Your browser doesn't support javascript.
loading
Within-host quantitation of anellovirus genome complexity from clinical samples.
Peng, Peng; Xu, Yanjuan; Aurora, Rajeev; Di Bisceglie, Adrian M; Fan, Xiaofeng.
Afiliación
  • Peng P; Division of Gastroenterology & Hepatology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, 63104, USA; Wuhan Pulmonary Hospital, Wuhan, 430030, Hubei, China.
  • Xu Y; Division of Gastroenterology & Hepatology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, 63104, USA.
  • Aurora R; Department of Microbiology & Immunology, Saint University School of Medicine, St. Louis, MO, 63104, USA.
  • Di Bisceglie AM; Division of Gastroenterology & Hepatology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, 63104, USA; Saint Louis University Liver Center, Saint Louis University School of Medicine, St. Louis, MO, 63104, USA.
  • Fan X; Division of Gastroenterology & Hepatology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, 63104, USA; Saint Louis University Liver Center, Saint Louis University School of Medicine, St. Louis, MO, 63104, USA. Electronic address: xiaofeng.fan@health.slu
J Virol Methods ; 302: 114493, 2022 04.
Article en En | MEDLINE | ID: mdl-35176352
Anellovirus (AV) is a ubiquitous and diverse virus in the human population. An individual can be infected with multiple AV genera and species that form a heterogeneous repertoire, called the anellome. Due to its exceptional genetic diversity, efficient evaluation of anellome complexity remains a methodological challenge. In the current study, AV genome was first enriched from patient serum samples through two-phase rolling circle amplification. Following Illumina sequencing, anellome was analyzed with an advanced bioinformatics pipeline, including read extraction at three similarity levels, de novo assembly, species assignment, and determination of relative abundance among AV variants. The method was validated in the mock sample and then applied to 21 hepatitis C virus (HCV) patients with and without hepatocellular carcinoma (HCC). Overall, there was a large variance regarding AV richness, ranging from 2 to 51 AV species. In contrast to HCV patients without HCC, HCC incidence was associated with reduced richness (12.6 ± 14.4 vs. 35.4 ± 13.6, p = 0.001) and Shannon entropy (0.4 ± 0.34 vs. 0.61 ± 0.12, p = 0.095) at the AV species level. Interestingly, AV genus beta and gamma expanded in the anellome in 7 of 10 HCC patients. These observations shed light on the potential association between anellome and HCC incidence in patients with chronic HCV infection. The method presented here represents a valuable tool to investigate the role of anellome in human health and disease.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hepatitis C / Carcinoma Hepatocelular / Anelloviridae / Neoplasias Hepáticas Límite: Humans Idioma: En Revista: J Virol Methods Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hepatitis C / Carcinoma Hepatocelular / Anelloviridae / Neoplasias Hepáticas Límite: Humans Idioma: En Revista: J Virol Methods Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos