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Protocol Name
DOI:10.17504/protocols.io.kw4cxgw RRID Copied  
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Berthold Bivigou-Mboumba, Sandrine François-Souquière, Luc Deleplancque, Jeanne Sica, Augustin Mouinga-Ondémé, Marie Amougou-Atsama, Marie Laure Chaix, Richard Njouom, François Rouet 2018. HBV DNA Real Time Quantification according to ARNS 12187 project. protocols.io dx.doi.org/10.17504/protocols.io.kw4cxgw
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Protocol Information

URL: https://dx.doi.org/10.17504/protocols.io.kw4cxgw

Authors: Berthold Bivigou-Mboumba, Sandrine François-Souquière, Luc Deleplancque, Jeanne Sica, Augustin Mouinga-Ondémé, Marie Amougou-Atsama, Marie Laure Chaix, Richard Njouom, François Rouet

Summary: HBV DNA Real Time Quantification according to ARNS 12187 projectUsing the Arrow extractor (NorDiag, Biotrin International, Ireland), DNA was extracted from 240 μl of plasma, pre-treated with10 μl of proteinase K, using the Arrow Viral NA extraction kit, according to the manufacturer’s instructions during 45 min. Template DNA was eluted into 60 μl of kit elution buffer. Besides clinical samples, quantification standard (Acrometrix HBV Panel, Acrometrix, Menica, CA, USA) was also extracted for each run with the same protocol and1:10 diluted (from 50,000,000IU/mL to50IU/mL). For amplification, we used a primers/probe set designed under the auspices of “Agence Nationale de Recherches sur le SIDA et les hépatites virales” (ANRS 12187 project) and targeting a conserved region in the HBVS gene (nucleotide (nt) positions, 379–426). All runs were performed in a 50-μl volume containing DNA extract (10 μl), Master Mix (Platinum UGD, USA) (25 μl), pure water (HyClone Pure Water, Thermo Fisher Scientific, Waltham, MAUSA)(12.5 μl), forward primHBV1 (5’-GTGTCTGCGGCGTT TTATCA-3’) and reverse primHBV2 (5’-AGGCATAGCAGCAGGAT GAA-3’) primers at 10 μM (1μl each) and probe (5’FAM-TGCGGCGTTTTATCAT-MGB3’) at 5μM (0.5 μl). Each reaction consisted of: 2min at50°C and 10min at95°C; followed by 50 cycles of 15sec at 95°C and 1 min at 60°C each. The lower limit of quantification (LLOQ) of our technique was 100IU/mL and the lower limit of detection (LLOD) was 50IU/mL.

Associated Publications: Bivigou-Mboumba B, Amougou-Atsama M, Zoa-Assoumou S, Kamdem HM, Nzengui-Nzengui GF, Ndojyi-Mbiguino A, Njouom R, François-Souquière S (2018) Hepatitis B infection among HIV infected individuals in Gabon: Occult hepatitis B enhances HBV DNA prevalence. PLoS ONE 13(1): e0190592. doi: 10.1371/journal.pone.0190592

Affiliations: Unité Mixte de Recherche VIH et Maladies Infectieuses Associées (UMR-VIH-MIA), Libreville, Gabon, Unité Mixte de Recherche VIH et Maladies Infectieuses Associées (UMR-VIH-MIA), Libreville, Gabon, Laboratoire de Rétrovirologie, Centre International de Recherches Médicales de Franceville (CIRMF), Franceville, Gabon, Centre de Traitement Ambulatoire (CTA), Franceville, Gabon, Laboratoire de Rétrovirologie, Centre International de Recherches Médicales de Franceville (CIRMF), Service de Virologie, Centre Pasteur du Cameroun, Yaoundé, Cameroun, Laboratoire de Virologie, AP-HP, Hôpital Saint Louis; INSERM U941,Université Paris Diderot; Laboratoire associé au Centre national de Référence du VIH, Paris, France, Service de Virologie, Centre Pasteur du Cameroun, Yaoundé, Cameroun, Laboratoire de Rétrovirologie, Centre International de Recherches Médicales de Franceville (CIRMF)

External URL: https://doi.org/10.1371/journal.pone.0190592

Version: 1

Publication Date: 2018

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Source: Protocols.io