INTRODUCTION

Coagulase-negative staphylococci (CoNS) are a frequent cause of nosocomial and bacterial infections, especially in patients with medical devices and immunocompromised patients [1]. CoNS are also the most frequently isolated pathogens in intravascular catheter-related infections and infections from other implanted devices [2]. Many isolates of CoNS are becoming resistant to most beta lactams due to the mecA gene. The mecA gene encoding methicillin resistance is located on a mobile genetic element, designated as staphylococcal cassette chromosome mec (SCCmec). These elements are widely disseminated among Staphylococcus species, which might be due to horizontal transmissions [3]. In addition to the mec gene complex (the mecA gene and its regulators), SCCmec is also contained in the ccr gene complex, where it encodes site-specific recombinases that are responsible for the integration and excision of the cassette in the bacterial genome [4,5].

SCCmec displays a more polymorphous structure in methicillin-resistant coagulase-negative staphylococci (MR-CoNS), which are more frequent carriers of SCCmec than Staphylococcus aureus. The ccr and mec genes may be combined together in CoNS from an unknown source, although frequent ccr-mec combinations have not been described in methicillin-resistant S. aureus (MRSA) [6–8]. Therefore, SC-Cmec transfers from MR-CoNS to methicillin-sensitive S. aureus may occur [9–11]. However, this mechanism is not known. Eleven different types and several subtypes of SCCmec have been identified. SCCmec types I, II, and III mainly cause nosocomial infections and are significantly larger than the other types. Community-associated MRSA mainly carries SCCmec types IV and V [12].

In recent years, the role of integrons and gene cassettes in the dissemination of antibiotic resistance among pathogenic bacteria has been well documented [13]. Several classes of integrons, based on the homology of their respective integrase genes, have been described from pathogenic gram-negative bacteria. Of these, the class 1 integrons are the most commonly found and widely distributed. These integrons form a gene capture and expression system that is known to be responsible for multidrug resistance. They consist of an integrase gene (intI), which encodes a site-specific recombinase enzyme; a primary recombination site called attI, which is recognized by the integrase; and a promoter region (promoter cassette), which directs transcription of the integrated genes [14]. These integrons can carry single or multiple gene cassettes, which become a part of the integron when integrated; these gene cassettes can be coded for resistance to different antibiotics [15].

Although class 1 integrons are widely distributed among clinically isolated gram-negative bacteria, they have also been observed in gram-positive bacteria, including Corynebacterium, Staphylococcus, Streptococcus, Enterococcus, Brevibacterium, and Aerococcus (mostly in Staphylococcus) [16]. Class 1 integron-positive, gram-negative bacteria include Enterobacteriaceae, Acinetobacter, Aeromonas, Alacaligenes, Burkholderia, Campy-lobacter, Pseudomonas, Stenotrophomonas, and Vibrio [17]. The presence of class 1 integrons in Enterobacteriaceae is higher than in nonfermenting bacteria.

A small number of studies about integrons have focused on clinical staphylococcal isolates. The presence of class 1 integrons in clinical staphylococcal isolates was shown in China and other countries at high rates in MR-CoNS strains [18–22]. Therefore, increasing antibiotic resistance mediated by integrons in gram-positive bacteria has become a serious public health concern worldwide. Integrons and SCCmec are the reservoirs of many types of genes and can be transferred from one strain to another; therefore, their simultaneous existence would likely speed up the genetic exchange and effectiveness of genome evolution in staphylococci. In this article, we aim to determine the occurrence and prevalence of MR-CoNS-associated integrons, as well as the SCCmec types, in a hospital setting during 2014–2015.

MATERIALS AND METHODS

1. Bacterial strains

During 2014–2015, 100 CoNS isolates of three staphylococcal species from human sources (Staphylococcus epidermidis, Staphylococcus haemolyticus, and Staphylococcus saprophyticus) were isolated from various clinical specimens in the microbiology laboratories of three major hospitals of Hamedan, Iran. The majority of the samples were blood (44%); the others were isolated from urine specimens (38%), wounds (4%), and catheters (14%). Specimens were cultured on blood agar and chocolate agar (Merck, Darmstadt, Germany) and isolates were identified by standard biochemical methods. Verified isolates were preserved at −70°C in Trypticase soy broth (Merck) containing 20% (v/v) glycerol for further analysis.

