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多杀性巴氏杆菌对培养的火鸡外周血单核细胞的黏附增强。

Enhanced adhesion of Pasteurella multocida to cultured turkey peripheral blood monocytes.

作者信息

Pruimboom I M, Rimler R B, Ackermann M R

机构信息

Avian and Swine Respiratory Diseases Research Unit, USDA Agricultural Research Service National Animal Disease Center, Ames, Iowa 50010, USA.

出版信息

Infect Immun. 1999 Mar;67(3):1292-6. doi: 10.1128/IAI.67.3.1292-1296.1999.

Abstract

Capsular hyaluronic acid (HA) mediates adhesion of serogroup A strains of Pasteurella multocida to elicited turkey air sac macrophages (TASM). In contrast, freshly isolated turkey peripheral blood monocytes (TPBM) do not bind serogroup A strains. Following culture of TPBM for 6 days in chamber slides, adhesion of the bacteria to TPBM increased gradually. Incubation in chamber slides coated with entactin-collagen IV-laminin (ECL) attachment matrix or exposure to phorbol myristate acetate (PMA) further enhanced the adhesion of P. multocida to TPBM. Addition of HA, but not Arg-Gly-Asp peptide, to TPBM culture inhibited bacterial adherence similarly to the inhibition previously reported for TASM. Exposure of TPBM to monoclonal antibody directed against HA-binding cell surface proteoglycan (CD44) decreased binding of P. multocida. Collectively, these findings indicate that P. multocida adhesion to TPBM is mediated by capsular HA and can be increased by culture on ECL attachment matrix or PMA exposure. Additionally, the findings suggest that the capsular mucopolysaccharide of serogroup A strains of P. multocida recognizes an isoform of CD44 expressed on cultured TPBM.

摘要

荚膜透明质酸(HA)介导多杀性巴氏杆菌A血清型菌株与诱导产生的火鸡气囊巨噬细胞(TASM)的黏附。相比之下,新鲜分离的火鸡外周血单核细胞(TPBM)不与A血清型菌株结合。在培养箱载玻片上培养TPBM 6天后,细菌与TPBM的黏附逐渐增加。在涂有巢蛋白-胶原蛋白IV-层粘连蛋白(ECL)附着基质的培养箱载玻片中孵育或暴露于佛波酯肉豆蔻酸酯乙酸酯(PMA)进一步增强了多杀性巴氏杆菌与TPBM的黏附。向TPBM培养物中添加HA而非精氨酸-甘氨酸-天冬氨酸肽,对细菌黏附的抑制作用与先前报道的对TASM的抑制作用相似。将TPBM暴露于针对HA结合细胞表面蛋白聚糖(CD44)的单克隆抗体可降低多杀性巴氏杆菌的结合。总的来说,这些发现表明多杀性巴氏杆菌与TPBM的黏附由荚膜HA介导,并且可以通过在ECL附着基质上培养或暴露于PMA而增加。此外,这些发现表明多杀性巴氏杆菌A血清型菌株的荚膜黏多糖识别培养的TPBM上表达的CD44同工型。

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