Diagnostic ability of myxovirus resistance-A in pediatric cases of viral-acute respiratory tract infections with vitamin A and zinc deficiencies

Q2 Medicine
Dian Kesumapramudya Nurputra , Amalia Setyati , Nur Arfian , Endy Paryanto Prawirohartono , Zulvikar Syambani Ulhaq
{"title":"Diagnostic ability of myxovirus resistance-A in pediatric cases of viral-acute respiratory tract infections with vitamin A and zinc deficiencies","authors":"Dian Kesumapramudya Nurputra ,&nbsp;Amalia Setyati ,&nbsp;Nur Arfian ,&nbsp;Endy Paryanto Prawirohartono ,&nbsp;Zulvikar Syambani Ulhaq","doi":"10.1016/j.medmic.2024.100119","DOIUrl":null,"url":null,"abstract":"<div><div>Acute respiratory tract infection (ARTI) rank among the top ten most common illnesses affecting children in Indonesia. Myxovirus resistance-A (MxA) protein, selectively induced by the activation of type I interferon in response to viral infections, has emerged as a promising biomarker to diagnose viral ARTI. Notably, the activation of interferons is thought to be influenced by plasma vitamin A and zinc levels. Therefore, our study aims to investigate the level of MxA expression in children with vitamin A and zinc deficiencies when experiencing viral ARTI. This cross-sectional study involved a total of 113 subjects, including 53 diagnosed with ARTI due to viral causes based on validated clinical scoring criteria, and 50 healthy controls. To determine the etiology, we conducted blood cultures and employed RT-PCR analysis on nasopharyngeal swabs. Additionally, we assessed plasma levels of vitamin A, zinc, and MxA protein expression. Our findings revealed that subjects with ARTI displayed elevated MxA expression compared to controls. Specifically, MxA expression levels in ARTI cases of viral origin were significantly higher than those in both control and bacterial origin. On closer examination, the vitamin A and zinc non-deficient group exhibited higher MxA expression levels in comparison to the deficient group. However, it is notable that the expression levels in the deficient group remained higher than those in the control group. In summary, MxA protein expression was found to be lower in children with vitamin A and zinc deficiencies when compared to those without deficiencies in cases of viral ARTI. Thus, MxA expression may serve as a diagnostic tool for distinguishing viral from bacterial ARTI, especially in populations where the prevalence of micronutrient-deficient children is high, such as in Indonesia.</div></div>","PeriodicalId":36019,"journal":{"name":"Medicine in Microecology","volume":"23 ","pages":"Article 100119"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine in Microecology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590097824000223","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Acute respiratory tract infection (ARTI) rank among the top ten most common illnesses affecting children in Indonesia. Myxovirus resistance-A (MxA) protein, selectively induced by the activation of type I interferon in response to viral infections, has emerged as a promising biomarker to diagnose viral ARTI. Notably, the activation of interferons is thought to be influenced by plasma vitamin A and zinc levels. Therefore, our study aims to investigate the level of MxA expression in children with vitamin A and zinc deficiencies when experiencing viral ARTI. This cross-sectional study involved a total of 113 subjects, including 53 diagnosed with ARTI due to viral causes based on validated clinical scoring criteria, and 50 healthy controls. To determine the etiology, we conducted blood cultures and employed RT-PCR analysis on nasopharyngeal swabs. Additionally, we assessed plasma levels of vitamin A, zinc, and MxA protein expression. Our findings revealed that subjects with ARTI displayed elevated MxA expression compared to controls. Specifically, MxA expression levels in ARTI cases of viral origin were significantly higher than those in both control and bacterial origin. On closer examination, the vitamin A and zinc non-deficient group exhibited higher MxA expression levels in comparison to the deficient group. However, it is notable that the expression levels in the deficient group remained higher than those in the control group. In summary, MxA protein expression was found to be lower in children with vitamin A and zinc deficiencies when compared to those without deficiencies in cases of viral ARTI. Thus, MxA expression may serve as a diagnostic tool for distinguishing viral from bacterial ARTI, especially in populations where the prevalence of micronutrient-deficient children is high, such as in Indonesia.
黏液病毒耐药性-A在儿童病毒性急性呼吸道感染伴维生素A和锌缺乏症中的诊断能力
急性呼吸道感染是影响印度尼西亚儿童的十大最常见疾病之一。黏液病毒耐药性- a (MxA)蛋白是在病毒感染反应中由I型干扰素激活选择性诱导产生的,已成为诊断病毒性ARTI的一种有前景的生物标志物。值得注意的是,干扰素的激活被认为受到血浆维生素A和锌水平的影响。因此,我们的研究旨在探讨维生素A和锌缺乏的儿童在经历病毒性ARTI时MxA的表达水平。这项横断面研究共涉及113名受试者,其中53名根据经过验证的临床评分标准诊断为由病毒引起的ARTI, 50名健康对照。为了确定病因,我们对鼻咽拭子进行了血培养和RT-PCR分析。此外,我们评估了血浆中维生素A、锌和MxA蛋白的表达水平。我们的研究结果显示,与对照组相比,ARTI患者的MxA表达升高。具体来说,病毒源性ARTI病例的MxA表达水平显著高于对照组和细菌源性ARTI病例。进一步研究发现,维生素A和锌不缺乏组的MxA表达水平高于缺乏组。然而,值得注意的是,缺陷组的表达水平仍然高于对照组。总之,在病毒性ARTI病例中,与不缺乏维生素A和锌的儿童相比,缺乏维生素A和锌的儿童的MxA蛋白表达较低。因此,MxA表达可以作为区分病毒性和细菌性ARTI的诊断工具,特别是在印度尼西亚等微量营养素缺乏儿童患病率高的人群中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Medicine in Microecology
Medicine in Microecology Medicine-Gastroenterology
CiteScore
5.60
自引率
0.00%
发文量
16
审稿时长
76 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信