| Literature DB >> 35779208 |
Mariana Sequetin Cunha1,2, Thaís de Moura Coletti3, Juliana Mariotti Guerra4, César Cliento Ponce4, Natalia Coelho Couto Azevedo Fernandes4, Rodrigo Albegaria Résio4, Ingra Morales Claro3, Flávia Salles3, Daniel Ferreira Lima Neto5, Ester Sabino3.
Abstract
Dengue infection is the most prevalent arthropod-borne viral disease in subtropical and tropical regions, whose primary vector is Aedes aegypti mosquitoes. The mechanisms of dengue virus (DENV) pathogenesis are little understood because we have no good disease models. Only humans develop symptoms (dengue fever, DF, or dengue hemorrhagic fever, DHF) and research has been limited to studies involving patients. Samples from serum, brain, cerebellum, heart, lungs, liver, and kidneys from a 13-year-old male patient that died with hemorrhagic manifestations were sent for differential diagnosis at Adolfo Lutz, using both classical virological methods (RT-qPCR, virus isolation, ELISA, and hemagglutination inhibition test) and immunohistochemistry (IHQ). A DENV serotype 4 was detected by a DENV multiplex RT-qPCR, and the C6/36 cell supernatant was used for NGS using Minion. Lesions were described in the heart, liver, lung, and kidney with positive IHQ in endothelial cells of the brain, cerebellum, heart, and kidney, and also in hepatocytes and Kuppfer cells. A whole genome was obtained, revealing a DENV-4 genotype II, with no evidence of secondary dengue infection.Entities:
Keywords: Dengue virus; Immunohistochemistry; Phylogeny; Whole-genome sequencing
Mesh:
Year: 2022 PMID: 35779208 PMCID: PMC9433511 DOI: 10.1007/s42770-022-00784-4
Source DB: PubMed Journal: Braz J Microbiol ISSN: 1517-8382 Impact factor: 2.214