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Background: The genetic diversity of Trypanosoma cruzi and the epidemiological characteristics of the environments in which the parasite occurs are essential for understanding infection dynamics and controlling Chagas disease. This systematic review aimed to: (i) identify and analyze studies that evaluated the genetic variability and epidemiological aspects of T. cruzi infection in the state of Rio Grande do Norte, Brazil; (ii) summarize the information reported in the literature; and (iii) suggest new control strategies tailored to the region's epidemiological profile.
Methods: Following the application of inclusion and exclusion criteria, 13 studies catalogued in PubMed, the Brazilian Virtual Health Library, Scopus, and the Web of Science were selected.
Results: T. cruzi isolates were primarily obtained from triatomine species Triatoma brasiliensis, Panstrongylus lutzi, and Triatoma pseudomaculata, as well as from wild mammals such as Euphractus sexcinctus, Galea spixii, and humans. A total of 295 T. cruzi isolates were genotyped: 46.5% (137) were identified as Discrete Typing Unit (DTU) I, 29.1% (86) as DTU II, and 20% (59) as DTU III. Mixed infections were detected in 4.4% (13/295) of hosts. Triatomine species were found in both peridomestic and intradomestic environments and were occasionally infected with T. cruzi.
Conclusions: This review provides a comprehensive overview of the circulation of distinct Trypanosoma cruzi genotypes (I, II, and III) in both wild and human-modified environments in Rio Grande do Norte.
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http://dx.doi.org/10.1590/0037-8682-0063-2025 | DOI Listing |
ChemMedChem
September 2025
Laboratorio de Síntesis Orgánica, Facultad de Farmacia, Universidad Central de Venezuela, Apartado 47206, Los Chaguaramos, Caracas, 1041-A, Venezuela.
Due to the advantages of drug repurposing, the discovery of new chemotherapeutic agents for the treatment of Chagas disease based on approved drugs has become a strategy for identifying new candidates. In this work, the antidepressant drug sertraline is reported, with an IC of 7.8 ± 1.
View Article and Find Full Text PDFmBio
September 2025
Department of Microbiology & Immunology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Fatty acid-binding protein 4 (FABP4) is a cytosolic lipid chaperone predominantly expressed in adipocytes. It has been shown that targets adipose tissues and resides in adipocytes. However, how manipulates adipocytes to redirect nutrients for its benefit remains unknown.
View Article and Find Full Text PDFJ Insect Physiol
September 2025
Instituto René Rachou, Avenida Augusto de Lima, 1715, CEP 30190-009, Belo Horizonte, Minas Gerais, Brazil. Electronic address:
Triatomines are vectors of Trypanosoma cruzi, the causative agent of Chagas disease. Their locomotor activity is influenced by endogenous and exogenous factors, but whether individual behavioral profiles persist across developmental stages remains unclear. This study evaluated non-oriented locomotor activity in Rhodnius prolixus under varying nutritional states (short-fasting, long-fasting, fed), developmental stages (5th instar nymphs and adults), sex (males and females), and light phase (photophase vs.
View Article and Find Full Text PDFGigaByte
August 2025
Centro de Estudios Parasitológicos y de Vectores (CEPAVE-CCT-La Plata-CONICET-UNLP), B1900 La Plata, Buenos Aires, Argentina.
Chagas disease is caused by , which is transmitted to mammals, including humans, mainly by insects of the subfamily Triatominae (Hemiptera: Reduviidae). Also known as "kissing bugs", the subfamily includes 159 species in 18 genera and five tribes. Although most species are in the Americas, here we present the first compilation of non-American triatomine occurrences.
View Article and Find Full Text PDFJ Inorg Biochem
September 2025
Área Química Inorgánica, Facultad de Química, Universidad de la República, Montevideo, Uruguay. Electronic address:
Chagas disease, caused by Trypanosoma cruzi, remains a major public health concern with limited therapeutic options and significant toxicity associated with current treatments. In this work, eight novel heteroleptic complexes of the type [M(L)(phen)], where M = Cu(II) or Zn(II), L = coumarin-thiosemicarbazone hybrid ligands, and phen = 1,10-phenanthroline, were synthesized and fully characterized in the solid state and in solution. For comparison, some homoleptic [Cu(HL)₂], [Zn(HL)₂], and [CuCl(HL)] complexes were also prepared.
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