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肠出血性大肠杆菌 O157:H7 的适应性放射抗性导致编码志贺毒素的噬菌体基因组丢失。

Adaptive Radioresistance of Enterohemorrhagic Escherichia coli O157:H7 Results in Genomic Loss of Shiga Toxin-Encoding Prophages.

机构信息

INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada.

Research Laboratories in Sciences Applied to Food, Canadian Irradiation Centre, INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, Québec, Canada.

出版信息

Appl Environ Microbiol. 2023 Apr 26;89(4):e0130622. doi: 10.1128/aem.01306-22. Epub 2023 Apr 4.

Abstract

Enterohemorrhagic Escherichia coli (EHEC) O157:H7 is a foodborne pathogen producing Shiga toxins (Stx1 and Stx2), which can cause hemorrhagic diarrhea and life-threatening infections. O157:H7 strain EDL933 carries prophages CP-933V and BP-933W, which encode Shiga toxin genes ( and , respectively). The aim of this work was to investigate the mechanisms of adaptive resistance of EHEC strain EDL933 to a typically lethal dose of gamma irradiation (1.5 kGy). Adaptive selection through six passages of exposure to 1.5 kGy resulted in the loss of CP-933V and BP-933W prophages from the genome and mutations within three genes: , , and Wt_02639 (). Three selected EHEC clones that became irradiation adapted to the 1.5-kGy dose (C1, C2, and C3) demonstrated increased resistance to oxidative stress, sensitivity to acid pH, and decreased cytotoxicity to Vero cells. To confirm that loss of prophages plays a role in increased radioresistance, clones C1 and C2 were exposed to bacteriophage-containing lysates. Although phage BP-933W could lysogenize C1, C2, and E. coli K-12 strain MG1655, it was not found to have integrated into the bacterial chromosome in C1-Φ and C2-Φ lysogens. Interestingly, for the E. coli K-12 lysogen (K-12-Φ), BP-933W DNA had integrated at the gene (K-12-Φ). Both C1-Φ and C2-Φ lysogens regained sensitivity to oxidative stress, were more effectively killed by a 1.5-kGy gamma irradiation dose, and had regained cytotoxicity and acid resistance phenotypes. Further, the K-12-Φ lysogen became cytotoxic, more sensitive to gamma irradiation and oxidative stress, and slightly more acid resistant. Gamma irradiation of food products can provide an effective means of eliminating bacterial pathogens such as enterohemorrhagic Escherichia coli (EHEC) O157:H7, a significant foodborne pathogen that can cause severe disease due to the production of Stx. To decipher the mechanisms of adaptive resistance of the O157:H7 strain EDL933, we evolved clones of this bacterium resistant to a lethal dose of gamma irradiation by repeatedly exposing bacterial cells to irradiation following a growth restoration over six successive passages. Our findings provide evidence that adaptive selection involved modifications in the bacterial genome, including deletion of the CP-933V and BP-933W prophages. These mutations in EHEC O157:H7 resulted in loss of and , loss of cytotoxicity to epithelial cells, and decreased resistance to acidity, critical virulence determinants of EHEC, concomitant with increased resistance to lethal irradiation and oxidative stress. These findings demonstrate that the potential adaptation of EHEC to high doses of radiation would involve elimination of the Stx-encoding phages and likely lead to a substantial attenuation of virulence.

摘要

肠出血性大肠杆菌(EHEC)O157:H7 是一种食源性病原体,可产生志贺毒素(Stx1 和 Stx2),引起出血性腹泻和威胁生命的感染。O157:H7 菌株 EDL933 携带 CP-933V 和 BP-933W 噬菌体,分别编码志贺毒素基因(和)。本研究旨在探讨 EHEC 菌株 EDL933 对典型致死剂量伽马辐射(1.5 kGy)的适应性耐药机制。通过 6 次暴露于 1.5 kGy 的适应性选择,导致 CP-933V 和 BP-933W 噬菌体从基因组中丢失,以及三个基因(,和 Wt_02639())内的突变。三个适应 1.5 kGy 剂量的选定 EHEC 克隆(C1、C2 和 C3)表现出对氧化应激的抵抗力增强、对酸性 pH 的敏感性增加和对 Vero 细胞的细胞毒性降低。为了确认噬菌体丢失在提高放射性抗性中的作用,将克隆 C1 和 C2 暴露于含有噬菌体的裂解物中。尽管噬菌体 BP-933W 可以使 C1、C2 和大肠杆菌 K-12 菌株 MG1655 溶原化,但在 C1-Φ和 C2-Φ溶原菌中未发现其整合到细菌染色体中。有趣的是,对于大肠杆菌 K-12 溶原菌(K-12-Φ),BP-933W DNA 整合到基因(K-12-Φ)中。C1-Φ和 C2-Φ 溶原菌均恢复对氧化应激的敏感性,对 1.5 kGy 伽马辐射剂量的杀伤效果更好,并恢复细胞毒性和耐酸性表型。此外,K-12-Φ 溶原菌变得具有细胞毒性,对伽马辐射和氧化应激更敏感,并且耐酸性略增强。食品辐照可有效消除肠出血性大肠杆菌(EHEC)O157:H7 等食源性病原体,该病原体因产生 Stx 而导致严重疾病。为了解释 O157:H7 菌株 EDL933 的适应性耐药机制,我们通过在六个连续传代中在细菌生长恢复后反复暴露于辐照下,使该细菌的克隆对致死剂量的伽马辐射产生抗性。我们的研究结果提供了证据,表明适应性选择涉及细菌基因组的修饰,包括 CP-933V 和 BP-933W 噬菌体的缺失。这些 EHEC O157:H7 的突变导致和的丢失,对上皮细胞的细胞毒性丧失,以及对酸度的抵抗力降低,这是 EHEC 的关键毒力决定因素,同时对致死辐射和氧化应激的抵抗力增强。这些发现表明,EHEC 对高剂量辐射的潜在适应可能涉及到 Stx 编码噬菌体的消除,并且可能导致毒力显著减弱。

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