Azam Mudsser, Jan Arif T, Haq Qazi M R
Microbiology Research Laboratory, Department of Biosciences, Jamia Millia Islamia New Delhi, India.
Molecular Biology Laboratory, School of Biotechnology, Yeungnam University Gyeongsan, South Korea.
Front Microbiol. 2016 Feb 23;7:176. doi: 10.3389/fmicb.2016.00176. eCollection 2016.
Natural environment influenced by anthropogenic activities creates selective pressure for acquisition and spread of resistance genes. In this study, we determined the prevalence of Extended Spectrum β-Lactamases producing gram negative bacteria from the River Yamuna, India, and report the identification and characterization of a novel CTX-M gene variant bla CTX-M-152 . Of the total 230 non-duplicate isolates obtained from collected water samples, 40 isolates were found positive for ESBL production through Inhibitor-Potentiation Disc Diffusion test. Based on their resistance profile, 3% were found exhibiting pandrug resistance (PDR), 47% extensively drug resistance (XDR), and remaining 50% showing multidrug resistant (MDR). Following screening and antimicrobial profiling, characterization of ESBLs (bla TEM and bla CTX-M ), and mercury tolerance determinants (merP, merT, and merB) were performed. In addition to abundance of bla TEM-116 (57.5%) and bla CTX-M-15 (37.5%), bacteria were also found to harbor other variants of ESBLs like bla CTX-M-71 (5%), bla CTX-M-3 (7.5%), bla CTX-M-32 (2.5%), bla CTX-M-152 (7.5%), bla CTX-M-55 (2.5%), along with some non-ESBLs; bla TEM-1 (25%) and bla OXY (5%). Additionally, co-occurrence of mercury tolerance genes were observed among 40% of isolates. In silico studies of the new variant, bla CTX-M-152 were conducted through modeling for the generation of structure followed by docking to determine its catalytic profile. CTX-M-152 was found to be an out-member of CTX-M-group-25 due to Q26H, T154A, G89D, P99S, and D146G substitutions. Five residues Ser70, Asn132, Ser237, Gly238, and Arg273 were found responsible for positioning of cefotaxime into the active site through seven H-bonds with binding energy of -7.6 Kcal/mol. Despite small active site, co-operative interactions of Ser237 and Arg276 were found actively contributing to its high catalytic efficiency. To the best of our knowledge, this is the first report of bla CTX-M-152 of CTX-M-group-25 from Indian subcontinent. Taking a note of bacteria harboring such high proportion of multidrug and mercury resistance determinants, their presence in natural water resources employed for human consumption increases the chances of potential risk to human health. Hence, deeper insights into mechanisms pertaining to resistance development are required to frame out strategies to tackle the situation and prevent acquisition and dissemination of resistance determinants so as to combat the escalating burden of infectious diseases.
受人为活动影响的自然环境为耐药基因的获得和传播创造了选择压力。在本研究中,我们测定了印度亚穆纳河中产生超广谱β-内酰胺酶的革兰氏阴性菌的流行情况,并报告了一种新型CTX-M基因变体bla CTX-M-152的鉴定和特征。在从采集的水样中获得的总共230株非重复分离株中,通过抑制剂增强纸片扩散试验发现40株分离株产ESBL呈阳性。根据它们的耐药谱,发现3%表现出泛耐药(PDR),47%表现出广泛耐药(XDR),其余50%表现出多重耐药(MDR)。在进行筛选和抗菌谱分析之后,对ESBLs(bla TEM和bla CTX-M)以及汞耐受性决定因素(merP、merT和merB)进行了鉴定。除了大量存在bla TEM-116(57.5%)和bla CTX-M-15(37.5%)之外,还发现细菌携带其他ESBLs变体,如bla CTX-M-71(5%)、bla CTX-M-3(7.5%)、bla CTX-M-32(2.5%)、bla CTX-M-152(7.5%)、bla CTX-M-55(2.5%),以及一些非ESBLs;bla TEM-1(25%)和bla OXY(5%)。此外,在40%的分离株中观察到汞耐受性基因的共现。通过建模生成结构然后进行对接以确定其催化特征,对新变体bla CTX-M-152进行了计算机模拟研究。由于Q26H、T154A、G89D、P99S和D146G替换,CTX-M-152被发现是CTX-M-25组的一个外围成员。发现五个残基Ser70、Asn132、Ser237、Gly238和Arg273通过七个氢键将头孢噻肟定位到活性位点,结合能为-7.6千卡/摩尔。尽管活性位点较小,但发现Ser237和Arg276的协同相互作用积极地促进了其高催化效率。据我们所知,这是来自印度次大陆的CTX-M-25组bla CTX-M-152的首次报告。鉴于携带如此高比例多重耐药和汞耐药决定因素的细菌,它们在用于人类消费的天然水资源中的存在增加了对人类健康产生潜在风险的可能性。因此,需要更深入地了解耐药性发展的机制,以制定应对策略,防止耐药决定因素的获得和传播,从而应对不断升级的传染病负担。