肠炎沙门氏菌对不同感染倍数的噬菌体处理的转录响应

Catherine W. Y. Wong, Siyun Wang
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摘要

肠炎沙门氏菌(S. enterica)是众多食源性疾病爆发的致病菌,而目前的工业措施的有效率可能低于 90%。因此,有人建议用噬菌体来抗菌治疗肠炎沙门氏菌,但目前还不清楚是否存在针对肠炎沙门氏菌的最佳噬菌体感染倍率(MOI)。将 MOI 分别为 1、10、100、1000 和 10,000 的两种噬菌体鸡尾酒共同接种到四种肠炎球菌菌株(肠炎球菌、纽波特肠炎球菌、门兴肠炎球菌和鼠伤寒肠炎球菌)上,并在第 0-3 天估算菌群数量。在噬菌体 SE14、SF5 和 SF6 处理后的第 0、1 和 3 天,从所有四种肠道菌株中提取 RNA,并进行 RT-qPCR 分析,以确定 20 个选定基因的表达情况。结果表明,MOI 为 1000 时,肠炎球菌 S5-483 和伤寒杆菌 S5-536 的肠炎球菌数量从第 0 天到第 3 天减少到检测不到的水平。 在 MOI 为 1000 和 10,000 时,肠炎球菌 S5-483 和伤寒杆菌 S5-536 的 cas1(SOS 响应)和 mod(DNA 修饰和重组)基因在第 0 天高度上调 2.5 至 5 倍。在第 3 天,MOI 为 1000 时,肠球菌 S5-483 的 hsdS(DNA 修饰和重组)上调了约 1 倍。了解最佳噬菌体 MOI 有助于在工业中实施有效和最佳的噬菌体处理。了解肠炎球菌在噬菌体处理后的转录反应可进一步了解肠炎球菌如何在噬菌体感染后存活下来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptional Response of Salmonella enterica to Bacteriophage Treatments with Differential Multiplicities of Infection
Salmonella enterica (S. enterica) is a causative agent of numerous foodborne outbreaks, as current industrial measures may be <90% effective. Therefore, bacteriophages have been suggested as an antimicrobial treatment against S. enterica, but it is currently unclear if there is an optimal bacteriophage multiplicity of infection (MOI) against S. enterica. Two bacteriophage cocktails at MOIs 1, 10, 100, 1000 and 10,000 were co-inoculated against four S. enterica strains (S. Enteritidis, S. Newport, S. Muenchen and S. Typhimurium), and populations were estimated on days 0–3. The transcriptional profiles of 20 genes previously indicated to be differentially expressed after bacteriophage treatment were studied by extracting RNA from all four S. enterica strains after bacteriophage SE14, SF5 and SF6 treatment on days 0, 1 and 3, and RT-qPCR was conducted to determine the expression of the 20 selected genes. The results showed that an MOI of 1000 was the most optimal in reducing S. Enteritidis populations to undetectable levels from day 0 to 3. The cas1 (SOS response) and mod (DNA modification and recombination) genes were highly upregulated between 2.5- and 5-fold on day 0 for S. Enteritidis S5-483 and S. Typhimurium S5-536 at MOIs of 1000 and 10,000. On day 3, hsdS (DNA modification and recombination) was upregulated by ~1-fold for S. enteritidis S5-483 after an MOI of 1000. Understanding an optimal bacteriophage MOI can be beneficial to implementing effective and optimal bacteriophage treatments in the industry. Knowledge of S. enterica’s transcriptional response after bacteriophage treatment provides further insight into how S. enterica can survive bacteriophage infection.
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