A time-resolved immunoassay to measure serum antibodies to the rotavirus VP6 capsid protein

Owen Kavanagh, Xi-Lei Zeng, Sasirekha Ramani, Indrani Mukhopadhya, Sue E. Crawford, Gagandeep Kang, Mary K. Estes

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)
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Abstract

The rotavirus (RV) inner capsid protein VP6 is widely used to evaluate immune response during natural infection and in vaccine studies. Recombinant VP6 from the most prevalent circulating rotavirus strains in each subgroup (SG) identified in a birth cohort of children in southern India [SGII (G1P[8]) and SGI (G10P[11])] were produced. The purified proteins were used to measure VP6-specific antibodies in a Dissociation-Enhanced Lanthanide Fluorometric Immunoassay (DELFIA). The ability of the assay to detect a ≥2 fold rise in IgG level in a panel of serum samples from a longitudinal study was compared to a gold standard virus-capture ELISA. A strong association was observed between the assays (p < 0.001; chi-squared test) with assay performances remaining similar when the samples were subdivided as having a fold change increase in VP6 antibody levels (a) within 90 days of RV RNA detection in stool or (b) if no RV RNA was detected within that time period. This study demonstrates the suitability of using recombinant proteins to measure anti-RV immune responses and serves as a “proof of principle” to examine the antibody responses generated to other recombinant RV proteins and thereby possibly identify a correlate of protection.
Original languageEnglish
Pages (from-to)228-231
Number of pages4
JournalJournal of Virological Methods
Volume189
Issue number1
Early online date23 Nov 2012
DOIs
Publication statusPublished - Apr 2013

Bibliographical note

This work was funded by The Wellcome Trust Trilateral Initiative for Infectious Diseases (grant no. 063144). The funding source had no role, in study design; in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.

Keywords

  • Rotavirus
  • Recombinant VP6
  • DELFIA
  • ELISA

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