Your browser doesn't support javascript.
loading
Application of a truncated ORF2 protein-based ELISA for diagnosis of hepatitis E in an endemic area.
Deshmukh, Tejaswini Mahesh; Dudhmal, Manisha Tukaram; Thorat, Neeta Changdeo; Sarje, Prakash Dnyaneshwar; Walimbe, Atul M; Lole, Kavita Satish.
Afiliação
  • Deshmukh TM; ICMR-National Institute of Virology, 130/1, Sus Road, Pashan, Pune, India, 411021. desh_tejas19@hotmail.com.
  • Dudhmal MT; ICMR-National Institute of Virology, 130/1, Sus Road, Pashan, Pune, India, 411021.
  • Thorat NC; ICMR-National Institute of Virology, 130/1, Sus Road, Pashan, Pune, India, 411021.
  • Sarje PD; ICMR-National Institute of Virology, 130/1, Sus Road, Pashan, Pune, India, 411021.
  • Walimbe AM; ICMR-National Institute of Virology, 130/1, Sus Road, Pashan, Pune, India, 411021.
  • Lole KS; ICMR-National Institute of Virology, 130/1, Sus Road, Pashan, Pune, India, 411021.
Appl Microbiol Biotechnol ; 106(24): 8259-8272, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36380192
ABSTRACT
Enterically transmitted waterborne hepatitis E (HE) caused due to hepatitis E virus (HEV) prevails as a significant public health problem endemic to India. Due to short-term viremia/fecal excretion and poor in vitro transmissibility of HEV, HE diagnosis depends on detection of specific IgM antibodies in serum. Present study evaluated performances of two in-house and six commercial IgM detection enzyme-linked immunosorbent assays (ELISAs) using sera collected from volunteers/acute hepatitis patients (n = 716). The in-house ELISAs were based on complete and truncated open reading frame 2 (ORF2) proteins containing neutralizing epitope/s region of genotype 1 HEV (ORF2p, 1-660 amino acid (a.a.) and T1NEp, 458-607 a.a., respectively). The commercial ELISAs included Wantai (China), MP Diagnostics (MPD) (Singapore), DIA.PRO Diagnostics (Italy), MBS (Italy), abia (Germany), and ImmunoVision (USA). T1NE ELISA showed 97.0% positive percent agreement (PPA), 99.4% negative percent agreement (NPA), and 98.6% concordance (κ = 0.97, P = 0.0000) with ORF2 ELISA. ORF2, T1NE, Wantai, and MPD ELISAs agreed on results for 88% of sera tested. Two percent sera showed reactivity in each combination of three and two of aforementioned four ELISAs. Remaining 8% sera were single ELISA reactive. PPA and NPA value ranges were 76.3-99.0% and 84.8-99.5%, respectively. Pairwise concordances between all the eight ELISAs ranged from 88.0 to 100% (κ 0.74-1.00). Both the in-house ELISAs agreed better with Wantai over MPD ELISA. In conclusion, both ORF2 and T1NE ELISAs were equally efficient in diagnosing HEV infections. T1NEp proved to be an excellent tool in HE sero-diagnosis and is worth exploring in development of simple rapid tests. KEY POINTS • In-house ELISA based on bacterially expressed neutralizing epitope/s region protein • In-house ELISA based on complete ORF2 protein expressed in insect cells • Comparison of two in-house and six commercial anti-HEV IgM antibody detection ELISAs.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite E Tipo de estudo: Diagnostic_studies Limite: Humans País como assunto: Asia / Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite E Tipo de estudo: Diagnostic_studies Limite: Humans País como assunto: Asia / Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article