Evidence map›Paper›PMID 31516090›Full record

ArticleEmerging microbes & infections2019

Occult HBV infection in Chinese blood donors: role of N-glycosylation mutations and amino acid substitutions in S protein transmembrane domains.

Lu Zhang, Le Chang, Syria Laperche, Huimin Ji, Junpeng Zhao, Xinyi Jiang, Lunan Wang, Daniel Candotti

Abstract read
In one paragraph

Article in Emerging microbes & infections, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

21 citing papers in PubMed.

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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

8 authors.

Lu ZhangNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology , Beijing , People's Republic of China.
Le ChangNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology , Beijing , People's Republic of China.
Syria LapercheNational Institute of Blood Transfusion, DATS, CNR RIT , Paris , France.
Huimin JiNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology , Beijing , People's Republic of China.
Junpeng ZhaoNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology , Beijing , People's Republic of China.
Xinyi JiangNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology , Beijing , People's Republic of China.
Lunan WangNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology , Beijing , People's Republic of China.
Daniel CandottiNational Institute of Blood Transfusion, DATS, CNR RIT , Paris , France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Occult hepatitis B virus infection (OBI) is a low-level asymptomatic phase of HBV infection. Evidence of OBI clinical relevance is emerging but the mechanisms of its occurrence remain unclear. In this study, the molecular characteristics of 97 confirmed OBI from Chinese blood donors were analyzed and relevant mutations were identified. Recombinant HBsAg bearing these mutations were expressed in vitro and the antigenicity and HBsAg secretion properties were analyzed. Results showed that 45 (46.4%) genotype B, 50 (51.5%) genotype C, and 2 (2.1%) genotype D sequences were identified. Two groups of mutations in the S gene were significantly associated with OBI. The first group included mutations creating new N-linked glycosylation sites at positions s116, s123, s130, and s131 + s133 or removing the existing one at s146. Mutations TCT123-125NCT/NFT were associated with reduced antigenicity, while TST116-118NST, GTS130-132NTS, and TSM131-133NSS/NYT/NST were associated with varying levels of impaired HBsAg secretion. N146 mutations had no effect on HBsAg production pattern. The second group included substitutions within the S transmembrane domains TMD1-3. Only mutations C85R, L87R, L88R, and C90R within TMD2 were associated with defective HBsAg production. These mutations appear to be rare and mostly strain specific but they may contribute to the multifactorial occurrence of OBI.

Indexed as

Blood DonorsMutation, MissenseProtein Processing, Post-TranslationalAmino Acid SubstitutionAsian PeopleAsymptomatic DiseasesGenotypeGlycosylationHepatitis BHepatitis B Surface AntigensHumansMutant ProteinsHepatitis B Surface AntigensMutant Proteinsblood donorsHBsAgHepatitis B virusN-linked glycosylationoccult infectiontransmembrane domain

Identifiers

PMID31516090
PMCPMC6758628

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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.