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本文引用的文献

1
Detecting and measuring small numbers of viable Coxiella burnetii.检测和测量少量存活的伯纳特立克次体。
FEMS Immunol Med Microbiol. 2012 Feb;64(1):61-5. doi: 10.1111/j.1574-695X.2011.00898.x. Epub 2011 Dec 5.
2
A comparison of methods for extracting DNA from Coxiella burnetii as measured by a duplex qPCR assay.比较用双 qPCR 法检测贝氏柯克斯体时从样品中提取 DNA 的方法。
Lett Appl Microbiol. 2011 May;52(5):514-20. doi: 10.1111/j.1472-765X.2011.03034.x. Epub 2011 Mar 18.
3
Coxiella burnetii isolates cause genogroup-specific virulence in mouse and guinea pig models of acute Q fever.伯纳特柯克斯体分离株在急性Q热的小鼠和豚鼠模型中引起特定基因组的毒力。
Infect Immun. 2009 Dec;77(12):5640-50. doi: 10.1128/IAI.00851-09. Epub 2009 Sep 28.
4
Attenuated Coxiella burnetii phase II causes a febrile response in gamma interferon knockout and Toll-like receptor 2 knockout mice and protects against reinfection.减毒的贝氏柯克斯体II期菌株在γ干扰素基因敲除小鼠和Toll样受体2基因敲除小鼠中引起发热反应,并能预防再次感染。
Infect Immun. 2007 Dec;75(12):5845-58. doi: 10.1128/IAI.00901-07. Epub 2007 Sep 24.
5
T cells are essential for bacterial clearance, and gamma interferon, tumor necrosis factor alpha, and B cells are crucial for disease development in Coxiella burnetii infection in mice.T细胞对于清除细菌至关重要,而γ干扰素、肿瘤坏死因子α和B细胞在小鼠感染伯纳特立克次体的疾病发展过程中起着关键作用。
Infect Immun. 2007 Jul;75(7):3245-55. doi: 10.1128/IAI.01767-06. Epub 2007 Apr 16.
6
Analysis of the O-antigen biosynthesis regions of phase II isolates of Coxiella burnetii.伯氏考克斯氏体II期分离株O抗原生物合成区域的分析
FEMS Microbiol Lett. 2007 Feb;267(1):102-7. doi: 10.1111/j.1574-6968.2006.00544.x. Epub 2006 Nov 29.
7
Comparative virulence of phase I and II Coxiella burnetii in immunodeficient mice.免疫缺陷小鼠中Ⅰ相和Ⅱ相伯纳特柯克斯体的相对毒力
Ann N Y Acad Sci. 2005 Dec;1063:167-70. doi: 10.1196/annals.1355.026.
8
A growth study of Coxiella burnetii Nine Mile Phase I and Phase II in fibroblasts.伯纳特柯克斯体九里株I期和II期在成纤维细胞中的生长研究
FEMS Immunol Med Microbiol. 2004 Nov 1;42(3):291-7. doi: 10.1016/j.femsim.2004.06.003.
9
SCID mouse model for lethal Q fever.致死性Q热的重症联合免疫缺陷(SCID)小鼠模型
Infect Immun. 2003 Aug;71(8):4717-23. doi: 10.1128/IAI.71.8.4717-4723.2003.
10
Identification and cloning potentially protective antigens of Coxiella burnetii using sera from mice experimentally infected with Nine Mile phase I.利用感染九英里一期株的小鼠血清鉴定和克隆伯氏考克斯氏体的潜在保护性抗原。
Ann N Y Acad Sci. 2003 Jun;990:510-20. doi: 10.1111/j.1749-6632.2003.tb07420.x.

贝氏柯克斯体衰减的 9 英里二期克隆 4/RSA439 株对严重联合免疫缺陷(SCID)小鼠具有高度毒力。

The attenuated nine mile phase II clone 4/RSA439 strain of Coxiella burnetii is highly virulent for severe combined immunodeficient (SCID) mice.

机构信息

Department of Microbiology, Pathology North-Hunter, NSW Health Pathology, John Hunter Hospital, Locked Bag 1, HRMC, Australia; Australian Rickettsial Reference Laboratory, Barwon Health, Geelong, Australia.

出版信息

Am J Trop Med Hyg. 2013 Oct;89(4):800-3. doi: 10.4269/ajtmh.12-0653. Epub 2013 Aug 19.

DOI:10.4269/ajtmh.12-0653
PMID:23958905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3795117/
Abstract

The Nine Mile phase II clone 4 (NMIIC4) strain of Coxiella burnetii is an attenuated phase II strain that has lost the genes for virulence determinant type 1 lipopolysaccharide. These bacteria were very virulent for severe combined immunodeficient (SCID) mice. The lethal dose 50 (LD50) was ~10 bacteria. Infected SCID mice died between Day 28 and Day 53 post-infection. At termination of the experiment (Day 60) only 5 of 24 mice had survived. The degree of splenomegaly was directly related to the bacterial load in the SCID mice spleens. The NMIIC4 was avirulent in immunocompetent wild mice and bacterial DNA copies in splenic tissue were extremely low. The SCID mice that were inoculated with high doses of heat inactivated NMIIC4 C. burnetii were all alive at Day 60 and without splenomegaly. It appears that the phase I lipopolysaccharide present in virulent Nine Mile phase I but not in attenuated NMIIC4 is not the only virulence factor for C. burnetii.

摘要

贝氏柯克斯体九英里二期克隆 4(NMIIC4)株是一种减毒的二期菌株,它失去了毒力决定因素 1 型脂多糖的基因。这些细菌对严重联合免疫缺陷(SCID)小鼠具有很强的毒性。半数致死量(LD50)约为 10 个细菌。感染的 SCID 小鼠在感染后第 28 天至第 53 天之间死亡。在实验结束时(第 60 天),24 只小鼠中只有 5 只存活。脾肿大的程度与 SCID 小鼠脾脏中的细菌负荷直接相关。NMIIC4 在免疫功能正常的野生小鼠中无致病性,且脾脏组织中的细菌 DNA 拷贝极低。接种高剂量热灭活 NMIIC4 贝氏柯克斯体的 SCID 小鼠在第 60 天都存活且无脾肿大。似乎存在于毒力九英里一期而非减毒 NMIIC4 中的一期脂多糖并非贝氏柯克斯体的唯一毒力因子。