Patel Mitul A, Pandey Aparna, Patel A C, Patel S S, Chauhan H C, Shrimali M D, Patel Pankaj A, Mohapatra S K, Chandel B S
Department of Biotechnology, Sankalchand Patel University, Visnagar, India.
Department of Biochemistry, Dental College, Sankalchand Patel University, Visnagar, India.
Front Microbiol. 2022 Oct 14;13:996214. doi: 10.3389/fmicb.2022.996214. eCollection 2022.
Worldwide dissemination of extended-spectrum -lactamase (ESBL)-producing constitutes an emerging global health issue, with animal food products contributing as potential reservoirs. ESBL infection is associated with the high mortality and mobility rate in developing countries due to less susceptibility to antibiotics. The present study aimed to elucidate the molecular characteristics and sequence-based analysis of ESBL in the Gujarat state of India. This study included 108 strains were isolated from different poultry farms (broiler and layer) in the Banaskantha District. PCR was employed to identify genotypic ESBL-producing antimicrobial resistance genes. Overall, a high occurrence of ESBL genes was found in poultry farms due to the high usage of antimicrobials. The PCR analysis revealed that 79.62% of isolates were detected positive with one or more ESBL genes. Among them, (63.88%) was found to be the predominant genotype, followed by (30.55%) and (28.70%). In the group, a higher occurrence was observed in (23.14%), followed by (24.07%) and (22.22%). We used the whole-genome sequencing (WGS) method to evaluate the antimicrobial resistance genes, virulence factors, single nucleotide polymorphisms (SNPs), plasmid replicons, and plasmid-mediated AMR genes of one ESBL isolated. We examined the genetic relatedness of a human pathogenic strain by comparing its sequence with the broad geographical reference sequences. ST 681 was determined using multi-locus sequence typing. We compared our findings to the reference sequence of str. K- 12 substr. MG1655. We found 24,937 SNPs with 21,792 in the genic region, 3,145 in the intergenic region, and six InDels across the genome. The WGS analysis revealed 46 antimicrobial resistance genes and seven plasmid-mediated AMR genes , , , , , , and . The ST 681 was found to have , , and virulence factors and two plasmid replicons, IncFII(pHN7A8) and IncI1-I(Alpha). This study revealed a higher occurrence of ESBL detected in poultry.
产超广谱β-内酰胺酶(ESBL)细菌在全球范围内的传播构成了一个新出现的全球健康问题,动物食品可能是其潜在储存宿主。由于对抗生素敏感性较低,ESBL细菌感染在发展中国家与高死亡率和高迁移率相关。本研究旨在阐明印度古吉拉特邦产ESBL细菌的分子特征并进行基于序列的分析。本研究纳入了从巴纳斯坎塔区不同家禽养殖场(肉鸡场和蛋鸡场)分离出的108株细菌。采用聚合酶链反应(PCR)来鉴定产ESBL基因型抗菌耐药基因。总体而言,由于抗菌药物的大量使用,家禽养殖场中ESBL基因的出现率很高。PCR分析显示,79.62%的分离株检测出一种或多种ESBL基因呈阳性。其中,blaCTX-M(63.88%)被发现是主要基因型,其次是blaTEM(30.55%)和blaSHV(28.70%)。在blaCTX-M组中,在ST1199(23.14%)中观察到更高的出现率,其次是ST155(24.07%)和ST167(22.22%)。我们使用全基因组测序(WGS)方法来评估一株产ESBL细菌的抗菌耐药基因、毒力因子、单核苷酸多态性(SNP)、质粒复制子和质粒介导的AMR基因。通过将一株人类致病性细菌菌株的序列与广泛的地理参考序列进行比较,我们检测了其遗传相关性。使用多位点序列分型确定为ST681。我们将我们的研究结果与大肠杆菌str. K-12 substr. MG1655的参考序列进行了比较。我们在全基因组中发现了24,937个SNP,其中21,792个在基因区域,3,145个在基因间区域,还有6个插入缺失。WGS分析揭示了46个抗菌耐药基因和7个质粒介导的AMR基因blaCTX-M、blaTEM、blaSHV、blaOXA-1、blaOXA-10、blaOXA-12、blaOXA-23。发现ST681具有ompT、fimH和papC毒力因子以及两个质粒复制子,IncFII(pHN7A8)和IncI1-I(Alpha)。本研究揭示在家禽中检测到的产ESBL细菌出现率较高。