Evidence map›Paper›PMID 24587360›Full record

ArticlePloS one2014

Molecular characterization of HBV strains circulating among the treatment-naive HIV/HBV co-infected patients of eastern India.

Debraj Saha, Ananya Pal, Avik Biswas, Rajesh Panigrahi, Neelakshi Sarkar, Dipanwita Das, Jayeeta Sarkar, Subhasish Kamal Guha, Bibhuti Saha, Sekhar Chakrabarti and 1 more

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
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

11 authors.

Debraj SahaICMR Virus Unit, Kolkata, ID & BG Hospital Campus, Kolkata, West Bengal, India.
Ananya PalICMR Virus Unit, Kolkata, ID & BG Hospital Campus, Kolkata, West Bengal, India.
Avik BiswasICMR Virus Unit, Kolkata, ID & BG Hospital Campus, Kolkata, West Bengal, India.
Rajesh PanigrahiDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana, United States of America.
Neelakshi SarkarICMR Virus Unit, Kolkata, ID & BG Hospital Campus, Kolkata, West Bengal, India.
Dipanwita DasICMR Virus Unit, Kolkata, ID & BG Hospital Campus, Kolkata, West Bengal, India.
Jayeeta SarkarCalcutta School of Tropical Medicine, Kolkata, West Bengal, India.
Subhasish Kamal GuhaCalcutta School of Tropical Medicine, Kolkata, West Bengal, India.
Bibhuti SahaCalcutta School of Tropical Medicine, Kolkata, West Bengal, India.
Sekhar ChakrabartiNational Institute of Cholera and Enteric Diseases, Kolkata, West Bengal, India.
Runu ChakravartyICMR Virus Unit, Kolkata, ID & BG Hospital Campus, Kolkata, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously we reported that the exposure to hepatitis B virus (HBV) infection serves as a major threat among the treatment naive HIV infected population of eastern India. Hence, molecular characterization of these strains is of utmost importance in order to identify clinically significant HBV mutations. A total of 85 treatment naive HIV/HBV co-infected participants were included of whom the complete basal core promoter/precore region, the core and the whole envelope gene could be successfully sequenced for 59, 57 and 39 isolates respectively. Following phylogenetic analysis, it was found that HBV/D was the predominant genotype with HBV/D2 (38.5%) being the most prevalent subgenotype followed by HBV/A1. The major mutations affecting HBeAg expression includes the A1762T/G1764A (13.6%), G1896A (22%) and G1862T mutation (33.9%) which was predominantly associated with HBV/A1. Moreover, the prevalence of G1896A was considerably high among the HBeAg negative HIV/HBV co-infected subjects compared to HBV mono-infection. The main amino acid substitutions within the MHC class II restricted T-cell epitope of HBcAg includes the T12S (15.8%) and T67N (12.3%) mutation and the V27I (10.5%) mutation in the MHC class I restricted T-cell epitope. PreS1/S2 deletion was detected in 3 isolates with all harboring the BCP double mutation. Furthermore, the frequently occurring mutations in the major hydrophilic loop of the S gene include the T125M, A128V and M133I/L. Therefore, this study is the first from India to report useful information on the molecular heterogeneity of the HBV strains circulating among the treatment naive HIV/HBV co-infected population and is thus clinically relevant.

Indexed as

HIVPhylogenyAdultCoinfectionFemaleGenetic HeterogeneityGenotypeHepatitis B, ChronicHepatitis B Core AntigensHepatitis B e AntigensHepatitis B virusHIV InfectionsHumansMaleMiddle AgedMolecular TypingHepatitis B Core AntigensHepatitis B e AntigensViral Core ProteinsViral Envelope Proteins

Identifiers

PMID24587360
PMCPMC3938687

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.