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Article

Prevalence and Characterization of Integrons in Multidrug Resistant Acinetobacter baumannii in Eastern China: A Multiple-Hospital Study

by
Jing Chen
1,2,
Hong Li
3,
Jinsong Yang
4,
Rong Zhan
1,
Aiping Chen
4 and
Yansheng Yan
2,4,*
1
Fujian Medical University Union Hospital, No. 29 Xinquan Road, Fuzhou 350001, China
2
School of Public Health, Fujian Medical University, No.1 Xueyuan Road, Shangjie Town, Minhou County, Fuzhou 350108, China
3
Department of Pharmaceuticals, Fujian Health College, No. 366 Guankou Road, Jingxi Town, Minhou County, Fuzhou 350101, China
4
Fujian Center for Disease Control and Prevention, 76 Jintai Road, Fuzhou 350001, China
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2015, 12(8), 10093-10105; https://doi.org/10.3390/ijerph120810093
Submission received: 26 June 2015 / Revised: 6 August 2015 / Accepted: 19 August 2015 / Published: 21 August 2015
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Abstract

:
Objective: The aim of this multiple-hospital study was to investigate the prevalence of integrons in multidrug-resistant Acinetobacter baumannii (MDRAB) in Eastern China, and characterize the integron-integrase genes, so as to provide evidence for the management and appropriate antibiotic use of MDRAB infections. Methods: A total of 425 clinical isolates of A. baumannii were collected from 16 tertiary hospitals in 11 cities of four provinces (Fujian, Jiangsu, Zhejiang and Shandong) from January 2009 to June 2012. The susceptibility of A. baumannii isolates to ampicillin/sulbactam, piperacillin/tazobactam, ceftazidime, ceftriaxone, cefepime, aztreonam, meropenem, amikacin, gentamicin, tobramycin, ciprofloxacin, levofloxacin, sulfamethoxazole/trimenthoprim, minocycline and imipenem was tested, and integrons and their gene cassettes were characterized in these isolates using PCR assay. In addition, integron-positive A. baumannii isolates were genotyped using pulsed-field gel electrophoresis (PFGE) assay, and intI1 gene cassette was sequenced. Results: intI1 gene was carried in 69.6% of total A. baumannii isolates, while intI2 and intI3 genes were not detected. The prevalence of resistance to ampicillin/sulbactam, piperacillin/tazobactam, ceftazidime, ceftriaxone, cefepime, aztreonam, imipenem, meropenem, amikacin, gentamicin, tobramycin, ciprofloxacin, levofloxacin and sulfamethoxazole/trimenthoprim was significantly higher in integron-positive A. baumannii isolates than in negative isolates (all p values <0.05), while no significant difference was observed in the prevalence of minocycline resistance (p > 0.05). PFGE assay revealed 27 PFGE genotypes and 4 predominant genotypes, P1, P4, P7 and P19. The PFGE genotype P1 contained 13 extensive-drug resistant and 89 non-extensive-drug resistant A. baumannii isolates, while the genotype P4 contained 34 extensive-drug resistant and 67 non-extensive-drug resistant isolates, appearing a significant antimicrobial resistance pattern (both p values <0.05). Sequencing analysis revealed two gene cassette assays of aacA4-catB8-aadA1 and dfrXII-orfF-aadA2 in MDRAB isolates. Conclusions: The results of this study demonstrate a high prevalence of class 1 integrons in MDRAB in Eastern China, and a greater prevalence of antimicrobial resistance in intI1 gene-positive MDRAB isolates than in negative isolates. Four predominant PFGE genotypes are identified in intI1 gene-positive MDRAB isolates, in which P4 is an epidemic PFGE genotype in Fujian Province, and it has a high proportion of extensive drug resistant A. baumannii. The gene cassette dfrXII-orfF-aadA2 is reported, for the first time, in A. baumannii strains isolated from Fujian Province, Eastern China.

1. Introduction

As a common opportunistic bacterial pathogen of hospital-acquired infections, Acinetobacter baumannii has a high ability to acquire resistance to multiple antibiotics and clonal spread [1,2,3]. Multiple-, extensive- or extreme-drug resistant A. baumannii is reported worldwide, and the outbreaks of infection with drug resistant strains have become a serious threat to global public health [4,5,6,7]. Integron is a specific integration and exercise system that allows the capture of a single or multiple exogenous gene cassettes, which is of a great significance in the emergence and spread of multidrug resistant A. baumannii (MDRAB) [8,9,10]. A regional variation has been detected in the type and gene cassette structure of integron in MDRAB strains [11,12,13]. Therefore, understanding of the epidemiological features and spread pattern may provide new insights into the management of A. baumannii infections and antibiotic resistance [14,15,16]. The major purposes of this multiple-hospital study were to investigate the prevalence of integrons in MDRAB strains isolated from 16 tertiary hospitals in Eastern China, and characterize the integron-integrase genes, in order to provide evidence for the management and appropriate antibiotic use of MDRAB infections.

