other sporadic strains.
Conclusions
MDR A. baumannii strains harboring bla OXA-23-like genes were widely circulating in this ICU. MLST was a powerful tool for identifying and epidemiologically typing our strains. Strict infection control measures must be implemented to contain the worldwide spread of MDR A. baumannii in ICUs.
Keywords
- MDR- A. baumannii
- bla OXA-23-like
- MLST
Background
The clinical care of intensive care unit (ICU) patients with infections has been complicated by the emergence and spread of extremely drug-resistant (XDR) Acinetobacter baumannii strains [1]. Due to scarce current therapeutic options; higher infection rates; poor patient outcomes because of life-threatening infections, including ventilator-related pneumonia, sepsis, urinary tract infections, and skin and soft tissue disorders may occur [1, 2].
Extensively drug-resistant (XDR) A. baumannii strains exhibiting resistance to three or more antibiotic classes, except for polymyxins, have been recently described in nosocomial outbreaks [2, 3]. The essential role of A. baumannii resistance to carbapenems, is mediated by oxacillinases (OXA-class D) and, less frequently, by metallo-β-lactamases (MBL-class B) [4, 5]. The class D carbapenemases are the most predominant carbapenemases in A. baumannii. They are categorized into six subclasses: intrinsic chromosomal OXA-51-like, the acquired OXA-23-like, OXA-24/40-like, OXA-58-like, OXA-143-like, and OXA-235-like β-lactamases [6]. In this study, we aimed to investigate the antimicrobial susceptibility, class D carbapenemases and clonal relationship of A. baumannii strains isolated from a tertiary care hospital ICU in Egypt.
Methods
The study was carried out in EL Sheikh Zayed hospital which provides tertiary care from specialists and consultants after referral (in orthopedic, trauma, neuro/spine surgeries) from primary care and secondary care hospitals in Egypt. A lab-based surveillance was performed over a period of 6 months (June–December 2015) after the isolation of five MDR A. baumannii strains in a period of 1 week showing the same phenotypic characteristics.
Bacterial strains
All clinical samples of the patients admitted during the above-mentioned period were processed at the microbiology unit. All samples were cultured on blood agar and MacConkey agar (Oxoid Co. England). All culture plates were incubated aerobically at 35 °C for 24–48 h. Identification of isolated organisms was performed by conventional biochemical reactions. During the experimental period, 50 A. baumannii non-duplicate strains were isolated.
Antimicrobial susceptibility testing
Susceptibility testing was performed by the disc diffusion method (Modified Kirby-Bauer technique) using Mueller–Hinton agar and aerobic incubation at 35 °C for 16–18 h. Antimicrobial discs containing imipenem (10 μg), meropenem (10 μg), gentamicin (10 μg), ciprofloxacin (5 μg), amikacin (30 μg), cotrimoxazole (25 μg), cefepime (30 μg), cefotaxime (30 μg), cefotaxime/clavulanic acid (30/10 μg), aztreonam (30 μg), ceftazidime (30 μg), ceftazidime/clavulanic acid (30/10 μg), amoxicillin/clavulanic acid (20/10 μg), and cefoxitin (30 μg) were obtained from Oxoid Co. (Oxoid Limited, Basingstoke, Hampshire, England) [7].
Multidrug resistance was defined in this analysis as resistance to three or more representatives of the following classes of antibiotics: fluoroquinolones, extended-spectrum cephalosporins, aminoglycosides, and carbapenems [8].
Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, and Staphylococcus aureus ATCC 29213 were used as reference strains for susceptibility testing per Clinical and Laboratory Standards Institute (CLSI, 2015) guidelines and interpretations [7].
Minimum inhibitory concentrations (MICs) were determined by broth microdilution and interpreted using CLSI, 2015 guidelines [7].
The presence of A. baumannii genes encoding oxacillinases (bla OXA-23-like, bla OXA-24-like, bla OXA-51-like, and bla OXA-58-like) was assessed in all 50 isolates using multiplex PCR.
Multiplex PCR assay
The sequences of bla OXA alleles encoding carbapenemases were aligned and group-specific regions were identified using BioEdit software (http://www.mbio.ncsu.edu/BioEdit/bioedit.html). The primers: 5′-TAA TGC TTT GATCGG CCT TG and 5′-TGG ATT GCA CTT CAT CTT GG were used to amplify a 353 bp fragment of genes encoding the intrinsic OXA-51-like enzymes of A. baumannii [9].
