| Literature DB >> 29313485 |
Aline Rimoldi Ribeiro1, Luciana Lima2, Larissa Aguiar de Almeida3, Joana Monteiro4, Cláudia Jassica Gonçalves Moreno5, Juliana Damieli Nascimento1, Renato Freitas de Araújo6, Fernanda Mello7, Luciamáre Perinetti Alves Martins8, Márcia Aparecida Silva Graminha3, Marta Maria Geraldes Teixeira2, Marcelo Sousa Silva9,5,4, Mário Steindel10, João Aristeu da Rosa3.
Abstract
Chagas disease affects between six and seven million people. Its etiological agent, Trypanosoma cruzi, is classified into six discrete typing units (DTUs). The biological study of 11 T. cruzi strains presented here included four parameters: growth kinetics, parasitemia curves, rate of macrophage infection, and serology to evaluate IgM, total IgG, IgG1, IgG2a, and IgG3. Sequencing of small subunit of ribosomal RNA (SSU rRNA)was performed and the T. cruzi strains were classified into three DTUs. When their growth in liver infusion tryptose medium was represented in curves, differences among the strains could be noted. The parasitemia profile varied among the strains from the TcI, TcII, and TcIII groups, and the 11 T. cruzi strains produced distinct parasitemia levels in infected BALB/c. The TcI group presented the highest rate of macrophage infection by amastigotes, followed by TcII and TcIII. Reactivity to immunoglobulins was observed in the TcI, TcII, and TcIII; all the animals infected with the different strains of T. cruzi showed anti-T. cruzi antibodies. The molecular study presented here resulted in the classification of the T. cruzi strains into the TcI (Bolivia, T lenti, Tm, SC90); TcII (Famema, SC96, SI8, Y); and TcIII (QMM3, QMM5, SI5) groups. These biological and molecular results from 11 T. cruzi strains clarified the factors involved in the biology of the parasite and its hosts. The collection of triatomine (vector) species, and the study of geographic distribution, as well as biological and molecular characterization of the parasite, will contribute to the reporting and surveillance measures in Brazilian states.Entities:
Mesh:
Year: 2018 PMID: 29313485 PMCID: PMC5929169 DOI: 10.4269/ajtmh.16-0200
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345