- Open Access
The impact of a single round of community mass treatment with azithromycin on disease severity and ocular Chlamydia trachomatis load in treatment-naïve trachoma-endemic island communities in West Africa
Parasites & Vectorsvolume 10, Article number: 624 (2017)
Trachoma, a neglected tropical disease, is caused by ocular infection with Chlamydia trachomatis (Ct). The World Health Organization (WHO) recommends three annual rounds of community mass drug treatment with azithromycin (MDA) if the prevalence of follicular trachoma in 1–9 year olds (TF1–9) exceeds 10% at district level to achieve an elimination target of district-level TF1–9 below 5% after. To evaluate this strategy in treatment-naïve trachoma-endemic island communities in Guinea Bissau, we conducted a cross-sectional population-based trachoma survey on four islands. The upper tarsal conjunctivae of each participant were clinically assessed for trachoma and conjunctival swabs were obtained (n = 1507). We used a droplet digital PCR assay to detect Ct infection and estimate bacterial load. We visited the same households during a second cross-sectional survey and repeated the ocular examination and obtained conjunctival swabs from these households one year after MDA (n = 1029).
Pre-MDA TF1–9 was 22.0% (136/618). Overall Ct infection prevalence (CtI) was 18.6% (25.4% in 1–9 year olds). Post-MDA (estimated coverage 70%), TF1–9 and CtI were significantly reduced (7.4% (29/394, P < 0.001) and 3.3% (34/1029, P < 0.001) (6.6% in 1–9 year olds, P < 0.001), respectively. Median ocular Ct load was reduced from 2038 to 384 copies/swab (P < 0.001). Following MDA cases of Ct infection were highly clustered (Moran’s I 0.27, P < 0.001), with fewer clusters of Ct infection overall, fewer clusters of cases with high load infections and less severe disease.
Despite a significant reduction in the number of clusters of Ct infection, mean Ct load, disease severity and presence of clusters of cases of high load Ct infection suggesting the beginning of trachoma control in isolated island communities, following a single round of MDA we demonstrate that transmission is still ongoing. These detailed data are useful in understanding the epidemiology of ocular Ct infection in the context of MDA and the tools employed may have utility in determining trachoma elimination and surveillance activities in similar settings.
Chlamydia trachomatis is the leading infectious cause of blindness globally [1,2,3]. Trachoma is caused by infection with ocular strains of C. trachomatis and manifests as distinct clinical syndromes, beginning with an acute self-limiting kerato-conjunctivitis which may progress to chronic inflammatory disease with subsequent conjunctival scarring and blinding sequelae.
The World Health Organization (WHO) advocates the implementation of the SAFE strategy (Surgery for trichiasis, Antibiotics for active infection, Facial cleanliness to prevent disease transmission and Environmental improvement to increase access to water and sanitation) for trachoma elimination. Mass drug treatment with azithromycin (MDA) to entire communities aims to treat individual cases of infection and reduce the reservoir of infection, interrupting transmission within communities. Repeated episodes of conjunctival infection with C. trachomatis are thought to be required to cause the blinding sequelae of trachoma [2, 4]. Community-wide MDA, as part of the SAFE strategy, therefore aims to interrupt transmission, thus reducing the number of infections that each individual is exposed to and eliminate blinding trachoma as a public health concern [2, 5].
The WHO recommends between three and five annual rounds of MDA if the baseline prevalence of follicular trachoma in 1–9 year olds (TF1–9) at district level is between 10 and 39%, and at least five annual rounds of MDA if TF1–9 ≥ 40%, to achieve a reduction of TF1–9 to below 5% following treatment [5, 6]. These recommendations were made in 2010 after previous guidance  was found to be insufficient to eliminate trachoma. According to WHO guidance, trachoma control programmes should aim to administer antibiotics to at least 80% of the population. Following completion of MDA an impact survey is recommended, the results from the impact survey informing decisions about continuing treatment or conducting surveillance. There are conflicting data from trachoma-endemic communities on the optimal duration and mode of administration required to achieve the elimination target.
