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南非新型隐球菌小儿分离株分析。

Analyses of pediatric isolates of Cryptococcus neoformans from South Africa.

机构信息

Department of Molecular Genetics and Microbiology, 207 Research Drive, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

J Clin Microbiol. 2011 Jan;49(1):307-14. doi: 10.1128/JCM.01277-10. Epub 2010 Oct 27.

Abstract

Compared to the incidence in adults, cryptococcosis is inexplicably rare among children, even in sub-Saharan Africa, which has the highest prevalence of coinfection with HIV and Cryptococcus neoformans. To explore any mycological basis for this age-related difference in the incidence of cryptococcosis, we investigated isolates of C. neoformans recovered from pediatric and adult patients during a 2-year period in South Africa. From reports to the Group for Enteric, Respiratory, and Meningeal Disease Surveillance in South Africa (GERMS-SA), we reviewed all cases of cryptococcosis in 2005 and 2006. We analyzed one isolate of C. neoformans from each of 82 pediatric patients (<15 years of age) and determined the multilocus sequence type (ST), mating type, ploidy, and allelic profile. This sample included isolates of all three molecular types of serotype A or C. neoformans var. grubii (molecular types VNI, VNII, and VNB) and one AD hybrid. Seventy-seven (94%) of the strains possessed the MATα mating type allele, and five were MATa. Seventy-five (91%) were haploid, and seven were diploid. A total of 24 different STs were identified. The ratios of each mating type and the proportion of haploids were comparable to those for the isolates that were obtained from 86 adult patients during the same period. Notably, the most prevalent pediatric ST was significantly associated with male patients. Overall, these pediatric isolates exhibited high genotypic diversity. They included a relatively large percentage of diploids and the rarely reported MATa mating type.

摘要

与成人相比,隐球菌病在儿童中发病率异常低,即使在 HIV 和新生隐球菌共感染率最高的撒哈拉以南非洲也是如此。为了探究儿童隐球菌病发病率的这种年龄相关差异的任何真菌学基础,我们调查了南非 2 年间从儿科和成年患者中分离的新生隐球菌分离株。根据南非肠道、呼吸道和脑膜疾病监测组织(GERMS-SA)的报告,我们回顾了 2005 年和 2006 年所有的隐球菌病病例。我们分析了 82 例儿科患者(<15 岁)的每一个新生隐球菌分离株,并确定了多位点序列型(ST)、交配型、倍性和等位基因谱。该样本包括血清型 A 或新生隐球菌变种格卢比的所有三种分子型(分子型 VNI、VNII 和 VNB)和一个 AD 杂种的分离株。77 株(94%)具有 MATα交配型等位基因,5 株为 MATa。75 株(91%)为单倍体,7 株为二倍体。总共鉴定出 24 种不同的 ST。每种交配型的比例和单倍体的比例与同期从 86 例成年患者中获得的分离株相似。值得注意的是,最常见的儿科 ST 与男性患者显著相关。总体而言,这些儿科分离株表现出高度的遗传多样性。它们包括相对较大比例的二倍体和罕见报道的 MATa 交配型。

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