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Actinobacillus pleuropneumoniae Iron Transport and Urease Activity: Effects on Bacterial Virulence and Host Immune Response

机译:胸膜肺炎放线杆菌铁运输和脲酶活性:对细菌毒力和宿主免疫反应的影响。

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Actinobacillus pleuropneumoniae, a porcine respiratory tract pathogen, has been shown to express transferrin-binding proteins and urease during infection. Both activities have been associated with virulence; however, their functional role for infection has not yet been elucidated. We used two isogenic A. pleuropneumoniaesingle mutants (ΔexbB and ΔureC) and a newly constructed A. pleuropneumoniae double (ΔureC ΔexbB) mutant in aerosol infection experiments. Neither the A. pleuropneumoniaeΔexbB mutant nor the double ΔureCΔexbB mutant was able to colonize sufficiently long to initiate a detectable humoral immune response. These results imply that the ability to utilize transferrin-bound iron is required for multiplication and persistence of A. pleuropneumoniae in the porcine respiratory tract. TheA. pleuropneumoniae ΔureC mutant and the parent strain both caused infections that were indistinguishable from one another in the acute phase of disease; however, 3 weeks postinfection the A. pleuropneumoniae ΔureCmutant, in contrast to the parent strain, could not be isolated from healthy lung tissue. In addition, the local immune response—as assessed by fluorescence-activated cell sorter and enzyme-linked immunosorbent spot analyses—revealed a significantly higher number ofA. pleuropneumoniae-specific B cells in the bronchoalveolar lavage fluid (BALF) of pigs infected with the A. pleuropneumoniae ΔureC mutant than in the BALF of those infected with the parent strain. These results imply thatA. pleuropneumoniae urease activity may cause sufficient impairment of the local immune response to slightly improve the persistence of the urease-positive A. pleuropneumoniaeparent strain.
机译:猪呼吸道病原菌胸膜肺炎放线杆菌在感染过程中表达转铁蛋白结合蛋白和脲酶。两种活动都与毒力有关。但是,它们在感染中的功能作用尚未阐明。我们使用了两个同基因的 A。胸膜肺炎单个突变体(Δ exbB 和Δ ureC )和一个新构建的 A。气溶胶感染实验中的胸膜肺炎双(Δ ureC Δ exbB )突变体。 A都没有。胸膜肺炎Δ exbB 突变体或双Δ ureC Δ exbB 突变体能够定植足够长的时间以启动可检测的体液免疫反应。这些结果暗示 A的繁殖和持久性需要利用运铁蛋白结合的铁的能力。猪呼吸道中的胸膜肺炎 A。胸膜肺炎Δ ureC 突变体和亲本菌株在疾病的急性期均引起相互之间无法区分的感染。但是, A感染后3周。与亲本菌株相比,胸膜肺炎Δ ureC 突变体无法从健康的肺组织中分离出来。另外,通过荧光激活的细胞分选仪和酶联免疫吸附点分析评估的局部免疫应答显示出显着更高数量的em。感染 A的猪的支气管肺泡灌洗液(BALF)中的胸膜肺炎特异性B细胞。胸膜肺炎Δ ureC 突变体比亲本菌株感染者的BALF中突变。这些结果表明 A。胸膜肺炎尿素酶的活性可能会引起局部免疫反应的充分损害,以稍微改善尿素酶阳性的 A的持久性。胸膜肺炎亲本菌株。

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