2. Antimicrobial susceptibility testing

Antimicrobial susceptibility testing was performed by the standard disk diffusion method according to the Clinical and Laboratory Standards Institute (CLSI) guidelines [23] for the following: chloramphenicol (30 μg), cefoxitin (30 μg), clindamycin (2 μg), doxycycline (30 μg), erythromycin (15 μg), gentamicin (10 μg), levofloxacin (5 μg), novobiocin (5 μg), rifampicin (5 μg), trimethoprim-sulfamethoxazole (25 μg), and vancomycin (30 μg) (MAST, Merseyside, UK). Isolates that were shown to be resistant to at least three different classes of antimicrobial agents were classified as multi-drug resistant. S. aureus ATCC33591 strain was used for controlling the test.

3. Template DNA preparation

Template DNA was prepared using a GeneMATRIX Quick Blood DNA Purification Kit (EURx Ltd., Gdansk, Poland) according to the manufacturer’s instructions.

4. Detection of the mecA gene and SCCmec typing

The presence of the mecA gene was detected in all isolates by polymerase chain reaction (PCR) using specific primers (Table 1 [5,24–27]). PCR primer sets (Table 1) were selected from published papers based on their specificity, compatibility, and the ability to target fragments of SCCmec types I–V. The 25-mL PCR mixtures consisted of 5 μL template DNA, 0.2 mM of each deoxynucleoside triphosphate, 10 pmol of each primer, 10 mM Tris–HCl, 1.5 mM MgCl₂; 50 mM KCl, and 1.5 U of Taq DNA polymerase.

Amplification involved an initial denaturation at 94°C for 15 minutes, followed by 30 cycles of denaturation (94°C for 30 seconds), annealing (57°C for 1.5 minutes), and extension (72°C for 1.5 minutes), with a final extension step (72°C for 10 minutes). The amplified DNA was separated by gel electrophoresis on 1% agarose and visualized under ultraviolet transillumination. For quality control, we used S. aureus ATCC29247 strains (for mecA gene), S. aureus NCTC 10442 (for Type I), S. aureus N315 (for Type II), S. aureus 85/2082(for Type III), S. aureus JCSC 4744 (for Type IV), and S. aureus WIS (for Type V).

5. Integron characterization and sequencing of resistance-encoding gene cassettes

The presence of integron genes and resistance-encoding gene cassettes associated with class 1 was investigated by PCR using specific primers (Table 1). PCR was performed in a reaction mixture with total volume of 25 μL, containing 2 μL template DNA, 0.2 mM of each deoxynucleoside triphosphate, 10 pmol of each primer, 10 mM Tris-HCl, 1.5 mM MgCl₂, 50 mM KCl, and 1.5 U of Taq DNA polymerase. PCR was performed with the Eppendorf and Biorad thermocycler (ASTEC Co., Hamadan, Iran).

Amplification was performed as follows: initial denaturation step at 94°C for 5 minutes, followed by 35 cycles consisting of denaturation (94°C for 30 seconds), annealing (55°C, 30 seconds for intI1, intI2, and 5′CS and 3′CS), and extension (72°C for 1 minute), followed by a final extension step. The PCR products of variable regions were cut out from the agarose gel and purified using a QIAquick gel extraction kit (Qiagen, Valencia, CA, USA). The sequencing of gene cassettes of class 1 integrons was performed using the ABI 3730× capillary sequencer (Genfanavaran and Macrogen, Seoul, Korea). Finally, sequence data were analyzed with Chromas software and aligned with the GenBank databases using the BLAST algorithm, which is available through the National Center for Biotechnology Information website (http://www.ncbi.nlm.nih.gov).

RESULTS

1. Antimicrobial susceptibility testing

The antimicrobial resistance of 100 CoNS isolates, including 56 isolates of S. epidermidis, 40 isolates of S. haemolyticus, and 4 isolates of S. saprophyticus, are presented in Table 2. In all, 64% (32 isolates) of MR-CoNS isolates and 18% (9 isolates) of methicillin-susceptible CoNS isolates were multi-drug resistant. All 20 integron-bearing MR-CoNS strains were resistant to cefoxitin (100%, n = 20), followed by trimethoprim/sulfamethoxazole (60%, n = 12) and doxycycline/erythromycin (25%, n = 5). The percentage of resistance to levofloxacin, clindamycin, gentamicin, tetracycline, and chloramphenicol ranged from 15 to 20% (Table 2). None of the tested isolates showed resistance to vancomycin, rifampicin, or novobiocin.

