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对流行型副溶血性弧菌 O3:K6 的荚膜多糖(K 抗原)和胞外多糖基因进行遗传分析。

Genetic analysis of the capsule polysaccharide (K antigen) and exopolysaccharide genes in pandemic Vibrio parahaemolyticus O3:K6.

机构信息

Department of Pathology, University of Florida, 1600 SW Archer Road, Gainesville, FL 32610, USA.

出版信息

BMC Microbiol. 2010 Nov 2;10:274. doi: 10.1186/1471-2180-10-274.

Abstract

BACKGROUND

Pandemic Vibrio parahaemolyticus has undergone rapid changes in both K- and O-antigens, making detection of outbreaks more difficult. In order to understand these rapid changes, the genetic regions encoding these antigens must be examined. In Vibrio cholerae and Vibrio vulnificus, both O-antigen and capsular polysaccharides are encoded in a single region on the large chromosome; a similar arrangement in pandemic V. parahaemolyticus would help explain the rapid serotype changes. However, previous reports on "capsule" genes are controversial. Therefore, we set out to clarify and characterize these regions in pandemic V. parahaemolyticus O3:K6 by gene deletion using a chitin based transformation strategy.

RESULTS

We generated different deletion mutants of putative polysaccharide genes and examined the mutants by immuno-blots with O and K specific antisera. Our results showed that O- and K-antigen genes are separated in V. parahaemolyticus O3:K6; the region encoding both O-antigen and capsule biosynthesis in other vibrios, i.e. genes between gmhD and rjg, determines the K6-antigen but not the O3-antigen in V. parahaemolyticus. The previously identified "capsule genes" on the smaller chromosome were related to exopolysaccharide synthesis, not K-antigen.

CONCLUSION

Understanding of the genetic basis of O- and K-antigens is critical to understanding the rapid changes in these polysaccharides seen in pandemic V. parahaemolyticus. This report confirms the genetic location of K-antigen synthesis in V. parahaemolyticus O3:K6 allowing us to focus future studies of the evolution of serotypes to this region.

摘要

背景

大流行副溶血性弧菌在 K 和 O 抗原上都经历了快速变化,使得爆发的检测更加困难。为了了解这些快速变化,必须检查编码这些抗原的遗传区域。在霍乱弧菌和创伤弧菌中,O 抗原和荚膜多糖都编码在大染色体上的单个区域;大流行副溶血性弧菌中类似的排列方式将有助于解释快速的血清型变化。然而,之前关于“荚膜”基因的报道存在争议。因此,我们着手使用基于几丁质的转化策略通过基因缺失来阐明和表征大流行副溶血性弧菌 O3:K6 中的这些区域。

结果

我们生成了推定多糖基因的不同缺失突变体,并使用 O 和 K 特异性抗血清通过免疫印迹检查突变体。我们的结果表明,O 抗原和 K 抗原基因在副溶血性弧菌 O3:K6 中是分开的;在其他弧菌中编码 O 抗原和荚膜生物合成的基因,即 gmhD 和 rjg 之间的基因,决定了 K6 抗原而不是副溶血性弧菌的 O3 抗原。较小染色体上先前鉴定的“荚膜基因”与外多糖合成有关,而与 K 抗原无关。

结论

了解 O 抗原和 K 抗原的遗传基础对于理解大流行副溶血性弧菌中这些多糖的快速变化至关重要。本报告证实了副溶血性弧菌 O3:K6 中 K 抗原合成的遗传位置,使我们能够将未来对血清型进化的研究集中在该区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db45/2987987/391d36e1abc1/1471-2180-10-274-1.jpg

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