• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

髓样分化因子88样衔接蛋白基因多态性rs8177374在调节巴基斯坦人群疟疾严重程度中的作用。

Role of MyD88-adaptor-like gene polymorphism rs8177374 in modulation of malaria severity in the Pakistani population.

作者信息

Rani Asima, Nawaz Syed Kashif, Irfan Shazia, Arshad Muhammad, Bashir Razia, Shaheen Najma

机构信息

University of Sargodha, Department of Zoology, Sargodha, Pakistan.

University of Sargodha, Department of Zoology, Sargodha, Pakistan.

出版信息

Braz J Infect Dis. 2017 Jul-Aug;21(4):418-423. doi: 10.1016/j.bjid.2017.04.002. Epub 2017 May 6.

DOI:10.1016/j.bjid.2017.04.002
PMID:28482182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9428015/
Abstract

INTRODUCTION

The present study was designed to investigate the association between rs8177374 polymorphism and malaria symptoms due to exposure of Plasmodium vivax and Plasmodium falciparum.

MATERIALS AND METHODS

A total of 454 samples were included in the study (228 malaria patients and 226 healthy individuals). Malaria patients, divided into P. vivax and P. falciparum groups on the basis of the causative species of Plasmodium, were categorized into mild and severe on the basis of clinical outcomes according to WHO criteria. Healthy individuals were used as controls. Allele specific PCR based strategy was used for the identification of rs8177374 SNP.

RESULTS

MyD88-adaptor-like gene polymorphism was associated with susceptibility to malaria (p<0.001). C allele frequency (0.74) was higher in the population compared to T allele frequency (0.26). CT genotype increased the susceptibility of malaria (OR: 2.661; 95% CI: 1.722-4.113) and was positively associated with mild malaria (OR: 5.609; 95% CI: 3.479-9.044, p=0.00). On the other hand, CC genotype was associated with severe malaria (OR: 3.116; 95% CI: 1.560-6.224, p=0.00). P. vivax infection rate was higher in CT genotype carriers compared to other genotypes (OR: 3.616; 95% CI: 2.219-5.894, p<0.001).

CONCLUSION

MyD88-adaptor-like/TIR domain containing adaptor protein polymorphism for single nucleotide polymorphism rs8177374 is related with the susceptibility of malaria.

摘要

引言

本研究旨在调查rs8177374多态性与间日疟原虫和恶性疟原虫感染所致疟疾症状之间的关联。

材料与方法

本研究共纳入454个样本(228例疟疾患者和226例健康个体)。疟疾患者根据疟原虫致病种类分为间日疟原虫组和恶性疟原虫组,并根据世界卫生组织标准依据临床结果分为轻症和重症。健康个体作为对照。采用基于等位基因特异性PCR的策略鉴定rs8177374单核苷酸多态性。

结果

MyD88衔接蛋白样基因多态性与疟疾易感性相关(p<0.001)。人群中C等位基因频率(0.74)高于T等位基因频率(0.26)。CT基因型增加了疟疾易感性(比值比:2.661;95%置信区间:1.722 - 4.113),并与轻症疟疾呈正相关(比值比:5.609;95%置信区间:3.479 - 9.044,p = 0.00)。另一方面,CC基因型与重症疟疾相关(比值比:3.116;95%置信区间:1.560 - 6.224,p = 0.00)。CT基因型携带者的间日疟原虫感染率高于其他基因型(比值比:3.616;95%置信区间:2.219 - 5.894,p<0.001)。

