Evaluation of Multiplex-Based Antibody Testing for Use in Large-Scale Surveillance for Yaws: a Comparative Study

Details

• Alternative Title:
  J Clin Microbiol
• Personal Author:
  Cooley, Gretchen M. ; Mitja, Oriol ; Goodhew, Brook ; Pillay, Allan ; Lammie, Patrick J. ; Castro, Arnold ; Moses, Penias ; Chen, Cheng ; Ye, Tun ; Ballard, Ronald ; Martin, Diana L.
• Description:
  WHO has targeted yaws for global eradication by 2020. The program goals are to interrupt the transmission in countries where yaws is endemic and to certify countries as yaws free where yaws was endemic in the past. No new rapid plasmin reagin (RPR) seroreactivity in young children is required for certification of elimination at a country level. We sought to evaluate whether antibody responses to specific treponemal antigens measured in a high-throughput multiplex bead array (MBA) assay differentiate past versus current infection and whether a nontreponemal lipoidal antigen test can be incorporated into the MBA. Serum and dried blood spot specimens collected for yaws surveillance projects in Ghana, Vanuatu, and Papua New Guinea (PNG) were run on MBA to measure antibodies against recombinant p17 (rp17) and treponemal membrane protein A (TmpA) treponemal antigens. Results were compared to standard treponemal laboratory (TPPA or TPHA [TPP(H)A]) and quantitative RPR test data. Of 589 specimens, 241 were TPP(H)A(+)/RPR(+), 88 were TPP(H)A(+)/RPR(-), 6 were TPP(H)A(-)/RPR(+), and 254 were negative for both tests. Compared to TPP(H)A, reactive concordance of rp17 was 93.7%, while reactive concordance of TmpA was only 81.9%. TmpA-specific reactivity showed good correlation with RPR titers (R(2) = 0.41; P < 0.0001). IgG responses to the lipoidal antigen used in RPR testing (cardiolipin) were not detected in the MBA. Our results suggest that TmpA can be used as a treponemal antigen marker for recent or active infection and potentially replace RPR in a high-throughput multiplex tool for large-scale yaws surveillance.
• Subjects:
  Epidemiology
• Source:
  J Clin Microbiol. 2016; 54(5):1321-1325.
• Pubmed ID:
  26962086
• Pubmed Central ID:
  PMC4844712
• Document Type:
  Journal Article
• Volume:
  54
• Issue:
  5
• Collection(s):
  CDC Public Access
• Main Document Checksum:
  urn:sha256:69ae867777f5a8c89ef7810f22ca0d2a44c823d1aac1a2b95f303f38c3a0398d
• Download URL:
  https://stacks.cdc.gov/view/cdc/39335/cdc_39335_DS1.pdf
• File Type:
  [PDF - 609.05 KB ]