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猩猩体内疟原虫的起源。

The origin of malarial parasites in orangutans.

机构信息

Center for Evolutionary Medicine and Informatics, the Biodesign Institute, Arizona State University, Tempe, Arizona, United States of America.

出版信息

PLoS One. 2012;7(4):e34990. doi: 10.1371/journal.pone.0034990. Epub 2012 Apr 20.

Abstract

BACKGROUND

Recent findings of Plasmodium in African apes have changed our perspectives on the evolution of malarial parasites in hominids. However, phylogenetic analyses of primate malarias are still missing information from Southeast Asian apes. In this study, we report molecular data for a malaria parasite lineage found in orangutans.

METHODOLOGY/PRINCIPAL FINDINGS: We screened twenty-four blood samples from Pongo pygmaeus (Kalimantan, Indonesia) for Plasmodium parasites by PCR. For all the malaria positive orangutan samples, parasite mitochondrial genomes (mtDNA) and two antigens: merozoite surface protein 1 42 kDa (MSP-1(42)) and circumsporozoite protein gene (CSP) were amplified, cloned, and sequenced. Fifteen orangutans tested positive and yielded 5 distinct mitochondrial haplotypes not previously found. The haplotypes detected exhibited low genetic divergence among them, indicating that they belong to one species. We report phylogenetic analyses using mitochondrial genomes, MSP-1(42) and CSP. We found that the orangutan malaria parasite lineage was part of a monophyletic group that includes all the known non-human primate malaria parasites found in Southeast Asia; specifically, it shares a recent common ancestor with P. inui (a macaque parasite) and P. hylobati (a gibbon parasite) suggesting that this lineage originated as a result of a host switch. The genetic diversity of MSP-1(42) in orangutans seems to be under negative selection. This result is similar to previous findings in non-human primate malarias closely related to P. vivax. As has been previously observed in the other Plasmodium species found in non-human primates, the CSP shows high polymorphism in the number of repeats. However, it has clearly distinctive motifs from those previously found in other malarial parasites.

CONCLUSION

The evidence available from Asian apes indicates that these parasites originated independently from those found in Africa, likely as the result of host switches from other non-human primates.

摘要

背景

最近在非洲猿类中发现的疟原虫改变了我们对人类疟原虫进化的看法。然而,灵长类疟原虫的系统发育分析仍然缺少来自东南亚猿类的信息。在这项研究中,我们报告了在猩猩中发现的疟原虫谱系的分子数据。

方法/主要发现:我们通过 PCR 从婆罗洲猩猩(印度尼西亚加里曼丹)的 24 个血液样本中筛选疟原虫。对所有疟原虫阳性的猩猩样本,扩增、克隆和测序了寄生虫线粒体基因组(mtDNA)和两种抗原:裂殖子表面蛋白 1 42kDa(MSP-1(42))和环子孢子蛋白基因(CSP)。15 只猩猩检测呈阳性,并产生了 5 种以前未发现的独特线粒体单倍型。检测到的单倍型之间遗传分化较低,表明它们属于一个物种。我们报告了使用线粒体基因组、MSP-1(42)和 CSP 的系统发育分析。我们发现,猩猩疟原虫谱系是一个单系群的一部分,包括所有在东南亚发现的已知非人类灵长类疟原虫;具体来说,它与 P. inui(猕猴寄生虫)和 P. hylobati(长臂猿寄生虫)有最近的共同祖先,这表明该谱系是由于宿主转换而起源的。猩猩 MSP-1(42)的遗传多样性似乎受到负选择的影响。这一结果与先前在与 P. vivax 密切相关的非人类灵长类疟原虫中的发现相似。与在其他非人类灵长类动物中发现的其他疟原虫一样,CSP 在重复次数上表现出高度多态性。然而,它具有与其他疟原虫先前发现的明显不同的特征。

结论

来自亚洲猿类的证据表明,这些寄生虫是独立于非洲发现的寄生虫起源的,可能是由于从其他非人类灵长类动物的宿主转换而来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee48/3335055/6820f00c9c42/pone.0034990.g001.jpg

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