Study on the pathogenesis of normal flora in respiratory tract infection and on the diagnostic methods for the flora
呼吸道感染正常菌群发病机制及菌群诊断方法研究
基本信息
- 批准号:10670555
- 负责人:
- 金额:$ 1.66万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1998
- 资助国家:日本
- 起止时间:1998 至 1999
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Streptococcus milleri group and anaerobes, recognized as normal flora in the mouth, were proved to be isolated from the patients of acute pneumonia, lung abscess and thoracic empyema by the methods of transthoracic needle aspiration, which could prevented the causative organisms from contamination with normal flora. This suggested that S. milleri group and anaerobes were important causative organisms in pulmonary infections.Studies on the mechanisms of their pathogenicity in the mice model of pneumonia showed that the higher mortality, longer survival in the lungs and more severe pathohistological changes in the mixed infection of S. milleri group and anaerobes than in the single infection, respectively. This suggested that there may be a synergistic effect between S. milleri group and anaerobes.In vitro studies demonstrated that S. milleri group strains isolated from the infectious lesions had stronger ability to inhibit the function of phagocytosis and phagocytic killing of human leukocytes against S. milleri group than that from normal flora. The degree of the inhibition depended on the presence of capsule of the bacteria. The addition of capsular material, mainly composed of mucopolysaccharide, could also inhibited the neutrophil function of phagocytic killing against S. milleri group. The presence of capsular material might be a pathogenicity of S. milleri group strains. On the other hand, the metabolic substances of anaerobes, short-chain fatty acids, inhibited the neutrophil function of phagocytosis and phagocytic killing against bacteria, while they could promoted the growth of S. milleri group.The problems from the view of clinical microbiology was the isolation and identification of S. milleri group. It was elucidated that it depended on what kind of blood agar plate and identification kit used.
经胸针吸法从急性肺炎、肺脓肿和胸胸脓肿患者的口腔中分离出正常菌群——milleri链球菌群和厌氧菌群,可防止病原菌与正常菌群的污染。提示米勒梭菌群和厌氧菌是肺部感染的重要致病菌。对其在肺炎小鼠模型中的致病性机制的研究表明,米勒梭菌组和厌氧菌混合感染分别比单一感染时死亡率更高,肺内存活时间更长,病理组织学改变更严重。这表明米勒梭菌群与厌氧菌群之间可能存在协同作用。体外研究表明,从感染性病变中分离的米勒氏菌群菌株对人白细胞的吞噬和杀伤功能的抑制能力强于正常菌群。抑菌效果与菌囊的存在程度有关。添加以粘多糖为主要成分的荚膜物质也能抑制嗜中性粒细胞对粟粒葡萄球菌组的吞噬杀伤功能。荚膜物质的存在可能是米勒氏葡萄球菌群菌株的致病性。另一方面,厌氧菌的代谢物质短链脂肪酸抑制了嗜中性粒细胞对细菌的吞噬和杀伤功能,而能促进米勒氏菌群的生长。从临床微生物学的角度来看,存在的问题是米勒氏菌群的分离和鉴定。结果表明,这取决于所使用的血琼脂平板和鉴定试剂盒。
项目成果
期刊论文数量(13)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
當山真人,斎藤 厚(本間日臣 編): "Streptococcus milleri group肺炎・膿胸(新しい肺法性肺炎・間質性肺炎の臨床)"克誠堂. 193 (1998)
Masato Toyama,Atsushi Saito(由 Hiomi Honma 编辑):“米勒链球菌群肺炎/脓胸(肺炎/间质性肺炎的新临床实践)”Kuseido 193(1998)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Saito A, Shinzato T: "The role of Streptococcus milleri in pulmonary infections"The Journal of Antimicrobial Chemotherapy. 44・Suppl A. 32-32 (1999)
Saito A,Shinzato T:“米勒链球菌在肺部感染中的作用”抗菌化疗杂志 44·Suppl A. 32-32 (1999)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
草野展周,新里 敬: "Streptococcus milleri groupの検査法"Newsletter Bact. 30. 1-5 (1999)
Nobu Shu Kusano,Kei Niisato:“米勒链球菌群的检测方法”Newsletter Bact. 30. 1-5 (1999)
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Saito A, Shinzato T: "The role of Streptococcus milleri in pulmonary infections"The Journal of Antimicrobial Chemotherapy. 44(Suppl A). 32 (1999)
Saito A,Shinzato T:“米勒链球菌在肺部感染中的作用”抗菌化疗杂志。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Kusano N, Shinzato T: "Laboratory approach for Streptococcus milleri group"Newsletter Bact. 30. 1-5 (1999)
Kusano N、Shinzato T:“米勒链球菌群的实验室方法”Newsletter Bact。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
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SAITO Atsushi其他文献
重症呼吸不全に対するECMOの最新知見
ECMO治疗严重呼吸衰竭的最新研究结果
- DOI:
- 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
SAITO Atsushi;INOUE Takashi;SUZUKI Shinsuke;EZURA Masayuki;UENOHARA Hiroshi;TOMINAGA Teiji;市場晋吾 - 通讯作者:
市場晋吾
SAITO Atsushi的其他文献
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{{ truncateString('SAITO Atsushi', 18)}}的其他基金
Development of 100 W-class superconducting transmit filter
开发100W级超导发射滤波器
- 批准号:
24560393 - 财政年份:2012
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The elucidation of the pathogenesis of dysphagia in amyotrophic lateral sclerosis -Using model mice-
阐明肌萎缩侧索硬化症吞咽困难的发病机制 -使用模型小鼠 -
- 批准号:
23791921 - 财政年份:2011
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
New therapeutic strategy with SMTP for acute cerebral ischemia
SMTP治疗急性脑缺血新策略
- 批准号:
23791582 - 财政年份:2011
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
A study on the mechanisms involved in the invasion of host cells by periodontal pathogens and the novel method for its regulation
牙周病原菌侵袭宿主细胞的机制及调控新方法研究
- 批准号:
22592317 - 财政年份:2010
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The analysis of the differentiation and function of the cells in central nervous system regulated by endoplasmic reticulum stress response.
内质网应激反应调控中枢神经系统细胞分化和功能的分析。
- 批准号:
22800049 - 财政年份:2010
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Research Activity Start-up
Development of high-performance transmit filter using superconducting bulk
使用超导体开发高性能发射滤波器
- 批准号:
21760246 - 财政年份:2009
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Expression of cellular protective factors in neuronal cells after cerebral ischemia
脑缺血后神经元细胞保护因子的表达
- 批准号:
21791344 - 财政年份:2009
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
The discovery research of the vulnerability factor, which is associated with schizophrenia, through familial clustering cases of both Hermansky-Pudlak syndrome and schizophrenia.
通过赫曼斯基-普德拉克综合征和精神分裂症的家族聚集性病例发现与精神分裂症相关的脆弱因素。
- 批准号:
20790857 - 财政年份:2008
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Study on the pathogenecity of tuberculosis in elderly people and development of its prevention
老年人结核病发病机制研究及防治进展
- 批准号:
15591061 - 财政年份:2003
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Studies on newly synthesized peptides having parasitocidal activity, and their mechanisms on host immune repsponses.
新合成的具有杀寄生虫活性的肽及其对宿主免疫反应的机制的研究。
- 批准号:
07406014 - 财政年份:1995
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
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