The Staphylococcus species are a group of Gram-positive, facultative, aerobic, and unencapsulated bacteria, which are responsible for a variety of skin and tissue infections (23). Of all the species, Staphylococcus aureus (S. aureus) has been most notable as a major human and animal pathogen responsible for a wide variety of infections, including skin infections, pneumonia, bacteraemia, and toxin-mediated food poisoning (9). Food poisoning caused by animal-derived S. aureus has been one of the most economically important food-borne diseases and a major threat to public health (14). In China, the production and consumption of pork has long been in great demand (20). However, with the increasing abuse of antibiotics on pig farms, multi-drug resistant (MDR) phenotypes of S. aureus are emerging and contaminate pork products as a result, which poses a great threat to human health (7).
The bacterial resistance mechanisms involved in the acquisition and spread of resistance genes have been illuminated in the past few years (19). These mainly resolve to one of two types: (i) mutations in preexisting or previously acquired resistance genes, and (ii) horizontal or lateral gene transfer, which is mediated by various types of genetic elements, such as transposons, plasmids, bacteriophages, pathogenicity islands, and integrons (1, 3). Among them, integrons are an important mechanism involved in acquisition and spreading of antibiotic resistance, which permit tandem integration and expression of various antibiotic-resistance genes (8).
Integrons contribute to horizontal gene transfer in association with transposons or plasmids. A complete integron is generally composed of three elements: the 5′ conserved segment (5′CS), an internal variable region containing one or more resistance gene cassettes, and a 3′ conserved segment (3′CS). The 5′CS contains an integrase gene (intI) that encodes an integrase (recombinase) responsible for site specific insertion of resistance-gene cassettes, a recombination site (attI), and a promoter (Pc) that is responsible for expression of the captured gene cassettes. The 3′CS contains a quaternary ammonium compound resistance gene (qacΔE-1), the sulphonamide resistance gene (sul1) and an open reading frame of unknown function (11). So far, five classes of mobile integrons have been identified and distinguished by differences in the intI sequences. Class 1, 2, and 3 integrons are relatively common and capture from and spread antibiotic-resistance gene cassettes to the same or other bacterial species by horizontal gene transfer (12). Class 4 and 5 integrons are relatively rare and they are involved in the development of trimethoprim resistance in Vibrio species (12).
Class 1 integrons are the most frequent type in clinical isolates, and most of the reported antibiotic-resistance gene cassettes are found in this class. Previously, class 1 integrons were identified in a large variety of clinical Gram-negative organisms. Recently, they were observed in a few Gram-positive bacteria as well (21). Although class 2 and 3 integrons have a similar organisation to that of class 1, they are less detected in bacteria from clinical samples and poorly studied (15). Studies have indicated that Gram-positive bacteria are also a major reservoir of integrons (6). In particular, class 1 integrons have been identified in S. aureus isolates from hospitals and cow’s milk (11, 24). Class 2 integrons have been identified in S. aureus clinical isolates in Tehran, Iran (15).
Pork is a major protein source in the Chinese diet. Pigs are raised on a very large scale in China, and S. aureus isolates from pigs are reported to be an important source of methicillin-resistant Staphylococcus aureus (MRSA) (5). To investigate the prevalence of MRSA strains and S. aureus isolates carrying class 1 and 2 integrons from pig farms in China, we report here the characterisation of the S. aureus isolates from local pig farms in Chongqing.
Material and Methods
Sample collection. A total of 724 samples were collected from 12 pig farms in 6 regions of Chongqing between November 2018 and January 2019. These samples included faecal swabs (n = 426), floor swabs (n = 215), water swabs (n = 22), feed swabs (n = 20), and air swabs (n = 41), which were randomly collected by the farmers from three pig houses of each farm.
Isolation and identification of S. aureus. Each swab was transferred into 15 mL of buffered peptone water (Land Bridge, China) and incubated at 37°C for 16 to 18 h for recovering S. aureus. A loopful of the recovered S. aureus suspensions was sub-cultured in 10 mL of 7.5% NaCl broth (Land Bridge) at 37°C for 18 to 24 h and another loopful was streaked onto Baird-Parker agar plate (Land Bridge) and chromogenic medium (CHROMagar, France), for isolation and direct differentiation, respectively. Finally, the specific genes femB and mecA were used for identifying S. aureus and MRSA by PCR and the subsequent DNA sequencing (13, 18).