2. Materials and Methods

2.1. A. baumannii Isolates

A total of 514 clinical bacterial isolates, identified as MDRAB using VITEK 2 (bioMérieux; Marcy l’Etoile, France), were collected from 16 tertiary hospitals in 11 cities of four Chinese provinces (Fujian, Jiangsu, Zhejiang and Shandong) during the period from January 2009 through June 2012. Then, a one-tube multiplex PCR assay was performed for rapid identification of A. baumannii using the method described previously [17]. Accordingly, 425 isolates were identified as A. baumannii (Table 1), while the other 89 isolates belonged to other species of Acinetobacter.
Table
Table 1. Number of A. baumannii strains isolated from 16 hospitals in eastern China.
Table 1. Number of A. baumannii strains isolated from 16 hospitals in eastern China.
ProvinceCityHospital CodeNumber of A. baumannii Strains Isolated
FujianFuzhouA254
B2
C20
D15
XiamenE25
F1
G3
QuanzhouH14
LongyanI5
NanpingJ56
JiangsuNanjingK3
ZhejiangHainingL3
HangzhouM17
TaizhouN2
WenzhouO2
ShandongYantaiP3
Total425

2.2. Antimicrobial Susceptibility Test

The susceptibility of A. baumannii to ampicillin/sulbactam, piperacillin/tazobactam, ceftazidime, ceftriaxone, cefepime, aztreonam, meropenem, amikacin, gentamicin, tobramycin, ciprofloxacin, levofloxacin, sulfamethoxazole/trimenthoprim, minocycline (National Institutes for Food and Drug Control, Beijing, China) and imipenem (Merck Sharp & Dohme Pharmaceutical Co., Ltd., Shanghai, China) was tested using the Clinical Laboratory Standard Institute (CLSI) recommended agar dilution method [18], and was evaluated using the CLSI interpretive criteria [19]. Escherichia coli ATCC25922 and Pseudomonas aeruginosa ATCC27853 (Shanghai Fuxiang Biotech Co., Ltd., Shanghai, China) served as quality control bacterial isolates.

2.3. Characterization of Integrons and Their Gene Cassettes

The bacterial colonies of A. baumannii were prepared into bacterial suspensions, boiled at 100 °C for 10 min in a DK-8D thermostatic water bath (Shanghai Boheng Scientific Instruments Co., Ltd., Shanghai, China), and then centrifuged at 8000 r/min for 10 min at room temperature. The supernatant was collected and used as a DNA template for the subsequent PCR assay.
Characterization of class 1 (intI1), 2 (intI2) and 3 (intI3) integron-integrase genes and intI1 gene cassette (intI CS) was done using a PCR assay in a 50 μL system containing 5 μL of 10 × PCR buffer, 1 μL of each forward and reverse primer reported previously (Table 2) [20], 4 μL of dNTPs (Takara, Dalian, China), 0.3 μL of Taq DNA polymerase (Takara), 5 μL of DNA template, and 33.7 μL of ddH2O. The conditions for PCR amplification were: initial denaturation at 95 °C for 5 min, followed by 30 cycles of denaturation at 95 °C for 30 s, primer annealing at 55 °C for intI1 and intI2, 50 °C for intI3 and 46 °C for intI CS for 30 s, and extension at 72 °C for 30 (for intI1 and intI2) or 60 s (for intI3 and intI CS), and final extension at 72 °C for 7 min. The PCR amplification products were checked with electrophoresis on a 1.5% agarose gel. In addition, the variable region of integrons was amplified using the specific primers targeting the 5’ and 3’ conserved regions, purified, and sequenced by the Shanghai Biosune Biotechnology Co., Ltd. (Shanghai, China). Then, the type and sequence of the gene cassette were identified through homology analysis using the software BLAST [21,22,23].
Table
Table 2. Primer sequences and PCR product size of integrase genes.
Table 2. Primer sequences and PCR product size of integrase genes.
Integrase GenePrimer SequencesPCR Product Size (bp)Reference
intl1F: 5’-CAG TGG ACA TAA GCC TGT TC-3’;16020
R: 5’-CCC GAG GCA TAG ACT GTA-3’
intl2F: 5’-TTG CGA GTA TCC ATA ACC TG-3’;28820
R: 5’-TTA CCT GCA CTG GAT TAA GC-3’
intl3F: 5’-GCCTCCGGCAGCGACTTTCAG-3’;104120
R: 5’-ACGGATCTGCCAAACCTGACT-3’
intl CSF: 5’-GGC ATC CAA GCA GCA AG-3’;Unknown20
R: 5’-AAGCAG ACT TGA CCT GA-3’