结论

含MyD88衔接蛋白样/TIR结构域衔接蛋白的单核苷酸多态性rs8177374与疟疾易感性相关。

相似文献

1
Role of MyD88-adaptor-like gene polymorphism rs8177374 in modulation of malaria severity in the Pakistani population.髓样分化因子88样衔接蛋白基因多态性rs8177374在调节巴基斯坦人群疟疾严重程度中的作用。
Braz J Infect Dis. 2017 Jul-Aug;21(4):418-423. doi: 10.1016/j.bjid.2017.04.002. Epub 2017 May 6.
2
Role of MyD88-Adaptor-Like (MAL) Gene Polymorphism rs8177374 and Cytokine (IFN-γ, TNF-α, IL-10, TGF-β) Levels in Diverse Malaria Manifestations upon P. falciparum and P. vivax Infections.MyD88 衔接子样(MAL)基因多态性 rs8177374 与疟原虫(Pf 和 Pv)感染后不同疟疾表现的细胞因子(IFN-γ、TNF-α、IL-10、TGF-β)水平的关系。
Jpn J Infect Dis. 2023 Nov 22;76(6):358-364. doi: 10.7883/yoken.JJID.2023.079. Epub 2023 Aug 31.
3
Role of S180L polymorphism in etiology of malaria caused by Plasmodium falciparum in a small group of Pakistani population.S180L多态性在一小部分巴基斯坦人群中由恶性疟原虫引起的疟疾病因中的作用。
Bosn J Basic Med Sci. 2015 Aug 19;15(4):20-3. doi: 10.17305/bjbms.2015.413.
4
Malaria Susceptibility and Severity: Influence of MyD88-Adaptor-Like Gene (rs8177374) Polymorphism.疟疾易感性与严重程度:髓样分化因子88样衔接蛋白基因(rs8177374)多态性的影响
Infect Drug Resist. 2022 Nov 28;15:6815-6827. doi: 10.2147/IDR.S387463. eCollection 2022.
5
Genetic variation of TLR-4, TLR-9 and TIRAP genes in Iranian malaria patients.伊朗疟疾患者 TLR-4、TLR-9 和 TIRAP 基因的遗传变异。
Malar J. 2011 Apr 4;10:77. doi: 10.1186/1475-2875-10-77.
6
Association of TLR variants with susceptibility to Plasmodium vivax malaria and parasitemia in the Amazon region of Brazil.巴西亚马逊地区TLR变体与间日疟原虫疟疾易感性及寄生虫血症的关联
PLoS One. 2017 Aug 29;12(8):e0183840. doi: 10.1371/journal.pone.0183840. eCollection 2017.
7
TIRAP rs8177374 gene polymorphism increased the risk of pulmonary tuberculosis in Zahedan, southeast Iran.TIRAP基因rs8177374位点多态性增加了伊朗东南部扎赫丹地区患肺结核的风险。
Asian Pac J Trop Med. 2014 Jun;7(6):451-5. doi: 10.1016/S1995-7645(14)60073-0.
8
Role of polymorphisms of toll-like receptor (TLR) 4, TLR9, toll-interleukin 1 receptor domain containing adaptor protein (TIRAP) and FCGR2A genes in malaria susceptibility and severity in Burundian children.布隆迪儿童疟疾易感性和严重程度中 TLR4、TLR9、TIRAP 和 FCGR2A 基因多态性的作用。
Malar J. 2012 Jun 12;11:196. doi: 10.1186/1475-2875-11-196.
9
Toll-like receptor polymorphisms in malaria-endemic populations.疟疾流行地区人群中的Toll样受体多态性
Malar J. 2009 Mar 24;8:50. doi: 10.1186/1475-2875-8-50.
10
Evidence for genetic linkage between a polymorphism in the GNAS gene and malaria in South Indian population.GNAS 基因多态性与南印度人群疟疾的遗传连锁证据。
Acta Trop. 2013 Dec;128(3):571-7. doi: 10.1016/j.actatropica.2013.08.005. Epub 2013 Aug 17.

