Fournier Pierre-Edouard, Robson Jenny, Zeaiter Zaher, McDougall Rodney, Byrne Shane, Raoult Didier
Unité des Rickettsies, CNRS UMR 6020, IFR 48, Faculté de Médecine, 27 Boulevard Jean Moulin, 13385 Marseille, France.
J Clin Microbiol. 2002 Oct;40(10):3620-4. doi: 10.1128/JCM.40.10.3620-3624.2002.
Over a 4-year period we detected Bartonella henselae isolates in 104 of 297 specimens (35.1%) from Australian patients clinically suspected of having cat scratch disease by amplification of a fragment of the htrA gene. We isolated 17 B. henselae strains (20.5%) from the 83 PCR-positive human specimens available for culture. Our culture method was based on prolonged incubation in a moist atmosphere of blood agar to which hemin was added. We obtained more B. henselae isolates than the number of all other isolates from lymph nodes reported in the literature. In order to identify and study the genetic variation of Australian B. henselae isolates, we determined the sequence of a fragment of the pap31 gene from our 17 human isolates and also from 8 Australian cat isolates. Thirteen of the human B. henselae isolates belonged to the Houston genotype, variant Houston-1 (76.5%), and four belonged to the Marseille genotype, variant CAL-1 (23.5%). In contrast, seven cat isolates were classified as B. henselae Marseille, variant CAL-1 (87.5%), and one was classified as B. henselae Houston, variant Houston-1 (12.5%). Our study describes an efficient culture method for the diagnosis of cat scratch disease and contributes to the description of the genotypic distribution of B. henselae in Australia.
在4年期间,我们通过扩增htrA基因片段,在297份来自临床疑似患有猫抓病的澳大利亚患者的标本中,检测到104份(35.1%)巴尔通体亨氏菌分离株。我们从83份可用于培养的PCR阳性人类标本中分离出17株亨氏巴尔通体菌株(20.5%)。我们的培养方法是在添加了血红素的血琼脂的潮湿环境中延长孵育时间。我们获得的亨氏巴尔通体分离株比文献中报道的来自淋巴结的所有其他分离株的数量都多。为了鉴定和研究澳大利亚亨氏巴尔通体分离株的遗传变异,我们测定了来自我们的17株人类分离株以及8株澳大利亚猫分离株的pap31基因片段的序列。13株人类亨氏巴尔通体分离株属于休斯顿基因型,变体休斯顿-1(76.5%),4株属于马赛基因型,变体CAL-1(23.5%)。相比之下,7株猫分离株被归类为亨氏巴尔通体马赛型,变体CAL-1(87.5%),1株被归类为亨氏巴尔通体休斯顿型,变体休斯顿-1(12.5%)。我们的研究描述了一种用于诊断猫抓病的有效培养方法,并有助于描述澳大利亚亨氏巴尔通体的基因型分布。