单核细胞增生李斯特菌的表型和系统发育分析显示临床分离株的胆汁耐受性增强。

IF 2
Mary Jane Lynch, Jialun Wu, Olivia McAuliffe, Conor P O'Byrne, Cormac G M Gahan
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引用次数: 0

摘要

介绍。单核细胞增生李斯特菌菌株的分子流行病学和表型分析可以帮助我们了解影响其传播的因素、毒力潜力和在食品或临床环境中控制病原体的能力。胆汁酸代表了宿主特异性的屏障,以阻止微生物在胃肠道定植,因此,在外部环境中不会遇到胆汁酸。我们验证了胆汁酸耐受性可能是L.单核增生克隆复合体(cc)的进化适应的假设,该假设随基因型和/或临床分离而变化。我们假设单增乳杆菌菌株在胆汁耐受性(一种潜在的毒力相关性状)方面可能存在差异,并根据CC、菌株来源和基因型对这一现象进行了研究。评估205株单增乳杆菌对猪胆汁酸的耐受性和胆盐水解酶(BSH)的活性。在模拟小肠环境的条件下暴露于猪胆汁酸后,测定了单核增生乳杆菌菌株的存活率。用琼脂平板解结法测定BSH对纯牛磺酸和糖去氧胆酸的活性。分析了已知胆汁耐受位点的基因组多态性。在模拟肠道环境的厌氧条件下,分离物表现出明显的个体间胆汁耐受性差异。从人类疾病病例中分离出来的菌株比从自然环境或食物中分离出来的菌株对胆汁的耐受性强得多。在BSH琼脂平板试验中,胆汁耐受性水平与胆汁沉淀区大小之间没有相关性。在分析已知或推测的胆汁耐受位点时,没有发现显著的模式;然而,自然发生sigB操纵子突变的个别菌株表现出胆汁耐受性降低。从李斯特菌病临床病例中分离出的单核细胞增生乳杆菌菌株表现出胆汁耐药性升高,这与在侵袭性疾病之前引起胃肠道感染的能力可能增强相一致。这些数据提示了单核增生乳杆菌感染中胆汁耐受性的潜在重要性,并强调了菌株在其自然胆汁耐受性水平上变化的潜在分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenotypic and phylogenetic analyses of Listeria monocytogenes strains reveal enhanced bile tolerance in clinical isolates.

Introduction. Molecular epidemiological and phenotypic analyses of Listeria monocytogenes strains can inform our understanding of factors that influence onward transmission, virulence potential and ability to control the pathogen in foods or in clinical settings. Bile acids represent a host-specific barrier to microbial colonization of the gastrointestinal tract and are, therefore, not encountered in the external environment. We tested the hypothesis that tolerance of bile acids may be an evolutionary adaptation across L. monocytogenes clonal complexes (CCs), which varies with genotype and/or is associated with clinical isolates.Hypothesis. We hypothesized that strains of L. monocytogenes may differ in bile tolerance (a potential virulence-associated trait) and herein examine this phenomenon according to CC, strain origin and genotype.Aim. To assess 205 genome-sequenced isolates of L. monocytogenes for tolerance of porcine bile acids and bile salt hydrolase (BSH) activity.Methodology. Survival of L. monocytogenes strains was determined following exposure to porcine bile acids under conditions that mimic the small intestinal environment. BSH activity was assayed against pure taurodeoxycholic acid and glycodeoxycholic acid using an agar plate deconjugation assay. Genomes were analysed for polymorphisms in known bile tolerance loci.Results. Isolates demonstrated distinct inter-individual variances in bile tolerance under anaerobic conditions that mimic the intestinal environment. Strains isolated from cases of human disease were significantly more bile-tolerant than those isolated from natural environments or foods. There was no correlation between levels of bile tolerance and the size of bile precipitation zones on the BSH agar plate assay. No significant patterns were seen upon analysis of known or putative bile tolerance loci; however, individual strains with naturally occurring sigB operon mutations demonstrated reduced bile tolerance.Conclusion. L. monocytogenes strains isolated from clinical cases of listeriosis demonstrated elevated bile resistance consistent with a likely enhanced capacity to cause gastrointestinal infection preceding invasive disease. The data suggest the potential importance of bile tolerance in L. monocytogenes infection and highlight underlying molecular mechanisms by which strains vary in their natural levels of bile tolerance.

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