2. Integron analysis

Of the 100 CoNS isolates, 16 isolates carried class 1(intI1) integrons and 4 isolates carried class 2 (intI2) integrons. Class 1 integrons were more frequent among CoNS isolates compared with class 2 integrons. All isolates that carried integrons had the mecA gene (100%). One type of gene cassette array was found in class 1 integrons. Sequence analysis of the integron variable regions indicated the presence of aminoglycoside 3′-adenyltransferase (aadA1; 1,000 bp). A total of 37.5% of MR-CoNS isolates (6 of 16 isolates) harbored aadA1 gene cassettes.

3. SCCmec typing

Fifty isolates of CoNS were positive for mecA and a certain type of SCCmec. The distribution of SCCmec types in the 50 MR-CoNS strains showed that SCCmec types III and V dominated among the tested strains (Tables 2 and 3). Of the 20 integron-bearing MR-CoNS strains, five strains had type III SCCmec, four strains had type V SCCmec, two strains had type II SCCmec, two strains had type I SCCmec, and seven strains were untypeable (Table 3). None of the tested strains had type IV. Of the 30 non-integron-bearing MR-CoNS strains, ten strains had type III SC-Cmec, eight strains had type V SCCmec, five strains had type II SCCmec, four strains had type IV SCCmec, and two strains had type I SCCmec, with five strains being untypeable (Table 4).

DISCUSSION

Despite the remarkable advances in therapeutic options and novel drug discovery efforts, the development of antimicrobial resistance in microorganism’s remains as a serious public health concern in the treatment of infectious diseases. The horizontal transmission of antimicrobial resistance genes via mobile elements, such as plasmids and transposons, plays an important role in the evolution and dissemination of multi-drug resistance [22,28].

In this study, we isolated three species of CoNS strains—S. epidermidis, S. saprophyticus, and S. haemolyticus—which were simultaneously carrying gene cassettes within a class 1 integron and SCCmec. We identified one type of gene cassette array and five different types of SCCmec. To our knowledge, this is the first report of CoNS strains that carry two mobile genetic elements, including class 1 and class 2 integrons and SCCmec, in Iran.

Integrons are now well known as a primary source of resistance genes, and they are suspected to facilitate the spread of antimicrobial resistance genes and the rapid evolution of resistance within microbial populations [16]. Integrons can harbor more than 100 different antibiotic resistance gene cassettes, which encode adaptations that extend beyond antibiotic resistance and pathogenicity. Other types of mobile genetic elements, such as plasmids, transposons, and even entire chromosomes, have been identified as major sources of integrons, which are able to facilitate the spread of genetic material between species or genera of bacteria [29].

In the present study of 100 CoNS isolates, 16 (16%) and 4 (4%) clinical isolates were found to carry class 1 integrons and class 2 integrons, respectively. These results indicate that class 1 integrons are more prevalent than class 2 integrons in clinical isolates. This is similar to the findings of a study of China from 2001 to 2006. In this study, 209 MRSA and 53 MR-CoNS strains were isolated from various clinical samples. Class 1 integrons were detected in 122 MRSA strains. None of the isolates contained class 2 or class 3 integrons [30]. In another study by Veise et al [31], 200 Staphylococcus isolates were isolated from nasal and throat swabs at Sanandaj Hospital in Iran. Class 1 integrons were detected in 81 isolates (40.1%), including 37 (40.1%) S. aureus, 35 (23.5%) S. epidermidis, and 9 (36.0%) S. saprophyticus strains. The results of this study indicate a high prevalence of integrons in Staphylococcus isolates. The differences in the prevalence of integron genes can be due to the differing geographic regions, the bacteria strains, or the indiscriminate use of antibiotics. The low prevalence of integrons in our study may be carried on other genetic elements [32].

