TY - JOUR
T1 - Study on the persistence of Zika virus (ZIKV) in body fluids of patients with ZIKV infection in Brazil
AU - and for the ZIKABRA Study Team
AU - Calvet, Guilherme Amaral
AU - Kara, Edna Oliveira
AU - Giozza, Silvana Pereira
AU - Bôtto-Menezes, Camila Helena Aguiar
AU - Gaillard, Philippe
AU - de Oliveira Franca, Rafael Freitas
AU - de Lacerda, Marcus Vinicius Guimarães
AU - da Costa Castilho, Marcia
AU - Brasil, Patrícia
AU - de Sequeira, Patrícia Carvalho
AU - de Mello, Maeve Brito
AU - Bermudez, Ximena Pamela Diaz
AU - Modjarrad, Kayvon
AU - Meurant, Robyn
AU - Landoulsi, Sihem
AU - Benzaken, Adele Schwartz
AU - de Filippis, Ana Maria Bispo
AU - Broutet, Nathalie Jeanne Nicole
AU - de Menezes, Ana Izabel Costa
AU - de Abreu, André Luiz
AU - Thorson, Anna
AU - Neto, Armando Menezes
AU - Brito, Carlos Alexandre Antunes
AU - Simões, Daniele
AU - Trautmann, Lydie
AU - Ghidinelli, Massimo
AU - Rolland, Morgane
AU - Habib, Ndema
AU - Formenty, Pierre
AU - Thomas, Rasmi
AU - de Jesus, Ronaldo
N1 - Funding Information:
Funding was provided by the Brazilian Ministry of Health, the World Health Organization, the UNDP-UNFPA-UNICEF-WHO-World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP) from the WHO, the Wellcome Trust and Walter Reed Army Institute of Research.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/1/22
Y1 - 2018/1/22
N2 - Background: Zika virus (ZIKV) has been identified in several body fluids of infected individuals. In most cases, it remained detected in blood from few days to 1 week after the onset of symptoms, and can persist longer in urine and in semen. ZIKV infection can have dramatic consequences such as microcephaly and Guillain-Barré syndrome. ZIKV sexual transmission has been documented. A better understanding of ZIKV presence and persistence across biologic compartments is needed to devise rational measures to prevent its transmission. Methods: This observational cohort study will recruit non-pregnant participants aged 18 years and above with confirmed ZIKV infection [positive reverse transcriptase-polymerase chain reaction (RT-PCR) test in blood and/or urine]: symptomatic men and women in ZIKV infection acute phase, and their symptomatic or asymptomatic household/sexual infected contacts. Specimens of blood, urine, semen, vaginal secretion/menstrual blood, rectal swab, oral fluids, tears, sweat, urine and breast milk (if applicable) will be collected at pre-established intervals and tested for ZIKV RNA presence by RT-PCR, other co-infection (dengue, Chikungunya, HIV, hepatitis B and C, syphilis), antibody response (including immunoglobulins M and G), plaque reduction neutralization test (if simultaneously positive for ZIKV and dengue), and ZIKV culture and RNA sequencing. Data on socio-demographic characteristics and comorbidities will be collected in parallel. Participants will be followed up for 12 months. Discussion: This prolonged longitudinal follow-up of ZIKV infected persons with regular biologic testing and data collection will offer a unique opportunity to investigate the presence and persistence of ZIKV in various biologic compartments, their clinical and immunological correlates as well as the possibility of ZIKV reactivation/reinfection over time. This valuable information will substantially contribute to the body of knowledge on ZIKV infection and serve as a base for the development of more effective recommendation on the prevention of ZIKV transmission. Trial registration:NCT03106714.
AB - Background: Zika virus (ZIKV) has been identified in several body fluids of infected individuals. In most cases, it remained detected in blood from few days to 1 week after the onset of symptoms, and can persist longer in urine and in semen. ZIKV infection can have dramatic consequences such as microcephaly and Guillain-Barré syndrome. ZIKV sexual transmission has been documented. A better understanding of ZIKV presence and persistence across biologic compartments is needed to devise rational measures to prevent its transmission. Methods: This observational cohort study will recruit non-pregnant participants aged 18 years and above with confirmed ZIKV infection [positive reverse transcriptase-polymerase chain reaction (RT-PCR) test in blood and/or urine]: symptomatic men and women in ZIKV infection acute phase, and their symptomatic or asymptomatic household/sexual infected contacts. Specimens of blood, urine, semen, vaginal secretion/menstrual blood, rectal swab, oral fluids, tears, sweat, urine and breast milk (if applicable) will be collected at pre-established intervals and tested for ZIKV RNA presence by RT-PCR, other co-infection (dengue, Chikungunya, HIV, hepatitis B and C, syphilis), antibody response (including immunoglobulins M and G), plaque reduction neutralization test (if simultaneously positive for ZIKV and dengue), and ZIKV culture and RNA sequencing. Data on socio-demographic characteristics and comorbidities will be collected in parallel. Participants will be followed up for 12 months. Discussion: This prolonged longitudinal follow-up of ZIKV infected persons with regular biologic testing and data collection will offer a unique opportunity to investigate the presence and persistence of ZIKV in various biologic compartments, their clinical and immunological correlates as well as the possibility of ZIKV reactivation/reinfection over time. This valuable information will substantially contribute to the body of knowledge on ZIKV infection and serve as a base for the development of more effective recommendation on the prevention of ZIKV transmission. Trial registration:NCT03106714.
KW - Arbovirus
KW - Body fluids
KW - Emerging infectious diseases
KW - Flavivirus
KW - Persistence
KW - Rt-Pcr
KW - Zika virus
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U2 - 10.1186/s12879-018-2965-4
DO - 10.1186/s12879-018-2965-4
M3 - Article
C2 - 29357841
AN - SCOPUS:85040861062
SN - 1471-2334
VL - 18
JO - BMC Infectious Diseases
JF - BMC Infectious Diseases
IS - 1
M1 - 49
ER -