首页> 美国卫生研究院文献>Journal of Bacteriology >Serotype Differences and Lack of Biofilm Formation Characterize Yersinia pseudotuberculosis Infection of the Xenopsylla cheopis Flea Vector of Yersinia pestis
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Serotype Differences and Lack of Biofilm Formation Characterize Yersinia pseudotuberculosis Infection of the Xenopsylla cheopis Flea Vector of Yersinia pestis

机译:血清型差异和缺乏生物被膜形成的特点是鼠疫耶尔森氏菌的鼠疫耶尔森菌假结核耶尔森氏菌结核病感染的特征。

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摘要

Yersinia pestis, the agent of plague, is usually transmitted by fleas. To produce a transmissible infection, Y. pestis colonizes the flea midgut and forms a biofilm in the proventricular valve, which blocks normal blood feeding. The enteropathogen Yersinia pseudotuberculosis, from which Y. pestis recently evolved, is not transmitted by fleas. However, both Y. pestis and Y. pseudotuberculosis form biofilms that adhere to the external mouthparts and block feeding of Caenorhabditis elegans nematodes, which has been proposed as a model of Y. pestis-flea interactions. We compared the ability of Y. pestis and Y. pseudotuberculosis to infect the rat flea Xenopsylla cheopis and to produce biofilms in the flea and in vitro. Five of 18 Y. pseudotuberculosis strains, encompassing seven serotypes, including all three serotype O3 strains tested, were unable to stably colonize the flea midgut. The other strains persisted in the flea midgut for 4 weeks but did not increase in numbers, and none of the 18 strains colonized the proventriculus or produced a biofilm in the flea. Y. pseudotuberculosis strains also varied greatly in their ability to produce biofilms in vitro, but there was no correlation between biofilm phenotype in vitro or on the surface of C. elegans and the ability to colonize or block fleas. Our results support a model in which a genetic change in the Y. pseudotuberculosis progenitor of Y. pestis extended its pre-existing ex vivo biofilm-forming ability to the flea gut environment, thus enabling proventricular blockage and efficient flea-borne transmission.
机译:鼠疫耶尔森氏菌通常通过跳蚤传播。为了产生可传播的感染,鼠疫耶尔森氏菌定居在跳蚤的中肠并在前庭瓣膜中形成生物膜,从而阻止了正常的血液供应。鼠疫耶尔森氏菌最近从其进化而来的肠病原性耶尔森氏菌假结核并不通过跳蚤传播。然而,鼠疫耶尔森氏菌和假结核耶尔森氏菌均形成附着在口外并阻止线虫秀丽隐杆线虫进食的生物膜,该生物膜被认为是鼠疫耶尔森菌-跳蚤相互作用的模型。我们比较了鼠疫耶尔森氏菌和假结核耶尔森氏菌感染大鼠跳蚤Xenopsylla cheopis并在跳蚤和体外产生生物膜的能力。 18种假结核耶尔森氏菌菌株中有5种,包括7种血清型,包括所有3种血清型O3菌株,都无法稳定地定居跳蚤中肠。其他菌株在跳蚤中肠内持续4周,但数量并未增加,并且18个菌株中没有一个定植在前胃或在跳蚤中产生生物膜。假结核耶尔森氏菌菌株在体外产生生物膜的能力上也有很大差异,但是在体外或秀丽隐杆线虫表面上的生物膜表型与定殖或阻断跳蚤的能力之间没有相关性。我们的结果支持一种模型,其中鼠疫耶尔森氏菌假结核耶尔森氏菌祖先的遗传变化将其先前存在的离体生物膜形成能力扩展到了跳蚤肠道环境,从而实现了小肠阻塞和有效的跳蚤传播。

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