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Hepatitis Delta Virus Clade 8 Is the Predominant Clade Circulating in Botswana amongst People Living with HIV.

Authors :
Baruti, Kabo
Choga, Wonderful T.
Motshosi, Patience C.
Phinius, Bonolo B.
Phakedi, Basetsana
Bhebhe, Lynnette N.
Mpebe, Gorata G. A.
Tsayang, Chanana D.
Ratsoma, Tsholofelo
Gaolathe, Tendani
Mosepele, Mosepele
Makhema, Joseph
Shapiro, Roger
Lockman, Shahin
Moyo, Sikhulile
Jongman, Mosimanegape
Anderson, Motswedi
Gaseitsiwe, Simani
Source :
Viruses (1999-4915); Oct2024, Vol. 16 Issue 10, p1568, 8p
Publication Year :
2024

Abstract

Hepatitis delta virus (HDV) co-infections more often result in severe hepatitis compared to hepatitis B virus (HBV) infections alone. Despite a high HDV prevalence (7.1%), information regarding circulating HDV clades is very limited in Botswana. We extracted total nucleic acid from confirmed HDV-positive samples and quantified their viral load. We then sequenced the large hepatitis delta antigen (L-HDAg) using Oxford Nanopore Technology (ONT). Genotyping was performed using the HDV Database, and HDV mutation profiling was performed on AliView. All participants with HBV genotypic information belonged to sub-genotype A1, and 80% (4/5) of them had a higher HDV viral load and a lower HBV viral load. We sequenced 75% (9/12) of the HDV-positive samples, which belonged to HDV clade 8. A total of 54 mutations were discovered, with the most prevalent being Q148R (16%), D149P (16%) and G151D (16%). Known mutations such as S117A, K131R, R139K and G151D were detected, while the other mutations were novel. Our results reveal that HDV clade 8 is the predominant clade in Botswana. The significance of all mutations remains unclear. Future studies with a larger sample size to detect other HDV clades that might be circulating in Botswana and functionally characterize the detected mutations are warranted. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19994915
Volume :
16
Issue :
10
Database :
Complementary Index
Journal :
Viruses (1999-4915)
Publication Type :
Academic Journal
Accession number :
180485823
Full Text :
https://doi.org/10.3390/v16101568