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本文引用的文献

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The largest Q fever outbreak ever reported.有史以来报告的最大规模的Q热疫情。
Neth J Med. 2010 Dec;68(12):380-1.
2
The Q fever epidemic in The Netherlands: history, onset, response and reflection.荷兰 Q 热疫情:历史、爆发、应对与反思。
Epidemiol Infect. 2011 Jan;139(1):1-12. doi: 10.1017/S0950268810002268. Epub 2010 Oct 5.
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Coxiella burnetii Nine Mile II proteins modulate gene expression of monocytic host cells during infection.考克斯体九英里 II 蛋白在感染过程中调节单核宿主细胞的基因表达。
BMC Microbiol. 2010 Sep 20;10:244. doi: 10.1186/1471-2180-10-244.
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Sex-related differences in gene expression following Coxiella burnetii infection in mice: potential role of circadian rhythm.感染柯克斯体后小鼠基因表达的性别差异:昼夜节律的潜在作用。
PLoS One. 2010 Aug 13;5(8):e12190. doi: 10.1371/journal.pone.0012190.
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A large Q fever outbreak in an urban school in central Israel.以色列中部一城市学校发生大规模 Q 热疫情。
Clin Infect Dis. 2010 Jun 1;50(11):1433-8. doi: 10.1086/652442.
6
Q fever in the Netherlands: an update on the epidemiology and control measures.荷兰的 Q 热:流行病学和控制措施的最新进展。
Euro Surveill. 2010 Mar 25;15(12):19520.
7
Q fever outbreak in Cheltenham, United Kingdom, in 2007 and the use of dispersion modelling to investigate the possibility of airborne spread.2007 年英国切尔滕纳姆 Q 热疫情爆发及使用扩散模型调查空气传播的可能性。
Euro Surveill. 2010 Mar 25;15(12):19521.
8
Investigation of a Q fever outbreak in a Scottish co-located slaughterhouse and cutting plant.苏格兰同地屠宰场和切割厂中 Q 热疫情的调查。
Zoonoses Public Health. 2010 Dec;57(7-8):493-8. doi: 10.1111/j.1863-2378.2009.01251.x.
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Q Fever.Q 热。
Vet Microbiol. 2010 Jan 27;140(3-4):297-309. doi: 10.1016/j.vetmic.2009.07.016. Epub 2009 Aug 8.
10
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.

Q热(伯纳特立克次体)的动物模型。

Animal models of Q fever (Coxiella burnetii).

作者信息

Bewley Kevin R

机构信息

Public Health England (PHE), Porton Down, Salisbury, Wiltshire, UK.

出版信息

Comp Med. 2013;63(6):469-76.

PMID:24326221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3866982/
Abstract

Q fever, caused by the pathogen Coxiella burnetii, is an acute disease that can progress to become a serious chronic illness. The organism leads an obligate, intracellular lifecycle, during which it multiplies in the phagolytic compartments of the phagocytic cells of the immune system of its hosts. This characteristic makes study of the organism particularly difficult and is perhaps one of the reasons why, more than 70 y after its discovery, much remains unknown about the organism and its pathogenesis. A variety of animal species have been used to study both the acute and chronic forms of the disease. Although none of the models perfectly mimics the disease process in humans, each opens a window onto an important aspect of the pathology of the disease. We have learned that immunosuppression, overexpression of IL10, or physical damage to the heart muscle in mice and guinea pigs can induce disease that is similar to the chronic disease seen in humans, suggesting that this aspect of disease may eventually be fully understood. Models using species from mice to nonhuman primates have been used to evaluate and characterize vaccines to protect against the disease and may ultimately yield safer, less expensive vaccines.

摘要

Q热由病原体贝纳柯克斯体引起,是一种急性疾病,可发展为严重的慢性疾病。该病原体具有专性细胞内生命周期,在此期间它在宿主免疫系统吞噬细胞的吞噬小室中繁殖。这一特性使得对该病原体的研究格外困难,这或许也是为什么在其被发现70多年后,人们对该病原体及其发病机制仍知之甚少的原因之一。多种动物物种已被用于研究该疾病的急性和慢性形式。尽管没有一种模型能完美模拟人类的疾病过程,但每种模型都为该疾病病理学的一个重要方面打开了一扇窗。我们已经了解到,小鼠和豚鼠的免疫抑制、IL10的过度表达或心肌的物理损伤可诱发与人类所见慢性疾病相似的疾病,这表明该疾病的这一方面最终可能会被完全理解。从小鼠到非人灵长类动物的各种物种模型已被用于评估和表征预防该疾病的疫苗,最终可能会产生更安全、更便宜的疫苗。