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光敏杆菌黏附修饰蛋白(Pam)结合细胞外多糖并改变细菌的附着。

Photorhabdus adhesion modification protein (Pam) binds extracellular polysaccharide and alters bacterial attachment.

机构信息

Department of Biology and Biochemistry, University of Bath, Claverton Down, Bath BA27AY, UK.

出版信息

BMC Microbiol. 2010 May 12;10:141. doi: 10.1186/1471-2180-10-141.

Abstract

BACKGROUND

Photorhabdus are Gram-negative nematode-symbiotic and insect-pathogenic bacteria. The species Photorhabdus asymbiotica is able to infect humans as well as insects. We investigated the secreted proteome of a clinical isolate of P. asymbiotica at different temperatures in order to identify proteins relevant to the infection of the two different hosts.

RESULTS

A comparison of the proteins secreted by a clinical isolate of P. asymbiotica at simulated insect (28 degrees C) and human (37 degrees C) temperatures led to the identification of a small and highly abundant protein, designated Pam, that is only secreted at the lower temperature. The pam gene is present in all Photorhabdus strains tested and shows a high level of conservation across the whole genus, suggesting it is both ancestral to the genus and probably important to the biology of the bacterium. The Pam protein shows limited sequence similarity to the 13.6 kDa component of a binary toxin of Bacillus thuringiensis. Nevertheless, injection or feeding of heterologously produced Pam showed no insecticidal activity to either Galleria mellonella or Manduca sexta larvae. In bacterial colonies, Pam is associated with an extracellular polysaccharide (EPS)-like matrix, and modifies the ability of wild-type cells to attach to an artificial surface. Interestingly, Surface Plasmon Resonance (SPR) binding studies revealed that the Pam protein itself has adhesive properties. Although Pam is produced throughout insect infection, genetic knockout does not affect either insect virulence or the ability of P. luminescens to form a symbiotic association with its host nematode, Heterorhabditis bacteriophora.

CONCLUSIONS

We studied a highly abundant protein, Pam, which is secreted in a temperature-dependent manner in P. asymbiotica. Our findings indicate that Pam plays an important role in enhancing surface attachment in insect blood. Its association with exopolysaccharide suggests it may exert its effect through mediation of EPS properties. Despite its abundance and conservation in the genus, we find no evidence for a role of Pam in either virulence or symbiosis.

摘要

背景

Photorhabdus 是一种革兰氏阴性的线虫共生和昆虫致病细菌。物种 Photorhabdus asymbiotica 能够感染人类和昆虫。我们研究了一个临床分离株 Photorhabdus asymbiotica 在不同温度下的分泌蛋白质组,以鉴定与两种不同宿主感染相关的蛋白质。

结果

比较临床分离株 Photorhabdus asymbiotica 在模拟昆虫(28°C)和人类(37°C)温度下分泌的蛋白质,鉴定出一种小而丰富的蛋白质 Pam,仅在较低温度下分泌。Pam 基因存在于所有测试的 Photorhabdus 菌株中,在整个属中高度保守,表明它既是属的祖先,也可能对细菌的生物学很重要。Pam 蛋白与苏云金芽孢杆菌二元毒素的 13.6 kDa 成分有有限的序列相似性。然而,注射或喂食异源生产的 Pam 对大蜡螟或烟青虫幼虫均无杀虫活性。在细菌菌落中,Pam 与一种细胞外多糖(EPS)样基质相关,并改变野生型细胞附着在人工表面的能力。有趣的是,表面等离子体共振(SPR)结合研究表明 Pam 蛋白本身具有粘附特性。尽管 Pam 在整个昆虫感染过程中都有产生,但基因敲除既不影响昆虫毒力,也不影响发光杆菌与其宿主线虫 Heterorhabditis bacteriophora 形成共生关系的能力。

结论

我们研究了一种高度丰富的蛋白质 Pam,它在 Photorhabdus asymbiotica 中以温度依赖的方式分泌。我们的发现表明 Pam 在增强昆虫血液中的表面附着方面发挥重要作用。它与外多糖的关联表明它可能通过调节 EPS 特性发挥作用。尽管它在属中丰富且保守,但我们没有发现 Pam 在毒力或共生中发挥作用的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3439/2878306/a7a51662d3f5/1471-2180-10-141-1.jpg

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