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Genetic Diversity and Resistance Genotype Profile in Infected Placental Samples Collected After Delivery in Ouagadougou. | LitMetric

AI Article Synopsis

  • Intermittent preventive treatment with sulfadoxine-pyrimethamine for malaria in pregnant women is crucial in Burkina Faso, but resistance to the drug needs further investigation due to insufficient data on genetic mutations.
  • A study conducted from April 2019 to March 2020 analyzed placentas from postpartum women in Ouagadougou to assess genetic diversity and mutation prevalence in malaria-causing parasites.
  • Findings revealed high rates of PCR-positive samples, widespread allelic families, and certain genetic mutations, indicating potential early warning signs for increasing resistance to sulfadoxine-pyrimethamine in the population.

Article Abstract

Purpose: Intermittent preventive treatment with sulfadoxine-pyrimethamine is widely used for the prevention of malaria in pregnant women in Africa. Known resistance cases of sulfadoxine-pyrimethamine during pregnancy need to be follow up to support IPTp implementation in Burkina Faso. However, data on the development and spread of resistance to this molecule are lacking. This study aimed to investigating the genetic diversity of and the mutation prevalence in the and genes infected from postpartum infected placentas.

Patients And Methods: This was a prospective and cross-sectional study conducted between April 2019 and March 2020 in four health districts of Ouagadougou capital city. From the placentas collected after delivery, detection and and polymorphism analysis were performed by nested PCR. The resistance profile was checked after analyzing the mutation point on and genes.

Results: PCR-positive samples were estimated at 96% for and 98% for . The polymorphism analysis showed that the RO33 and 3D7 allelic families were the most widespread with 62.5% and 91.83%, respectively. Multiple infections by and were frequent with 12.50% and 92.92%, respectively. The prevalence of individual mutation point, 51I, 108A, and 59R, was 1.96, 15.68, and 7.84, respectively, and the mutation point, 437G, was 3.92. There is no detected mutation at the point 164L and 540E. The triple (51I+108A+59R) in and quadruple (51I+108A+59R+ 437G) mutation were not found.

Conclusion: The results showed that has a high genetic diversity of and . This suggests that and mutant genotypes are potential early warning factors in the increase in the sulfadoxine-pyrimethamine resistance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578158PMC
http://dx.doi.org/10.2147/IDR.S420004DOI Listing

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