Antibiotic susceptibility testing. Antibiotic susceptibility of all S. aureus isolates against 11 subclasses of antimicrobial agents was determined by the Kirby–Bauer disk diffusion method (2) and interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guidelines (4). The tested antimicrobials (Hangzhou Microbial Reagent Co, China) included penicillin (10 U), gentamicin (10 μg), tetracycline (30 μg), erythromycin (15 μg), clindamycin (2 μg), trimethoprim/sulphamethoxazole (25 μg), chloramphenicol (30 μg), ciprofloxacin (5 μg), teicoplanin (30 μg), rifampicin (5 μg), nitrofurantoin (300 μg), levofloxacin (5 μg), and oxacillin (1 μg). Escherichia coli (ATCC25922) was used as a quality control. The S. aureus isolates resistant to more than three subclasses of antimicrobial agents were defined as MDR isolates.
Extraction of S. aureus plasmid and genomic DNA. The plasmid DNA of S. aureus was extracted by using an E.Z.N.A. Plasmid Mini Kit I (Omega Bio-Tek, USA) according to the manufacturer’s instructions. The genomic DNA was extracted by the boiling method as previously described (24). Briefly, the overnight cultures of S. aureus in 7.5% NaCl broth were suspended in 100 μL of TE buffer (10 mM Tris; 1 mM EDTA, pH 8), and then boiled for 10 min, vortexed for 10 s, and finally centrifuged at 9,000 × g for 5 min. The supernatant containing genomic DNA of S. aureus was collected and stored at −20°C until use.
Detection of three classes of integrons. The presence of class 1, 2, and 3 integrons in MDR S. aureus was confirmed by PCR amplification of integrase genes (intI1, intI2, and intI3) with their specific primers (Table 1) as described in previous studies (16). PCR mixtures were in the volume of 25 μL and PCR amplifications were performed in a T100 thermocycler (Bio-Rad, USA). The reaction conditions for detection of intI1 were as follows: initial denaturation at 94°C for 5 min, 35 cycles of denaturation at 94°C for 1 min, annealing at 58°C for 30 s, and extension at 72°C for 1 min, and a final extension at 72°C for 10 min. Conditions for detection of intI2 and intI3 were: initial denaturation at 94°C for 5 min, 35 cycles of denaturation at 94°C for 1 min, annealing at 55°C for 30 s, and extension at 72°C for 1 min, and a final extension at 72°C for 10 min. Furthermore, the two genes located in the 3′CS of class 1 integrons conferring resistance to sul1 and qacΔE-1 were also confirmed by PCR as protocolled in a previous report (25).
Primers used in this study
|Primer||Target gene||Sequence (5′–3′)||Product size (bp)|
|intl1-k||variable region 1||ACCGAAACCTTGCGCTCGT||Variable|
|variable region 2||GATTTGTA||Variable|
Detection of integron-associated gene cassettes. All integron-positive MDR S. aureus isolates were tested for the presence of internal gene cassettes. The PCR for detecting gene cassette arrays in class 1 integrons employed the primers intl1-k and lnB (Table 1) as previously described (24). The reaction conditions were initial denaturation at 94°C for 4 min and 10 touchdown cycles of denaturation at 94°C for 1 min, annealing at 62–53°C for 30 s (decreasing by 1°C/cycle) and extension at 72°C for 2 min, followed by 24 cycles of denaturation at 94°C for 30 s, annealing at 52°C for 30 s and extension at 72°C for 2 min, with a final extension at 72°C for 7 min. A PCR also detected gene cassette arrays in class 2 integrons. The primers hep74 and hep51 (Table 1) were used as previously published (25). The reaction conditions were initial denaturation at 94°C for 5 min, 12 cycles of denaturation at 94°C for 50 s, annealing at 68–57°C for 50 s (decreasing by 1°C/cycle) and extension at 72°C for 4 min, followed by 30 cycles of denaturation at 94°C for 30 s, annealing at 57°C for 30 s and extension at 72°C for 4 min, with a final extension at 72°C for 5 min.
