Molecular aspects of Chikungunya virus infections in cancer patients

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,...

Full description

Bibliographic Details
Main Authors: Débora Familiar-Macedo, Bianca Ervatti Gama, Vanessa Erichsen Emmel, Gabriela Vera-Lozada, Eliana Abdelhay, Ianick Souto Martins, Rocio Hassan
Format: Article
Language:English
Published: Fundação Oswaldo Cruz (FIOCRUZ) 2022-04-01
Series:Memorias do Instituto Oswaldo Cruz
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762022000101103&tlng=en
_version_ 1827847018709516288
author Débora Familiar-Macedo
Bianca Ervatti Gama
Vanessa Erichsen Emmel
Gabriela Vera-Lozada
Eliana Abdelhay
Ianick Souto Martins
Rocio Hassan
author_facet Débora Familiar-Macedo
Bianca Ervatti Gama
Vanessa Erichsen Emmel
Gabriela Vera-Lozada
Eliana Abdelhay
Ianick Souto Martins
Rocio Hassan
author_sort Débora Familiar-Macedo
collection DOAJ
description 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.
first_indexed 2024-03-12T09:24:50Z
format Article
id doaj.art-fa9456bbac6440a99c7bf88f095448f6
institution Directory Open Access Journal
issn 1678-8060
language English
last_indexed 2024-03-12T09:24:50Z
publishDate 2022-04-01
publisher Fundação Oswaldo Cruz (FIOCRUZ)
record_format Article
series Memorias do Instituto Oswaldo Cruz
spelling doaj.art-fa9456bbac6440a99c7bf88f095448f62023-09-02T14:21:06ZengFundação Oswaldo Cruz (FIOCRUZ)Memorias do Instituto Oswaldo Cruz1678-80602022-04-0111710.1590/0074-02760210383Molecular aspects of Chikungunya virus infections in cancer patientsDébora Familiar-Macedohttps://orcid.org/0000-0002-9229-5912Bianca Ervatti GamaVanessa Erichsen EmmelGabriela Vera-LozadaEliana AbdelhayIanick Souto MartinsRocio Hassan 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762022000101103&tlng=enCHIKVoncological patientsviral loadECSA
spellingShingle Débora Familiar-Macedo
Bianca Ervatti Gama
Vanessa Erichsen Emmel
Gabriela Vera-Lozada
Eliana Abdelhay
Ianick Souto Martins
Rocio Hassan
Molecular aspects of Chikungunya virus infections in cancer patients
Memorias do Instituto Oswaldo Cruz
CHIKV
oncological patients
viral load
ECSA
title Molecular aspects of Chikungunya virus infections in cancer patients
title_full Molecular aspects of Chikungunya virus infections in cancer patients
title_fullStr Molecular aspects of Chikungunya virus infections in cancer patients
title_full_unstemmed Molecular aspects of Chikungunya virus infections in cancer patients
title_short Molecular aspects of Chikungunya virus infections in cancer patients
title_sort molecular aspects of chikungunya virus infections in cancer patients
topic CHIKV
oncological patients
viral load
ECSA
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762022000101103&tlng=en
work_keys_str_mv AT deborafamiliarmacedo molecularaspectsofchikungunyavirusinfectionsincancerpatients
AT biancaervattigama molecularaspectsofchikungunyavirusinfectionsincancerpatients
AT vanessaerichsenemmel molecularaspectsofchikungunyavirusinfectionsincancerpatients
AT gabrielaveralozada molecularaspectsofchikungunyavirusinfectionsincancerpatients
AT elianaabdelhay molecularaspectsofchikungunyavirusinfectionsincancerpatients
AT ianicksoutomartins molecularaspectsofchikungunyavirusinfectionsincancerpatients
AT rociohassan molecularaspectsofchikungunyavirusinfectionsincancerpatients