引用本文的文献

1
Malaria Susceptibility and Severity: Influence of MyD88-Adaptor-Like Gene (rs8177374) Polymorphism.疟疾易感性与严重程度:髓样分化因子88样衔接蛋白基因(rs8177374)多态性的影响
Infect Drug Resist. 2022 Nov 28;15:6815-6827. doi: 10.2147/IDR.S387463. eCollection 2022.
2
Paradoxical Roles of the MAL/Tirap Adaptor in Pathologies.MAL/Tirap衔接蛋白在病理学中的矛盾作用
Front Immunol. 2020 Sep 25;11:569127. doi: 10.3389/fimmu.2020.569127. eCollection 2020.

本文引用的文献

1
TIRAP rs8177374 gene polymorphism increased the risk of pulmonary tuberculosis in Zahedan, southeast Iran.TIRAP基因rs8177374位点多态性增加了伊朗东南部扎赫丹地区患肺结核的风险。
Asian Pac J Trop Med. 2014 Jun;7(6):451-5. doi: 10.1016/S1995-7645(14)60073-0.
2
Strain-specific innate immune signaling pathways determine malaria parasitemia dynamics and host mortality.特异性先天免疫信号通路决定疟疾寄生虫血症动态和宿主死亡率。
Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):E511-20. doi: 10.1073/pnas.1316467111. Epub 2014 Jan 13.
3
Prevalence and distribution of human Plasmodium infection in Pakistan.巴基斯坦人体疟原虫感染的流行状况和分布。
Malar J. 2013 Aug 28;12:297. doi: 10.1186/1475-2875-12-297.
4
A Plasmodium-encoded cytokine suppresses T-cell immunity during malaria.疟原虫编码的细胞因子在疟疾期间抑制 T 细胞免疫。
Proc Natl Acad Sci U S A. 2012 Jul 31;109(31):E2117-26. doi: 10.1073/pnas.1206573109. Epub 2012 Jul 9.
5
Role of polymorphisms of toll-like receptor (TLR) 4, TLR9, toll-interleukin 1 receptor domain containing adaptor protein (TIRAP) and FCGR2A genes in malaria susceptibility and severity in Burundian children.布隆迪儿童疟疾易感性和严重程度中 TLR4、TLR9、TIRAP 和 FCGR2A 基因多态性的作用。
Malar J. 2012 Jun 12;11:196. doi: 10.1186/1475-2875-11-196.
6
Biology of human malaria plasmodia including Plasmodium knowlesi.人类疟原虫生物学,包括疟原虫 knowlesi。
Mediterr J Hematol Infect Dis. 2012;4(1):e2012013. doi: 10.4084/MJHID.2012.013. Epub 2012 Mar 10.
7
Genetic variation of TLR-4, TLR-9 and TIRAP genes in Iranian malaria patients.伊朗疟疾患者 TLR-4、TLR-9 和 TIRAP 基因的遗传变异。
Malar J. 2011 Apr 4;10:77. doi: 10.1186/1475-2875-10-77.
8
Toll-like receptor and TIRAP gene polymorphisms in pulmonary tuberculosis patients of South India.印度南部肺结核患者 Toll 样受体和 TIRAP 基因多态性。
Tuberculosis (Edinb). 2010 Sep;90(5):306-10. doi: 10.1016/j.tube.2010.08.001. Epub 2010 Aug 24.
9
Low frequency of the TIRAP S180L polymorphism in Africa, and its potential role in malaria, sepsis, and leprosy.非洲TIRAP S180L多态性的低频率及其在疟疾、败血症和麻风病中的潜在作用。
BMC Med Genet. 2009 Jul 14;10:65. doi: 10.1186/1471-2350-10-65.
10
Heterozygosity for the S180L variant of MAL/TIRAP, a gene expressing an adaptor protein in the Toll-like receptor pathway, is associated with lower risk of developing chronic Chagas cardiomyopathy.MAL/TIRAP基因的S180L变体杂合性与慢性恰加斯心肌病的发病风险降低有关,该基因在Toll样受体途径中表达一种衔接蛋白。
J Infect Dis. 2009 Jun 15;199(12):1838-45. doi: 10.1086/599212.