Abstract

BackgroundThis cross-sectional study was conducted to characteriseP. falciparuminfections matched in peripheral, placental and cord blood among Congolese women at delivery receiving 1, 2 or more doses of sulfadoxine-pyrimethamine. The cross-sectional study was conducted in a Southern district of Brazzaville, Republic of the Congo, between March 2014 and April 2015.MethodsPeripheral and placental blood samples were collected forP. falciparuminfection investigation by microscopy and nested polymerase chain reaction (PCR), usingP. falciparummerozoite surface protein-2 (msp2) gene as marker.ResultsOf the 370 pregnant women recruited, only 7.3% peripheral and 2.7% placental blood samples were found smear-positive forP. falciparumby microscopy. All isolates from cord blood were microscopy-negative. However, the prevalences of submicroscopicP. falciparuminfections (detectable only by PCR) were 25.4%, 16.7% and 9.4% in peripheral, placental and cord blood respectively. The frequency of 3D7 msp2 alleles was the highest (>60%) whatever the blood considered. We found a high prevalence of submicroscopic infection in pregnant women associated with a high genetic diversity ofP. falciparumisolates. The multiplicity of infection ranged between 1.2 and 1.4 irrespective of the blood compartment, and it showed no significant association with maternal age (p=0.3), gravidity (p=0.1) or sulfadoxine-pyrimethamine (p=0.3).ConclusionIn summary, this study showed that there is a high prevalence of submicroscopic infection and a high genetic diversity ofPlasmodium falciparumstrains in Congo. This diversity varies according to maternal, placental and umbilical cord blood. Age, gravidity and doses of preventive treatment based on sulfadoxine-pyrimethamine do not interfere with the multiplicity of infections.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.