新出现的人畜共患病原体厦门雪旺氏菌的基因组研究。

Ci ji yi xue za zhi = Tzu-chi medical journal Pub Date : 2019-06-13 eCollection Date: 2020-04-01 DOI:10.4103/tcmj.tcmj_69_19
Jui-Hsing Wang, Shu-Ying Tseng, Kwong-Chung Tung
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引用次数: 0

摘要

目的:厦门雪旺氏菌(Shewanella xiamenensis)是一种新出现的人畜共患病原体,常见于水生生态系统。簇状规则间隔短回文重复序列(CRISPR)和(CRISPR)相关基因系统是原核生物的适应性免疫系统。最近,越来越多的证据表明它们在细菌毒力和抗药性方面发挥作用。尽管厦门嗜血杆菌在医学上具有重要意义,但人们对其基因组特征知之甚少:菌株 ZYW6 分离自 Epinephelus awoara。我们对 16S rRNA 基因进行了测序,并与 GenBank 细菌数据库进行了比对。抗生素敏感性测试和解释由自动 VITEK 2 系统完成。我们使用 QIAGEN Genomic-tip 100/G 试剂盒和 QIAGEN Genomic DNA Buffer Set 提取基因组 DNA。使用 Illumina MiSeq 测序仪进行了全基因组枪式测序。为了鉴定厦门酵母菌 ZYW6 基因组中的 CRISPR-Cas 系统,使用了 Integrated Microbial Genomes and Microbiomes 和 CRISPRFinder:结果:我们鉴定了一株厦门芽孢杆菌(S. xiamenensis)的基因组。基因组长度为 4,765,190 bp,编码 4262 个开放阅读框。鉴定了 I 型 CRISPR-Cas 系统和丝氨酸生物合成基因:结论:我们的研究结果证明了厦门金丝猴的 CRISPR-Cas 系统、丝氨酸合成和氧青霉素酶的基因结构。本研究中抗生素耐药性基因的报告可能表明食用动物中可能存在抗菌药物耐药性基因库,从而导致潜在的感染源。这些发现有助于深入了解厦门金眼鲷中CRISPR-Cas系统的结构和组成,为今后的生物学验证奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genomic investigation of emerging zoonotic pathogen <i>Shewanella xiamenensis</i>.

Genomic investigation of emerging zoonotic pathogen <i>Shewanella xiamenensis</i>.

Genomic investigation of emerging zoonotic pathogen Shewanella xiamenensis.

Objective: Shewanella xiamenensis is an emerging zoonotic pathogen commonly found in aquatic ecosystem. Clustered regularly interspaced short palindromic repeats (CRISPR) and (CRISPR)-associated gene systems act as adaptive immune system of prokaryotes. Recently, growing evidence suggested their role in bacterial virulence and resistance. Despite its medical importance, little is known about the genomic characteristics of S. xiamenensis.

Materials and methods: Strain ZYW6 was isolated from Epinephelus awoara. We sequenced the 16S rRNA gene and blast against the GenBank bacterial database. Antibiotic susceptibility tests and interpretation were performed by automatic VITEK 2 system. We extracted the genomic DNA with QIAGEN Genomic-tip 100/G kit and QIAGEN Genomic DNA Buffer Set. Whole-genome shotgun sequencing was performed using the Illumina MiSeq sequencer. To identify the CRISPR-Cas System in the genome of S. xiamenensis ZYW6, the Integrated Microbial Genomes and Microbiomes and CRISPRFinder were used.

Results: We characterized the genome of a S. xiamenensis strain. The genome is 4,765,190 bp in length and encodes 4262 open-reading frames. Type I CRISPR-Cas system and serine biosynthesis genes were identified.

Conclusion: Our results demonstrate the genetic structure of CRISPR-Cas system, l-serine synthesis, and oxacillinase in S. xiamenensis. The report of antibiotics resistance genes in the study might indicate a possible reservoir of antimicrobial drug resistance determinants in food animal, resulting in potential infection source. The findings provide insights into the structure and composition of CRISPR-Cas system in S. xiamenensis and foundation for future biological validation.

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