We also found one gene cassette in intI1-positive isolates, including aadA1—an encoded protein that may contribute to the bacterial isolates’ resistance to aminoglycosides (streptomycin/spectinomycin). In our study, the class 1 integron containing the aadA1 gene was similar to that found in gram-negative bacteria [33]. Therefore, the transfer of resistance genes that may occur between ram-positive and gram-negative organisms could lead to the construction of diverse resistance to the usual antibiotics [34]. All integron-positive isolates had more resistance to antibiotics than integron-negative isolates, and resistant phenotypes usually correlated with the presence of integrons. Furthermore, a considerably large number of the MR-CoNS isolates (20 out of 50; 40%) carried class 1 integrons. Our results suggest that the identification of and screening for integrons may assist in guiding treatment regimens and could complement existing antibiotic resistance surveillance programs by providing information about antibiotic resistance and widespread dissemination among bacterial populations.

Our study also addressed the role of SCCmec in the transmission of MR-CoNS strains. The SCCmec element is a mobile genetic element that carries the mecA gene and is widely distributed among MR-CoNS species. Among 50 MR-CoNS strains, SCCmec types III and V dominated. Similar results were previously described in a study performed by Murugesan et al [35] in South India, in which types I and IV SCCmec dominated among the tested strains. Xu et al [36] found types I, II, and V SCCmec to be the most common in China.

Integrons and SCCmec can serve as reservoirs for different resistance genes. Therefore, they might act as a vehicle for the exchange of useful genes and resistance genes to improve the survival for staphylococci in various environments. The transfer of these genes is dependent on the host species, the environment, and the geographical location. As is generally accepted, the indiscriminate use of antibiotics can proliferate the emergence and selection of antibiotic-associated mobile genetic elements, which to some extent is reflected by the domination of nosocomial SC-Cmec and the prevalence of integrons. In fact, these elements act as a reservoir for many kinds of genes and are able to exchange genes between species; for this reason, bacteria can adapt to environmental and stressful conditions [22].

In Iran, antibiotic resistance is increasing due to the indiscriminate use of antibiotics and poor performance of regulations on the clinical use of antibiotics. The widespread occurrence of integrons and SCCmec will be a major challenge in the treatment and control of infectious diseases.

Acknowledgements

ACKNOWLEDGMENTS

This study was supported by the fund of the vice chancellor of Hamadan University of Medical Sciences. The authors thank the members of the Department of Microbiology at Hamedan University of Medical Sciences for their assistance in data analysis and providing bacterial strains.