2.4. Strain Typing of Integron-Positive A. baumannii Isolates

The integron-positive A. baumannii isolates were genotyped using pulsed-field gel electrophoresis (PFGE) [24], while Salmonella serotype Braenderup H9812 strain (PulseNet China, Beijing, China) served as a standard quality control isolate. Briefly, genomic DNA was extracted from integron-positive A. baumannii isolates, and digested with restriction endonuclease Apa I (New England Biolabs, Inc., Beverly, MA, USA). Electrophoresis was performed at 14 °C on a 1% Seakem Gold agarose gel (Lonza, Rockland, ME, USA) in the CHEF Mapper® Pulsed Field Electrophoresis System (Bio-Rad, Hercules, CA, USA) for 19 h under the following conditions: switching time of 5 to 20 s, 120° field angle, and voltage of 6 V/cm. Gel images were captured using the Gel Doc XR+ imaging system (Bio-Rad), and all PFGE profiles were processed using the software BioNumerics version 6.0 (Applied Maths, Inc., Austin, TX, USA). Similarities were obtained using the Dice coefficient at a 1.5% tolerance, and a dendrogram was constructed with the unweighted-pair group method using average linkages (UPGMA) clustering method. A mean similarity of <90% indicated various PFGE genotypes, whereas a similarity of 90% or greater was defined as the same PFGE genotype [24].

2.5. Ethical Statement

This study was approved by the institutional review board of Fujian Medical University Union Hospital and Fujian Medical University. All experimental procedures performed in this study complied with all laws and regulations in China.

2.6. Statistical Analysis

All antimicrobial susceptibility testing results were analyzed using the software WHONET version 5.6, and all statistical analyses were performed with the statistical software SPSS 14.0 (SPSS Inc., Chicago, IL, USA). The differences of the prevalence of antimicrobial resistance were compared with chi-square test. A P value <0.05 was considered statistically significant.

3. Results

3.1. Prevalence of intI1, intI2 and intI3 Genes in A. baumannii

Among the 425 clinical isolates of MDRAB, there were 296 isolates (69.6%) positive for intI1 gene, while intI2 and intI3 genes were not detected (Figure 1).
Ijerph 12 10093 g001 1024
Figure 1. Electrophoresis of the PCR amplification products of intI1 gene. M, DL 2000 DNA Marker; 1–23, A. baumannii isolates; 24, Negative control isolate. Positive bands show the PCR products of intI1 gene.
Figure 1. Electrophoresis of the PCR amplification products of intI1 gene. M, DL 2000 DNA Marker; 1–23, A. baumannii isolates; 24, Negative control isolate. Positive bands show the PCR products of intI1 gene.
Ijerph 12 10093 g001

3.2. Comparison of the Prevalence of Antimicrobial Resistance between Integron-Positive and -Negative A. baumannii Isolates

A significantly higher prevalence of resistance to ampicillin/sulbactam, piperacillin/tazobactam, ceftazidime, ceftriaxone, cefepime, aztreonam, imipenem, meropenem, amikacin, gentamicin, tobramycin, ciprofloxacin, levofloxacin and sulfamethoxazole/trimenthoprim was detected in integron-positive A. baumannii isolates than in integron-negative isolates (all p values <0.05); however, no significant difference was observed in the prevalence of minocycline resistance between these two groups isolates (Table 3).
Table
Table 3. Comparison of the prevalence of antimicrobial resistance between integron-positive and -negative Acinetobacter baumannii isolates.
Table 3. Comparison of the prevalence of antimicrobial resistance between integron-positive and -negative Acinetobacter baumannii isolates.
AntimicrobialIntegron-Positive A. baumannii Isolates (n = 296)Integron-Negative A. baumannii Isolates (n = 129)p Value
Ampicillin/sulbactam89.9%62.4%<0.05
Piperacillin/tazobactam92.7%65.2%<0.05
Ceftazidime98.5%75.4%<0.05
Ceftriaxone100%98%<0.05
Cefepime94.3%74.6%<0.05
Aztreonam99.6%93.1%<0.05
Imipenem86.6%65.8%<0.05
Meropenem89.9%57.6%<0.05
Amikacin87.8%42.7%<0.05
Gentamicin98.1%71.7%<0.05
Tobramycin93.3%62.7%<0.05
Ciprofloxacin98.7%77.7%<0.05
Levofloxacin86.2%55.4%<0.05
Sulfamethoxazole/trimenthoprim98.3%85.3%<0.05
Minocycline39.3%28.8%0.119

