基因组和转录组比较分析揭示了临床和水生动物来源的副溶血性弧菌分离物对缺氧的不同反应策略

IF 3 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Huihui Xu, Beiyu Zhang, Pan Yu, Meng Sun, Lu Xie, Lanming Chen
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引用次数: 0

摘要

副溶血性弧菌是全球主要的海产品传播病原体。本研究旨在破译临床和水产动物来源的副溶血性弧菌分离物对缺氧条件的反应机制,因为缺氧条件对细菌在宿主和环境中的生存构成挑战。在不同的压力条件(渗透压、酸、温度和氧气浓度)下,研究了临床和水生动物来源的副溶血性弧菌分离株(n = 5)的生长曲线。利用 Illumina 测序技术确定了副溶血性弧菌分离株的基因组草案。通过比较基因组分析,确定并验证了与耐缺氧相关的基因。副溶血性弧菌分离株具有氧浓度依赖性生长模式,在 37 ℃ 的 TSB 培养基(pH 8.5,3% NaCl)中培养时,10% 的氧气条件强烈抑制细菌生长。意想不到的是,与正常的 21% 氧气条件形成鲜明对比的是,10% 氧气处理 24 小时会显著增加副溶血性弧菌分离物的生物膜形成(p < 0.05)。测定了四种水生动物源副溶血性弧菌分离株的基因组序列草案(4.914-5.3530 Mb),其中携带移动遗传因子(n = 12-29)。进一步研究了缺氧条件引发的全基因组基因表达变化。转录组比较分析揭示了该细菌为减轻缺氧对细胞造成的损伤而采用的多种分子策略。值得注意的是,致病性副溶血性弧菌 ATCC17802 下调和/或关闭了十种代谢途径,以降低细胞活力并维持缺氧应激下的细胞结构。这项研究结果填补了副溶血性弧菌对缺氧条件反应机制方面的空白。对低氧的不同耐受性导致了致病性副溶血性弧菌在壁龛中的持续存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative genomic and transcriptomic analyses reveal distinct response strategies to hypoxia by Vibrio parahaemolyticus isolates of clinical and aquatic animal origins
Vibrio parahaemolyticus is a leading seafood borne pathogen worldwide. The aim of this study was to decipher the response mechanism of V. parahaemolyticus isolates of clinical and aquatic animal origins to the hypoxic condition, which challenges the bacterial survival in the host and in the environment. Growth profiles of V. parahaemolyticus isolates (n = 5) of clinical and aquatic animal origins were examined at different stress conditions (osmolality, acid, temperature, and O2 concentrations). Draft genomes of the V. parahaemolyticus isolates were determined using the Illumina sequencing technique. Comparative genomic analysis were performed to identify and validate the hypoxic tolerance-related genes. The V. parahaemolyticus isolates had an oxygen concentration-dependent growth mode, and the 10% O2 condition strongly inhibited the bacterial growth, when incubated in TSB medium (pH 8.5, 3% NaCl) at 37 °C. Unexpectedly, in marked contrast to the normal 21% O2 condition, the 10% O2 treatment for 24 h significantly increased biofilm formation of V. parahaemolyticus isolates (p < 0.05). Draft genome sequences of four V. parahaemolyticus isolates of aquatic animal origins were determined (4.914–5.3530 Mb), which carried mobile genetic elements (n = 12–29). Genome-wide gene expression changes triggered by the hypoxic condition were further examined. Comparative transcriptomic analyses unveiled multiple molecular strategies employed by the bacterium to mitigate the cell damage caused by the hypoxia. Of note, the pathogenic V. parahaemolyticus ATCC17802 down-regulated and/or shut down ten metabolic pathways to reduce cell viability and maintain cell structure under the hypoxic stress. The results of this study fill prior gaps in the response mechanism of V. parahaemolyticus to the hypoxic condition. Different tolerance to hypoxia contributes to the persistence of pathogenic V. parahaemolyticus in the niches.
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来源期刊
Annals of Microbiology
Annals of Microbiology 生物-生物工程与应用微生物
CiteScore
6.40
自引率
0.00%
发文量
41
审稿时长
3.2 months
期刊介绍: Annals of Microbiology covers these fields of fundamental and applied microbiology: general, environmental, food, agricultural, industrial, ecology, soil, water, air and biodeterioration. The journal’s scope does not include medical microbiology or phytopathological microbiology. Papers reporting work on bacteria, fungi, microalgae, and bacteriophages are welcome. Annals of Microbiology publishes Review Articles, Original Articles, Short Communications, and Editorials. Originally founded as Annali Di Microbiologia Ed Enzimologia in 1940, Annals of Microbiology is an official journal of the University of Milan.
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