钩虫β-微管蛋白基因苯并咪唑耐药相关突变的系统综述

IF 1.8 3区 医学 Q2 PARASITOLOGY Parasitology Research Pub Date : 2024-12-09 DOI:10.1007/s00436-024-08432-6
Jan Clyden B Tenorio, Muhammad Fikri Heikal, Alok Kafle, Prasert Saichua, Sutas Suttiprapa
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引用次数: 0

摘要

越来越多的研究报道了多种寄生虫β-微管蛋白同型1基因中出现与苯并咪唑耐药相关的单核苷酸多态性(snp),引起了兽医和公共卫生的关注。然而,尚未对其发生情况及其对钩虫产生苯并咪唑抗性的贡献进行全面分析。本系统综述的目的是总结和综合有关钩虫耐药相关突变发生的同行评审证据,记录其地理分布,并评估其对赋予表型耐药的贡献。使用特定的关键词系统地检索了三个数据库。评估钩虫中苯并咪唑耐药相关snp发生的研究,报道这些snp地理分布的论文,以及调查snp耐药相关表型效应的研究都被纳入综述。非钩虫研究、非英语论文、文献综述和书籍章节均被排除在外。使用关键评估清单来确定所选论文的偏倚风险。从选定的研究中提取数据并进行分析。普洛斯彼罗系统评价方案注册号:: CRD42024510924。共纳入并分析了29项研究。其中,4项是在实验室环境中进行的,8项描述了SNP检测方法的开发和验证,其余17项涉及实地研究。据报道,在Q134H、F167Y、E198A、E198K、E198V、F200Y和F200L 4个位点上发现了7个snp诱导的氨基酸替换。在美国、加拿大、巴西、海地、澳大利亚、新西兰、肯尼亚、加纳、莫桑比克和坦桑尼亚的分离株中已经报道了单核苷酸多态性。在亚洲尚未有耐药性突变的报道。据报道,E198A和F200L在蓝球钩虫中具有实验室诱导抗性。F167Y和Q134H经体外调查和现场鉴定,对犬盲犬产生抗性。没有足够的经同行评审的证据来证明SNP的发生与耐药性之间的关联。β-微管蛋白同型基因1的突变使犬单钩绦虫和黄单钩绦虫对苯并咪唑产生耐药性,但对其他人类钩虫缺乏类似的证据。通过进一步研究了解苯并咪唑耐药性可以更好地为治疗、预防和控制策略提供信息。
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Benzimidazole Resistance-Associated Mutations in the β-tubulin Gene of Hookworms: A Systematic Review.

There is a growing number of reports on the occurrence of benzimidazole resistance-associated single nucleotide polymorphisms (SNPs) in the β-tubulin isotype 1 gene of various helminths of veterinary, and public health concerns. However, a comprehensive analysis of their occurrence, and their contributions to conferring benzimidazole resistance among hookworms has yet to be done. The objectives of this systematic review are to summarize and synthesize peer-reviewed evidence on the occurrence of these resistance-associated mutations in hookworms, document their geographical distribution, and assess their contributions to conferring phenotypic resistance. Three databases were systematically searched using specific keywords. Research that assessed the occurrence of benzimidazole resistance-associated SNPs in hookworms, papers that reported the geographical distribution of these SNPs, and studies that investigated the SNPs' resistance-associated phenotypic effects were included in the review. Research that was not done in hookworms, papers not in the English language, and literature reviews and book chapters were excluded. Critical appraisal checklists were used to determine the risk of bias in the selected papers. Data were extracted from the selected studies and analyzed. PROSPERO Systematic Review Protocol Registration No.: CRD42024510924. A total of 29 studies were included and analyzed. Of these, four were conducted in a laboratory setting, eight described the development and validation of SNP detection methods, and the remaining 17 involved field research. Seven SNP-induced amino acid substitutions at four loci were reported among several hookworm species: Q134H, F167Y, E198A, E198K, E198V, F200Y, and F200L. SNPs have been reported in isolates occurring in the United States, Canada, Brazil, Haiti, Australia, New Zealand, Kenya, Ghana, Mozambique, and Tanzania. Resistance mutations have not been reported in Asia. E198A and F200L were reported in Ancylostoma ceylanicum with laboratory-induced resistance. F167Y and Q134H conferred resistance in A. caninum, as revealed by in vitro investigations and field assessments. There is insufficient peer-reviewed evidence to prove the association between SNP occurrence and resistance. Mutations in the β-tubulin isotype 1 gene confer benzimidazole resistance in A. caninum and A. ceylanicum, but similar evidence is lacking for other human hookworms. Understanding benzimidazole resistance through further research can better inform treatment, prevention, and control strategies.

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来源期刊
Parasitology Research
Parasitology Research 医学-寄生虫学
CiteScore
4.10
自引率
5.00%
发文量
346
审稿时长
6 months
期刊介绍: The journal Parasitology Research covers the latest developments in parasitology across a variety of disciplines, including biology, medicine and veterinary medicine. Among many topics discussed are chemotherapy and control of parasitic disease, and the relationship of host and parasite. Other coverage includes: Protozoology, Helminthology, Entomology; Morphology (incl. Pathomorphology, Ultrastructure); Biochemistry, Physiology including Pathophysiology; Parasite-Host-Relationships including Immunology and Host Specificity; life history, ecology and epidemiology; and Diagnosis, Chemotherapy and Control of Parasitic Diseases.
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