3.3. PFGE Analysis of intI1 Gene-Positive A. baumannii Isolates

PFGE assay of 296 intI1 gene-positive A. baumannii isolates revealed 27 PFGE genotypes, and there were 4 genotypes containing 10 or more A. baumannii isolates, including genotypes P1 (102 isolates), P4 (101 isolates), P7 (25 isolates) and P19 (10 isolates) (Figure 2).
Ijerph 12 10093 g002 1024
Figure 2. PFGE profile of 296 A. baumannii isolates positive for intl1 gene.
Figure 2. PFGE profile of 296 A. baumannii isolates positive for intl1 gene.
Ijerph 12 10093 g002

3.4. Distribution of intI1 Gene-Positive A. baumannii Isolates

The intI1 gene was detected in the clinical strains of A. baumannii isolated from 15 hospitals. The PFGE genotype P1, which contained 102 A. baumannii isolates, was detected in the A. baumannii strains isolated from hospitals A (48%) and J (43.1%) (Figure 3). The PFGE genotype P4, which contained 101 A. baumannii isolates, was found in the A. baumannii strains isolated from four hospitals in two cities (Figure 4), 96% of which was detected in the A. baumannii strains isolated from A hospital. The PFGE genotype P7, which contained 25 A. baumannii isolates, was prevalent in the A. baumannii strains isolated from four hospitals in three cities (Figure 5), 64% of which was detected in the A. baumannii strains isolated from hospital E. The PFGE genotype P9 contained 10 A. baumannii strains, which were isolated from hospitals A (seven isolates), I (two isolates) and D (one isolate).
Ijerph 12 10093 g003 1024
Figure 3. Distribution of A. baumannii isolates with PFGE genotype P1.
Figure 3. Distribution of A. baumannii isolates with PFGE genotype P1.
Ijerph 12 10093 g003
Ijerph 12 10093 g004 1024
Figure 4. Distribution of A. baumannii isolates with PFGE genotype P4.
Figure 4. Distribution of A. baumannii isolates with PFGE genotype P4.
Ijerph 12 10093 g004
Ijerph 12 10093 g005 1024
Figure 5. Distribution of A. baumannii isolates with PFGE genotype P5.
Figure 5. Distribution of A. baumannii isolates with PFGE genotype P5.
Ijerph 12 10093 g005

3.5. Antimicrobial Resistance Pattern of intI1 Gene-Positive A. baumannii Isolates with PFGE Genotypes P1 and P4

PFGE assay revealed that P1 and P4 were the predominant PFGE genotypes in the 296 intI1 gene-positive A. baumannii isolates. The PFGE genotype P1 contained 13 extensive-drug resistant and 89 non-extensive-drug resistant A. baumannii isolates, and the PFGE genotype P4 contained 34 extensive-drug resistant and 67 non-extensive-drug resistant A. baumannii isolates. There were significant differences observed in the antimicrobial resistance pattern (both p values <0.05).

3.6. Sequencing of int I Gene Cassette

The variable region of integrons was detected in 115 A. baumannii isolates positive for intI1 gene, in which two arrays of cassettes, with 2.3 kb (97 isolates) and 1.8 kb (18 isolates) in lengths, were detected. Sequence alignment revealed that the sequences of these two arrays of gene cassettes had both 99% homology with the sequences of the two cassettes (GenBank accession number: AY557339 and AB154407) within the variable regions of class I integron of A. baumannii, which encoded the drug resistance gene cassettes aacA4-catB8-aadA1 and dfrXII-orfF-aadA2.