A set of primers were designed to amplify OXA-23-like genes (501 bp: 5′-GAT CGG ATT GGA GAA CCAGA and 5′-ATT TCT GAC CGC ATT TCC AT), OXA-24-like genes (246 bp: 5′-GGT TAG TTG GCC CCC TTA AA and 5′-AGT TGA GCG AAA AGG GGA TT), and OXA-58-like genes (599 bp: 5′-AAG TAT TGG GGC TTG TGC TG and 5′-CCCCTCTGCGCTCTACATAC) [9]. The primers were evaluated separately against control strains and then in a multiplex format. The amplification conditions were: initial denaturation at 94 °C for 5 min, 30 cycles of 94 °C for 25 s, 52 °C for 40 s, and 72 °C for 50 s, and a final elongation at 72 °C for 6 min [9].
Multilocus sequence typing
MLST analysis was performed per the protocol of the Pasteur Institute. Fragments of seven internal housekeeping genes (gltA, gyrB, gdhB, recA, cpn60, gpi, and rpoD) were amplified and sequenced as previously described [10]. Briefly, PCR amplifications were performed with a MasterCycler Nexus (Eppendorf, Hamburg, Germany) with an initial denaturation at 94 °C for 5 min, followed by 35 cycles of denaturation at 94 °C for 1 min, annealing at 55 °C for 1 min, and extension at 72 °C for 2 min, and a 4-min final extension at 72 °C. The amplicons were verified by agarose gel electrophoresis and were subsequently purified for bidirectional Sanger sequencing reactions. Multiple allele sequences were assigned for each locus with an arbitrary allele number to obtain characterization of sequence types (STs) for each A. baumannii isolate. Each sequence was compared with sequences deposited in the Institute of Pasteur MLST schema (http://pubmlst.org/perl/bigsdb/bigsdb.pl?db=pubmlst_abaumannii_pasteur_seqdef).
Results
Patient’s data
Age (mean ± SD) | Sex % | APACHE % | Length of stay (mean ± SD) | More than one device inserted % | |||
|---|---|---|---|---|---|---|---|
Male | Female | <15% | >15% | ||||
VAP | (42.62 ± 17.63) | 72% | 28% | 40% | 60% | (48.96 ± 77.3) | (100%) |
CLABSI | (41 ± 23.4) | 88.8% | 11.1% | 33.3% | 66.6% | (22.33 ± 11.4) | (55.55%) |
CAUTI | (44.53 ± 22.1) | 76.9% | 23.0% | 38.4% | 61.5% | (82.307 ± 67.8) | (100%) |
P value | 0.900 | 0.535 | 0.880 | 0.131 | 0.00 | ||
Results of multiplex PCR for detection of bla OXA-51-like, bla OXA-23-like, bla OXA-24-like, and bla OXA-58-like genes. Lane 1 100 bp DNA Ladder, Lane 2 positive control, Lanes 3–6 A. baumannii clinical isolates showing bla OXA-51-like and bla OXA-23-like positivity (353 and 501 bp, respectively). bla OXA-24-like and bla OXA-58-like were not detected at (246 and 599 bp) respectively. Lane 7 negative control
Sequence types (STs), allele profiles of 50 carbapenem-resistant A. baumannii isolates, carbapenem-hydrolyzing class D β-lactamase genes, minimum inhibitory concentration (MIC), site of isolation and patient outcome
Sample ID | Site of isolation | Allele profile | ST | Carbapenem-hydrolyzing class D β-lactamase genes | MIC R ≥ 8 (mg/L) | Patient outcome | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
gltA | gyrB | gdhB | recA | cpn60 | gpi | rpoD | bla OXA-51 | bla OXA-23 | bla OXA-24 | bla OXA-58 | IMI | |||||
A. baumannii | 21 | ETA | 1 | 3 | 3 | 2 | 2 | 96 | 3 | 195 | + | + | − | − | 25 | Deceased |
A. baumannii | 22 | ETA | 1 | 3 | 3 | 2 | 2 | 96 | 3 | 195 | + | + | – | – | 20 | Deceased |
A. baumannii | 30 | ETA | 1 | 3 | 3 | 2 | 2 | 97 | 3 | 208 | + | + | – | – | 25 | Deceased |
A. baumannii | 33 | ETA | 1 | 3 | No gene | 2 | 2 | 97 | 3 | NA | + | + | – | – | 25 | Deceased |
A. baumannii | 34 | ETA | 1 | 3 | 3 | 2 | 2 | 97 | 3 | 208 | + | – | – | – | 35 | Deceased |
A. baumannii | 36 | ETA | 1 | 3 | 3 | 2 | 2 | 97 | 3 | 208 | + | + | – | – | 20 | Deceased |
A. baumannii | 37 | ETA | 1 | 3 | 3 | 2 | 2 | 97 | 3 | 208 | + | + | – | – | 30 | Deceased |
A. baumannii | 44 | Blood | 1 | 3 | 3 | 2 | 2 | 97 | 3 | 208 | + | + | – | – | 25 | Deceased |
A. baumannii | 46 | Urine | 1 | 3 | 3 | 2 | 2 | 97 | 3 | 208 | + | + | – | – | 25 | Deceased |
A. baumannii | 47 | Urine | 1 | 3 | No gene | 2 | 2 | 97 | 3 | NA | + | + | – | – | 30 | Discharged |
A. baumannii | 49 | Urine | 1 | 3 | 3 | 2 | 2 | 96 | 3 | 195 | + | + | – | – | 25 | Deceased |
A. baumannii | 5 | ETA | 1 | 12 | 3 | 2 | 2 | 79 | 3 | 1114 | + | + | – | – | 20 | Deceased |
A. baumannii | 29 | ETA | 1 | 87 | 3 | 2 | 2 | 96 | 3 | 13929a | + | + | – | – | 20 | Discharged |