Oral azithromycin, even as a single dose delivered as a mass administration to communities, has significantly reduced the burden of active disease and in some populations has eliminated infection with C. trachomatis entirely . However, the evidence-base relating to optimal frequency of MDA that will be effective in eliminating trachoma is not fully understood and may vary between settings .
In trachoma-endemic populations with an extremely high baseline prevalence of TF1–9, despite high coverage of MDA under research study conditions, levels of infection and disease, although reduced, can persist or return to pre-treatment levels. Longitudinal studies in Tanzania suggest that with present WHO protocols, hyperendemic countries may need yearly mass treatment for over ten years, which has significant economic and logistic impact on national trachoma programmes, non-government organisations and donors of azithromycin . Similarly in Ethiopia, despite more than seven annual rounds of treatment in some regions showing that the prevalence of disease and infection can be reduced, but that on cessation of treatment, disease and infection return to baseline prevalence levels . Despite adequate MDA coverage in line with WHO recommendations, disease elimination at 18 months post-MDA may not be sustained and re-emergence of disease within households has been demonstrated .
In some regions where annual treatment appears to have had little impact, even biannual treatment that has been implemented under research study conditions has failed to reduce TF prevalence in 1–9 year olds to less than 5% . These data are supported by findings from a recent study, suggesting that extended MDA timelines may be required to interrupt transmission to meet elimination targets .
The dynamics of C. trachomatis transmission, particularly in the context of MDA, is complex and not well understood. Trachoma endemicity is likely to be important, as disease can disappear spontaneously from hypoendemic (TF1–9 5–10%) communities [15,16,17,18,19] or disappear after a single round of MDA [8, 19]. In meso-endemic (TF1–9 10–20%) populations disease prevalence may stabilize following MDA , and in hyper-endemic (TF1–9 > 20%) populations disease and infection persist despite multiple rounds of MDA .
The trachoma-endemic populations of the Bijagós Archipelago of Guinea-Bissau we have observed a strong association between C. trachomatis bacterial load and disease severity with spatial clustering of high load infections [20, 21]. In the current study we sought to assess the impact of a single round of MDA in these isolated treatment-naïve island communities on the prevalence of clinical trachoma and ocular C. trachomatis infection and investigate its effect on C. trachomatis load, disease severity and spatial clustering of C. trachomatis infection one year following MDA.
Study design and study population
The cross-sectional population-based trachoma survey methodology and this study population have been described previously [20,21,22,23,24,25]. Briefly, we used first stage cluster random sampling with geospatial representation on four islands at village-level to randomly select households for inclusion in the survey at baseline. A sample size of 1000 (including a design effect of 2 to account for anticipated household clustering) yields adequate power to estimate TF1–9 5% ± 3% precision . Two hundred and ninety-three households from all 38 villages were enrolled in the survey at baseline. Data were geo-coded at household and village level [20, 21]. One year following MDA we sought to follow up the households enrolled at baseline. A de facto census of each household was conducted at baseline and follow-up, from which individuals were enrolled.