Cloning, sequencing, and analysis of amplified integron gene cassettes. To analyse the sequences of the gene cassettes, PCR amplicons of the representative cassettes that had a unique size when visualised on the gel were purified with a Gel Extraction Kit (Omega Bio-Tek) and then ligated into the pMD-19T vector (TaKaRa Biomedical Technology, China). After transformation, three positive clones carrying recombinant pMD-19T plasmids were sequenced by the Sanger method. The resulting nucleotide sequences were analysed and compared with the available sequences both in GenBank by the BLAST programme (http://www.ncbi.nlm.nih.gov/blast/) and in the Integron Database (INTEGRALL) (http://integrall.bio.ua.pt/).
Statistical analysis. Comparison of the detection rates of class 1 and 2 integrons between plasmid and genomic DNA was analysed by χ2 test in SPSS software (IBM SPSS, USA). P < 0.05 was considered statistically significant.
Prevalence and antibiotic susceptibility of S. aureus isolates. A total of 68 S. aureus isolates were recovered from 724 samples collected on pig farms in Chongqing, which includes 43/426 (10.1%) from faecal samples, 11/215 (5.1%) from floor samples, 3/22 (13.6%) from water samples, 6/20 (30.0%) from feed samples, and 5/41 (12.2%) from air samples (Table 2). Of these, 57 (83.8%) isolates were further confirmed as MRSA strains based on the presence of the mecA gene. This gene was contained in 35/43 (81.4%) isolates from faecal samples, 9/11 (81.8%) isolates from floor samples, 2/3 (66.7%) from water samples, 6/6 (100%) from feed samples, and 5/5 (100%) from air samples (Table 2). Subsequently, 13 antimicrobial agents were used to test the antibiotic susceptibility of the 68 S. aureus isolates. It showed that high levels of resistance to antibiotics were found in these isolates. Resistance to penicillin, tetracycline, and erythromycin were observed in all 68 S. aureus isolates. Additionally, 60/68 (88.2%) of these isolates were resistant to oxacillin, 46/68 (67.6%) to chloramphenicol, 15/68 (22.1%) to trimethoprim/ sulphamethoxazole, and 7/68 (10.3%) to clindamycin. Low resistance rates to rifamycin (2.9%), gentamicin (1.5%), ciprofloxacin (1.5%), levofloxacin (1.5%), nitrofurantoin (0%), and teicoplanin (0%) were noted among the isolates (Table 3).
The prevalence of pig farm-derived S. aureus
|Sample sources||Number of samples from each source||Number of positive isolates (%)||Number of MRSA strains among the positive isolates (%)|
|Faeces||426||43 (10.1%)||35 (81.4%)|
|Floor||215||11 (5.1%)||9 (81.8%)|
|Water||22||3 (13.6%)||2 (66.7%)|
|Feed||20||6 (30.0%)||6 (100%)|
|Air||41||5 (12.2%)||5 (100%)|
|Total||724||68 (9.4%)||57 (83.8%)|
Antibiotic-resistant phenotypes and genotypes of S. aureus in this study
|Antimicrobial subclass||Antimicrobial agent||Phenotypes (n = 68)||Genotypes (number of isolates containing different resistance gene cassettes)|
|Number of resistant isolates (%)||Number of sensitive isolates||Class 1 integron (n = 60)||Class 2 integron (n = 68)|
|aadA1c or aadA1||dfrA1||blaTEM-1|
|Folate pathway||15 (22.1)||-||-||2||-|
Detection and characterisation of class 1, 2, and 3 integrons. All the 68 S. aureus isolates were screened with a specific PCR for the presence of class 1, 2, and 3 integrons. Sixty of the 68 isolates (88.2%) were positive for class 1 integrons with an amplicon of 280 bp, while all 68 isolates had class 2 integrons with an amplicon of 233 bp. No class 3 integrons were found in any isolates (data not shown). In addition, there were significant differences in the detection rate of integrons between the bacterial chromosome and plasmid. It was found that in the S. aureus isolates, the positive rates for plasmids carrying class 1 and 2 integrons (88.2% and 100%, respectively) were significantly higher than those for chromosomes carrying them (36.8%, 45.6%, respectively) (Table 4). Moreover, all integrons on chromosomes were also found on the plasmids of the corresponding S. aureus strains (data not shown).
