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Molecular aspects of Chikungunya virus infections in cancer patients
Familiar-Macedo, Débora; Gama, Bianca Ervatti; Emmel, Vanessa Erichsen; Vera-Lozada, Gabriela; Abdelhay, Eliana; Martins, Ianick Souto; Hassan, Rocio.
  • Familiar-Macedo, Débora; Instituto Nacional de Câncer. Centro de Transplante de Medula Óssea. Laboratório de Oncovirologia. Rio de Janeiro. BR
  • Gama, Bianca Ervatti; Instituto Nacional de Câncer. Centro de Transplante de Medula Óssea. Laboratório de Oncovirologia. Rio de Janeiro. BR
  • Emmel, Vanessa Erichsen; Instituto Nacional de Câncer. Centro de Transplante de Medula Óssea. Laboratório de Oncovirologia. Rio de Janeiro. BR
  • Vera-Lozada, Gabriela; Instituto Nacional de Câncer. Centro de Transplante de Medula Óssea. Laboratório de Oncovirologia. Rio de Janeiro. BR
  • Abdelhay, Eliana; Instituto Nacional de Câncer. Centro de Transplante de Medula Óssea. Laboratório de Células-Tronco. Rio de Janeiro. BR
  • Martins, Ianick Souto; Instituto Nacional de Câncer. Comissão de Controle de Infecções Hospitalares. Rio de Janeiro. BR
  • Hassan, Rocio; Instituto Nacional de Câncer. Centro de Transplante de Medula Óssea. Laboratório de Oncovirologia. Rio de Janeiro. BR
Mem. Inst. Oswaldo Cruz ; 117: e210383, 2022. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1375925
ABSTRACT
BACKGROUND Chikungunya virus (CHIKV) is an arbovirus that can cause chronic and debilitating manifestations. The first autochthonous case in Rio de Janeiro state was diagnosed in 2015, and an outbreak was declared in 2016. OBJECTIVE The aim of this work was to evaluate CHIKV viral load in serum, plasma and urine in cancer patients to determine the best sample for diagnosis, as well as perform molecular characterisation and phylogenetic analysis of circulating strains. METHODS Paired serum, plasma and urine collected from 31 cancer patients were tested by real-time quantitative polymerase chain reaction (qPCR) and a segment of the CHIKV E1 gene was sequenced. FINDINGS We detected 11 CHIKV+ oncological patients. Paired samples analyses of nine patients showed a different pattern of detection. Also, a higher viral load in plasma (6.84 log10) and serum (6.07 log10) vs urine (3.76 log10) was found. Phylogenetic analysis and molecular characterisation revealed East/Central/Southern Africa (ECSA) genotype circulation and three amino acids substitutions (E1-K211T, E1-M269V, E1-T288I) in positive patients. MAIN CONCLUSION The results indicate the bioequivalence of serum and plasma for CHIKV diagnosis, with urine being an important complement. ECSA genotype was circulating among patients in the period of the 2016 outbreak with K211T, M269V and T288I substitution.


Full text: Available Index: LILACS (Americas) Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2022 Type: Article Affiliation country: Brazil Institution/Affiliation country: Instituto Nacional de Câncer/BR

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Full text: Available Index: LILACS (Americas) Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2022 Type: Article Affiliation country: Brazil Institution/Affiliation country: Instituto Nacional de Câncer/BR