Clinical examination and conjunctival sampling
Clinical examination and conjunctival sampling were conducted at baseline and one year following treatment using standardised methods [20, 23]. A single validated physician examiner assessed each participant using the WHO simplified  and modified FPC  grading systems. In the modified FPC system, follicles (F), papillary hypertrophy (inflammation) (P) and conjunctival scarring (C) are each assigned a separate grade from 0 to 3. FPC grades of F2/3 or P3 equate to a diagnosis of active trachoma [TF (Trachomatous inflammation-Follicular) or TI (Trachomatous inflammation-Intense) by the WHO simplified system] and a grade of C2/3 (and in some cases C1) equates to a diagnosis of TS (Trachomatous Scarring). Clinical grading of the upper tarsal conjunctivae was conducted in the field as described previously [20,21,22,23]. The trachoma grader achieved an inter grader agreement (Cohen’s Kappa) score of > 0.9 against an international expert trachoma grader. Samples were taken using a polyester-tipped swab from the left upper tarsal conjunctiva of each participant using a well-tolerated standardized procedure [20,21,22,23]. Quality control swabs (pre-marked and drawn at random from the swab dispenser in the field) were passed 10 cm in front of the eye but without touching the eye were collected and treated in the same way as the conjunctival swabs for field and laboratory quality control. Our ddPCR assay enabled us to detect a human target (Homo sapiens RNase P/MRP 30-kDa subunit (RPP30) gene) to ensure that control swabs had not come into contact with the conjunctival surface and that swabs collected from participants were adequate samples (using strict minimum RPP30 detection criteria as described previously ). We found no evidence of cross-contamination using these methods; all control swabs were negative for C. trachomatis DNA and all conjunctival specimens were deemed adequate for inclusion in the analysis.
Community mass treatment
A single height-based dose of oral azithromycin was offered by the national trachoma control programme distribution teams to all individuals in all communities participating in the study in accordance with WHO and national policy. Alternative treatment with tetracycline eye ointment was offered if there were contraindications to treatment with azithromycin. District-level coverage was estimated by the national trachoma control programme following the MDA using data from their MDA treatment registers and the most recent Electoral Census (2009).
Detection and quantitation of C. trachomatis
DNA was extracted from swabs using QIAamp DNA Mini kit (Qiagen, Manchester, UK) and C. trachomatis DNA was detected and quantitated using droplet digital PCR (ddPCR) (Bio-Rad Laboratories, Hemel Hempstead, UK) as described previously [20, 22, 23]. Briefly, C. trachomatis plasmid-based ddPCR was used to detect DNA and diagnose infection and a single-copy pathogen chromosomal gene (omcB) was used to estimate pathogen load in each plasmid-positive sample [22, 23]. Estimated quantities of omcB (C. trachomatis load) are expressed as copies/swab.
Chlamydia trachomatis quantitation data were processed as described previously [22, 23]. Data were double entered into a customised database (Microsoft Access 2007) and discrepancies resolved through source documents. Data were cleaned and analysed in STATA 13 (Stata Corporation, College Station, Texas USA). Statistical significance was determined at the 5% level.
We estimated the variance due to between-household, village and island clustering using null models for both active trachoma and C. trachomatis infection adjusted for age and gender in multivariable null models including all three cluster variables as previously described .
We examined trachoma and C. trachomatis infection prevalence data at baseline and follow-up using a Chi-square test of proportions. Chlamydia trachomatis load data were loge-transformed where indicated. Median load comparisons were made between baseline and follow-up using Kruskall-Wallis test. Associations between load and detailed clinical phenotype (defined by F and P scores using the modified FPC trachoma grading system) were examined using multivariable mixed effects linear and logistic regression models accounting for clustering detected in previous studies [20, 21] and adjusting for household C. trachomatis infection status at baseline in the follow-up analysis.
Geo-coded data were projected into UTM Zone 28 N and analysed in ArcGIS 10.1 (ESRI Inc., USA) . A statistical measure of clustering (Moran’s I) was calculated at baseline and follow-up to evaluate the effect of MDA on the global spatial distribution of active trachoma and C. trachomatis infection. A local indicator of spatial association (Local (Anselin) Moran’s I) was used to identify clusters and outliers of C. trachomatis infection by load at baseline and follow-up. This method detects statistically significant clusters or outliers related to C. trachomatis load based on the calculation of z-scores for the distribution. Cluster types identified (relative to their z-score and P-value) include HH (high loads associated with other high loads), LL (low loads associated with other low loads), HL (a high load outlier associated with other predominantly lower loads) and LH (a low load outlier associated with other predominantly high loads). The geostatistical methods used are discussed fully elsewhere . Briefly, we used the zone of indifference to define adjacency. This method assumes that each observation (individual C. trachomatis load) has local influence that decreases with distance beyond a critical distance cut-off, resulting in an adapted model of impedance, or distance decay, such that all features have an impact on all other features, but this impact decreases with distance. The crucial cut-off used in this study is derived from the distance over which spatial autocorrelation occurs in these data and relates to the village boundaries, assuming impedance as described above .
