Malaria Research Centre, Faculty of Medicine & Health Sciences, Universiti Malaysia Sarawak, 94300, Kota Samarahan, Sarawak, Malaysia.
Faculty of Resource Science & Technology, Universiti Malaysia Sarawak, 94300, Kota Samarahan, Sarawak, Malaysia.
BMC Evol Biol. 2018 Apr 10;18(1):49. doi: 10.1186/s12862-018-1170-9.
Non-human primates have long been identified to harbour different species of Plasmodium. Long-tailed macaques (Macaca fascicularis), in particular, are reservoirs for P. knowlesi, P. inui, P. cynomolgi, P. coatneyi and P. fieldi. A previous study conducted in Sarawak, Malaysian Borneo, however revealed that long-tailed macaques could potentially harbour novel species of Plasmodium based on sequences of small subunit ribosomal RNA and circumsporozoite genes. To further validate this finding, the mitochondrial genome and the apicoplast caseinolytic protease M genes of Plasmodium spp. were sequenced from 43 long-tailed macaque blood samples.
Apart from several named species of malaria parasites, long-tailed macaques were found to be potentially infected with novel species of Plasmodium, namely one we refer to as "P. inui-like." This group of parasites bifurcated into two monophyletic clades indicating the presence of two distinct sub-populations. Further analyses, which relied on the assumption of strict co-phylogeny between hosts and parasites, estimated a population expansion event of between 150,000 to 250,000 years before present of one of these sub-populations that preceded that of the expansion of P. knowlesi. Furthermore, both sub-populations were found to have diverged from a common ancestor of P. inui approximately 1.5 million years ago. In addition, the phylogenetic analyses also demonstrated that long-tailed macaques are new hosts for P. simiovale.
Malaria infections of long-tailed macaques of Sarawak, Malaysian Borneo are complex and include a novel species of Plasmodium that is phylogenetically distinct from P. inui. These macaques are new natural hosts of P. simiovale, a species previously described only in toque monkeys (Macaca sinica) in Sri Lanka. The results suggest that ecological factors could affect the evolution of malaria parasites.
非人类灵长类动物长期以来一直被认为携带有不同种的疟原虫。长尾猕猴(Macaca fascicularis)尤其被认为是 P. knowlesi、P. inui、P. cynomolgi、P. coatneyi 和 P. fieldi 的宿主。然而,之前在马来西亚婆罗洲的沙捞越进行的一项研究表明,长尾猕猴可能携带有新型疟原虫,这是基于小亚基核糖体 RNA 和环子孢子蛋白基因序列的发现。为了进一步验证这一发现,对来自 43 只长尾猕猴血液样本的疟原虫 spp. 的线粒体基因组和质体天冬氨酸蛋白酶 M 基因进行了测序。
除了几种已知的疟原虫外,长尾猕猴还可能感染了新型疟原虫,我们称之为“P. inui 样”。这组寄生虫分为两个单系枝,表明存在两个不同的亚种群。进一步的分析,依赖于宿主和寄生虫之间严格的共进化假设,估计其中一个亚种群的种群扩张事件发生在 15 万至 25 万年前,早于 P. knowlesi 的扩张。此外,两个亚种群都与大约 150 万年前的 P. inui 共同祖先分化而来。此外,系统发育分析还表明,长尾猕猴是 P. simiovale 的新宿主。
马来西亚婆罗洲沙捞越的长尾猕猴的疟疾感染很复杂,包括一种与 P. inui 在系统发育上截然不同的新型疟原虫。这些猕猴是 P. simiovale 的新天然宿主,P. simiovale 以前只在斯里兰卡的戴帽猕猴(Macaca sinica)中被描述过。这些结果表明,生态因素可能会影响疟原虫的进化。