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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.
Afiliação
  • Garand M; Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Huang SSY; Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Goessling LS; Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Santillan DA; Department of Obstetrics and Gynecology, University of Iowa, Iowa City, IA 52242, USA.
  • Santillan MK; Department of Obstetrics and Gynecology, University of Iowa, Iowa City, IA 52242, USA.
  • Brar A; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Wylie TN; McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Wylie KM; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Eghtesady P; McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.
Microorganisms ; 10(10)2022 Sep 28.
Article em En | MEDLINE | ID: mdl-36296201
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article