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本文引用的文献

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Ecology of Vibrio parahaemolyticus and Vibrio vulnificus in the coastal and estuarine waters of Louisiana, Maryland, Mississippi, and Washington (United States).美国路易斯安那州、马里兰州、密西西比州和华盛顿州沿海和河口水域副溶血性弧菌和创伤弧菌的生态学研究。

Appl Environ Microbiol. 2012 Oct;78(20):7249-57. doi: 10.1128/AEM.01296-12. Epub 2012 Aug 3.

2

Decreased expression of type 1 fimbriae by a pst mutant of uropathogenic Escherichia coli reduces urinary tract infection.尿路致病性大肠埃希菌 pst 突变株致 1 型菌毛表达减少可降低尿路感染。

Infect Immun. 2012 Aug;80(8):2802-15. doi: 10.1128/IAI.00162-12. Epub 2012 Jun 4.

3

Kanagawa-negative, tdh- and trh-positive Vibrio parahaemolyticus isolated from fresh oysters marketed in Fortaleza, Brazil.从巴西福塔雷萨市销售的新鲜牡蛎中分离出的 kanagawa 阴性、tdh 和 trh 阳性副溶血性弧菌。

Curr Microbiol. 2011 Aug;63(2):126-30. doi: 10.1007/s00284-011-9945-x. Epub 2011 May 28.

4

Use of OmpU porins for attachment and invasion of Crassostrea gigas immune cells by the oyster pathogen Vibrio splendidus.利用 OmpU 孔蛋白附着和入侵牡蛎病原体灿烂弧菌对虾贻贝类免疫细胞。

Proc Natl Acad Sci U S A. 2011 Feb 15;108(7):2993-8. doi: 10.1073/pnas.1015326108. Epub 2011 Jan 31.

5

The Vibrio parahaemolyticus Type III Secretion Systems manipulate host cell MAPK for critical steps in pathogenesis.副溶血性弧菌 III 型分泌系统操纵宿主细胞的丝裂原活化蛋白激酶（MAPK），以完成致病过程中的关键步骤。

BMC Microbiol. 2010 Dec 30;10:329. doi: 10.1186/1471-2180-10-329.

6

Distribution of type III secretion systems in Vibrio parahaemolyticus from the northern Gulf of Mexico.墨西哥湾北部副溶血性弧菌 III 型分泌系统的分布。

J Appl Microbiol. 2010 Sep;109(3):953-62. doi: 10.1111/j.1365-2672.2010.04722.x.

7

Contribution of Vibrio parahaemolyticus virulence factors to cytotoxicity, enterotoxicity, and lethality in mice.副溶血性弧菌毒力因子对小鼠细胞毒性、肠毒性和致死性的贡献。

Infect Immun. 2010 Apr;78(4):1772-80. doi: 10.1128/IAI.01051-09. Epub 2010 Jan 19.

8

Phase variation, capsular polysaccharide, pilus and flagella contribute to uptake of Vibrio vulnificus by the Eastern oyster (Crassostrea virginica).相变、荚膜多糖、菌毛和鞭毛有助于创伤弧菌被美国东海岸牡蛎（弗吉尼亚巨蛎）摄取。

Environ Microbiol. 2009 Aug;11(8):1934-44. doi: 10.1111/j.1462-2920.2009.01916.x.

9

Vibrio biofilms: so much the same yet so different.弧菌生物膜：如此相似却又如此不同。

Trends Microbiol. 2009 Mar;17(3):109-18. doi: 10.1016/j.tim.2008.12.004. Epub 2009 Feb 21.

10

Role of type IV pilins in persistence of Vibrio vulnificus in Crassostrea virginica oysters.IV型菌毛蛋白在创伤弧菌于弗吉尼亚海湾扇贝中持续存在的作用。

Appl Environ Microbiol. 2007 Aug;73(15):5041-4. doi: 10.1128/AEM.00641-07. Epub 2007 Jun 8.

副溶血弧菌在太平洋牡蛎中的持续存在是一个多因素的过程，涉及菌毛和鞭毛，但不涉及 III 型分泌系统或相位变异。

Persistence of Vibrio parahaemolyticus in the Pacific oyster, Crassostrea gigas, is a multifactorial process involving pili and flagella but not type III secretion systems or phase variation.

机构信息

Department of Biomedical Sciences, Oregon State University, Corvallis, OR, USA.

出版信息

Appl Environ Microbiol. 2013 May;79(10):3303-5. doi: 10.1128/AEM.00314-13. Epub 2013 Mar 8.

DOI:10.1128/AEM.00314-13

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3685240/

Abstract

Vibrio parahaemolyticus can resist oyster depuration, suggesting that it possesses specific factors for persistence. We show that type I pili, type IV pili, and both flagellar systems contribute to V. parahaemolyticus persistence in Pacific oysters whereas type III secretion systems and phase variation do not.

摘要

副溶血性弧菌可以抵抗牡蛎的净化作用，这表明它具有特定的持久生存因素。我们表明，I 型菌毛、IV 型菌毛和两个鞭毛系统有助于副溶血性弧菌在太平洋牡蛎中持久存在，而 III 型分泌系统和相位变异则没有。