Molecular Identification and Drug Susceptibility of Leishmania spp. Clinical Isolates Collected from Two Regions of Oaxaca, Mexico

被引:0
作者
Moreno-Rodriguez, Adriana [1 ]
del Campo-Colin, Ada Sarai Martin [2 ]
Dominguez-Diaz, Luis Roberto [3 ]
Posadas-Jimenez, Ana Livia [4 ]
Matadamas-Martinez, Felix [2 ]
Yepez-Mulia, Lilian [2 ]
机构
[1] Univ Autonoma Benito Juarez Oaxaca, Fac Ciencias Quim, Lab Estudios Epidemiol Clin Disenos Expt & Invest, Ave Univ S-N, Oaxaca 68120, Mexico
[2] Inst Mexicano Seguro Social, UMAE Hosp Pediat, Ctr Med Nacl Siglo XXI, Unidad Invest Med Enfermedades Infecciosas & Paras, Mexico City 06720, Mexico
[3] Univ Sierra Sur, Ctr Patol Clin, UNSIS, Ciencias Biomed, Guillermo Rojas S-N Esq Ave Univ, Oaxaca 70800, Mexico
[4] Serv Salud Oaxaca, Dept Prevenc & Control Enfermedades Transmitidas V, Programa Prevenc & Control Enfermedad Chagas, Oaxaca 68000, Mexico
关键词
skin smears; ITS1; PCR; drug susceptibility; AMERICAN CUTANEOUS LEISHMANIASIS; GEOGRAPHIC DISTRIBUTIONS; VISCERAL LEISHMANIASIS; TREATMENT FAILURE; KALA-AZAR; ANTIMONY; TRANSMISSION; DIAGNOSIS; VECTORS; BRAZIL;
D O I
10.3390/microorganisms13020220
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pentavalent antimonials are the first line for leishmaniasis treatment, although they induce many adverse side effects and treatment failure and parasite resistance have been detected. Cutaneous leishmaniasis is the main clinical manifestation of the disease in Oaxaca State, Mexico; however, its presence is under-registered, and information about the Leishmania species that circulate and cause the disease in the region is limited. In this study, the presence of Leishmania was analyzed in 24 skin smears and 2 biopsies from lesions suspicious for leishmaniasis in inhabitants of the Tehuantepec Isthmus and Papaloapan Basin regions, Oaxaca State. By ITS1-PCR, the species of clinical isolates were identified. Moreover, the susceptibility of clinical isolates to leishmanicidal drugs was assessed. Skin smears were negative for the presence of Leishmania spp.; meanwhile, parasite amastigotes were observed in tissue biopsies; however, by ITS1-PCR, 46% of the samples were determined to be positive for the parasite. Six clinical isolates were identified as L. mexicana and had lower susceptibility to Miltefosine and Amphotericin B than the L. mexicana reference strain. No leishmanicidal activity of Glucantime was detected. Further studies with increased patient sample sizes and genotypic studies will describe in detail parasite susceptibility to reference drugs in the region.
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