Reyes-Montes M R, Bobadilla-Del Valle M, Martínez-Rivera M A, Rodríguez-Arellanes G, Maravilla E, Sifuentes-Osornio J, Taylor M L
Departamento de Microbiología-Parasitología, Facultad de Medicina, UNAM, Mexico City, Mexico.
J Clin Microbiol. 1999 May;37(5):1404-8. doi: 10.1128/JCM.37.5.1404-1408.1999.
The present paper analyzes the histoplasmin electrophoretic profiles and the randomly amplified polymorphic DNA (RAPD) patterns of the fungus Histoplasma capsulatum isolated from Mexican patients with AIDS-associated histoplasmosis. Clinical isolates from Guatemala, Colombia, and Panama, as well as H. capsulatum isolates from different sources in nature, were also processed. All histoplasmin samples shared four antigenic fractions of 200, 49, 10.5, and 8.5 kDa in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). According to their percentage of relatedness, based on SDS-PAGE histoplasmin electrophoretic image analysis, H. capsulatum isolates were divided in two groups: group A contained all AIDS-associated isolates studied and two human reference strains from Mexican histoplasmosis patients without AIDS; group B included bat guano, infected bat, and cock excreta isolates from the State of Guerrero, Mexico, plus three human histoplasmosis strains from Guatemala, Panama, and Colombia. Polymorphic DNA patterns evaluated by RAPD-PCR showed three major bands of 4.4, 3.2, and 2.3 kb in most H. capsulatum isolates studied. Four groups were related by DNA polymorphisms: group I was formed by most of the AIDS-associated H. capsulatum isolates studied, one human histoplasmosis strain from Colombia, two human reference strains from Mexican patients without AIDS, and one human histoplasmosis strain from Guatemala. Group II consisted of only a single strain from Panama. Group III included three strains: one from a Mexican patient with AIDS and two isolated from nature in Guerrero (cock excreta and bat guano). The last, group IV, consisted of only one strain isolated from an infected bat, captured in Guerrero. A tight relationship between phenotypic and genotypic characterization was observed, and both analyses could be useful tools for typing H. capsulatum from different sources and geographic origins.
本文分析了从患有艾滋病相关组织胞浆菌病的墨西哥患者中分离出的荚膜组织胞浆菌的组织胞浆菌素电泳图谱和随机扩增多态性DNA(RAPD)模式。还对来自危地马拉、哥伦比亚和巴拿马的临床分离株以及自然界不同来源的荚膜组织胞浆菌分离株进行了处理。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)中,所有组织胞浆菌素样品均具有200、49、10.5和8.5 kDa的四个抗原组分。根据基于SDS-PAGE组织胞浆菌素电泳图像分析的相关性百分比,荚膜组织胞浆菌分离株分为两组:A组包含所有研究的艾滋病相关分离株以及来自墨西哥无艾滋病组织胞浆菌病患者的两株人类参考菌株;B组包括来自墨西哥格雷罗州的蝙蝠粪便、感染蝙蝠和公鸡排泄物分离株,以及来自危地马拉、巴拿马和哥伦比亚的三株人类组织胞浆菌病菌株。通过RAPD-PCR评估的多态性DNA模式在大多数研究的荚膜组织胞浆菌分离株中显示出4.4、3.2和2.3 kb的三条主要条带。根据DNA多态性可将其分为四组:I组由大多数研究的艾滋病相关荚膜组织胞浆菌分离株、一株来自哥伦比亚的人类组织胞浆菌病菌株、两株来自墨西哥无艾滋病患者的人类参考菌株和一株来自危地马拉的人类组织胞浆菌病菌株组成。II组仅由来自巴拿马的一个菌株组成。III组包括三个菌株:一个来自墨西哥艾滋病患者,两个从格雷罗州的自然界分离(公鸡排泄物和蝙蝠粪便)。最后,IV组仅由从格雷罗州捕获的一只感染蝙蝠中分离出的一个菌株组成。观察到表型和基因型特征之间存在紧密关系,两种分析都可能是对来自不同来源和地理区域的荚膜组织胞浆菌进行分型的有用工具。