Evidence map›Paper›PMID 17567705›Full record

ArticleJournal of virology2007

Critical role of the 36-nucleotide insertion in hepatitis B virus genotype G in core protein expression, genome replication, and virion secretion.

Ke Li, Fabien Zoulim, Christian Pichoud, Karen Kwei, Stéphanie Villet, Jack Wands, Jisu Li, Shuping Tong

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
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

24 citing papers in PubMed, 39 citations in OpenAlex.

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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 at 4 institutions in 2 countries.

Ke LiLiver Research Center, Rhode Island Hospital, Brown University, Providence, Rhode Island 02903, USA.
Fabien Zoulim
Christian Pichoud
Karen Kwei
Stéphanie Villet
Jack Wands
Jisu Li
Shuping Tong
Brown University · USInserm · FRRhode Island Hospital · USUniversité Claude Bernard Lyon 1 · FR

Funding

PATHOGENESIS, IMMUNODIAGNOSIS AND THERAPY OF HCCR37CA035711 · NCI · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 2000 to 2008
$2.9M
BIOPHYSICAL PRINCIPLES OF PERISTALTIC PHENOMENAR01DK028614 · NIDDK · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI BIANCANI, PIERO · 1986 to 2006
$2.4M
Molecular Target(s) for Interruption of HBV InfectionR01CA109733 · NCI · RHODE ISLAND HOSPITAL · PI LI, JISU · 2005 to 2009
$1.1M
Role of Glycine Decarboxylase in hepadnaviral infectionR21CA095490 · NCI · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI LI, JISU · 2002 to 2003
$308k
Hepatitis C virus core protein and cell proliferationR21DK066950 · NIDDK · RHODE ISLAND HOSPITAL · PI LI, JISU · 2004 to 2005
$308k
PATHOGENESIS, IMMUNODIAGNOSIS, AND THERAPY OF HCCR01CA035711 · NCI · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI WANDS, JACK R · 1985 to 1999
–
NCI NIH HHS CA109733NCI NIH HHS CA35711NCI NIH HHS CA95490NCI NIH HHS R01 CA035711NCI NIH HHS R01 CA109733NCI NIH HHS R37 CA035711NIDDK NIH HHS DK066950NIDDK NIH HHS DK28614NIDDK NIH HHS R01 DK028614NIDDK NIH HHS R21 DK066950
6 · The paper itself

Abstract

Frequent coinfection of hepatitis B virus genotype G with genotype A suggests that genotype G may require genotype A for replication or transmission. In this regard, genotype G is unique in having a 12-amino-acid extension in the core protein due to a 36-nucleotide insertion near the core gene translation initiation codon. The insertion alters base pairing in the lower stem of the pregenome encapsidation signal, which harbors the core gene initiator, and thus has the potential to affect both core protein translation and pregenomic RNA encapsidation. Genotype G is also unusual for possessing two nonsense mutations in the precore region, which together with the core gene encode a secreted nonstructural protein called hepatitis B e antigen (HBeAg). We found that genotype G clones were indeed incapable of HBeAg expression but were competent in RNA transcription, genome replication, and virion secretion. Interestingly, the 36-nucleotide insertion markedly increased the level of core protein, which was achieved at the level of protein translation but did not involve alteration in the mRNA level. Consequently, the variant core protein was readily detectable in patient blood. The 12-amino-acid insertion also enhanced the genome maturity of secreted virus particles, possibly through less efficient envelopment of core particles. Cotransfection of genotypes G and A did not lead to mutual interference of genome replication or virion secretion. Considering that HBeAg is an immunotolerogen required for the establishment of persistent infection, its lack of expression rather than a replication defect could be the primary determinant for the rare occurrence of genotype G monoinfection.

Indexed as

Recombination, GeneticVirionCell LineDNA, ViralGenotypeHepatitis BHepatitis B e AntigensHepatitis B virusHumansMolecular Sequence DataProtein BiosynthesisRNA, MessengerRNA, ViralTranscription, GeneticVirus AssemblyVirus ReplicationDNA, ViralHepatitis B e AntigensRNA, MessengerRNA, Viral

Identifiers

PMID17567705
PMCPMC1951435
OpenAlexW2134562820

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.