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Title: Optimization of a rapid test for antibodies to the Chlamydia trachomatis antigen Pgp3. Author: Gwyn S, Mkocha H, Randall JM, Kasubi M, Martin DL. Journal: Diagn Microbiol Infect Dis; 2019 Apr; 93(4):293-298. PubMed ID: 30709562. Abstract: Serological surveillance for trachoma could allow monitoring of transmission levels in areas that have achieved elimination targets. Platforms that allow testing in basic laboratories or testing of easy-to-manage samples such as dried blood spots would contribute to the feasibility of serologic testing. Blood from 506 1-12-year-olds in 2 villages in Kongwa district, Tanzania, was tested for antibodies against the antigen Pgp3. Whole blood, plasma, and dried blood spots (DBS) were tested in lab and field settings using a cassette-enclosed Pgp3 lateral flow assay (LFA-cassette) and a pared-back "dipstick" assay (LFA-dipstick). DBS were also tested with a bead-based multiplex assay (MBA). There was no significant difference in antibody positivity between the MBA and either LFA format (ranging from 42.5% to 48.4%). Interrater agreement between an expert rater and 3 different raters in field and lab settings was uniformly good, with Cohen's kappa >0.81 in all cases.[Abstract] [Full Text] [Related] [New Search]