Koepfli Cristian, Robinson Leanne J, Rarau Patricia, Salib Mary, Sambale Naomi, Wampfler Rahel, Betuela Inoni, Nuitragool Wang, Barry Alyssa E, Siba Peter, Felger Ingrid, Mueller Ivo
Walter and Eliza Hall Institute, Population Health and Immunity Division, Parkville, Victoria, Australia; University of Melbourne, Department of Medical Biology, Parkville, Victoria, Australia.
Walter and Eliza Hall Institute, Population Health and Immunity Division, Parkville, Victoria, Australia; University of Melbourne, Department of Medical Biology, Parkville, Victoria, Australia; Papua New Guinea Institute of Medical Research, Vector Borne Diseases Unit, Madang, Papua New Guinea.
PLoS One. 2015 May 21;10(5):e0126747. doi: 10.1371/journal.pone.0126747. eCollection 2015.
A better understanding of human-to-mosquito transmission is crucial to control malaria. In order to assess factors associated with gametocyte carriage, 2083 samples were collected in a cross-sectional survey in Papua New Guinea. Plasmodium species were detected by light microscopy and qPCR and gametocytes by detection of pfs25 and pvs25 mRNA transcripts by reverse-transcriptase PCR (qRT-PCR). The parasite prevalence by PCR was 18.5% for Plasmodium falciparum and 13.0% for P. vivax. 52.5% of all infections were submicroscopic. Gametocytes were detected in 60% of P. falciparum-positive and 51% of P. vivax-positive samples. Each 10-fold increase in parasite density led to a 1.8-fold and 3.3-fold increase in the odds of carrying P. falciparum and P. vivax gametocytes. Thus the proportion of gametocyte positive and gametocyte densities was highest in young children carrying high asexual parasite densities and in symptomatic individuals. Dilution series of gametocytes allowed absolute quantification of gametocyte densities by qRT-PCR and showed that pvs25 expression is 10-20 fold lower than pfs25 expression. Between 2006 and 2010 parasite prevalence in the study site has decreased by half. 90% of the remaining infections were asymptomatic and likely constitute an important reservoir of transmission. However, mean gametocyte densities were low (approx. 1-2 gametocyte/μL) and it remains to be determined to what extent low-density gametocyte positive individuals are infective to mosquitos.
更好地了解人蚊传播对于控制疟疾至关重要。为了评估与配子体携带相关的因素,在巴布亚新几内亚进行了一项横断面调查,收集了2083份样本。通过光学显微镜和定量聚合酶链反应(qPCR)检测疟原虫种类,通过逆转录聚合酶链反应(qRT-PCR)检测pfs25和pvs25 mRNA转录本来检测配子体。通过PCR检测,恶性疟原虫的寄生虫感染率为18.5%,间日疟原虫为13.0%。所有感染中有52.5%为亚显微感染。在60%的恶性疟原虫阳性样本和51%的间日疟原虫阳性样本中检测到了配子体。寄生虫密度每增加10倍,携带恶性疟原虫和间日疟原虫配子体的几率分别增加1.8倍和3.3倍。因此,配子体阳性比例和配子体密度在无性寄生虫密度高的幼儿和有症状个体中最高。配子体的稀释系列允许通过qRT-PCR对配子体密度进行绝对定量,并表明pvs25表达比pfs25表达低10 - 20倍。2006年至2010年期间,研究地点的寄生虫感染率下降了一半。其余感染中有90%无症状,可能构成重要的传播源。然而,配子体平均密度较低(约1 - 2个配子体/微升),低密度配子体阳性个体对蚊子的感染程度还有待确定。