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Forward Genetic Approaches in Chlamydia trachomatis
Published on: October 23, 2013
Optimization of a rapid test for antibodies to the Chlamydia trachomatis antigen Pgp3
Sarah Gwyn1, Harran Mkocha2, Jessica Morgan Randall1
1Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Insights
Serological surveillance for trachoma can be monitored using dried blood spots (DBS) and lateral flow assays (LFAs). These methods are reliable for tracking disease transmission in elimination programs.
Area of Science:
- Ophthalmology
- Infectious Diseases
- Public Health
Background:
- Serological surveillance is crucial for monitoring trachoma transmission, especially after elimination targets are met.
- Feasible testing platforms are needed for resource-limited settings.
- Dried blood spots (DBS) offer a convenient sample type for serologic testing.
Purpose of the Study:
- To evaluate the feasibility and accuracy of different serologic testing platforms for trachoma surveillance.
- To assess antibody prevalence against the Pgp3 antigen in a Tanzanian population.
- To compare the performance of lateral flow assays (LFAs) with a bead-based multiplex assay (MBA) using DBS.
Main Methods:
- Blood samples (whole blood, plasma, DBS) were collected from 506 children aged 1-12 years in Tanzania.
- Antibodies against Pgp3 antigen were tested using a cassette-enclosed LFA (LFA-cassette), a dipstick LFA (LFA-dipstick), and a bead-based multiplex assay (MBA).
- Testing was conducted in both laboratory and field settings, with interrater agreement assessed.
Main Results:
- Antibody positivity rates against Pgp3 were similar across all tested formats (MBA, LFA-cassette, LFA-dipstick), ranging from 42.5% to 48.4%.
- There were no significant differences in positivity between the multiplex assay and either lateral flow assay format.
- Excellent interrater agreement (Cohen's kappa >0.81) was observed between expert and field raters across all settings.
Conclusions:
- Lateral flow assays, including a simple dipstick format, are reliable for serological surveillance of trachoma using DBS.
- These platforms are suitable for monitoring trachoma transmission in basic laboratory or field conditions.
- The findings support the use of accessible serologic tools for ongoing trachoma control efforts.
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.
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