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A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman

Human pegivirus (HPgV) is best known for persistent, presumably non-pathogenic, infection and a propensity to co-infect with human immunodeficiency virus or hepatitis C virus. However, unique attributes, such as the increased risk of malignancy or immune modulation, have been recently recognized for...

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Autores principales: Garand, Mathieu, Huang, Susie S. Y., Goessling, Lisa S., Santillan, Donna A., Santillan, Mark K., Brar, Anoop, Wylie, Todd N., Wylie, Kristine M., Eghtesady, Pirooz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610878/
https://www.ncbi.nlm.nih.gov/pubmed/36296201
http://dx.doi.org/10.3390/microorganisms10101925
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author Garand, Mathieu
Huang, Susie S. Y.
Goessling, Lisa S.
Santillan, Donna A.
Santillan, Mark K.
Brar, Anoop
Wylie, Todd N.
Wylie, Kristine M.
Eghtesady, Pirooz
author_facet Garand, Mathieu
Huang, Susie S. Y.
Goessling, Lisa S.
Santillan, Donna A.
Santillan, Mark K.
Brar, Anoop
Wylie, Todd N.
Wylie, Kristine M.
Eghtesady, Pirooz
author_sort Garand, Mathieu
collection PubMed
description Human pegivirus (HPgV) is best known for persistent, presumably non-pathogenic, infection and a propensity to co-infect with human immunodeficiency virus or hepatitis C virus. However, unique attributes, such as the increased risk of malignancy or immune modulation, have been recently recognized for HPgV. We have identified a unique case of a woman with high levels HPgV infection in two pregnancies, which occurred 4 years apart and without evidence of human immunodeficiency virus or hepatitis C virus infection. The second pregnancy was complicated by congenital heart disease. A high level of HPgV infection was detected in the maternal blood from different trimesters by RT-PCR and identified as HPgV type 1 genotype 2 in both pregnancies. In the second pregnancy, the decidua and intervillous tissue of the placenta were positive for HPgV by PCR but not the chorion or cord blood (from both pregnancies), suggesting no vertical transmission despite high levels of viremia. The HPgV genome sequence was remarkably conserved over the 4 years. Using VirScan, sera antibodies for HPgV were detected in the first trimester of both pregnancies. We observed the same anti-HPgV antibodies against the non-structural NS5 protein in both pregnancies, suggesting a similar non-E2 protein humoral immune response over time. To the best of our knowledge, this is the first report of persistent HPgV infection involving placental tissues with no clear indication of vertical transmission. Our results reveal a more elaborate viral-host interaction than previously reported, expand our knowledge about tropism, and opens avenues for exploring the replication sites of this virus.
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spelling pubmed-96108782022-10-28 A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman Garand, Mathieu Huang, Susie S. Y. Goessling, Lisa S. Santillan, Donna A. Santillan, Mark K. Brar, Anoop Wylie, Todd N. Wylie, Kristine M. Eghtesady, Pirooz Microorganisms Brief Report Human pegivirus (HPgV) is best known for persistent, presumably non-pathogenic, infection and a propensity to co-infect with human immunodeficiency virus or hepatitis C virus. However, unique attributes, such as the increased risk of malignancy or immune modulation, have been recently recognized for HPgV. We have identified a unique case of a woman with high levels HPgV infection in two pregnancies, which occurred 4 years apart and without evidence of human immunodeficiency virus or hepatitis C virus infection. The second pregnancy was complicated by congenital heart disease. A high level of HPgV infection was detected in the maternal blood from different trimesters by RT-PCR and identified as HPgV type 1 genotype 2 in both pregnancies. In the second pregnancy, the decidua and intervillous tissue of the placenta were positive for HPgV by PCR but not the chorion or cord blood (from both pregnancies), suggesting no vertical transmission despite high levels of viremia. The HPgV genome sequence was remarkably conserved over the 4 years. Using VirScan, sera antibodies for HPgV were detected in the first trimester of both pregnancies. We observed the same anti-HPgV antibodies against the non-structural NS5 protein in both pregnancies, suggesting a similar non-E2 protein humoral immune response over time. To the best of our knowledge, this is the first report of persistent HPgV infection involving placental tissues with no clear indication of vertical transmission. Our results reveal a more elaborate viral-host interaction than previously reported, expand our knowledge about tropism, and opens avenues for exploring the replication sites of this virus. MDPI 2022-09-28 /pmc/articles/PMC9610878/ /pubmed/36296201 http://dx.doi.org/10.3390/microorganisms10101925 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Garand, Mathieu
Huang, Susie S. Y.
Goessling, Lisa S.
Santillan, Donna A.
Santillan, Mark K.
Brar, Anoop
Wylie, Todd N.
Wylie, Kristine M.
Eghtesady, Pirooz
A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman
title A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman
title_full A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman
title_fullStr A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman
title_full_unstemmed A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman
title_short A Case of Persistent Human Pegivirus Infection in Two Separate Pregnancies of a Woman
title_sort case of persistent human pegivirus infection in two separate pregnancies of a woman
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610878/
https://www.ncbi.nlm.nih.gov/pubmed/36296201
http://dx.doi.org/10.3390/microorganisms10101925
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