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Short-term malaria reduction by single-dose azithromycin during mass drug administration for trachoma, Tanzania

  • Stephen E. Schachterle
  • , George Mtove
  • , Joshua P. Levens
  • , Emily Clemens
  • , Lirong Shi
  • , Amrita Raj
  • , J. Stephen Dumler
  • , Beatriz Munoz
  • , Shelia West
  • , David J. Sullivan

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Single-dose mass drug administration of azithromycin (AZT) is underway to eliminate trachoma worldwide. Studies in Ethiopia showed a reduction in all-cause childhood deaths after administration. To examine the effect of singledose AZ MDA on prevalent malaria infections in a large prospective cohort of children and parents in Dodoma Province, Tanzania, we quantified the temporal prevalence of malaria parasitemia by real-time PCR for 6 months after single-dose AZT. In the first month after treatment but not in subsequent months, Plasmodium falciparum infections were reduced by 73% (95% CI 43%-89%) in treatment versus control villages and differences remained significant (p = 0.00497) in multivariate models with village-level random effects. Genetic sequencing of P. falciparum ribosomal L4 protein showed no mutations associated with AZT resistance. AZT mass drug administration caused a transient, 1-month antimalarial effect without selecting for P. falciparum ribosomal L4 resistance mutations in a region with a 10-year history of treating trachoma with this drug.

Original languageEnglish
Pages (from-to)941-949
Number of pages9
JournalEmerging Infectious Diseases
Volume20
Issue number6
DOIs
StatePublished - Jun 2014

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