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A study on the effects of some laboratory-derived genetic mutations on biofilm formation by Listeria monocytogenes

机译:实验室衍生的某些基因突变对单核细胞增生性李斯特菌生物膜形成的影响的研究

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摘要

Biofilms formed by the human pathogen Listeria monocytogenes in food-processing environments can be a potential source of contamination. In this study, we investigated the ability of L. monocytogenes wild type and its laboratory-derived isogenic mutants in cwhA, prfA, agrA, flaA, degU, ami and sigB to adhere to and form biofilms on abiotic surfaces. The results suggest that inactivation of the two component regulatory system degU completely abolished biofilm formation, while inactivation of the flagellar gene flaA, two component response regulator agrA and the autolysin-adhesin gene ami lead to severe impairment of initial attachment and the subsequent development of a mature biofilm by L. monocytogenes. Mutants in the global regulator of virulence prfA and the alternative sigma factor sigB were unaffected and formed biofilms similar to wild type L. monocytogenes.
机译:人类病原体单核细胞增生李斯特氏菌在食品加工环境中形成的生物膜可能是潜在的污染源。在这项研究中,我们调查了单核细胞增生李斯特菌野生型及其在cwhA,prfA,agrA,flaA,degU,ami和sigB中实验室衍生的同基因突变体粘附并形成非生物表面生物膜的能力。结果表明,两组分调节系统degU的失活完全消除了生物膜的形成,而鞭毛基因flaA,两组分响应调节剂agrA和自溶素-粘附素基因ami的失活导致了初始附着的严重损害以及随后的a单核细胞增生李斯特氏菌的成熟生物膜。在全球毒力prfA和替代sigma因子sigB的全球监管机构中的突变不受影响,并形成类似于野生型单核细胞增生李斯特菌的生物膜。

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