猪、家禽和小反刍动物支原体定殖核酸酶活性的标准化分析。

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Manon Vastel, Patrice Gaurivaud, Florence Tardy, Anne V Gautier-Bouchardon
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引用次数: 0

摘要

分泌的核酸酶,无论是细胞附着的还是在环境中释放的,在感染期间细菌-宿主相互作用中发挥着不同的作用。它们通过降解宿主核酸帮助提供细菌生长所必需的核苷酸,参与细胞外陷阱的降解,从而参与免疫逃避,并且可以在宿主细胞中具有直接的细胞毒性活性。迄今为止,对支原体属细菌中核酸酶的表达研究甚少。本研究采用一套标准化的方法检测了主要动物支原体的体外核酸酶活性。猪(猪肺炎支原体、猪鼻支原体和絮凝支原体)和禽(鸡毒支原体、爱奥华支原体和滑膜支原体)中均检测到核酸酶,而小反刍亚种mycoides亚种中未检测到核酸酶。卡普里和卡普里亚种。山羊。在猪种中,在细胞颗粒和上清液中都检测到核酸酶活性,而在家禽种中,结果变化较大。我们发现,在我们的实验条件下,核酸酶活性的检测-在M. iowae和M. synoviae中存在/不存在-是菌株依赖的。来自巨噬细胞胞外陷阱的DNA进一步被证明是支原体表达核酸酶的底物,这表明一些感染动物的支原体物种和/或菌株可以以产生的核苷酸为食,从而逃脱陷阱,这两个特征有助于感染的持续存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Standardized analysis of nuclease activities in Mycoplasma species colonizing swine, poultry, and small ruminants.

Secreted nucleases, either cell-attached or released in the environment, play varied roles in bacteria-host interactions during an infection. They help to provide nucleotides essential for bacterial growth by degrading host nucleic acids, are involved in the degradation of extracellular traps and hence in immune evasion, and can have direct cytotoxic activity in host cells. Nuclease expression in bacteria of the Mycoplasma genus has been poorly studied so far. In this study, a standardized set of methods was used to detect the in vitro nuclease activities of major animal mycoplasmas. Nucleases were detected in swine (Mycoplasma (M.) hyopneumoniae, M. hyorhinis, and M. flocculare) as well as avian (M. gallisepticum, M. iowae, and M. synoviae) species, but not in the small ruminant subspecies M. mycoides subsp. capri and M. capricolum subsp. capricolum. In swine species, nuclease activity was detected in both the cell pellet and the supernatant, whereas in poultry species, the results were more variable. We showed that detection of nuclease activity-in terms of presence/absence in our experimental conditions-was strain dependent in M. iowae and M. synoviae. The DNA from macrophage extracellular traps was further demonstrated to be a substrate for mycoplasma-expressed nucleases, suggesting that several Mycoplasma species and/or strains infecting animals could feed on resulting nucleotides and hence escape the traps, two features contributing to persistence of the infection.

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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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