Surveillance for peri-elimination trachoma recrudescence: Exploratory studies in Ghana.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
09 2021
Historique:
received: 19 05 2021
accepted: 18 08 2021
revised: 15 10 2021
pubmed: 21 9 2021
medline: 15 12 2021
entrez: 20 9 2021
Statut: epublish

Résumé

To date, eleven countries have been validated as having eliminated trachoma as a public health problem, including Ghana in 2018. Surveillance for recrudescence is needed both pre- and post-validation but evidence-based guidance on appropriate strategies is lacking. We explored two potential surveillance strategies in Ghana. Amongst randomly-selected communities enrolled in pre-validation on-going surveillance between 2011 and 2015, eight were identified as having had trachomatous-inflammation follicular (TF) prevalence ≥5% in children aged 1-9 years between 2012 and 2014. These eight were re-visited in 2015 and 2016 and neighbouring communities were also added ("TF trigger" investigations). Resident children aged 1-9 years were then examined for trachoma and had a conjunctival swab to test for Chlamydia trachomatis (Ct) and a dried blood spot (DBS) taken to test for anti-Pgp3 antibodies. These investigations identified at least one community with evidence of probable recent Ct ocular transmission. However, the approach likely lacks sufficient spatio-temporal power to be reliable. A post-validation surveillance strategy was also evaluated, this reviewed the ocular Ct infection and anti-Pgp3 seroprevalence data from the TF trigger investigations and from the pre-validation surveillance surveys in 2015 and 2016. Three communities identified as having ocular Ct infection >0% and anti-Pgp3 seroprevalence ≥15.0% were identified, and along with three linked communities, were followed-up as part of the surveillance strategy. An additional three communities with a seroprevalence ≥25.0% but no Ct infection were also followed up ("antibody and infection trigger" investigations). DBS were taken from all residents aged ≥1 year and ocular swabs from all children aged 1-9 years. There was evidence of transmission in the group of communities visited in one district (Zabzugu-Tatale). There was no or little evidence of continued transmission in other districts, suggesting previous infection identified was transient or potentially not true ocular Ct infection. There is evidence of heterogeneity in Ct transmission dynamics in northern Ghana, even 10 years after wide-scale MDA has stopped. There is added value in monitoring Ct infection and anti-Ct antibodies, using these indicators to interrogate past or present surveillance strategies. This can result in a deeper understanding of transmission dynamics and inform new post-validation surveillance strategies. Opportunities should be explored for integrating PCR and serological-based markers into surveys conducted in trachoma elimination settings.

Identifiants

pubmed: 34543293
doi: 10.1371/journal.pntd.0009744
pii: PNTD-D-21-00720
pmc: PMC8519445
doi:

Substances chimiques

Antibodies, Bacterial 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0009744

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Laura Senyonjo (L)

Research Team, Sightsavers, Haywards Heath, United Kingdom.
Clinical Research Department, London School of Hygiene & Tropical Medicine, London, United Kingdom.

James Addy (J)

Eye Health Department, Ghana Health Service, Accra, Ghana.

Diana L Martin (DL)

Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, United States of America.

David Agyemang (D)

Sightsavers Ghana, Accra, Ghana.

Dorothy Yeboah-Manu (D)

Bacteriology Department, Noguchi Memorial Institute for Medical Research, Accra, Ghana.

Sarah Gwyn (S)

Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, United States of America.

Benjamin Marfo (B)

Neglected Tropical Diseases Division, Ghana Health Service, Accra, Ghana.

Adwoa Asante-Poku (A)

Bacteriology Department, Noguchi Memorial Institute for Medical Research, Accra, Ghana.

Agatha Aboe (A)

Sightsavers Ghana, Accra, Ghana.

Ernest Mensah (E)

NTD team, FHI360, Accra, Ghana.

Anthony W Solomon (AW)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Robin L Bailey (RL)

Clinical Research Department, London School of Hygiene & Tropical Medicine, London, United Kingdom.

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