Chlamydia trachomatis Pgp3 Antibody Population Seroprevalence before and during an Era of Widespread Opportunistic Chlamydia Screening in England (1994-2012)

PLoS One. 2017 Jan 27;12(1):e0152810. doi: 10.1371/journal.pone.0152810. eCollection 2017.

Abstract

Background: Opportunistic chlamydia screening of <25 year-olds was nationally-implemented in England in 2008 but its impact on chlamydia transmission is poorly understood. We undertook a population-based seroprevalence study to explore the impact of screening on cumulative incidence of chlamydia, as measured by C.trachomatis-specific antibody.

Methods: Anonymised sera from participants in the nationally-representative Health Surveys for England (HSE) were tested for C.trachomatis antibodies using two novel Pgp3 enzyme-linked immunosorbent assays (ELISAs) as a marker of past infection. Determinants of being seropositive were explored using logistic regression among 16-44 year-old women and men in 2010 and 2012 (years when sexual behaviour questions were included in the survey) (n = 1,402 women; 1,119 men). Seroprevalence trends among 16-24 year-old women (n = 3,361) were investigated over ten time points from 1994-2012.

Results: In HSE2010/2012, Pgp3 seroprevalence among 16-44 year-olds was 24.4% (95%CI 22.0-27.1) in women and 13.9% (11.8-16.2) in men. Seroprevalence increased with age (up to 33.5% [27.5-40.2] in 30-34 year-old women, 18.7% [13.4-25.6] in 35-39 year-old men); years since first sex; number of lifetime sexual partners; and younger age at first sex. 76.7% of seropositive 16-24 year-olds had never been diagnosed with chlamydia. Among 16-24 year-old women, a non-significant decline in seroprevalence was observed from 2008-2012 (prevalence ratio per year: 0.94 [0.84-1.05]).

Conclusion: Our application of Pgp3 ELISAs demonstrates a high lifetime risk of chlamydia infection among women and a large proportion of undiagnosed infections. A decrease in age-specific cumulative incidence following national implementation of opportunistic chlamydia screening has not yet been demonstrated. We propose these assays be used to assess impact of chlamydia control programmes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Antibodies, Bacterial / genetics
  • Antibodies, Bacterial / immunology
  • Antibodies, Bacterial / isolation & purification
  • Antigens, Bacterial / genetics
  • Antigens, Bacterial / immunology
  • Antigens, Bacterial / isolation & purification*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / immunology
  • Bacterial Proteins / isolation & purification*
  • Chlamydia Infections / epidemiology*
  • Chlamydia Infections / genetics
  • Chlamydia Infections / transmission
  • Chlamydia trachomatis / genetics
  • Chlamydia trachomatis / isolation & purification*
  • Chlamydia trachomatis / pathogenicity
  • England / epidemiology
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Humans
  • Male
  • Opportunistic Infections / epidemiology*
  • Opportunistic Infections / genetics
  • Opportunistic Infections / transmission
  • Risk Factors
  • Seroepidemiologic Studies
  • Sexual Behavior
  • Sexual Partners
  • Young Adult

Substances

  • Antibodies, Bacterial
  • Antigens, Bacterial
  • Bacterial Proteins
  • pgp3 protein, Chlamydia

Grants and funding

The Health Survey for England was funded by the Health and Social Care Information Centre. Testing of stored sera was funded by the Health Protection Agency (now Public Health England). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.