Prevalence of trachoma and C. trachomatis infection
Participant enrolment and follow-up are illustrated in Fig. 1. MDA was conducted following the baseline survey and coverage was estimated at 70% (using district-level data provided by the national trachoma control programme) across the study islands. Socio-demographic characteristics did not significantly differ between individuals seen at baseline or at follow-up, nor were population-based estimates of the prevalence of scarring trachoma (TS) and trachomatous trichiasis (TT) (Table 1). The prevalence of TF and ocular C. trachomatis infection were statistically significantly reduced following treatment (Table 2). The prevalence of TF in 1–9 year olds was reduced from 22.0% (95% confidence interval, CI: 18.9–25.5%) to 7.4% (95% CI: 4.8–9.9%) (P < 0.001). The prevalence of TI in this age group was also reduced: from 2.9% (95% CI: 1.4–4.1%) to 1.5% (95% CI: 0.3–2.7%). The prevalence of ocular C. trachomatis infection was reduced in the population from 18.6% to 3.3% (P < 0.001) and in 1–9 year olds from 25.4% to 6.6% (P < 0.001). Figure 2 shows the household prevalence of C. trachomatis infection in 1–9 year olds in the households seen at both time points demonstrating that the follow-up prevalence is much reduced compared to baseline in the majority of households. However 13% (37/293) households were lost to follow-up, and of those almost half (18/37) were households where C. trachomatis infection was detected in 1–9 year olds at baseline.
Clustering of active trachoma and C. trachomatis infection
There was evidence of increased clustering at follow-up of active trachoma and C. trachomatis infection at village-level and infection at household level (Table 3). The Moran’s I for C. trachomatis infection at baseline was 0.06 (z = 2.10, P = 0.0353) and 0.27 (z = 3.85, P = 0.0001) at follow-up indicating increased clustering following MDA.
Chlamydia trachomatis ocular load and disease severity
Median estimated load of C. trachomatis infection in infected individuals was significantly reduced from 2038 omcB copies/swab to 348 omcB copies/swab (χ 2 = 6.21, P = 0.0127) (Fig. 3). At follow-up almost all infections occurred in children under the age of 10 years, with 59% (20/34) occurring in children aged 0–5 years. At baseline a greater proportion of individuals with TS or normal conjunctivae were infected, indicating that infection was more widely spread in the population (Fig. 4).
In those with C. trachomatis infection, inflammatory disease was less severe at follow-up, most markedly with respect to conjunctival inflammation. There was a shift from higher proportions of P2 and P3 scoring disease at baseline to greater proportions of P0 and P1 scoring disease at follow-up (Fig. 5). However, age-adjusted mixed effect linear regression models accounting for household clustering and household C. trachomatis infection status at baseline demonstrate that a strong association remains between C. trachomatis load and conjunctival inflammation (P score), though the association is weaker at follow-up (ORadj 11.65, 95% CI: 1.89–71.76) compared to baseline (ORadj 27.6, 95% CI: 6.8–111.8) (Table 4).
Spatial clustering of high load C. trachomatis infections
Maps were generated using the local Moran’s I statistic. These demonstrated clustering of C. trachomatis infection by load and found that at baseline there were a larger number of clusters of high load infections (HH clusters) than at follow-up. High load outliers (HL) were not present at follow-up. The HH clusters present at follow-up were at different locations compared to baseline. One HH cluster at follow-up was present in a location where there was an HL outlier prior to MDA. A second HH cluster was located where there was previously no clustering related to bacterial load. Clustering of low load (LL clusters) infections was not evident at either time point. Cluster-outlier maps at baseline and follow-up are presented in Fig. 6. The minimum value of C. trachomatis load observed within any HH cluster in this data set is ~10,000 omcB copies/swab irrespective of time point.