4. Discussion

The long-term extensive use of antimicrobial agents may lead to the emergence of antimicrobial resistance [25]. Elucidation of the mechanism underling the antimicrobial resistance would be of great importance for the prevention and control of the spread of drug-resistant bacteria [26]. Under the selective pressure of antibiotics, MDRAB may emerge due to gene mutations and acquisition of exogenous drug resistance genes [27]. Horizontal transfer of drug resistance genes may occur within and among bacterial species [28], and integron-mediated horizontal transfer of drug resistance genes has been paid more and more attention [29,30]. It is reported that integrons play a vital role in the horizontal transfer of drug resistance genes in Gram-negative bacilli [31].
Integrons are classified according to the sequence of the integrase gene. Currently, class 1 and 2 integrons are the most common types detected in Gram-negative bacteria, and class 1 integron shows the highest prevalence in A. baumannii [32]. It has been shown that there are 40%–92% of A. baumannii strains carrying class 1 integrons, with a low prevalence of class 2 integrons detected, and class 1 integrons and their gene cassettes are a major contributor to the emergence of MDRAB [11,33,34]. Detection of integrons is therefore considered to serve as an indicator to assess the epidemics of A. baumannii [8,9,10]. In the present study, 69.6% of MDRAB isolates were found to carry intI1 gene, with no intI2 gene detected, and PFGE assay of the intI1 gene-positive A. baumannii isolates revealed four predominant epidemic clones, including genotypes P1, P4, P7 and P19, which were epidemic in 10 hospitals sampled from seven cities. Since a large number of A. baumannii strains were isolated from hospital A during a long period of time, the intI1 gene-positive A. baumannii clinical isolates from hospital A were characterized 14 PFGE genotypes, and a high proportion of P1 and P4 genotypes was detected, notably P4 (96%). In relative to other PFGE genotypes, the clinical A. baumannii isolates with P1 genotype were distributed in seven hospitals from five cities. Hospital A is a large tertiary teaching hospital, and critically ill patients throughout Fujian Province are admitted to the hospital, which results in the inter-hospital spread of intI1 gene-positive MDRAB.
It has been proved that integrons are involved in the development of MDR in A. baumannii [12,15,30]. A higher prevalence of antibiotic resistance is detected in integron-positive MDRAB than in negative strains [34,35]. Detection of 48 epidemic clinical strains of A. baumannii isolated from 11 hospitals showed a 50% carriage of integrons in the tested bacterial strains, and a greater prevalence of MDR was detected in integron-positive strains than in negative strains, demonstrating the important role of integrons in antibiotic resistance and thereby in the epidemic behavior of A. baumannii [36]. Our findings showed a significantly greater prevalence of resistance to ampicillin/sulbactam, piperacillin/tazobactam, ceftazidime, ceftriaxone, cefepime, aztreonam, imipenem, meropenem, amikacin, gentamicin, tobramycin, ciprofloxacin, levofloxacin and sulfamethoxazole/trimenthoprim was detected in integron-positive A. baumannii isolates than in negative isolates (all p values <0.05), which was in agreement with previous reports [34,35,36]. In addition, we compared the antimicrobial resistance pattern of P1 and P4 clones, two predominant PFGE genotypes in the 296 intl1 gene-positive A. baumannii isolates, and significant differences were found (both p values <0.05). The PFGE genotype P4 contained more extensive-drug resistant A. baumannii isolates, and this clone was found to be the predominant epidemic genotype in hospital A. Therefore, the strengthening of the implementation of interventions targeting the management of MDRAB infections and appropriate use of antibiotics are required.
The category and number of integron-carried gene cassettes are strongly associated with the development of MDR in A. baumannii [9,15]. The regional variation of epidemic MDRAB clones leads to various epidemic characteristics of their drug resistance gene cassettes. Among the 65 A. baumannii isolates collected from four regional hospitals in northern Taiwan in 2009, approximately 72% carriage of intI1 genes was detected in the A. baumannii isolates, which mainly carried three gene cassette arrays of aacC1-orfX-orfX-orfX’-aadA1a, aacA4-catB8-aadA1 and dfrXII-orfF-aadA2 [37]. Detection of class 1 and class 2 integrons in A. baumannii isolates from nine hospitals in Turkey showed 6.4% (18/281) prevalence of class 1 integrons and absence of class 2 integrons in the A. baumannii isolates, and the gene cassettes of class 1 integrons AacC1-AAC(3)I-aadA1, AacC1-aadA1, AAC(3)-I, AAC(3)-I-AAC(3)-I-aadA1, TEM-1, AAC(3)-I-aadA1-AAC(3)-I-AAC(3)-I, AAC(3)-I-AAC(3)-I-AAC(3)-I-aadA1, AAC(3)-I-aadA1, AAC(3)-I- AAC(3)-I, AAC(3)-I-aadA1-AAC(3)-I-aadA1 and AAC(3)-I-AAC(3)-I-aadA1-AAC(3)-I-aadA1 were detected in 18 isolates [22]. In the United Kingdom, class 1 integrons were found in all of the outbreak isolates of A. baumannii but in none of the sporadic isolates, and integrons were recognized as useful markers for the outbreak of epidemic strains of A. baumannii; in addition, four integron cassette arrays were reported, including aacA4, aacA4-catB8-aadA1, aacC1-orfX-orfX’-aadA1a and aacC1-orfX- orfX-orfX’-aadA1a [11], which have been found in other outbreak strains of A. baumannii from Taiwan [37], Italia [38] and some other European countries [39]. In addition, class 1 integrons were detected 52.8% of the A. baumannii isolates collected from Nanjing, China, which mainly carried gene cassette arrays of orf1-aadA1 and aacA4-catB8-aadA1. In the current study, the gene cassette arrays of aacA4-catB8-aadA1 and dfrXII-orfF-aadA2 were detected. The aacA4-catB8-aadA1 is a common gene cassette worldwide; however, dfrXII-orfF-aadA2 is only epidemic in eastern China [40]. This is the first report of the gene cassette dfrXII-orfF-aadA2 in A. baumannii strains isolated from Fujian Province, Eastern China. In these two gene cassettes, aacA4 encodes aminoglycoside 6’-N-acetyltransferase, which results in the resistance to amikacin, netilmicin, and tobramycin; aadA1 encodes aminoglycoside nucleotidyltransferase, which induces the resistance to streptomycin and spectinomycin; catB8 encodes chloramphenicol acetyltransferase, which leads to the resistance to chloromycetin; orfF is a gene with unknown function; dhfrXII is a dihyrofolate reductase gene, which mediates the resistance to trimethoprim and streptomycin; and aadA2 is a streptomycin adenylyltransferase gene, which is involved in the resistance to streptomycin and spectinomycin. Therefore, the drug resistance genes carried by these two gene cassettes are involved in the development of resistance to aminoglycosides and sulfonamides. However, no drug resistance genes involved in the resistance to carbapenems were detected in these two gene cassettes, inferring the complex mechanisms of antimicrobial resistance in A. baumannii.