A. baumannii | 24 | ETA | 1 | 107 | 12 | 10 | 23 | 195 | 26 | 723 | + | + | – | – | 25 | Deceased |
A. baumannii | 25 | ETA | 1 | 107 | 12 | 10 | 23 | 195 | 26 | 723 | + | + | – | – | 25 | Deceased |
A. baumannii | 38 | ETA | 1 | 107 | 12 | 10 | 23 | 195 | 26 | 723 | + | + | – | – | 30 | Deceased |
A. baumannii | 48 | urine | 1 | 107 | 12 | 10 | 23 | 195 | 26 | 723 | + | + | – | – | 25 | Deceased |
A. baumannii | 1 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 30 | Deceased |
A. baumannii | 3 | ETA | 10 | 12 | 4 | 11 | 4 | 79 | 5 | 945 | + | + | – | – | 15 | Deceased |
A. baumannii | 4 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 35 | Discharged |
A. baumannii | 8 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 35 | Deceased |
A. baumannii | 11 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 20 | Deceased |
A. baumannii | 14 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 20 | Deceased |
A. baumannii | 16 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 25 | Discharged |
A. baumanii | 18 | ETA | 10 | 12 | No gene | 11 | 4 | 98 | 5 | NA | + | + | – | – | 20 | Deceased |
A. baumanii | 19 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 20 | Deceased |
A. baumannii | 20 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 20 | Deceased |
A. baumannii | 23 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 15 | Deceased |
A. baumannii | 26 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 25 | Deceased |
A. baumannii | 27 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 20 | Deceased |
A. baumannii | 28 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 20 | Deceased |
A. baumannii | 31 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 25 | Deceased |
A. baumannii | 32 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 20 | Deceased |
A. baumannii | 35 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 25 | Deceased |
A. baumannii | 40 | ETA | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 25 | Deceased |
A. baumannii | 41 | Blood | 10 | 12 | 4 | 11 | 4 | 100 | 5 | 441 | + | + | – | – | 25 | Discharged |
A. baumannii | 45 | ETA | 10 | 12 | 4 | 11 | 4 | 98 | 5 | 231 | + | + | – | – | 20 | Deceased |
A. baumannii | 12 | ETA | 12 | 17 | 12 | 1 | 29 | 102 | 39 | 236 | + | + | – | – | 35 | Deceased |
A. baumannii | 17 | ETA | 12 | 17 | 12 | 1 | 29 | 102 | 39 | 236 | + | + | – | – | 35 | Deceased |
A. baumannii | 2 | ETA | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 20 | Discharged |
A. baumannii | 6 | ETA | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 25 | Deceased |
A. baumannii | 7 | ETA | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 20 | Deceased |
A. baumannii | 13 | ETA | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 15 | Deceased |
A. baumannii | 15 | ETA | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 15 | Deceased |
A. baumannii | 39 | ETA | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 35 | Deceased |
A. baumannii | 42 | Blood | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 25 | Deceased |
A. baumannii | 50 | Swab | 24 | 92 | 96 | 11 | 49 | 162 | 26 | 499 | + | + | – | – | 20 | Deceased |
A. baumannii | 43 | Blood | 28 | 38 | 45 | 1 | 16 | 66 | 2 | 1089 | + | – | – | – | 25 | Deceased |
A. baumannii | 9 | ETA | 44 | 73 | No gene | 11 | 44 | ‡ | 4 | NA | + | + | – | – | 40 | Deceased |
A. baumannii | 10 | ETA | 44 | 73 | No gene | 11 | 44 | ‡ | 4 | NA | + | + | – | – | 20 | Discharged |
Phylogenetic tree of 50 A. baumannii strains built based on the maximum likelihood algorithm in the MEGA6 software [11] and the concatenated alleles of seven housekeeping genes with bootstrap values. The phylogenetic analysis identified ST195, ST208, ST231, ST441, ST499, and ST723 and the new sequence type ST13929. The numbers in the branches depict the sample ID of A. baumannii
Discussion
MDR A. baumannii is a problematic, multidrug-resistant pathogen identified in healthcare settings worldwide, especially in ICUs [12]. A. baumannii has a notable ability to capture and express resistance genes. All resistance mechanisms including target modification, efflux pump expression, and enzymatic inactivation have been described in A. baumannii [13].