The WHO recommends that MDA aim for 80% coverage to be considered adequate for trachoma control programmes . However, due to the significant logistic challenges that exist in this remote area it was only possible to deliver MDA to an estimated 70% of the population. Our data suggest that in these island communities, despite initial high disease and infection prevalence and suboptimal MDA coverage, we observed a dramatic reduction in prevalence of both TF in 1–9 year olds and ocular C. trachomatis infection (overall and in 1–9 year olds) one year after MDA. This type of dramatic reduction has been observed previously in treatment-naïve settings following azithromycin MDA .
Active trachoma and C. trachomatis infection (particularly those with the highest bacterial loads) were most prevalent in children under 10 years of age at both baseline and follow-up. Following MDA C. trachomatis infection virtually disappeared in adults and was reduced in those with scarred or normal conjunctivae. The presence of C. trachomatis infection across all age groups and clinical phenotypes at baseline is likely to represent the distribution typical of chronic endemic trachoma before MDA . The reduction in the prevalence of infection and change in distribution by age and disease suggests a shift in the epidemiology of ocular C. trachomatis infection in these communities and may mark the beginning of control of transmission.
The significantly lower median ocular C. trachomatis load following MDA was consistent with findings from other studies suggesting that from 2 to 12 months following MDA the prevalence and load of infections remain low .
The number of clusters of high load infections detected using local spatial statistics was reduced and there was an absence of high load outlying infections amidst other low load infections after MDA. This phenomenon may be due to reduced chlamydial diversity in the population following MDA. The role of chlamydial strain diversity in transmission is unclear but greater diversity is likely to represent more successful transmission. There is some evidence that following MDA in other settings the number of C. trachomatis strains defined by ompA genotyping  or multi-locus sequence typing  was substantially reduced.
These data support the previous suggestion that C. trachomatis load is important in transmission of infection and its maintenance in the population [18, 21]. At both time points the minimum C. trachomatis load that we observed within an HH cluster was ~10,000 omcB copies/swab, supporting the hypothesis that there may be a threshold load important to sustain transmission, as suggested by Chidambaram et al. . The change from an HL outlier prior to MDA to an HH cluster, and the appearance of a new HH cluster were there was previously none, following treatment suggests that there is likely to be ongoing transmission within this population. This particular location has a mobile population, being populated by fishermen and their families from Guinea Conakry, Sierra Leone and other islands on the archipelago. There are limited amenities in this settlement and it is possible that infection has been reintroduced. Introduction of infection following migration events has been documented in The Gambia . In general, these island communities less susceptible to in-migration due to their isolated geographical location and therefore represent a unique opportunity to evaluate the effect of MDA in treatment-naïve trachoma-endemic populations.
Clustering of disease and infection was more apparent following MDA. Increased clustering of cases of C. trachomatis infection in treated communities has been described elsewhere . In this study the strongest clustering of C. trachomatis infection was present at village level following MDA. This may be relevant in the context of previous spatial analyses conducted in this population suggesting that the village may an important unit of transmission in addition to the household in these communities and that the dynamics of transmission are different before and after MDA .
We used the detailed conjunctival grading system to investigate associations between infection, bacterial load and disease severity following MDA. A strong association between C. trachomatis load and inflammatory trachoma has been described previously [21, 28, 35]. The reduced association between infection and P score following MDA may reflect the decreased burden of circulating infection and decreased infection loads. It is likely that repeated episodes of infection are reduced following MDA due to a decrease in circulating C. trachomatis and subsequently reduced transmission. Moreover, in populations undergoing MDA there is evidence that clinical signs of trachoma become less specific for C. trachomatis infection [36, 37], suggesting that only the more severe phenotypes remain predictive of C. trachomatis infection. Azithromycin exhibits immunomodulatory effects that may be associated with reduced levels of inflammation , although at one year after a single dose this effect is unlikely to play a major role.
