High prevalence of plasmid-mediated quinolone resistance (PMQR) among E. coli from aquatic environments in Bangladesh

被引:20
作者
Amin, Mohammed Badrul [1 ]
Saha, Sumita Rani [1 ]
Islam, Md Rayhanul [1 ]
Haider, S. M. Arefeen [1 ]
Hossain, Muhammed Iqbal [1 ]
Chowdhury, A. S. M. Homaun Kabir [1 ]
Rousham, Emily K. [2 ]
Islam, Mohammad Aminul [1 ,3 ]
机构
[1] Int Ctr Diarrhoeal Dis Res Bangladesh Icddr B, Lab Sci & Serv Div, Lab Food Safety & One Hlth, Dhaka, Bangladesh
[2] Loughborough Univ, Ctr Global Hlth & Human Dev, Sch Sport Exercise & Hlth Sci, Loughborough, Leics, England
[3] Washington State Univ, Paul G Allen Sch Global Hlth, Pullman, WA 99164 USA
来源
PLOS ONE | 2021年 / 16卷 / 12期
基金
英国生物技术与生命科学研究理事会;
关键词
ESCHERICHIA-COLI; ANTIBIOTIC-RESISTANCE; MULTIDRUG-RESISTANCE; GENES; PUMP;
D O I
10.1371/journal.pone.0261970
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluro(quinolones) is an important class of antibiotic used widely in both human and veterinary medicine. Resistance to fluro(quinolones) can be acquired by either chromosomal point mutations or plasmid-mediated quinolone resistance (PMQR). There is a lack of studies on the prevalence of PMQR in organisms from environmental sources in Bangladesh. In this study, we investigated the occurrence of PMQR genes in E. coli from various water sources and analysed associations between multi-drug resistance (MDR) and resistance to extended spectrum beta-lactam antibiotics. We analysed 300 E. coli isolates from wastewaters of urban live-bird markets (n = 74) and rural households (n = 80), rural ponds (n = 71) and river water samples (n = 75) during 2017-2018. We isolated E. coli by filtering 100 ml of water samples through a 0.2 mu m cellulose membrane and incubating on mTEC agar media followed by identification of isolated colonies using biochemical tests. We selected one isolate per sample for detection of PMQR genes by multiplex PCR and tested for antibiotic susceptibility by disc diffusion. Clonal relatedness of PMQR-positive isolates was evaluated by enterobacterial repetitive intergenic consensus-PCR (ERIC-PCR). About 66% (n = 199) of E. coli isolates harbored PMQR-genes, predominantly qnrS (82%, n = 164) followed by aac(6')-lb-cr (9%, n = 17), oqxAB (7%, n = 13), qnrB (6%, n = 11) and qepA (4%, n = 8). Around 68% (n = 135) of PMQR-positive isolates were MDR and 92% (n = 183) were extended spectrum beta-lactamase (ESBL)-producing of which the proportion of positive samples was 87% (n = 159) for bla(CTX-M-1)' 34% (n = 62) for bla(TEM), 9% (n = 16) for bla(OXA-1), bla(OXA-47) and bla(CMY-2), and 2% (n = 4) for bla(SHV). Further, 16% (n = 32) of PMQR-positive isolates were resistant to carbapenems of which 20 isolates carried bla(NDM-1). Class 1 integron (int1) was found in 36% (n = 72) of PMQR-positive E. coli isolates. PMQR genes were significantly associated with ESBL phenotypes (p <= 0.001). The presence of several PMQR genes were positively associated with ESBL and carbapenemase encoding genes such as qnrS with bla(CTXM-1) (p<0.001), qnrB with bla(TEM) (p<0.001) and bla(OXA-1) (p = 0.005), oqxAB and aac(6')-lb-cr with bla(SHV) and bla(OXA-1) (p<0.001), qnrB with bla(NDM-1) (p<0.001), aac(6')-lb-cr with bla(OXA-47) (p<0.001) and bla(NDM-1) (p = 0.002). Further, int1 was found to correlate with qnrB (p<0.001) and qepA (p = 0.011). ERIC-PCR profiles allowed identification of 84 of 199 isolates with 85% matching profiles which were further grouped into 33 clusters. Only 5 clusters had isolates (n = 11) with identical ERIC-PCR profiles suggesting that PMQR-positive E. coli isolates are genetically heterogeneous. Overall, PMQR-positive MDR E. coli were widely distributed in aquatic environments of Bangladesh indicating poor wastewater treatment and highlighting the risk of transmission to humans and animals.
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