Article information

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

REFERENCES

• 1. Ben-Ami R, Navon-Venezia S, Schwartz D, et al. Infection of a ventriculoatrial shunt with phenotypically variable Staphylococcus epidermidis masquerading as polymicrobial bacteremia due to various coagulase-negative Staphylococci and Kocuria varians. J Clin Microbiol 2003;41:2444−7. https://doi.org/10.1128/JCM.41.6.2444-2447.2003. PMID: 10.1128/JCM.41.6.2444-2447.2003. PMID: 12791862.ArticlePubMedPMC
• 2. Nouwen JL, van Belkum A, de Marie S, et al. Clonal expansion of Staphylococcus epidermidis strains causing Hickman catheter-related infections in a hemato-oncologic department. J Clin Microbiol 1998;36:2696−702. PMID: 9705416.ArticlePubMedPMC
• 3. Archer GL, Niemeyer DM. Origin and evolution of DNA associated with resistance to methicillin in staphylococci. Trends Microbiol 1994;2:343−7. https://doi.org/10.1016/0966-842X(94)90608-4. PMID: 10.1016/0966-842X(94)90608-4. PMID: 7850198.ArticlePubMed
• 4. Katayama Y, Ito T, Hiramatsu K. A new class of genetic element, staphylococcus cassette chromosome mec, encodes methicillin resistance in Staphylococcus aureus. Antimicrob Agents Chemother 2000;44:1549−55. https://doi.org/10.1128/AAC.44.6.1549-1555.2000. PMID: 10.1128/AAC.44.6.1549-1555.2000. PMID: 10817707.ArticlePubMedPMC
• 5. Zhang K, McClure JA, Elsayed S, et al. Novel multiplex PCR assay for characterization and concomitant subtyping of staphylococcal cassette chromosome mec types I to V in methicillin-resistant Staphylococcus aureus. J Clin Microbiol 2005;43:5026−33. https://doi.org/10.1128/JCM.43.10.5026-5033.2005. PMID: 10.1128/JCM.43.10.5026-5033.2005. PMID: 16207957.ArticlePubMedPMC
• 6. Schaumburg F, Köck R, Mellmann A, et al. Population dynamics among methicillin-resistant Staphylococcus aureus isolates in Germany during a 6-year period. J Clin Microbiol 2012;50:3186−92. https://doi.org/10.1128/JCM.01174-12. PMID: 10.1128/JCM.01174-12. PMID: 22814464.ArticlePubMedPMC
• 7. Basset P, Prod’hom G, Senn L, et al. Very low prevalence of meticillin-resistant Staphylococcus aureus carrying the mecC gene in western Switzerland. J Hosp Infect 2013;83:257−9. https://doi.org/10.1016/j.jhin.2012.12.004. PMID: 10.1016/j.jhin.2012.12.004. PMID: 23384824.ArticlePubMed
• 8. Hanssen AM, Kjeldsen G, Sollid JU. Local variants of Staphylococcal cassette chromosome mec in sporadic methicillin-resistant Staphylococcus aureus and methicillin-resistant coagulase-negative Staphylococci: evidence of horizontal gene transfer? Antimicrob Agents Chemother 2004;48:285−96. https://doi.org/10.1128/AAC.48.1.285-296.2004. PMID: 10.1128/AAC.48.1.285-296.2004. PMID: 14693553.ArticlePubMedPMC
• 9. Shore AC, Deasy EC, Slickers P, et al. Detection of staphylococcal cassette chromosome mec type XI carrying highly divergent mecA, mecI, mecR1, blaZ, and ccr genes in human clinical isolates of clonal complex 130 methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother 2011;55:3765−73. https://doi.org/10.1128/AAC.00187-11. PMID: 10.1128/AAC.00187-11. PMID: 21636525.ArticlePubMedPMC
• 10. Paterson GK, Morgan FJ, Harrison EM, et al. Prevalence and properties of mecC methicillin-resistant Staphylococcus aureus (MRSA) in bovine bulk tank milk in Great Britain. J Antimicrob Chemother 2014;69:598−602. https://doi.org/10.1093/jac/dkt417. PMID: 10.1093/jac/dkt417. PMID: 24155057.ArticlePubMed
• 11. Harrison EM, Paterson GK, Holden MT, et al. Whole genome sequencing identifies zoonotic transmission of MRSA isolates with the novel mecA homologue mecC. EMBO Mol Med 2013;5:509−15. https://doi.org/10.1002/emmm.201202413. PMID: 10.1002/emmm.201202413. PMID: 23526809.ArticlePubMedPMC
