Prevalence of multi drug resistance malaria among patients aged 0 – 14 years attending murtala muhammad specialist hospital Kano State, Nigeria

None Ummukulsum Mustapha, None Ado Shehu, None Attahir Sa’ad Ayuba, None Hayat Gomma, None Saleh Ngaski Garba, None Usman Sunusi Usman, None Bar. Baffa Alasan, None Muftahu Sa’adu, None Fatima Balarabe Garba, None Abba Jidda Harun, None Yunusa A, None Sagir Magaji, None Salihu Abubakar Dauda
{"title":"Prevalence of multi drug resistance malaria among patients aged 0 – 14 years attending murtala muhammad specialist hospital Kano State, Nigeria","authors":"None Ummukulsum Mustapha, None Ado Shehu, None Attahir Sa’ad Ayuba, None Hayat Gomma, None Saleh Ngaski Garba, None Usman Sunusi Usman, None Bar. Baffa Alasan, None Muftahu Sa’adu, None Fatima Balarabe Garba, None Abba Jidda Harun, None Yunusa A, None Sagir Magaji, None Salihu Abubakar Dauda","doi":"10.53771/ijbpsa.2023.6.2.0089","DOIUrl":null,"url":null,"abstract":"The Plasmodium falciparum multidrug resistance gene 1 (pfmdr1) is a molecular marker of parasite susceptibility to anti-malarial drugs. This study aimed to evaluate multidrug resistance resistance gene 1 (MDR1) mutation in 0-14years old malaria patients attending Murtala Muhammad Specialist Hospital, Kano, Nigeria. Samples from 100 children with malaria were examined to confirm the malaria parasite density and further genotyped via BigDye (v3.1) terminator cycle sequencing for the presence of two SNPs in pfmdr1on samples with high and moderate parasite densities. All data were analyzed using Pearson Chi square and Fisher’s exact (FE) tests. Of the 100 patients, 57% had low (+) malaria parasite density, 28% had moderate (++) and 15% had high (+++) malaria parasite densities of the 100 samples, 31 samples were successfully amplified and analyzed for the pfmdr1 gene located at codon 86 with amplicon size of 534bp while only 7 samples were successfully amplified for the pfmdr1 gene located at codon 1246.Pfmdr1-N86Y mutation was detected in 1 (3.2%) sample. In addition, only 1 (3.2%) sample with allelic change at 1246Y was detected in mutant pfmdr1gene. The result also showed that sex had no significant association (P = 0.4237) with pfmdr1SNP mutation. However, significant association (P = 0.0043) between the age groups (1 month to 14 years) represented in the study and pfmdr1mutation. The present study suggests that strains of P. falciparum with reduced sensitivity to the artemisinin component of artemisinin-based combination therapy (ACT) exist in Kano state, northern Nigeria. Methods: sample Collection Finger prick filter paper blood samples were collected from patients below the age of 5 years. However, 2 mL of venous blood was drawn using sterile syringe and needle from children aged 6 and 14 years. Safety procedures were adopted in the collection of blood samples by swabbing the area to be sampled with disinfectant and allowing it to dry before collection.","PeriodicalId":400966,"journal":{"name":"International Journal of Biological and Pharmaceutical Sciences Archive","volume":"116 ","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Biological and Pharmaceutical Sciences Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53771/ijbpsa.2023.6.2.0089","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The Plasmodium falciparum multidrug resistance gene 1 (pfmdr1) is a molecular marker of parasite susceptibility to anti-malarial drugs. This study aimed to evaluate multidrug resistance resistance gene 1 (MDR1) mutation in 0-14years old malaria patients attending Murtala Muhammad Specialist Hospital, Kano, Nigeria. Samples from 100 children with malaria were examined to confirm the malaria parasite density and further genotyped via BigDye (v3.1) terminator cycle sequencing for the presence of two SNPs in pfmdr1on samples with high and moderate parasite densities. All data were analyzed using Pearson Chi square and Fisher’s exact (FE) tests. Of the 100 patients, 57% had low (+) malaria parasite density, 28% had moderate (++) and 15% had high (+++) malaria parasite densities of the 100 samples, 31 samples were successfully amplified and analyzed for the pfmdr1 gene located at codon 86 with amplicon size of 534bp while only 7 samples were successfully amplified for the pfmdr1 gene located at codon 1246.Pfmdr1-N86Y mutation was detected in 1 (3.2%) sample. In addition, only 1 (3.2%) sample with allelic change at 1246Y was detected in mutant pfmdr1gene. The result also showed that sex had no significant association (P = 0.4237) with pfmdr1SNP mutation. However, significant association (P = 0.0043) between the age groups (1 month to 14 years) represented in the study and pfmdr1mutation. The present study suggests that strains of P. falciparum with reduced sensitivity to the artemisinin component of artemisinin-based combination therapy (ACT) exist in Kano state, northern Nigeria. Methods: sample Collection Finger prick filter paper blood samples were collected from patients below the age of 5 years. However, 2 mL of venous blood was drawn using sterile syringe and needle from children aged 6 and 14 years. Safety procedures were adopted in the collection of blood samples by swabbing the area to be sampled with disinfectant and allowing it to dry before collection.
尼日利亚卡诺州murtala muhammad专科医院0 - 14岁患者多药耐药疟疾患病率
恶性疟原虫多药耐药基因1 (pfmdr1)是疟原虫对抗疟药物敏感性的分子标记。本研究旨在评估尼日利亚卡诺Murtala Muhammad专科医院0-14岁疟疾患者的多药耐药基因1 (MDR1)突变情况。对来自100名疟疾儿童的样本进行检测,以确定疟原虫密度,并通过BigDye (v3.1)终止周期测序进一步进行基因分型,在疟原虫高密度和中等密度的pfmdr1on样本中存在两个snp。所有数据均采用皮尔逊卡方检验和费雪精确检验(FE)进行分析。100例患者中,57%为低(+)疟原虫密度,28%为中等(++)疟原虫密度,15%为高(+++)疟原虫密度。成功扩增到密码子86位pfmdr1基因的样本有31份,扩增子大小为534bp,成功扩增到密码子1246位pfmdr1基因的样本只有7份。Pfmdr1-N86Y突变1例(3.2%)。此外,在突变体pfmdr1基因中,仅检测到1例(3.2%)等位基因在1246Y发生改变。结果还显示,性别与pfmdr1SNP突变无显著相关性(P = 0.4237)。然而,研究中所代表的年龄组(1个月至14岁)与pfmdr1突变之间存在显著相关性(P = 0.0043)。目前的研究表明,尼日利亚北部卡诺州存在对青蒿素为基础的联合疗法(ACT)中青蒿素成分敏感性降低的恶性疟原虫菌株。方法:采集5岁以下患者手指穿刺滤纸血样。用无菌注射器和针抽取6岁和14岁儿童静脉血2 mL。采集血样时采用了安全程序,用消毒剂擦拭待采样区域,待其干燥后再采集。
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
自引率
0.00%
发文量
0
×
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