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在李斯特菌浮游细胞和生物膜细胞中,一些关键应激反应和毒力相关基因的差异表达存在明显的菌株间异质性。

Marked inter-strain heterogeneity in the differential expression of some key stress response and virulence-related genes between planktonic and biofilm cells in Listeria monocytogenes.

机构信息

Laboratory of Food Microbiology and Hygiene, Department of Food Science and Nutrition, School of the Environment, University of the Aegean, 81400 Myrina, Lemnos, Greece.

Laboratory of Food Microbiology and Hygiene, Department of Food Science and Nutrition, School of the Environment, University of the Aegean, 81400 Myrina, Lemnos, Greece.

出版信息

Int J Food Microbiol. 2023 Apr 2;390:110136. doi: 10.1016/j.ijfoodmicro.2023.110136. Epub 2023 Feb 13.

Abstract

Listeria monocytogenes is a facultatively intracellular pathogenic bacterium that can provoke invasive listeriosis, a severe foodborne infection in humans. Outside the host, this is capable to survive for long periods in soil, and water, as well as on plants, while, like many other microorganisms, this can also attach to abiotic surfaces, such as food contact ones, forming biofilms on them. It has been suggested that inside those sessile communities, L. monocytogenes cells not only display an increased stress tolerance but may also boost their pathogenicity. In this work, the expression of ten key stress response and/or virulence-related genes (i.e., groEL, hly, iap, inlA, inlB, lisK, mdrD, mdrL, prfA, and sigB) was studied in three different L. monocytogenes strains (AAL20066, AAL20107, and PL24), all isolated from foods and each belonging to a different listeriosis-associated serovar (1/2a, 1/2b, and 1/2c, respectively). For this, each strain was initially left to develop a mature biofilm on a model polystyrene surface (Petri dish) by incubating for 144 h (6 days) at 20 °C in tryptone soya broth (with medium renewal every 48 h). Following incubation, both biofilm and the surrounding free-swimming (planktonic) cells were recovered, and their gene expressions were comparatively evaluated through targeted reverse transcription-quantitative polymerase chain reactions (RT-qPCR). Results revealed a strain-dependent differential gene expression between the two cell types. Thus, for instance, in strain AAL20107 (ser. 1/2b) biofilm growth worryingly resulted in a significant overexpression of all the studied genes (P < 0.05), whereas in strain PL24 (ser. 1/2c), the expression of most genes (8/10) did not change upon biofilm growth, with only two of them (groEL and hly) being again significantly upregulated. Such transcriptomic strain variability in stress adaptation and/or virulence induction should be generally considered in the physiological studies of pathogenic biofilms and preferably upon designing and implementing novel and more efficient eradication methods.

摘要

李斯特菌是一种兼性细胞内病原体,可以引起侵袭性李斯特菌病,这是一种严重的食源性感染。在宿主外,它能够在土壤、水中以及植物上长时间存活,并且像许多其他微生物一样,它也可以附着在非生物表面上,如食品接触表面,在其上形成生物膜。有人认为,在这些固定群落中,李斯特菌细胞不仅表现出更高的应激耐受性,而且可能增强其致病性。在这项工作中,研究了三种不同李斯特菌菌株(AAL20066、AAL20107 和 PL24)中十个关键应激反应和/或毒力相关基因(即 groEL、hly、iap、inlA、inlB、lisK、mdrD、mdrL、prfA 和 sigB)的表达情况,这些菌株均从食品中分离出来,分别属于不同的李斯特菌相关血清型(1/2a、1/2b 和 1/2c)。为此,将每种菌株最初在模型聚苯乙烯表面(培养皿)上培养 144 小时(6 天),在 20°C 的胰蛋白酶大豆肉汤中孵育(每 48 小时更换培养基),以形成成熟的生物膜。孵育后,回收生物膜和周围的自由游动(浮游)细胞,并通过靶向逆转录定量聚合酶链反应(RT-qPCR)比较评估它们的基因表达。结果显示,两种细胞类型之间存在菌株依赖性的差异基因表达。例如,在菌株 AAL20107(血清型 1/2b)中,生物膜生长令人担忧地导致所有研究基因的过度表达(P < 0.05),而在菌株 PL24(血清型 1/2c)中,大多数基因(8/10)的表达在生物膜生长时没有改变,只有其中两个(groEL 和 hly)再次被显著上调。在应激适应和/或毒力诱导方面,这种转录组菌株变异性应在致病性生物膜的生理研究中得到普遍考虑,最好在设计和实施新的、更有效的根除方法时考虑。

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