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心内膜炎和猫抓病中出现的新型汉赛巴尔通体血清型。

New serotype of Bartonella henselae in endocarditis and cat-scratch disease.

作者信息

Drancourt M, Birtles R, Chaumentin G, Vandenesch F, Etienne J, Raoult D

机构信息

Unité des Richettsies CNRS EP J0054, Marseille, France.

出版信息

Lancet. 1996 Feb 17;347(8999):441-3. doi: 10.1016/s0140-6736(96)90012-4.

Abstract

BACKGROUND

The fastidious nature of Bartonella henselae is such that demonstration of clinical infection relies mainly on serological or molecular biological methods. Only five isolates have been obtained from patients with cat-scratch disease (CSD) and none from endocarditis.

METHODS

We isolated B henselae from a CSD patient and, for the first time, from a patient with endocarditis. The isolates were characterised on the basis of morphology, biochemistry, cell-wall fatty-acid analysis, PCR-restriction fragment length polymorphism analysis of the 16-23S intragenic spacer region, and 16S rRNA gene sequences. Characterisation of these isolates indicated them to belong to a new serogroup, which we have called "Marseille", and to a new genotype based on the 16S rRNA gene sequence. The new variant was incorporated into an immuno-fluorescence antibody test (IFAT), which was used to reassess serum samples from 113 CSD patients who were seronegative with the conventional IFAT.

FINDINGS

18 (16%) of these apparently seronegative patients yielded significantly raised titres. 20 CSD patients who were seropositive as judged by the conventional IFAT remained seropositive with the new IFAT.

INTERPRETATION

Antigenic variability within the species is one possible reason for inconsistent results in the serological diagnosis of CSD.

摘要

背景

汉赛巴尔通体苛求的特性使得临床感染的证明主要依赖血清学或分子生物学方法。仅从猫抓病(CSD)患者中获得了5株分离株,而从心内膜炎患者中未获得任何分离株。

方法

我们从一名CSD患者以及首次从一名心内膜炎患者中分离出汉赛巴尔通体。基于形态学、生物化学、细胞壁脂肪酸分析、16 - 23S基因间隔区的PCR - 限制性片段长度多态性分析以及16S rRNA基因序列对分离株进行了鉴定。这些分离株的鉴定表明它们属于一个新的血清群,我们将其命名为“马赛”,并且基于16S rRNA基因序列属于一个新的基因型。将这个新变种纳入免疫荧光抗体试验(IFAT),该试验用于重新评估113例用传统IFAT检测血清学阴性的CSD患者的血清样本。

结果

这些明显血清学阴性的患者中有18例(16%)产生了显著升高的滴度。20例经传统IFAT判断为血清学阳性的CSD患者用新的IFAT检测仍为血清学阳性。

解读

该物种内的抗原变异性是CSD血清学诊断结果不一致的一个可能原因。

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