The Malaria Institute at Macha, PO Box 630166, Choma, Zambia.
Malar J. 2013 Dec 19;12:453. doi: 10.1186/1475-2875-12-453.
The emergence of parasite drug resistance, especially Plasmodium falciparum, persists as a major obstacle for malaria control and elimination. To develop effective public health containment strategies, a clear understanding of factors that govern the emergence and spread of resistant parasites in the field is important. The current study documents selection for chloroquine-sensitive malaria parasites by wild Anopheles arabiensis in southern Zambia.
In a 2,000-sq km region, mosquitoes were collected from human sleeping rooms using pyrethrum spray catches during the 2006 malaria transmission season. After morphological examination and molecular confirmation, vector mosquitoes were dissected to separate head and thorax from the abdominal section, followed by PCR screening for P. falciparum infection. Human residents of all ages were tested for P. falciparum parasitaemia by microscopy and PCR. Plasmodium falciparum infections were genotyped at the chloroquine resistance-conferring amino acid codon 76 of the PfCRT gene, using PCR and restriction enzyme digestion.
In the human population there was nearly 90% prevalence of the chloroquine-resistant PfCRT K76T mutant, with no significant differences in polymorphism among smear-positive and smear-negative (submicroscopic) infections (p = 0.323, n = 128). However, infections in both abdominal and salivary gland phases of the An. arabiensis vector exhibited wild type K76-bearing parasites with up to 9X higher odds (OR (95% CI): 9 (3.7-20.2), p < 0.0005, n = 125), despite having been acquired from humans within a few weeks.
Anopheles arabiensis selects for wild-type K76-bearing P. falciparum during both abdominal and salivary gland phases of parasite development. The rapid vectorial selection, also recently seen with antifolate resistance, is evidence for parasite fitness cost in the mosquito, and may underpin regional heterogeneity in the emergence, spread and waning of drug resistance. Understanding the nature and direction of vector selection could be instrumental for rational curtailment of the spread of drug resistance in integrated malaria control and elimination programmes.
寄生虫耐药性的出现,尤其是恶性疟原虫的耐药性,仍然是疟疾控制和消除的主要障碍。为了制定有效的公共卫生控制策略,清楚地了解控制寄生虫在现场出现和传播的因素非常重要。本研究记录了赞比亚南部野生阿拉伯按蚊对氯喹敏感的疟原虫的选择。
在 2000 平方公里的区域内,在 2006 年疟疾传播季节,使用除虫菊酯喷雾捕获法从人睡房内收集蚊子。经过形态学检查和分子确认后,将媒介蚊子解剖,将头和胸部与腹部分开,然后进行 PCR 筛选以检测疟原虫感染。对所有年龄段的人类居民进行显微镜检查和 PCR 检测疟原虫寄生虫血症。使用 PCR 和限制性内切酶消化法对氯喹耐药性相关的 PfCRT 基因的 76 位氨基酸密码子的疟原虫感染进行基因分型。
人群中氯喹耐药 PfCRT K76T 突变体的流行率接近 90%,在涂片阳性和涂片阴性(亚微观)感染之间没有明显的多态性差异(p = 0.323,n = 128)。然而,在按蚊的腹部和唾液腺阶段的感染中,均发现了野生型 K76 携带寄生虫,其优势比(OR(95%CI))高达 9 倍(9(3.7-20.2),p <0.0005,n = 125),尽管这些寄生虫是在数周内从人类身上获得的。
在疟原虫发育的腹部和唾液腺阶段,按蚊均选择野生型 K76 携带的疟原虫。最近在抗叶酸耐药性中也发现了这种快速的媒介选择,这表明寄生虫在蚊子中的适应性成本,并且可能是药物耐药性在区域内出现、传播和消失的异质性的基础。了解媒介选择的性质和方向对于理性控制综合疟疾控制和消除计划中耐药性的传播可能具有重要意义。