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FORMATION OF SEROLOGICALLY REACTIVE DEXTRANS BY STREPTOCOCCI FROM SUBACUTE BACTERIAL ENDOCARDITIS.链球菌引起亚急性细菌性心内膜炎时形成的血清反应性右旋糖酐。
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Clonal diversity and turnover of Streptococcus mitis bv. 1 on shedding and nonshedding oral surfaces of human infants during the first year of life.婴儿出生后第一年口腔有菌和无菌表面上缓症链球菌1型克隆多样性及更替情况
Clin Diagn Lab Immunol. 2005 Oct;12(10):1184-90. doi: 10.1128/CDLI.12.10.1184-1190.2005.
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Prerequisites for dextran production by Streptococcus bovis.牛链球菌生产右旋糖酐的先决条件。
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Establishment of streptococci in the upper respiratory tract: longitudinal changes in the mouth and nasopharynx up to 2 years of age.上呼吸道中链球菌的定植:2岁以下儿童口腔和鼻咽部的纵向变化
J Med Microbiol. 2002 Sep;51(9):723-730. doi: 10.1099/0022-1317-51-9-723.
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Population dynamics of Streptococcus mitis in its natural habitat.口腔微生态环境中缓症链球菌的种群动态
Infect Immun. 2001 Oct;69(10):6055-63. doi: 10.1128/IAI.69.10.6055-6063.2001.
6
Structures of two cell wall-associated polysaccharides of a Streptococcus mitis biovar 1 strain. A unique teichoic acid-like polysaccharide and the group O antigen which is a C-polysaccharide in common with pneumococci.缓症链球菌1型菌株两种细胞壁相关多糖的结构。一种独特的类磷壁酸多糖以及与肺炎球菌共有的C多糖O抗原。
Eur J Biochem. 2000 Dec;267(24):7147-57. doi: 10.1046/j.1432-1327.2000.01821.x-i2.
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Genetic approaches to the identification of the mitis group within the genus Streptococcus.用于鉴定链球菌属内轻链菌群的遗传学方法。
Microbiology (Reading). 1999 Sep;145 ( Pt 9):2605-2613. doi: 10.1099/00221287-145-9-2605.
8
Humoral immunity to commensal oral bacteria in human infants: salivary secretory immunoglobulin A antibodies reactive with Streptococcus mitis biovar 1, Streptococcus oralis, Streptococcus mutans, and Enterococcus faecalis during the first two years of life.人类婴儿对口腔共生菌的体液免疫:生命最初两年期间唾液中与缓症链球菌生物变种1、口腔链球菌、变形链球菌和粪肠球菌反应的分泌型免疫球蛋白A抗体
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Survival of oral bacteria.口腔细菌的存活
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Clonal diversity of Streptococcus mitis biovar 1 isolates from the oral cavity of human neonates.来自人类新生儿口腔的缓症链球菌1型分离株的克隆多样性。
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人出生后第一年口腔中缓症链球菌1型的生理及血清学变异

Physiological and serological variation in Streptococcus mitis biovar 1 from the human oral cavity during the first year of life.

作者信息

Kirchherr Jennifer L, Bowden George H, Cole Michael F, Kawamura Yoshiaki, Richmond Dorothy A, Sheridan Michael J, Wirth Katherine A

机构信息

Department of Microbiology and Immunology, Georgetown University Medical Center, Washington, DC, USA.

出版信息

Arch Oral Biol. 2007 Jan;52(1):90-9. doi: 10.1016/j.archoralbio.2006.07.003. Epub 2006 Oct 12.

DOI:10.1016/j.archoralbio.2006.07.003
PMID:17045561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1861816/
Abstract

OBJECTIVE

The purpose of the study was to explore the physiological and antigenic diversity of a large number of Streptococcus mitis biovar 1 isolates in order to begin to determine whether these properties contribute to species persistence.

DESIGN

S. mitis biovar 1 was collected from four infants from birth to the first year of age. At each of eight to nine visits, 60 isolates each were obtained from the cheeks, tongue and incisors (once erupted) yielding 4440 in total. These were tested for production of neuraminidase, beta1-N-acetylglucosaminidase, beta1-N-acetylgalactosaminidase, IgA1 protease and amylase-binding. Antigenic diversity was examined by ELISA and Western immunoblotting using antisera raised against S. mitis biovar 1 NCTC 12261(T) and SK145.

RESULTS

Three thousand three hundred and thirty (75%) of the isolates were identified as S. mitis biovar 1 and 3144 (94.4%) could be divided into four large phenotypic groups based on glycosidase production. Fifty-four percent of the isolates produced IgA1 protease, but production was disproportionate among the phenotypes. Between one-third and one-half of the strains of each phenotype bound salivary alpha-amylase. Antisera against strains NCTC 12261(T) and SK145 displayed different patterns of reactivity with randomly selected representatives of the four phenotypes.

CONCLUSIONS

S. mitis biovar 1 is physiologically and antigenically diverse, properties which could aid strains in avoiding host immunity and promote re-colonization of a habitat or transfer to a new habitat.

摘要

目的

本研究旨在探索大量缓症链球菌1型菌株的生理和抗原多样性,以便初步确定这些特性是否有助于该菌种的持续存在。

设计

从4名婴儿出生至1岁期间收集缓症链球菌1型菌株。在8至9次访视中的每次访视时,分别从脸颊、舌头和已萌出的门牙获取60株菌株,共获得4440株。检测这些菌株的神经氨酸酶、β1-N-乙酰氨基葡萄糖苷酶、β1-N-乙酰半乳糖苷酶、IgA1蛋白酶和淀粉酶结合活性。通过酶联免疫吸附测定(ELISA)和使用针对缓症链球菌1型NCTC 12261(T)和SK145制备的抗血清进行的Western免疫印迹分析来检测抗原多样性。

结果

3330株(75%)菌株被鉴定为缓症链球菌1型,基于糖苷酶产生情况,3144株(94.4%)可分为四个大的表型组。54%的菌株产生IgA1蛋白酶,但在各表型中产生情况不均衡。每个表型的三分之一至二分之一的菌株结合唾液α-淀粉酶。针对NCTC 12261(T)和SK145菌株的抗血清与随机选择的四个表型代表显示出不同的反应模式。

结论

缓症链球菌1型在生理和抗原方面具有多样性,这些特性有助于菌株逃避宿主免疫并促进在栖息地的重新定殖或转移至新的栖息地。