揭示大肠埃希菌的抗生素耐药性和毒力基因谱:临床和环境分离物比较研究

IF 1 Q4 GENETICS & HEREDITY
Zimam Mahmud , Syeda Antara Shabnam , Israt Dilruba Mishu , Abdus Sadique , Laila N. Islam , Munirul Alam
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引用次数: 0

摘要

耐多药(MDR)大肠埃希菌引起腹泻,耐抗生素基因和毒力基因通过水生 MDR 菌株传播,是全球临床关注的一个主要问题。在这项研究中,我们检测了从孟加拉国腹泻患者和水生环境中分离出的大肠埃希菌菌株的毒力基因含量和耐多药流行率。研究对象包括来自 Mathbaria 的临床分离株,以及来自孟加拉国达卡(淡水和废水)和吉大港(海水)的环境分离株。其中,抗生素耐药性采用了盘扩散法进行检测,毒力基因的筛选则通过 PCR 法进行。结果表明,临床分离物中多重耐药性(MDR)的发生率很高,90.91%的分离物具有多重耐药性。在所有临床分离株中都发现了对红霉素的耐药性,而对美西林的敏感性为 100%。在临床分离物中,氨苄西林、阿奇霉素和磺胺甲噁唑-三甲氧苄啶(70%)也出现了明显的耐药性。在环境分离物中,87.64%被鉴定为耐药菌,其中红霉素、氨苄西林和阿奇霉素的耐药率较高。达卡和吉大港之间的耐药性模式存在地域差异,达卡对某些抗生素的耐药性较高,如庆大霉素(CN)、四环素(TE)、环丙沙星(CIP)、氨苄西林(AMP)、头孢克肟(CFM)和美西林(MEL)。临床和环境分离物的病毒基因流行率不同,临床样本中以肠道致毒大肠杆菌(ETEC)为主,环境样本中以肠道侵袭性大肠杆菌(EIEC)为主。年轻患者的毒力基因发生率明显高于年长者。在抗生素耐药性和毒力方面,没有观察到明显的性别差异。比较分析表明,兰普拉分离物的耐药性最高,米尔布尔分离物的毒力基因流行率最高。与河水分离物相比,污水样本的抗生素耐药性明显更高。在吉大港,来自 Chatkhil 和 Patenga 1 区的样本耐药性差异明显,而病毒基因流行率差异不大。总之,本研究强调了临床大肠杆菌分离物中耐药菌株占多数,以及环境分离物中大量的抗生素耐药性和毒力基因,尤其是在非沿海水源中。因此,有效的抗生素管理计划对孟加拉国临床和环境中抗药性的防治至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unveiling the spectrum of antibiotic resistance and virulence genes in Escherichia coli: A comparative study of clinical and environmental isolates

Unveiling the spectrum of antibiotic resistance and virulence genes in Escherichia coli: A comparative study of clinical and environmental isolates

Multidrug resistant (MDR) Escherichia coli causing diarrhea and the spread of antibiotic resistance genes as well as virulence genes through aquatic MDR strains represent a major clinical concern worldwide. In this study, we examined the virulence gene contents and prevalence of multidrug resistance among Escherichia coli strains isolated from diarrheal patients and aquatic environment of Bangladesh. Clinical isolates from Mathbaria and environmental isolates from Dhaka (freshwater and wastewater) and Chittagong (marine-water) in Bangladesh were included. Herein, antibiotic resistance was examined using the disc diffusion method, while the screening of virulence genes was conducted through PCR assay. The results showed a high prevalence of multidrug resistance (MDR) among clinical isolates, with 90.91 % exhibiting MDR. Erythromycin resistance was observed in all clinical isolates, while mecillinam showed 100 % sensitivity. Significant resistance was also seen for ampicillin, azithromycin, and sulfamethoxazole-trimethoprim (>70 %) in clinical isolates. Among environmental isolates, 87.64 % were identified as MDR, with high resistance rates for erythromycin, ampicillin, and azithromycin. Geographic variations in resistance patterns were observed between Dhaka and Chittagong, with higher resistance in Dhaka for certain antibiotics such as Gentamycin (CN), Tetracycline (TE), Ciprofloxacin (CIP), Ampicillin (AMP), Cefixime (CFM), Mecillinam (MEL). Virulence gene prevalence differed between clinical and environmental isolates, with entero-toxigenic E. coli (ETEC) being dominant in clinical samples and Entero-invasive E. coli (EIEC) in environmental samples. Younger patients had significantly higher occurrence of virulence genes than older ones. No significant gender biasness was observed for the prevalence of antibiotic resistance and virulence. Comparative analysis showed Rampura isolates had the highest resistance and Mirpur isolates had the highest virulence gene prevalence. Results from sewerage samples showed significantly higher antibiotic resistance compared to river water isolates. In Chittagong, significant difference in resistance was noticed for the samples from Chatkhil and Patenga 1 zones, while virulence gene prevalence did not vary significantly. Overall, this study highlights the preponderance of MDR in clinical E. coli isolates and substantial antibiotic resistance and virulence genes in environmental isolates, particularly in non-coastal water sources. Therefore, effective antibiotic stewardship programs are crucial to combat resistance in clinical and environmental settings in Bangladesh.

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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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