Although these are interesting data, the analysis is limited by the potential impact of loss to follow-up after MDA. 13% of households were not available at follow-up, and almost half of these were households where we found individuals with C. trachomatis infection at baseline. Clearly this may represent responder bias. The characteristics of the population in terms of age distribution, gender and chronic sequelae (trachomatous trichiasis) suggest that the follow-up sample is adequately representative of the baseline sample. However, the prevalence of conjunctival scarring in the cohort at follow-up was higher, possibly due to selective drop out of less severely affected individuals. This may affect the overall prevalence of C. trachomatis infection found at follow-up, as the prevalence of infection in conjunctival scarring is likely to be higher than in those with no clinical signs of trachoma . Additional limitations of the study include the programmatic implementation of SAFE. We did not evaluate the implementation of the ‘F’ and ‘E’ components of SAFE to improve hygiene and sanitation alongside MDA in this study. Nor did we have access to accurate MDA coverage estimates, at individual or household level. At the time of the study there was limited implementation of ‘F’ and ‘E’ components of SAFE in Guinea Bissau, but there may still have been some effect in these communities that we could not evaluate . Evaluating C. trachomatis load and clinical disease severity in cross-sectional studies is limited in the assumption that the duration of infection and the host conjunctival immune response are present in a steady state. To fully investigate the dynamics of C. trachomatis transmission more detailed longitudinal study is required, ideally in the context of individual or household level MDA coverage.
In summary, through investigating the micro-epidemiology of C. trachomatis infection and its relationship with bacterial load and disease severity, these data suggest that MDA is likely to be having a significant impact on transmission of ocular C. trachomatis in these communities. However, further monitoring is required, as this geospatial analysis suggests that that there may be on-going transmission and risk of reintroduction of infection to communities despite MDA. The loss to follow-up in the population following MDA is also a concern and may indicate that these data underestimate the current burden of circulating ocular C. trachomatis infection and trachoma. Further longitudinal study, utilising mathematical models and high-resolution chlamydial genotyping and geospatial analysis, is necessary to provide a more complete picture of the relationship between disease severity, chlamydial load, transmission and elimination thresholds in communities undergoing MDA. These tools may improve our understanding of disease pathogenesis and transmission and may be useful in trachoma surveillance in post-MDA settings to identify clusters of infection and thresholds of C. trachomatis bacterial load that may be important foci of transmission.
- Ct :
Droplet digital PCR
Follicles, Papillary hypertrophy, Conjunctival scarring
Mass drug treatment with azithromycin
Surgery for trichiasis, Antibiotics for active infection, Facial hygiene, Environmental improvements
Trachomatous inflammation – Follicular
- TF1–9 :
TF prevalence in 1–9 year olds
Trachomatous inflammation – Intense
Universal Transverse Mercator coordinate system
World Health Organization
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We extend our thanks to our colleagues in the Programa Nacional de Saúde de Visão in Bissau and to the communities of the Bijagós Archipelago, our field research team and all study participants in Guinea Bissau. Azithromycin was donated for treatment of trachoma on the islands by Pfizer Inc. through application via the International Trachoma Initiative.
This work was supported by the Wellcome Trust (grant number 097330/Z/11/Z).
Availability of data and materials
All important data that support the conclusions of this article are included within the article.
Ethics approval and consent to participate
This study was conducted in accordance with the declaration of Helsinki. Ethical approval was obtained from the Comitê Nacional de Ética e Saúde (Guinea Bissau), the LSHTM Ethics Committee (UK) and The Gambia Government/Medical Research Council Unit, The Gambia Joint Ethics Committee (The Gambia). Written (thumbprint or signature) informed consent was obtained from all study participants or their guardians as appropriate. All individual data were anonymised for the analysis presented in the manuscript. Following this study all communities on the study islands received further treatment with oral azithromycin in accordance with WHO and national protocols.
Consent for publication
The authors declare that they have no competing interests.
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