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在推测的链球菌分组中,产α毒素的产气荚膜梭菌与链球菌CAMP因子表现出的协同溶血现象。

Synergistic hemolysis phenomenon shown by an alpha-toxin-producing Clostridium perfingens and streptococcal CAMP factor in presumptive streptococcal grouping.

作者信息

Gubash S M

出版信息

J Clin Microbiol. 1978 Nov;8(5):480-8. doi: 10.1128/jcm.8.5.480-488.1978.

DOI:10.1128/jcm.8.5.480-488.1978
PMID:215600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC275283/
Abstract

A new phenomenon of synergistic hemolysis by Clostridium perfringens alpha-toxin and the streptococcal CAMP factor on human and guinea pig erythrocytes is described. A possible mode of action of the CAMP factors is suggested. On human blood agar all of the tested isolates of group B streptococci gave an arrowhead-shaped zone of hemolysis; 74% of group A gave a crescent-shaped lytic zone, whereas all isolates of groups C and G and the remaining 26% of group A streptococci gave a bullet-shaped lytic zone. By comparison, in the CAMP test incubated aerobically and anaerobically, 70 and 91%, respectively, of streptococci other than group B gave positive, arrowhead-shaped lytic zones. If all intermediate positive reactions in the CAMP tests were read as negative after aerobic incubation, only 89% of group B streptococci would be properly identified. The synergistic hemolysis phenomenon, using an alpha-toxin-producing C. perfringens and human blood agar, provided a reliable test for presumptive identification of group B streptococci, with promising potential to differentiate in the same test group A streptococci from other groups.

摘要

本文描述了产气荚膜梭菌α毒素与链球菌CAMP因子对人和豚鼠红细胞的协同溶血新现象,并提出了CAMP因子可能的作用模式。在人血琼脂上,所有检测的B组链球菌分离株均产生箭头状溶血区;74%的A组链球菌产生新月形溶解区,而所有C组和G组分离株以及其余26%的A组链球菌产生子弹形溶解区。相比之下,在需氧和厌氧培养的CAMP试验中,除B组外,分别有70%和91%的链球菌产生阳性箭头状溶解区。如果需氧培养后将CAMP试验中的所有中间阳性反应判为阴性,那么只有89%的B组链球菌能被正确鉴定。利用产生α毒素的产气荚膜梭菌和人血琼脂的协同溶血现象,为B组链球菌的初步鉴定提供了可靠试验,在同一试验中区分A组链球菌与其他组链球菌具有良好潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/9323f1332edc/jcm00196-0031-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/e490e6fff205/jcm00196-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/46302dae3010/jcm00196-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/eadf61a3ac35/jcm00196-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/a84253c0d114/jcm00196-0030-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/9323f1332edc/jcm00196-0031-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/e490e6fff205/jcm00196-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/46302dae3010/jcm00196-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/eadf61a3ac35/jcm00196-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/a84253c0d114/jcm00196-0030-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a8/275283/9323f1332edc/jcm00196-0031-a.jpg

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