5. Conclusions

A high prevalence of class 1 integrons is detected in MDRAB in Eastern China, and the prevalence of antimicrobial resistance is greater in intI1 gene-positive MDRAB isolates than in negative isolates. There are four predominant PFGE genotypes in intI1 gene-positive MDRAB isolates, in which P4 is an epidemic PFGE genotype in Fujian Province, and it has a high proportion of extensive drug resistant A. baumannii. We report the gene cassette dfrXII-orfF-aadA2, for the first time, in A. baumannii strains isolated from Fujian Province, Eastern China.

Acknowledgements

Many thanks are addressed to all participants for their kind cooperation.

Author Contributions

Yansheng Yan and Jing Chen designed the study; Jing Chen, Hong Li, Jinsong Yang, Rong Zhan, and Aiping Chen conducted the study, collected the data and performed analysis of data. Jing Chen wrote the manuscript; Yansheng Yan revised and finalized the manuscript. All authors read and approved the final version of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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MDPI and ACS Style

Chen, J.; Li, H.; Yang, J.; Zhan, R.; Chen, A.; Yan, Y. Prevalence and Characterization of Integrons in Multidrug Resistant Acinetobacter baumannii in Eastern China: A Multiple-Hospital Study. Int. J. Environ. Res. Public Health 2015, 12, 10093-10105. https://doi.org/10.3390/ijerph120810093

AMA Style

Chen J, Li H, Yang J, Zhan R, Chen A, Yan Y. Prevalence and Characterization of Integrons in Multidrug Resistant Acinetobacter baumannii in Eastern China: A Multiple-Hospital Study. International Journal of Environmental Research and Public Health. 2015; 12(8):10093-10105. https://doi.org/10.3390/ijerph120810093

Chicago/Turabian Style

Chen, Jing, Hong Li, Jinsong Yang, Rong Zhan, Aiping Chen, and Yansheng Yan. 2015. "Prevalence and Characterization of Integrons in Multidrug Resistant Acinetobacter baumannii in Eastern China: A Multiple-Hospital Study" International Journal of Environmental Research and Public Health 12, no. 8: 10093-10105. https://doi.org/10.3390/ijerph120810093

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