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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
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