• 12. Turlej A, Hryniewicz W, Empel J. Staphylococcal cassette chromosome mec (Sccmec) classification and typing methods: an overview. Pol J Microbiol 2011;60:95−103. PMID: 21905625.ArticlePubMed
• 13. Stokes HW, Hall RM. A novel family of potentially mobile DNA elements encoding site-specific gene-integration functions: integrons. Mol Microbiol 1989;3:1669−83. https://doi.org/10.1111/j.1365-2958.1989.tb00153.x. PMID: 10.1111/j.1365-2958.1989.tb00153.x. PMID: 2560119.ArticlePubMed
• 14. Koczura R, Mokracka J, Barczak A, et al. Association between the presence of class 1 integrons, virulence genes, and phylogenetic groups of Escherichia coli isolates from river water. Microb Ecol 2013;65:84−90. https://doi.org/10.1007/s00248-012-0101-3. PMID: 10.1007/s00248-012-0101-3. PMID: 22903163.ArticlePubMed
• 15. Khosravi Y, Tay ST, Vadivelu J. Analysis of integrons and associated gene cassettes of metallo-β-lactamase-positive Pseudomonas aeruginosa in Malaysia. J Med Microbiol 2011;60:988−94. https://doi.org/10.1099/jmm.0.029868-0. PMID: 10.1099/jmm.0.029868-0. PMID: 21436370.ArticlePubMed
• 16. Deng Y, Bao X, Ji L, et al. Resistance integrons: class 1, 2 and 3 integrons. Ann Clin Microbiol Antimicrob 2015;14:45https://doi.org/10.1186/s12941-015-0100-6. PMID: 10.1186/s12941-015-0100-6. PMID: 26487554.ArticlePubMedPMC
• 17. Köseoğlu O. Integrons. Mikrobiyol Bul 2004;38:305−12. In Turkish. PMID: 15490852.PubMed
• 18. Shi L, Zheng M, Xiao Z, et al. Unnoticed spread of class 1 integrons in gram-positive clinical strains isolated in Guangzhou, China. Microbiol Immunol 2006;50:463−7. https://doi.org/10.1111/j.1348-0421.2006.tb03815.x. PMID: 10.1111/j.1348-0421.2006.tb03815.x. PMID: 16785718.ArticlePubMed
• 19. Xu Z, Shi L, Zhang C, et al. Nosocomial infection caused by class 1 integron-carrying Staphylococcus aureus in a hospital in South China. Clin Microbiol Infect 2007;13:980−4. https://doi.org/10.1111/j.1469-0691.2007.01782.x. PMID: 10.1111/j.1469-0691.2007.01782.x. PMID: 17803751.ArticlePubMed
• 20. Xu Z, Li L, Alam MJ, et al. First confirmation of integron-bearing methicillin-resistant Staphylococcus aureus. Curr Microbiol 2008;57:264−8. https://doi.org/10.1007/s00284-008-9187-8. PMID: 10.1007/s00284-008-9187-8. PMID: 18594909.ArticlePubMed
• 21. Xu Z, Li L, Shirtliff ME, et al. Resistance class 1 integron in clinical methicillin-resistant Staphylococcus aureus strains in southern China, 2001–2006. Clin Microbiol Infect 2011;17:714−8. https://doi.org/10.1111/j.1469-0691.2010.03379.x. PMID: 10.1111/j.1469-0691.2010.03379.x. PMID: 21521411.ArticlePubMed
• 22. Loncaric I, Stalder GL, Mehinagic K, et al. Comparison of ESBL--and AmpC producing Enterobacteriaceae and methicillin-resistant Staphylococcus aureus (MRSA) isolated from migratory and resident population of rooks (Corvus frugilegus) in Austria. PLoS One 2013;8:e84048https://doi.org/10.1371/journal.pone.0084048. PMID: 10.1371/journal.pone.0084048. PMID: 24391878.ArticlePubMedPMC
• 23. Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing; twenty-first informaional supplement. CLSI document M100-S21. Wayne, PA: Clinical and Laboratory Standards Institute; 2011.
• 24. Koeleman JG, Stoof J, Van Der Bijl MW, et al. Identification of epidemic strains of Acinetobacter baumannii by integrase gene PCR. J Clin Microbiol 2001;39:8−13. https://doi.org/10.1128/JCM.39.1.8-13.2001. PMID: 10.1128/JCM.39.1.8-13.2001. PMID: 11136740.ArticlePubMedPMC
• 25. Lévesque C, Piché L, Larose C, et al. PCR mapping of integrons reveals several novel combinations of resistance genes. Antimicrob Agents Chemother 1995;39:185−91. https://doi.org/10.1128/AAC.39.1.185. PMID: 10.1128/AAC.39.1.185. PMID: 7695304.ArticlePubMedPMC
• 26. Milheiriço C, Oliveira DC, de Lencastre H. Update to the multiplex PCR strategy for assignment of mec element types in Staphylococcus aureus. Antimicrob Agents Chemother 2007;51:3374−7. https://doi.org/10.1128/AAC.00275-07. PMID: 10.1128/AAC.00275-07. PMID: 17576837.ArticlePubMedPMC
