Urassa Aloyce P, Kudra Mwanaidi P, Kaaya Robert D, Kajeguka Debora Charles, Mkumbaye Sixbert Isdory
Department of Microbiology and Immunology, Faculty of Medicine, Kilimanjaro Christian Medical University College.
Department of Clinical laboratory, Kilimanjaro Christian Medical Centre.
Rwanda J Med Health Sci. 2023 Jul 31;6(2):175-183. doi: 10.4314/rjmhs.v6i2.8. eCollection 2023 Jul.
Monitoring gametocytes in the population can inform about the human infective reservoir, which greatly aids malaria transmission, and provide relevant data for transmission models. Using molecular techniques in preference to light microscopy to detect gametocytes may lead to most reliable results. Effective determination of gametocytes is inevitable to achieve the transmission-blocking interventions as a prime target to end malaria. We aimed to determine the prevalence of P. falciparum gametocytes in malaria-positive cases from Korogwe district hospital.
Archived DNA samples collected from Korogwe district hospital collected in a cross-sectional study were used to determine the prevalence of P. falciparum gametocytes using specific primers for cPCR targeting a Pfg27 gene. Demographic data, including blood slides data were retrieved from the database for statistical analysis.
With light microscopy, prevalence of P. falciparum gametocytes was 9.8%; sensitivity and specificity were 35.6% and 99.2% respectively. The cPCR gave a prevalence of 25.9%, with a sensitivity of 94.1% and specificity of 81.5%. The cPCR was diagnostically found to be significantly superior over light microscopy technique (X=45.780, P < 0.001).
cPCR is superior to light microscopy technique in detecting P. falciparum gametocytes when one considers a successive malaria transmission-blocking intervention.
监测人群中的配子体可了解人类感染源,这对疟疾传播有很大帮助,并为传播模型提供相关数据。优先使用分子技术而非光学显微镜检测配子体可能会得出最可靠的结果。有效确定配子体对于实现作为终结疟疾主要目标的传播阻断干预措施而言是必不可少的。我们旨在确定科罗格韦区医院疟疾阳性病例中恶性疟原虫配子体的流行率。
在一项横断面研究中,从科罗格韦区医院收集的存档DNA样本被用于使用针对Pfg27基因的cPCR特异性引物来确定恶性疟原虫配子体的流行率。人口统计学数据,包括血涂片数据,从数据库中检索出来用于统计分析。
通过光学显微镜检查,恶性疟原虫配子体的流行率为9.8%;敏感性和特异性分别为35.6%和99.2%。cPCR得出的流行率为25.9%,敏感性为94.1%,特异性为81.5%。经诊断发现,cPCR在诊断方面明显优于光学显微镜技术(X=45.780,P < 0.001)。
在考虑连续的疟疾传播阻断干预措施时,cPCR在检测恶性疟原虫配子体方面优于光学显微镜技术。