Evidence map›Paper›PMID 30205537›Full record

ArticleGenes2018

Molecular Characterization of Near Full-Length Genomes of Hepatitis B Virus Isolated from Predominantly HIV Infected Individuals in Botswana.

Motswedi Anderson, Wonderful Tatenda Choga, Sikhulile Moyo, Trevor Graham Bell, Tshepiso Mbangiwa, Bonolo Bonita Phinius, Lynnette Bhebhe, Theresa Kibirige Sebunya, Shahin Lockman, Richard Marlink and 5 more

Abstract read
In one paragraph

Article in Genes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Motswedi AndersonBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. motswedi.anderson@gmail.com.
Wonderful Tatenda ChogaBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. wtchoga@gmail.com.
Sikhulile MoyoBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. smoyo@bhp.org.bw.ORCID 0000-0003-3821-4592
Trevor Graham BellHepatitis Virus Diversity Research Unit (HVDRU), Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2050, South Africa. TrevorGrahamBell@gmail.com.ORCID 0000-0003-2630-7513
Tshepiso MbangiwaBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. mbangiwat@gmail.com.
Bonolo Bonita PhiniusBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. bphinius@gmail.com.
Lynnette BhebheBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. lynnettebhebhe@gmail.com.
Theresa Kibirige SebunyaDepartment of Biological Sciences, Faculty of Science, University of Botswana, Gaborone, Botswana. sebunyat@gmail.com.
Shahin LockmanBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. shahin.lockman@gmail.com.
Richard MarlinkBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. rmarlink@globalhealth.rutgers.edu.
Anna KramvisHepatitis Virus Diversity Research Unit (HVDRU), Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2050, South Africa. Anna.Kramvis@wits.ac.za.ORCID 0000-0001-6006-3765
Max EssexBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. messex@hsph.harvard.edu.
Rosemary Mubanga MusondaBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. rmusonda@bhp.org.bw.
Jason Tory BlackardCollege of Medicine, University of Cincinnati, Cincinnati, OH 45627, USA. jason.blackard@uc.edu.ORCID 0000-0003-2876-3811
Simani GaseitsiweBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana. sgaseitsiwe@bhp.org.bw.

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Theresa Alenghat · 2007 to 2026
$24.4M
Partnership for Global Health Research Training Program (Renewal)-Supplement for OBSSR, NCI, NCI-AIDS and NIDCDD43TW010543 · FIC · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Wafaie W Fawzi, DAVIDSON HOWES HAMER · 2017 to 2026
$12.1M
Training in HIV Genomics, Treatment, and Cure Research in BotswanaD43TW009610 · FIC · THE BOTSWANA HARVARD HEALTH PARTNERSHIP · PI SHAHIN LOCKMAN, Joseph Moeketsi Makhema · 2013 to 2026
$4.4M
Mentoring in Patient-Oriented HIV Research in the Era of Universal ARTK24AI131928 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI SHAHIN LOCKMAN · 2017 to 2026
$1.9M
FIC NIH HHS D43 TW009610FIC NIH HHS D43 TW010543National Institutes of Health (NIH) Fogarty International Center 5D43TW009610NIAID NIH HHS K24 AI131928NIDDK NIH HHS P30 DK078392Southern Africa Consortium for Research Excellence 087537/F/08/ZThe research was also partly funded by the Sub-Saharan African Network for TB/HIV Research Excellence (SANTHE),a DELTAS Africa Initiative grant number DEL-15-006. The DELTAS Africa Initiative is an independent funding scheme of the African Academy of Scie DEL-15-006
6 · The paper itself

Abstract

The World Health Organization plans to eliminate hepatitis B and C Infections by 2030. Therefore, there is a need to study and understand hepatitis B virus (HBV) epidemiology and viral evolution further, including evaluating occult (HBsAg-negative) HBV infection (OBI), given that such infections are frequently undiagnosed and rarely treated. We aimed to molecularly characterize HBV genomes from 108 individuals co-infected with human immunodeficiency virus (HIV) and chronic hepatitis B (CHB) or OBI identified from previous HIV studies conducted in Botswana from 2009 to 2012. Full-length (3.2 kb) and nearly full-length (~3 kb) genomes were amplified by nested polymerase chain reaction (PCR). Sequences from OBI participants were compared to sequences from CHB participants and GenBank references to identify OBI-unique mutations. HBV genomes from 50 (25 CHB and 25 OBI) individuals were successfully genotyped. Among OBI participants, subgenotype A1 was identified in 12 (48%), D3 in 12 (48%), and E in 1 (4%). A similar genotype distribution was observed in CHB participants. Whole HBV genome sequences from Botswana, representing OBI and CHB, were compared for the first time. There were 43 OBI-unique mutations, of which 26 were novel. Future studies using larger sample sizes and functional analysis of OBI-unique mutations are warranted.

Indexed as

AfricaBotswanachronic hepatitis BHBVmutationsoccult hepatitis B

Identifiers

PMID30205537
PMCPMC6162474

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.