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非洲恶性疟原虫分离株的增殖率较低,且增殖率和红细胞选择性与疟疾毒力之间缺乏关联。

Low multiplication rates of African Plasmodium falciparum isolates and lack of association of multiplication rate and red blood cell selectivity with malaria virulence.

作者信息

Deans Anne-Marie, Lyke Kirsten E, Thera Mahamadou A, Plowe Christopher V, Koné Abdoulaye, Doumbo Ogobara K, Kai Oscar, Marsh Kevin, Mackinnon Margaret J, Raza Ahmed, Rowe J Alexandra

机构信息

Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

Am J Trop Med Hyg. 2006 Apr;74(4):554-63.

PMID:16606983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2738946/
Abstract

Two potential malaria virulence factors, parasite multiplication rate (PMR) and red blood cell selectivity (measured as selectivity index [SI]), were assessed in Plasmodium falciparum clinical isolates from Mali and Kenya. At both sites, PMRs were low (Kenya median = 2.2, n = 33; Mali median = 2.6, n = 61) and did not differ significantly between uncomplicated and severe malaria cases. Malian isolates from hyperparasitemic patients had significantly lower PMRs (median = 1.8, n = 19) than other Malian isolates (uncomplicated malaria median = 3.1, n = 23; severe malaria median = 2.8, n = 19; P = 0.03, by Kruskal-Wallis test). Selective invasion occurred at both sites (Kenya geometric mean SI = 1.9, n = 98; Mali geometric mean SI = 1.6, n = 104), and there was no significant association between the SI and malaria severity. Therefore, in contrast to previous results from Thailand, we found no association of PMR and SI with malaria severity in African children. This raises the possibility of differences in the mechanisms of malaria virulence between sub-Saharan Africa and Asia.

摘要

对来自马里和肯尼亚的恶性疟原虫临床分离株评估了两个潜在的疟疾毒力因子,即寄生虫增殖率(PMR)和红细胞选择性(以选择性指数[SI]衡量)。在这两个地点,PMR均较低(肯尼亚中位数 = 2.2,n = 33;马里中位数 = 2.6,n = 61),且单纯性疟疾和重症疟疾病例之间无显著差异。来自高疟原虫血症患者的马里分离株的PMR(中位数 = 1.8,n = 19)显著低于其他马里分离株(单纯性疟疾中位数 = 3.1,n = 23;重症疟疾中位数 = 2.8,n = 19;经Kruskal-Wallis检验,P = 0.03)。在这两个地点均发生了选择性侵袭(肯尼亚几何平均SI = 1.9,n = 98;马里几何平均SI = 1.6,n = 104),且SI与疟疾严重程度之间无显著关联。因此,与泰国先前的结果相反,我们发现在非洲儿童中PMR和SI与疟疾严重程度无关联。这增加了撒哈拉以南非洲和亚洲之间疟疾毒力机制存在差异的可能性。

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本文引用的文献

1
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Evolution. 1999 Jun;53(3):689-703. doi: 10.1111/j.1558-5646.1999.tb05364.x.
2
A Study of Induced Malignant Tertian Malaria.诱导性恶性三日疟的研究
Proc R Soc Med. 1932 Jun;25(8):1153-86. doi: 10.1177/003591573202500801.
3
Calculation of liver-to-blood inocula, parasite growth rates, and preerythrocytic vaccine efficacy, from serial quantitative polymerase chain reaction studies of volunteers challenged with malaria sporozoites.通过对感染疟原虫子孢子的志愿者进行系列定量聚合酶链反应研究,计算肝脏与血液接种量、寄生虫生长率以及疟原虫感染前期疫苗效力。
J Infect Dis. 2005 Feb 15;191(4):619-26. doi: 10.1086/427243. Epub 2005 Jan 7.
4
Parasite ligand-host receptor interactions during invasion of erythrocytes by Plasmodium merozoites.疟原虫裂殖子侵入红细胞过程中的寄生虫配体-宿主受体相互作用。
Int J Parasitol. 2004 Dec;34(13-14):1413-29. doi: 10.1016/j.ijpara.2004.10.010.
5
Protection against clinical malaria by heterologous immunoglobulin G antibodies against malaria-infected erythrocyte variant surface antigens requires interaction with asymptomatic infections.通过针对疟疾感染红细胞变异表面抗原的异源免疫球蛋白G抗体预防临床疟疾需要与无症状感染相互作用。
J Infect Dis. 2004 Nov 1;190(9):1527-33. doi: 10.1086/424675. Epub 2004 Sep 22.
6
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Infect Immun. 2004 Oct;72(10):5630-7. doi: 10.1128/IAI.72.10.5630-5637.2004.
7
Virulence in malaria: an evolutionary viewpoint.疟疾的毒力:一种进化视角
Philos Trans R Soc Lond B Biol Sci. 2004 Jun 29;359(1446):965-86. doi: 10.1098/rstb.2003.1414.
8
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Vaccine. 2004 Aug 13;22(23-24):3169-74. doi: 10.1016/j.vaccine.2004.01.054.
9
Association of intraleukocytic Plasmodium falciparum malaria pigment with disease severity, clinical manifestations, and prognosis in severe malaria.恶性疟原虫疟疾色素在白细胞内与重症疟疾的疾病严重程度、临床表现及预后的关联
Am J Trop Med Hyg. 2003 Sep;69(3):253-9.
10
Cross-species regulation of Plasmodium parasitemia in semi-immune children from Papua New Guinea.巴布亚新几内亚半免疫儿童中疟原虫血症的跨物种调节
Trends Parasitol. 2003 Jun;19(6):271-7. doi: 10.1016/s1471-4922(03)00116-8.