In the current study, five MDR A. baumannii strains were isolated over 1 week from the same ICU. All isolates showed the same phenotypic characteristics which prompted us to start a survey study of the antimicrobial susceptibility and clonal relationship of A. baumannii strains isolated from this ICU.
All our isolates were resistant to imipenem. The main role of the A. baumannii resistance to carbapenems is mediated by oxacillinases and, less frequently, by metallo-β-lactamases [4, 5].
bla OXA-23-like, bla OXA-24/40-like, and bla OXA-58-like genes have been repetitively reported in A. baumannii outbreaks from diverse parts of the world. The localization of numerous β-lactamase genes on plasmids facilitates their horizontal mobilization from one bacterium to another [13, 14].
All our isolates harbored the bla OXA-51-like gene, which is ubiquitous in A. baumannii [15]. bla OXA-23 was the most universally identified gene, while bla OXA-24-like and bla OXA-58-like genes were not detected in any strain. bla OXA-23 is the most prevalent carbapenemase-encoding gene in the Mediterranean region. This might be explained by the higher carbapenemase activity of bla OXA-23 and/or acquisition of carbapenem resistance through horizontal gene transfer [16–18]. The bla OXA-23 gene was either encoded on the chromosome or on plasmids and was associated with four dissimilar genetic structures, with the most common being transposons Tn2006. bla OXA-23 has been reported in different regions of the Middle East, The United Arab Emirates, Algeria, Libya, Bahrain, and recently, Qatar [16, 19].
Mugnier et al. found an isolate from Egypt harboring plasmid containing bla OXA-23. This finding might indicate the prevalence of the genetic environment of bla OXA-23 in Egyptian isolates [16]. Moreover, a recent study including three Egyptian hospitals revealed the emergence and spread of bla NDM-1 and bla OXA-23 in addition to the co-occurrence of 16S rRNA methylase armA with bla NDM-1 and bla OXA-23 in 27 distinct sequence types, 11 of which were novel among A. baumannii clinical isolates [20].
Per MLST results, ST195, ST208, ST231, ST441, ST499, and ST723 were the most prevalent isolates. Another Egyptian study illustrated the large diversity found within the strains where ten distinct sequence types (STs) were identified, ST408–ST414, ST331, ST108, and ST208 [21]. However, a study showed that the most prevalent sequence types in the gulf area were ST195, ST208, ST229, ST436, ST450, ST452, and ST499 [22].
Taking into consideration that ST208 is the ancestor strain of several STs including ST89, ST88, ST190, ST225, and ST75, it has been identified in different parts of the world such as Japan, China, Thailand, Korea, Italy, Australia, Portugal, and the Czech Republic [23].
In conclusion, MDR A. baumannii strains harboring the bla OXA 23-like gene were widely circulating in our ICU. MLST provided us with a powerful tool for identifying and epidemiologically typing our strains. Studying the epidemiology of HAIs is urgent to prevent the clonal dissemination of antibiotic-resistant pathogens, not only in hospital settings, but in the community, as well. Strict infection control measures and antimicrobial stewardship programs are necessary to contain the worldwide spread of MDR A. baumannii. Proving the clonal relation between clinical isolates emphasizes the importance of surveillance programs and strict IC measures that would influence decision-making and health policy.
Declarations
Authors’ contributions
DG, and MA conceived and designed the study, carried out the collection of the bacterial strains, participated in antibiotic sensitivity and molecular genetic studies. DG drafted the manuscript. MZ participated in antibiotic sensitivity, and MHA. EA and RB carried out the MLST and participated in the design of the study. OA participated in the antimicrobial sensitivity testing and multiplex PCR. All authors read and approved the final manuscript.
Acknowledgements
The authors extend their appreciation to the Deanship of Scientific Research at King Saud University for funding the study through research group project no. RGP-038.
Competing interests
The authors declare that they have no competing interests.
Availability of data and materials
The raw data of this research can be made available to the interested researchers if requested.
Ethics approval
Ethical Committee of faculty of medicine, Cairo University approved the study and a written informed consent was not obtained from patients because the bacterial isolates studied were collected from the routine work of microbiology laboratory for patient care and no additional clinical specimens were collected for the study. It is a standard practice not to get written informed consent for use of bacterial isolates unlinked to patient identity from the routine clinical laboratory.
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Authors’ Affiliations
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