@article {1566,
	title = {Ongoing transmission of trachoma in low prevalence districts in Mozambique: results from four cross-sectional enhanced impact surveys, 2022.},
	journal = {Sci Rep},
	volume = {14},
	year = {2024},
	month = {2024 Oct 15},
	pages = {22842},
	abstract = {<p>Mozambique is making progress towards elimination of trachoma as a public health problem, but in some districts trachomatous inflammation-follicular (TF) prevalence remains above the 5\% elimination threshold despite years of various interventions, including antibiotic mass drug administration. To characterize transmission in four districts, we incorporated testing of ocular infection and serology into routine trachoma impact surveys (TIS) in August 2022. We examined residents aged >= 1 year for trachoma and collected information on household water, sanitation, and hygiene. Among children aged 1-9 years, we tested conjunctival swabs for Chlamydia trachomatis nucleic acid and dried blood spots for C. trachomatis antibodies. We modeled age-dependent seroprevalence to estimate seroconversion rate (SCR). We examined 4841 children aged 1-9 years. TF prevalence ranged between 1.1 and 6.0\% with three districts below the 5\% threshold. PCR-confirmed infection prevalence ranged between 1.1 and 4.8\%, and Pgp3 seroprevalence ranged between 8.8 and 24.3\%. Pgp3 SCR was 1.9 per 100 children per year in the district with the lowest TF prevalence. Two other districts with TF < 5\% had SCR of 5.0 and 4.7. The district with TF >= 5\% had a SCR of 6.0. This enhanced TIS furthered understanding of transmission in these districts and provides information on additional indicators for monitoring trachoma programs.</p>},
	keywords = {Antibodies, Bacterial, Child, Child, Preschool, Chlamydia trachomatis, Cross-Sectional Studies, Female, Humans, Infant, Male, Mozambique, Prevalence, Seroepidemiologic Studies, Trachoma},
	issn = {2045-2322},
	doi = {10.1038/s41598-024-71201-z},
	author = {Sitoe, Henis Mior and Oswald, William E and Zita, Felizmina and Fall, Mawo and Momade, Tamimo and Adams, Molly W and Flueckiger, Rebecca M and McPherson, Scott and Eyob, Sabrina and Doan, Thuy and Lietman, Thomas M and Arnold, Benjamin F and Wickens, Karana and Gwyn, Sarah and Martin, Diana L and Kasubi, Mabula and Boyd, Sarah and Bakhtiari, Ana and Jimenez, Cristina and Solomon, Anthony W and Harding-Esch, Emma M and Mwingira, Upendo J and Ngondi, Jeremiah M}
}
@article {931,
	title = {Effect of biannual azithromycin distribution on antibody responses to malaria, bacterial, and protozoan pathogens in Niger.},
	journal = {Nat Commun},
	volume = {13},
	year = {2022},
	month = {2022 02 21},
	pages = {976},
	abstract = {<p>The MORDOR trial in Niger, Malawi, and Tanzania found that biannual mass distribution of azithromycin to children younger than 5 years led to a 13.5\% reduction in all-cause mortality (NCT02048007). To help elucidate the mechanism for mortality reduction, we report IgG responses to 11 malaria, bacterial, and protozoan pathogens using a multiplex bead assay in pre-specified substudy of 30 communities in the rural Niger placebo-controlled trial over a three-year period (n = 5642 blood specimens, n = 3814 children ages 1-59 months). Mass azithromycin reduces Campylobacter spp. force of infection by 29\% (hazard ratio = 0.71, 95\% CI: 0.56, 0.89; P = 0.004) but serological measures show no significant differences between groups for other pathogens against a backdrop of high transmission. Results align with a recent microbiome study in the communities. Given significant sequelae of Campylobacter infection among preschool aged children, our results support an important mechanism through which biannual mass distribution of azithromycin likely reduces mortality in Niger.</p>
},
	issn = {2041-1723},
	doi = {10.1038/s41467-022-28565-5},
	author = {Arzika, Ahmed M and Maliki, Ramatou and Goodhew, E Brook and Rogier, Eric and Priest, Jeffrey W and Lebas, Elodie and O{\textquoteright}Brien, Kieran S and Le, Victoria and Oldenburg, Catherine E and Doan, Thuy and Porco, Travis C and Keenan, Jeremy D and Lietman, Thomas M and Martin, Diana L and Arnold, Benjamin F}
}
