Trypanosoma cruzi: Biological characterization of lineages I and II supports the predominance of lineage I in Colombia |
| |
Authors: | Mejía-Jaramillo Ana María Peña Víctor Hugo Triana-Chávez Omar |
| |
Affiliation: | Grupo de Chagas, Universidad de Antioquia, Calle 67 No. 53-108, AA 1226, Medellín, Antioquia, Colombia |
| |
Abstract: | The causes of the particular distribution of both Trypanosoma cruzi lineages throughout the American continent remain unknown. In Colombia, T. cruzi I is the predominant group in both domestic and sylvatic cycles. Here, we present the biological characterization of T. cruzi parasites belonging to both T. cruzi I and T. cruzi IIb groups. Our results show the inability of the T. cruzi IIb clones to infect mammalian cells, produce trypomastigotes and replicate in Rhodnius prolixus, the main vector species in this country. Moreover, this result was confirmed when other species from the same genus, such as R. pallescens and R. robustus, were infected with the same TcIIb clone and its parental strain, while the infection in other genera such as Triatoma and Panstrongylus was successful. Furthermore, the growth kinetics and duplication time in vitro suggest that the high prevalence of T. cruzi I in Colombia results from more successful interactions between parasite lineage, vector, and host species. This type of study may help to understand the factors influencing the particular epidemiological patterns of Chagas disease transmission in different endemic regions. |
| |
Keywords: | Chagas disease Trypanosoma cruzi (Kinetoplastida Trypanosomatidae) Rhodnius prolixus Rhodnius pallescens Rhodnius robustus Panstrongylus geniculatus Triatoma dimidiata Triatoma infestans (Reduviidae: Triatominae) Colombia TcI, T. cruzi I TcIIb, T. cruzi IIb Z1, zymodeme 1 Z2, zymodeme 2 Z3, zymodeme 3 BNZ, benznidazole LIT, liver infusion tryptose FCS, fetal calf serum DNA, deoxyribonucleic acid SL, spliced leader PCR, polymerase chain reaction bp, base pair dNTP, deoxyribonucleotide triphosphate TBE, 89 mM Tris borate, 2 mM EDTA [pH 8.3] UV, ultraviolet kDNA, kinetoplast DNA LSSP-PCR, low stringency single primer-PCR PBS, phosphate-buffered saline EC50, effective concentration 50 %I, percentage of inhibition MTT, 3(4.5-dimethylthiazol-2-yl)-2,5diphenyltetrazolium bromide |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|