Grimaldi G, David J R, McMahon-Pratt D
Am J Trop Med Hyg. 1987 Mar;36(2):270-87. doi: 10.4269/ajtmh.1987.36.270.
Five hundred thirty stocks of Leishmania isolated from human and domestic and wild reservoir hosts, representing a wide geographic distribution of endemic foci of American cutaneous (ACL) and visceral leishmaniases (AVL) were characterized and identified at species and/or subspecies levels based on their reactivity to a cross-panel of specific monoclonal antibodies using a radioimmune binding assay. This study confirms and extends our preliminary results on the high specificity of some of these monoclonals for the L. braziliensis, L. mexicana, and L. donovani complexes. This study also demonstrates the relative stability of these molecular markers and the general usefulness of the method for parasite identification. Two hundred ninety-two of 420 isolates of ACL were classified as members of the L. braziliensis complex. Two hundred twenty-seven were L. b. braziliensis; these showed the widest geographical distribution (Brazil: Amazonas, Bahia, Ceara, Espirito Santo, Goias, Minas Gerais, Para, Paraiba, Rio de Janeiro, and Sao Paulo; Honduras: Santa Barbara and Yoko; Peru: Ancash, Piura, and Ucayali; and Venezuela: Cojedes, Distrito Federal, Lara, Portuguesa, Vale Hondo, Yaracuy, and Zulia). Forty-one stocks were identified as L. b. guyanensis (from North Brazil: Amazonas, Amapa, Para, and Rondonia). Twenty-one stocks were identified as L. b. panamensis (from Costa Rica: Alajuela, Guanacasten, Limon, Puntarenas, and San Jose; and Honduras: El Paraiso, and Olancho). Out of 128 isolates classified as members of the L. mexicana complex, 74 were differentiated as L. m. amazonensis (from Bolivia; Brazil: Amazonas, Bahia, Ceara, Goias, Maranhao, Mato Grosso do Norte, and Para; Peru: Pasco Forest and Van Humboldt; and Venezuela: Carabobo, Guarico, and Merida). Forty-four stocks were identified as L. m. venezuelensis (from Venezuela: Lara). Six stocks were L. m. mexicana (from Belize; and Mexico: Campeche [corrected] and Quintana Roo, Yucatan). One hundred ten isolates from AVL were identified as L. donovani chagasi (from Brazil: Bahia, Ceara, Maranhao, Minas Gerais, Mato Grosso do Sul, Piaui, Rio de Janeiro, and Sergipe; and Honduras: Valle). The implications of these results with respect to both the clinical and epidemiological data (including the detection of seven unusual characterized stocks) are discussed.
从人类、家养和野生储存宿主中分离出530株利什曼原虫,这些原虫代表了美洲皮肤利什曼病(ACL)和内脏利什曼病(AVL)流行病灶的广泛地理分布。基于它们对一组特异性单克隆抗体的反应性,采用放射免疫结合试验在种和/或亚种水平对其进行了特征鉴定和识别。本研究证实并扩展了我们关于其中一些单克隆抗体对巴西利什曼原虫、墨西哥利什曼原虫和杜氏利什曼原虫复合体具有高特异性的初步结果。本研究还证明了这些分子标记的相对稳定性以及该方法在寄生虫鉴定中的普遍实用性。420株ACL分离株中有292株被归类为巴西利什曼原虫复合体的成员。227株为巴西利什曼原虫指名亚种;它们的地理分布最广(巴西:亚马逊州、巴伊亚州、塞阿拉州、圣埃斯皮里图州、戈亚斯州、米纳斯吉拉斯州、帕拉州、帕拉伊巴州、里约热内卢州和圣保罗州;洪都拉斯:圣巴巴拉和约科;秘鲁:安卡什、皮乌拉和乌卡亚利;委内瑞拉:科赫德斯州、联邦区、拉腊州、葡萄牙萨州、瓦尔洪多州、亚拉库伊州和苏利亚州)。41株被鉴定为圭亚那利什曼原虫(来自巴西北部:亚马逊州、阿马帕州、帕拉州和朗多尼亚州)。21株被鉴定为巴拿马利什曼原虫(来自哥斯达黎加:阿拉胡埃拉、瓜纳卡斯特、利蒙、蓬塔雷纳斯和圣何塞;洪都拉斯:埃尔帕拉伊索和奥兰乔)。在128株被归类为墨西哥利什曼原虫复合体成员的分离株中,74株被鉴定为亚马逊利什曼原虫(来自玻利维亚;巴西:亚马逊州、巴伊亚州、塞阿拉州、戈亚斯州、马拉尼昂州、北马托格罗索州和帕拉州;秘鲁:帕斯科森林和范洪堡;委内瑞拉:卡拉沃沃、瓜里科和梅里达)。44株被鉴定为委内瑞拉利什曼原虫(来自委内瑞拉:拉腊州)。6株为墨西哥利什曼原虫(来自伯利兹;墨西哥:坎佩切[更正]和金塔纳罗奥州、尤卡坦州)。110株AVL分离株被鉴定为恰加斯杜氏利什曼原虫(来自巴西:巴伊亚州、塞阿拉州、马拉尼昂州、米纳斯吉拉斯州、南马托格罗索州、皮奥伊州、里约热内卢州和塞尔希培州;洪都拉斯:山谷)。讨论了这些结果在临床和流行病学数据方面的意义(包括检测到7株特征异常的菌株)。