• 27. Kondo Y, Ito T, Ma XX, et al. Combination of multiplex PCRs for staphylococcal cassette chromosome mec type assignment: rapid identification system for mec, ccr, and major differences in junkyard regions. Antimicrob Agents Chemother 2007;51:264−74. https://doi.org/10.1128/AAC.00165-06. PMID: 10.1128/AAC.00165-06. PMID: 17043114.ArticlePubMed
• 28. Arabestani MR, Fazzeli H, Nasr Esfahani B. Identification of the most common pathogenic bacteria in patients with suspected sepsis by multiplex PCR. J Infect Dev Ctries 2014;8:461−8. https://doi.org/10.3855/jidc.3856. PMID: 10.3855/jidc.3856. PMID: 24727512.ArticlePubMed
• 29. Rowe-Magnus DA, Mazel D. Integrons: natural tools for bacterial genome evolution. Curr Opin Microbiol 2001;4:565−9. https://doi.org/10.1016/S1369-5274(00)00252-6. PMID: 10.1016/S1369-5274(00)00252-6. PMID: 11587934.ArticlePubMed
• 30. Deng Y, Liu J, Peters BM, et al. Antimicrobial resistance investigation on Staphylococcus strains in a local hospital in Guangzhou, China, 2001–2010. Microb Drug Resist 2015;21:102−4. https://doi.org/10.1089/mdr.2014.0117. PMID: 10.1089/mdr.2014.0117. PMID: 25299244.ArticlePubMedPMC
• 31. Veise P, Ramazanzadeh R, Khiababi ZD, et al. Identification of class I integrons gene in staphylococcus strains isolated from clinical samples. Cell Biol 2013;1:24−7. https://doi.org/10.11648/j.cb.20130103.11. PMID: 10.11648/j.cb.20130103.11.Article
• 32. Xu Z, Li L, Shi L, et al. Class 1 integron in staphylococci. Mol Biol Rep 2011;38:5261−79. https://doi.org/10.1007/s11033-011-0676-7. PMID: 10.1007/s11033-011-0676-7. PMID: 21258866.ArticlePubMedPMC
• 33. Zeighami H, Haghi F, Hajiahmadi F. Molecular characterization of integrons in clinical isolates of betalactamase-producing Escherichia coli and Klebsiella pneumoniae in Iran. J Chemother 2015;27:145−51. https://doi.org/10.1179/1973947814Y.0000000180. PMID: 10.1179/1973947814Y.0000000180. PMID: 24571248.ArticlePubMed
• 34. Chen B, Zheng W, Yu Y, et al. Class 1 integrons, selected virulence genes, and antibiotic resistance in Escherichia coli isolates from the Minjiang River, Fujian Province, China. Appl Environ Microbiol 2011;77:148−55. https://doi.org/10.1128/AEM.01676-10. PMID: 10.1128/AEM.01676-10. PMID: 21057021.ArticlePubMed
• 35. Murugesan S, Perumal N, Mahalingam SP, et al. Analysis of antibiotic resistance genes and its associated SCCmec types among nasal carriage of methicillin resistant coagulase negative staphylococci from community settings, chennai, Southern India. J Clin Diagn Res 2015;9:DC01−5. https://doi.org/10.7860/JCDR/2015/11733.6307. PMID: 26435940.Article
• 36. Xu Z, Shi L, Alam MJ, et al. Integron-bearing methicillin-resistant coagulase-negative staphylococci in South China, 2001–2004. FEMS Microbiol Lett 2008;278:223−30. https://doi.org/10.1111/j.1574-6968.2007.00994.x. PMID: 10.1111/j.1574-6968.2007.00994.x. PMID: 18096018.ArticlePubMed

Figure & Data

References

Citations

Citations to this article as recorded by  

• Prevalence and Potential Risk Factors for the Acquisition of Antibiotic-Resistant Staphylococcus spp. Bacteria Among Pastoralist Farmers in Kajiado Central Subcounty, Kenya
  Edidah Ong’era, John Kagira, Naomi Maina, Daniel Kiboi, Kenneth Waititu, Lynda Michira, Maina Ngotho, Mejdi Snoussi
  BioMed Research International.2023; 2023: 1.     CrossRef
• Investigation of SCCmec types I–IV in clinical isolates of methicillin-resistant coagulase-negative staphylococci in Ahvaz, Southwest Iran
  Effat Abbasi Montazeri, Sakineh Seyed-Mohammadi, Aram Asarehzadegan Dezfuli, Azar Dokht Khosravi, Maryam Dastoorpoor, Mitra Roointan, Morteza Saki
  Bioscience Reports.2020;[Epub]     CrossRef