Comparison of detection rates of class 1 and 2 integrons in plasmid and genomic DNA in pig farm-derived S. aureus
|Types of DNA||Class 1 integrons||Class 2 integrons|
|Number of positive (negative) strains||Positive rate (%)||Number of positive (negative) strains||Positive rate (%)|
|Genomic DNA||25 (43)||36.8||31 (37)||45.6|
|Plasmid DNA||60 (8)||88.2||68 (0)||100|
PCR amplification of the gene cassette indicated that antibiotic-resistance gene cassettes could be detected in 66.7% (40/60) of class 1 integrons and 85.3% (58/68) of class 2 integrons (Table 5). Sequence analysis of the representative PCR amplicons identified several gene cassettes with product sizes of about 700 bp, 1,200 bp and 2,000 bp (Table 5). In class 1 integrons, three kinds of resistance gene cassette arrays (aadA1c; dfrA1 + aadA1; and aadA1c, dfrA1 + aadA1) were detected in folate pathway inhibitors and aminoglycoside-susceptible isolates (Table 3). Of these, the gene cassette arrays aadA1c (aminoglycosides) and aadA1c, dfrA1 + aadA1 (aminoglycosides and folate pathway inhibitors) were found to be the most common arrays, which were carried in 25 and 14 class 1 integron-positive isolates, respectively; the dfrA1 + aadA1 array was only found in one class 1 integron-positive isolate. In class 2 integron-positive isolates, only one kind of cassette array (blaTEM-1) related to β-lactam resistance was observed in 58 class 2 integrons of these isolates (Table 5). For better presentation, a schematic representation of the different cassette arrays found in class 1 and class 2 integrons is shown in Fig. 1.
Different types of gene cassette amplicons among the integron-bearing S. aureus
|Types of integrons||Number of isolates carrying different cassettes (%)||Approximate sizes of amplicon (bp)||Inserted cassette(s)|
|Integron 1||1 (1.7%)||2,000||dfrA1 + aadA1|
|14 (23.3%)||1,200, 2,000||aadA1c, dfrA1 + aadA1|
|Integron 2||58 (85.3%)||700||blaTEM-1|
The prevalence and characterisation of class 1 integrons in Gram-negative bacteria have been well documented; however, the presence of integrons in Gram-positive bacteria has been reported less so far. To our knowledge, this is the first report of the characterisation of class 1 and 2 integrons and their associated gene cassettes in MDR S. aureus isolates from pig farms in China. Our data indicated that MDR isolates and the class 1 and 2 integrons were widespread among pig farm–derived S. aureus isolates in Chongqing. The most common pattern of the isolates’ resistance was insusceptibility to β-lactams, tetracyclines, and macrolides. In addition, most (83.8%) MDR isolates were also MRSA isolates.
Unexpectedly, all S. aureus isolates were positive for class 2 integrons, and the majority (88.2%) of these isolates carried class 1 integrons. However, in previous reports, the proportion of class 1 integrons in S. aureus isolates from either farms (10%–25%) or hospitals (42.5% and 53%) was apparently much lower than that reported here (17, 22, 24). The proportion of class 2 integrons (100%) in this study was also much higher than that (35.2%) in S. aureus isolates from hospitals in Tehran, Iran (15). This is also the first time that a report is published of class 2 integrons in S. aureus isolates from farm animals. The high prevalence of class 1 and 2 integrons in S. aureus on pig farms may reflect that the integrons have played an important role in disseminating antimicrobial resistance in bacterial populations.
