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牛肺疫巴氏杆菌病:牛外周血白细胞对活的和灭活的溶血巴氏杆菌、多杀性巴氏杆菌及大肠杆菌的化学发光反应

Bovine pneumonic pasteurellosis: chemiluminescent response of bovine peripheral blood leukocytes to living and killed Pasteurella haemolytica, Pasteurella multocida, and Escherichia coli.

作者信息

Chang Y F, Renshaw H W, Augustine J L

出版信息

Am J Vet Res. 1985 Nov;46(11):2266-71.

PMID:3907434
Abstract

A luminol-dependent chemiluminescence (LDCL) assay was used to evaluate the response of bovine polymorphonuclear leukocytes; (neutrophils [PMN]) to living and heat-killed Escherichia coli, Pasteurella multocida (type A, serotype 3), and P haemolytica (biotype A, serotype 1), and to heat-killed P haemolytica and sterile culture supernatant from living P haemolytica. Control cultures containing PMN that had not been phagocytically stimulated with bacteria had a modest increase in LDCL during the initial 10 minutes of incubation, followed by a gradual decline throughout the 120-minute incubation period. Bovine PMN emitted LDCL more efficiently when the cells were exposed to living E coli or P multocida than when they were exposed to the same bacteria killed by heat. The mean LDCL values for reaction mixtures containing living E coli or P multocida peaked at 30 minutes of incubation and remained above values for mixtures containing the same heat-killed bacteria. Kinetics of the LDCL response of bovine PMN to heat-killed P haemolytica were similar (although reduced in amplitude) to that observed with killed E coli or P multocida. The LDCL response of bovine PMN to living P haemolytica was not like that for E coli or P multocida, and was characterized by the development of a peak response at 10 minutes followed by a precipitous decrease in responsiveness and a subsequent complete cessation of LDCL. Addition of sterile culture supernatant from living P haemolytica to test samples containing heat-killed P haemolytica induced a response similar to that obtained with the living microorganism.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用鲁米诺依赖性化学发光(LDCL)分析方法评估牛多形核白细胞(即中性粒细胞[PMN])对活的和热灭活的大肠杆菌、多杀巴斯德菌(A型3血清型)、溶血巴斯德菌(生物型A,血清型1)的反应,以及对热灭活的溶血巴斯德菌和活的溶血巴斯德菌无菌培养上清液的反应。含有未受细菌吞噬刺激的PMN的对照培养物在孵育最初10分钟内LDCL有适度增加,随后在整个120分钟孵育期逐渐下降。当细胞暴露于活的大肠杆菌或多杀巴斯德菌时,牛PMN发出LDCL的效率高于暴露于相同热灭活细菌时。含有活的大肠杆菌或多杀巴斯德菌的反应混合物的平均LDCL值在孵育30分钟时达到峰值,并保持高于含有相同热灭活细菌的混合物的值。牛PMN对热灭活的溶血巴斯德菌的LDCL反应动力学与热灭活的大肠杆菌或多杀巴斯德菌相似(尽管幅度降低)。牛PMN对活的溶血巴斯德菌的LDCL反应与大肠杆菌或多杀巴斯德菌不同,其特征是在10分钟时出现峰值反应,随后反应性急剧下降,随后LDCL完全停止。将活的溶血巴斯德菌的无菌培养上清液添加到含有热灭活的溶血巴斯德菌的测试样品中,诱导出与活微生物相似的反应。(摘要截短于250字)

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