Publications by authors named "M Bentahir"

The Biological Light Fieldable Laboratory for Emergencies (B-LiFE) is a box-based modular laboratory with the capacity to quickly deploy on-site in cases of uncontrolled spread of infectious disease. During the 2014-2015 West Africa Ebola outbreak, this tent laboratory provided diagnostic support to the N'Zerekore Ebola Treatment Center (ETC), Guinea, for three months. One of the objectives of B-LiFE deployment was to contribute, as much as possible, to national capacity building by training local scientists.

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Article Synopsis
  • COVID-19 is an infectious disease caused by the SARS-CoV-2 virus, which emerged in 2019 and continues to impact lives and the economy worldwide.
  • A mobile laboratory in Piedmont, Italy, conducted serological testing from June to July 2020 among local first responders to assess COVID-19 seroconversion and identify asymptomatic cases.
  • The study found a roughly 5% prevalence of SARS-CoV-2 antibodies among 6,013 tested individuals, indicating moderate agreement between different testing methods, but emphasized that seroprevalence testing is not diagnostic and is primarily useful for vaccination screening.
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Four isothermal recombinase polymerase amplification (RPA) assays were developed for fast in-field identification of The RPA assays targeted three specific sequences (i.e., the BA_5345 chromosomal marker, the lethal factor [from pXO1], and the capsule-biosynthesis-related [from pXO2]) and a conserved sequence in the adenylate cyclase gene () for the group.

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The ectodomain of matrix protein 2 is a universal influenza A virus vaccine candidate that provides protection through antibody-dependent effector mechanisms. Here we compared the functional engagement of Fcγ receptor (FcγR) family members by two M2e-specific monoclonal antibodies (MAbs), MAb 37 (IgG1) and MAb 65 (IgG2a), which recognize a similar epitope in M2e with similar affinities. The binding of MAb 65 to influenza A virus-infected cells triggered all three activating mouse Fcγ receptors , whereas MAb 37 activated only FcγRIII.

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