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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
Institution: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    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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