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Vertical transmission of African-lineage Zika virus through the fetal membranes in a rhesus macaque (Macaca mulatta) model.
Koenig, Michelle R; Mitzey, Ann M; Zeng, Xiankun; Reyes, Leticia; Simmons, Heather A; Morgan, Terry K; Bohm, Ellie K; Pritchard, Julia C; Schmidt, Jenna A; Ren, Emily; Leyva Jaimes, Fernanda B; Winston, Eva; Basu, Puja; Weiler, Andrea M; Friedrich, Thomas C; Aliota, Matthew T; Mohr, Emma L; Golos, Thaddeus G.
  • Koenig MR; Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Mitzey AM; Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Zeng X; Pathology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
  • Reyes L; Department of Pathobiological Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Simmons HA; Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Morgan TK; Department of Obstetrics and Gynecology, Oregon Health and Science University, Portland, Oregon, United States of America.
  • Bohm EK; Department of Veterinary and Biomedical Sciences, University of Minnesota, Twin Cities, St. Paul, Minnesota, United States of America.
  • Pritchard JC; Department of Veterinary and Biomedical Sciences, University of Minnesota, Twin Cities, St. Paul, Minnesota, United States of America.
  • Schmidt JA; Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Ren E; Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Leyva Jaimes FB; Department of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Winston E; Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Basu P; Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Weiler AM; Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Friedrich TC; Department of Pathobiological Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Aliota MT; Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
  • Mohr EL; Department of Veterinary and Biomedical Sciences, University of Minnesota, Twin Cities, St. Paul, Minnesota, United States of America.
  • Golos TG; Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
PLoS Pathog ; 19(8): e1011274, 2023 08.
Article en En | MEDLINE | ID: mdl-37549143
ABSTRACT
Zika virus (ZIKV) can be transmitted vertically from mother to fetus during pregnancy, resulting in a range of outcomes including severe birth defects and fetal/infant death. Potential pathways of vertical transmission in utero have been proposed but remain undefined. Identifying the timing and routes of vertical transmission of ZIKV may help us identify when interventions would be most effective. Furthermore, understanding what barriers ZIKV overcomes to effect vertical transmission may help improve models for evaluating infection by other pathogens during pregnancy. To determine the pathways of vertical transmission, we inoculated 12 pregnant rhesus macaques with an African-lineage ZIKV at gestational day 30 (term is 165 days). Eight pregnancies were surgically terminated at either seven or 14 days post-maternal infection. Maternal-fetal interface and fetal tissues and fluids were collected and evaluated for ZIKV using RT-qPCR, in situ hybridization, immunohistochemistry, and plaque assays. Four additional pregnant macaques were inoculated and terminally perfused with 4% paraformaldehyde at three, six, nine, or ten days post-maternal inoculation. For these four cases, the entire fixed pregnant uterus was evaluated with in situ hybridization for ZIKV RNA. We determined that ZIKV can reach the MFI by six days after infection and infect the fetus by ten days. Infection of the chorionic membrane and the extraembryonic coelomic fluid preceded infection of the fetus and the mesenchymal tissue of the placental villi. We did not find evidence to support a transplacental route of ZIKV vertical transmission via infection of syncytiotrophoblasts or villous cytotrophoblasts. The pattern of infection observed in the maternal-fetal interface provides evidence of paraplacental vertical ZIKV transmission through the chorionic membrane, the outer layer of the fetal membranes.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complicaciones Infecciosas del Embarazo / Virus Zika / Infección por el Virus Zika Límite: Animals / Female / Humans / Pregnancy Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complicaciones Infecciosas del Embarazo / Virus Zika / Infección por el Virus Zika Límite: Animals / Female / Humans / Pregnancy Idioma: En Año: 2023 Tipo del documento: Article