The class 1 integrons have long been considered the most universal integrons and they have the capability to integrate nearly all the antibiotic-resistance genes, such as those imparting resistance to β-lactams, aminoglycosides, chloramphenicol and others (12). In our study, we found that only aminoglycoside resistance genes (aadA1c and aadA1) and folate pathway inhibitor resistance determinant (dfrA1) were identified in class 1 integrons. The composition of the resistance gene cassette arrays was simple and only three kinds of arrays (aadA1c; dfrA1 + aadA1; and aadA1c, dfrA1 + aadA1) were observed. However, previous studies have documented many more antibiotic-resistance genes among S. aureus isolates from farms or hospitals, such as an assortment of 12 resistance genes (dhfrV, dfrA1, dfrA12, aadA1, aadA5, aadA4, aadA24, aacA4, aadA2, aadB, cmlA6, and qacH) found in isolates from Chinese dairy farms (11) or a 10-strong variety of resistance determinants (aadA1, aadA2, aadB, aacA4, dfrA12, oxa2, orfD, orfF, catB3, and cmlA6) reported in isolates from hospitals (15, 22).
Most reported class 2 integrons carry the three specific gene cassettes dfrA1, sat1, and aadA1, which confer resistance to trimethoprim, streptothricin and streptomycin/spectinomycin, respectively (8, 10). In this study, only the gene for resistance to β-lactams, blaTEM-1, was screened in the class 2 integrons of the isolated strains, which had not been reported previously among S. aureus strains. It can be seen that the diversity of gene cassettes in class 2 integrons was lower than that in class 1 integrons. The low diversity of integrated gene cassettes in class 2 integrons was probably owing to the non-functional intl2 generated by the replacement of its internal termination codon with a codon for glutamic acid, which could not excise existing cassettes or insert novel ones (21). In addition, the gene cassettes observed in this study could not correspond to the resistance phenotypes observed (e.g. tetracycline, erythromycin, or chloramphenicol) among the S. aureus isolates (Table 3). This suggested that resistance of S. aureus to tetracycline, erythromycin, and chloramphenicol may not be associated with integron-mediated antimicrobial resistance. Other resistance mechanisms beyond this research’s scope may be responsible for generating these resistant phenotypes. Subsequent genome-wide sequencing analysis will likely elucidate the mechanism for generation of these resistant phenotypes.
This is the first report of the presence and characterisation of class 1 and 2 integrons in S. aureus isolates from farmed swine in Chongqing, China. The results showed that high occurrence rates (88.2% and 100%) of class 1 and 2 integrons were observed in all 68 S. aureus isolates. Of these, 58 isolates carrying class 2 integrons were positive for the presence of the β-lactam resistance gene blaTEM-1 and 40 isolates carrying class 1 integrons harboured the aadA1c, aadA1 or dfrA1 genes. Out of concerns for public health, the presence of class 1 and 2 integrons and their associated resistance gene cassettes in S. aureus isolates from pig farms should be paid special attention and close surveillance of that presence should be mounted.
Conflict of Interest
Conflict of Interests Statement: The authors declare that there is no conflict of interests regarding the publication of this article.
Financial Disclosure Statement: This study was supported by the National Key Research and Development Program of China (2018YFD0500500), the Fundamental Research Funds for the Central Universities (XDJK2019B012, SWU118072), the Chongqing Science & Technology Commission (cstc2018jscx-msybX0302), the National Agricultural Product Quality and Safety Risk Assessment Project (GJFP2019007), the fund for China Agriculture Research System (CARS-37), and the Beibei Science & Technology Commission (No. 2018-20). The funding bodies had no role in the study design, data collection or analysis and decision to publish or preparation.
Alibayov B., Baba-Moussa L., Sina H., Zdeňková K., Demnerová K.: Staphylococcus aureus mobile genetic elements. Mol Biol Rep 2014, 41, 5005–5018.
Bauer A.W., Kirby W.M., Sherris J.C., Turck M.: Antibiotic susceptibility testing by a standardized single disk method. Am J Clin Pathol 1966, 45, 493–496.
Boerlin P., Reid-Smith R.J.: Antimicrobial resistance: its emergence and transmission. Anim Health Res Rev 2008, 9, 115–126.
Clinical and Laboratory Standards Institute: M02 Performance standards for antimicrobial disk susceptibility tests, 13th ed. CLSI, Wayne, 2018.
