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鱼类病原菌屈挠杆菌 MS-FC-4 株产生的铁载体对于其毒力并非必需。

Siderophores Produced by the Fish Pathogen Flavobacterium columnare Strain MS-FC-4 Are Not Essential for Its Virulence.

机构信息

Department of Biological Sciences, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin, USA.

National Center for Cool and Cold Water Aquaculture, Agricultural Research Service, U.S. Department of Agriculture, Kearneysville, West Virginia, USA.

出版信息

Appl Environ Microbiol. 2022 Sep 13;88(17):e0094822. doi: 10.1128/aem.00948-22. Epub 2022 Aug 15.

Abstract

Flavobacterium columnare causes columnaris disease in wild and aquaculture-reared freshwater fish. F. columnare virulence mechanisms are not well understood, and current methods to control columnaris disease are inadequate. Iron acquisition from the host is important for the pathogenicity and virulence of many bacterial pathogens. F. columnare iron acquisition has not been studied in detail. We identified genes predicted to function in siderophore production for ferric iron uptake. Genes predicted to encode the proteins needed for siderophore synthesis, export, uptake, and regulation were deleted from F. columnare strain MS-FC-4. The mutants were examined for defects in siderophore production, for growth defects in iron-limited conditions, and for virulence against zebrafish and rainbow trout. Mutants lacking all siderophore activity were obtained. These mutants displayed growth defects when cultured under iron-limited conditions, but they retained virulence against zebrafish and rainbow trout similar to that exhibited by the wild type, indicating that the F. columnare MS-FC-4 siderophores are not required for virulence under the conditions tested. Columnaris disease, which is caused by Flavobacterium columnare, is a major problem for freshwater aquaculture. Little is known regarding F. columnare virulence factors, and control measures are limited. Iron acquisition mechanisms such as siderophores are important for virulence of other pathogens. We identified F. columnare siderophore biosynthesis, export, and uptake genes. Deletion of these genes eliminated siderophore production and resulted in growth defects under iron-limited conditions but did not alter virulence in rainbow trout or zebrafish. The results indicate that the F. columnare strain MS-FC-4 siderophores are not critical virulence factors under the conditions tested but may be important for survival under iron-limited conditions in natural aquatic environments or aquaculture systems.

摘要

柱状屈挠杆菌引起野生和养殖淡水鱼类的柱状病。柱状屈挠杆菌的毒力机制尚未得到很好的理解,目前控制柱状病的方法也不充分。从宿主获取铁对于许多细菌病原体的致病性和毒力很重要。柱状屈挠杆菌的铁获取尚未得到详细研究。我们鉴定了预测在铁摄取方面具有功能的铁载体产生基因。预测编码铁载体合成、外排、摄取和调节所需蛋白质的基因从柱状屈挠杆菌菌株 MS-FC-4 中缺失。检查了突变体在铁载体产生、铁限制条件下的生长缺陷以及对斑马鱼和虹鳟鱼的毒力方面的缺陷。获得了缺乏所有铁载体活性的突变体。这些突变体在铁限制条件下培养时表现出生长缺陷,但它们对斑马鱼和虹鳟鱼的毒力与野生型相似,表明在测试条件下,F. columnare MS-FC-4 铁载体对毒力不是必需的。

由柱状屈挠杆菌引起的柱状病是淡水水产养殖的一个主要问题。关于 F. columnare 毒力因子的了解甚少,控制措施也有限。铁获取机制(如铁载体)对于其他病原体的毒力很重要。我们鉴定了 F. columnare 铁载体生物合成、外排和摄取基因。这些基因的缺失消除了铁载体的产生,并导致在铁限制条件下的生长缺陷,但没有改变在虹鳟或斑马鱼中的毒力。结果表明,在测试条件下,F. columnare 菌株 MS-FC-4 铁载体不是关键的毒力因子,但在自然水生环境或水产养殖系统中可能对铁限制条件下的生存很重要。

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