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首例杂交全基因组揭示了来自人类临床样本的染色体介导的新型结构变异。

First hybrid complete genome of reveals chromosome-mediated novel structural variant from a human clinical sample.

作者信息

Ragupathi Naveen Kumar Devanga, Sethuvel Dhiviya Prabaa Muthuirulandi, Anandan Shalini, Murugan Dhivya, Asokan Kalaiarasi, Neethi Mohan Ramya Gajaraj, Vasudevan Karthick, D Thirumal Kumar, C George Priya Doss, Veeraraghavan Balaji

机构信息

Department of Clinical Microbiology, Christian Medical College, Vellore - 632004, India.

School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore - 632014, India.

出版信息

Access Microbiol. 2020 Feb 17;2(4):acmi000103. doi: 10.1099/acmi.0.000103. eCollection 2020.

DOI:10.1099/acmi.0.000103
PMID:33005867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7523623/
Abstract

Recent findings demonstrate the origin of the plasmid-mediated colistin resistance gene from aeromonads. The present study aimed to screen for plasmid-mediated colistin resistance among 30 clinical multidrug-resistant (MDR) spp. PCR was used to screen for the presence of , , and , which revealed in a colistin-susceptible isolate (FC951). All other isolates were negative for . Sequencing of FC951 revealed that the () identified was different from previously reported variants and had 95.62 and 95.28 % nucleotide similarity with and . Hybrid assembly using IonTorrent and MinION reads revealed structural genetic information for with an insertion of IS within the gene. Due to this, was non-expressive, which makes FC951 susceptible to colistin. Further, sequence and protein structural analysis confirmed the new variant. To the best of our knowledge, this is the first report on a novel variant from India. The significant role of -like genes in different species remains unknown and requires additional investigation to obtains insights into the mechanism of colistin resistance.

摘要

最近的研究结果表明,质粒介导的黏菌素耐药基因起源于气单胞菌。本研究旨在筛选30株临床多重耐药(MDR)菌中的质粒介导黏菌素耐药性。采用聚合酶链反应(PCR)筛选mcr-1、mcr-2、mcr-3和mcr-4的存在情况,结果在一株对黏菌素敏感的分离株(FC951)中发现了mcr-1。所有其他分离株的mcr-1均为阴性。对FC951进行测序发现,鉴定出的mcr-1与先前报道的变体不同,与mcr-1和mcr-3的核苷酸相似性分别为95.62%和95.28%。使用IonTorrent和MinION读数进行混合组装,揭示了mcr-1的结构遗传信息,该基因内插入了一段插入序列(IS)。因此,mcr-1无表达,这使得FC951对黏菌素敏感。此外,mcr-1序列和蛋白质结构分析证实了这一新变体。据我们所知,这是印度首次报道新型mcr-1变体。类mcr-1基因在不同气单胞菌物种中的重要作用尚不清楚,需要进一步研究以深入了解黏菌素耐药机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbf6/7523623/cf452c04a60f/acmi-2-103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbf6/7523623/87ddb7713df9/acmi-2-103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbf6/7523623/cf452c04a60f/acmi-2-103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbf6/7523623/87ddb7713df9/acmi-2-103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbf6/7523623/cf452c04a60f/acmi-2-103-g002.jpg

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