Cui S., Li J., Hu C., Jin S., Li F., Guo Y., Ran L., Ma Y.: Isolation and characterization of methicillin-resistant Staphylococcus aureus from swine and workers in China. J Antimicrob Chemother 2009, 64, 680–683.
Deng Y., Liang Y., Cui H., Zhao X., Zhong N., Li Y., Chen D., Bian H., Li Y., Yu G.: Roles of integrons in the antimicrobial resistance of Gram-positive microorganisms. Rev Med Microbiol 2015, 26, 26–31.
Guo D., Liu Y., Han C., Chen Z., Ye X.: Phenotypic and molecular characteristics of methicillin-resistant and methicillin-susceptible Staphylococcus aureus isolated from pigs: implication for livestock-association markers and vaccine strategies. Infect Drug Resist 2018, 11, 1299–1307.
- Export Citation
Guo D., Liu Y., Han C., Chen Z., Ye X.: Phenotypic and molecular characteristics of methicillin-resistant and methicillin-susceptible)| false Staphylococcus aureusisolated from pigs: implication for livestock-association markers and vaccine strategies. Infect Drug Resist 2018, 11, 1299–1307. 30197527 10.2147/IDR.S173624
Hansson K., Sundström L., Pelletier A., Roy P.H.: IntI2 integron integrase in Tn7. J Bacteriol 2002, 184, 1712–1721.
Hardy K.J., Hawkey P.M., Gao F., Oppenheim B.A.: Methicillin resistant Staphylococcus aureus in the critically ill. Br J Anaesth 2004, 92, 121–130.
Labbate M., Case R.J., Stokes H.W.: The integron/gene cassette system: an active player in bacterial adaptation. Methods Mol Biol 2009, 532, 103–125.
Li L., Zhao X.: Characterization of the resistance class 1 integrons in Staphylococcus aureus isolates from milk of lactating dairy cattle in Northwestern China. BMC Vet Res 2018, 14, 59.
Mehrotra M., Wang G., Johnson W.M.: Multiplex PCR for detection of genes for Staphylococcus aureus enterotoxins, exfoliative toxins, toxic shock syndrome toxin 1, and methicillin resistance. J Clin Microbiol 2000, 38, 1032–1035.
- Export Citation
Mehrotra M., Wang G., Johnson W.M.: Multiplex PCR for detection of genes for)| false Staphylococcus aureusenterotoxins, exfoliative toxins, toxic shock syndrome toxin 1, and methicillin resistance. J Clin Microbiol 2000, 38, 1032–1035. 10.1128/JCM.38.3.1032-1035.2000 10698991
Miao J., Chen L., Wang J., Wang W., Chen D., Li L., Li B., Deng Y., Xu Z.: Current methodologies on genotyping for nosocomial pathogen methicillin-resistant Staphylococcus aureus (MRSA). Microb Pathog 2017, 107, 17–28.
Mostafa M., Siadat S.D., Shahcheraghi F., Vaziri F., Japoni-Nejad A., Vand Yousefi J., Rajaei B., Harifi Mood E., Ebrahimzadeh N., Moshiri A., Seyed Siamdoust S.A., Rahbar M.: Variability in gene cassette patterns of class 1 and 2 integrons associated with multi drug resistance patterns in Staphylococcus aureus clinical isolates in Tehran-Iran. BMC Microbiol 2015, 15, 152.
- Export Citation
Mostafa M., Siadat S.D., Shahcheraghi F., Vaziri F., Japoni-Nejad A., Vand Yousefi J., Rajaei B., Harifi Mood E., Ebrahimzadeh N., Moshiri A., Seyed Siamdoust S.A., Rahbar M.: Variability in gene cassette patterns of class 1 and 2 integrons associated with multi drug resistance patterns in)| false Staphylococcus aureusclinical isolates in Tehran-Iran. BMC Microbiol 2015, 15, 152. 10.1186/s12866-015-0488-3 26228695
Moura A., Henriques I., Ribeiro R., Correia A.: Prevalence and characterization of integrons from bacteria isolated from a slaughterhouse wastewater treatment plant. J Antimicrob Chemother 2007, 60, 1243–1250.
