Novel Genetic Constructs for Production of Recombinant HTLV-1/2 Antigens and Evaluation of Their Reactivity to Plasma Samples from HTLV-1-Infected Patients.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
19 03 2021
Historique:
received: 25 10 2020
accepted: 20 01 2021
pubmed: 29 1 2021
medline: 9 7 2021
entrez: 28 1 2021
Statut: epublish

Résumé

Human T-cell leukemia virus type 1 (HTLV-1) can cause life-threatening diseases for which there are no effective treatments. Prevention of HTLV-1 infection requires massive testing of pregnant women, blood for transfusion, and organs for transplantation, as well as safe sex. In this context, serological assays are widely used for monitoring HTLV-1 infections. Despite the necessity for recombinant antigens to compose serological tests, there is little information available on procedures to produce recombinant HTLV-1/2 antigens for serological diagnostic purposes. In this work, we tested a series of genetic constructions to select those more amenable for production in bacterial systems. To overcome the constraints in expressing sections of viral envelope proteins in bacteria, we have used the p24 segment of the gag protein as a scaffold to display the immunogenic regions of gp46 and gp21. Nine recombinant antigenic proteins derived from HTLV-1 and five derived from HTLV-2 were successfully purified. The HTLV-1 antigens showed high efficiency in discriminating HTLV-positive samples from HTLV-negative samples using enzyme-linked immunosorbent assays. Interestingly, HTLV-1-positive samples showed a high level of cross-reaction with HTLV-2 antigens. This finding is explained by the high sequence conservation between the structural proteins of these two highly related viruses. In summary, the results presented in this work provide a detailed description of the methods used to produce recombinant HTLV-1 and HTLV-2 antigens, and they demonstrate that the HTLV-1 antigens show strong potential for serological diagnosis of HTLV-1 infections.

Identifiants

pubmed: 33504592
pii: JCM.02701-20
doi: 10.1128/JCM.02701-20
pmc: PMC8092729
pii:
doi:

Substances chimiques

Gene Products, gag 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2021 American Society for Microbiology.

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Auteurs

Ueriton Dias de Oliveira (UD)

Laboratory of Structural Biology and Protein Engineering, Carlos Chagas Institute, Oswaldo Cruz Foundation, Curitiba, Paraná, Brazil.
Cellular and Molecular Biology Postgraduate Program, Federal University of Paraná, Curitiba, Paraná, Brazil.

Fred Luciano Neves Santos (FLN)

Advanced Public Health Laboratory, Gonçalo Moniz Institute, Fiocruz, Salvador, Bahia, Brazil.

Bernardo Galvão-Castro (B)

Advanced Public Health Laboratory, Gonçalo Moniz Institute, Fiocruz, Salvador, Bahia, Brazil.
Integrated and Multidisciplinary HTLV Center, Bahiana School of Medicine and Public Health, Salvador, Bahia, Brazil.

Marco Aurelio Krieger (MA)

Molecular Biology Institute of Paraná, Curitiba, Paraná, Brazil.

Nilson Ivo Tonin Zanchin (NIT)

Laboratory of Structural Biology and Protein Engineering, Carlos Chagas Institute, Oswaldo Cruz Foundation, Curitiba, Paraná, Brazil nilson.zanchin@fiocruz.br.

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Classifications MeSH