Nandi S., Maurer J.J., Hofacre C., Summers A.O.: Gram-positive bacteria are a major reservoir of class 1 antibiotic resistance integrons in poultry litter. Proc Natl Acad Sci USA 2004, 101, 7118–7122.
Paterson G.K., Larsen A.R., Robb A., Edwards G.E., Pennycott T.W., Foster G., Mot D., Hermans K., Baert K., Peacock S.J., Parkhill J., Zadoks R.N., Holmes M.A.: The newly described mecA homologue, mecA LGA251, is present in methicillin-resistant Staphylococcus aureus isolates from a diverse range of host species. J Antimicrob Chemother 2012, 67, 2809–2813.
- Export Citation
Paterson G.K., Larsen A.R., Robb A., Edwards G.E., Pennycott T.W., Foster G., Mot D., Hermans K., Baert K., Peacock S.J., Parkhill J., Zadoks R.N., Holmes M.A.: The newly described)| false mecAhomologue, mecA LGA251, is present in methicillin-resistant Staphylococcus aureusisolates from a diverse range of host species. J Antimicrob Chemother 2012, 67, 2809–2813. 22941897 10.1093/jac/dks329
Stalder T., Barraud O., Casellas M., Dagot C., Ploy M.C.: Integron involvement in environmental spread of antibiotic resistance. Front Microbiol 2012, 3, 119.
Wang H., Wang T., Luo Q., Huo X., Wang L., Liu T., Xu X., Wang Y., Lu F., Lun Z., Yu L., Shen J.: Prevalence and genotypes of Toxoplasma gondii in pork from retail meat stores in Eastern China. Int J Food Microbiol 2012, 157, 393–397.
- Export Citation
Wang H., Wang T., Luo Q., Huo X., Wang L., Liu T., Xu X., Wang Y., Lu F., Lun Z., Yu L., Shen J.: Prevalence and genotypes of)| false Toxoplasma gondiiin pork from retail meat stores in Eastern China. Int J Food Microbiol 2012, 157, 393–397. 10.1016/j.ijfoodmicro.2012.06.011 22781578
Xu Z., Li L., Shirtliff M.E., Peters B.M., Li B., Peng Y., Alam M.J., Yamasaki S., Shi L.: Resistance Class 1 integron in clinical methicillin resistant Staphylococcus aureus strains in southern China, 2001–2006. Clin Microbiol Infect 2011, 17, 714–718.
- Export Citation
Xu Z., Li L., Shirtliff M.E., Peters B.M., Li B., Peng Y., Alam M.J., Yamasaki S., Shi L.: Resistance Class 1 integron in clinical methicillin resistant)| false Staphylococcus aureusstrains in southern China, 2001–2006. Clin Microbiol Infect 2011, 17, 714–718. 21521411 10.1111/j.1469-0691.2010.03379.x
Xu Z., Shi L., Alam M.J., Li L., Yamasaki S.: Integron-bearing methicillin-resistant coagulase-negative staphylococci in South China, 2001–2004. FEMS Microbiol Lett 2008, 278, 223–230.
Xu Z., Shi L., Zhang C., Zhang L., Li X., Cao Y., Li L., Yamasaki S.: Nosocomial infection caused by class 1 integron-carrying Staphylococcus aureus in a hospital in South China. Clin Microbiol Infect 2007, 13, 980–984.
Zhang H., Shi L., Li L., Guo S., Zhang X., Yamasaki S., Miyoshi S., Shinoda S.: Identification and characterization of class 1 integron resistance gene cassettes among Salmonella strains isolated from healthy humans in China. Microbiol Immunol 2004, 48, 639–645.
- Export Citation
Zhang H., Shi L., Li L., Guo S., Zhang X., Yamasaki S., Miyoshi S., Shinoda S.: Identification and characterization of class 1 integron resistance gene cassettes among)| false Salmonellastrains isolated from healthy humans in China. Microbiol Immunol 2004, 48, 639–645. 10.1111/j.1348-0421.2004.tb03473.x 15383699