马线虫抗虫现状的系统回顾和荟萃分析:全球视角。

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Enjia Cai , Rongzheng Wu , Yuhong Wu , Yu Gao , Yiping Zhu , Jing Li
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引用次数: 0

摘要

背景:驱虫药在马体内的广泛应用已导致马棘球绦虫和马副绦虫产生相当大的抗药性。已有文献表明,对苯并咪唑和吡喃嘧啶的耐药性在cyathostomins和equorum Parascaris中广泛存在。由于在过去40年中没有引入新的驱虫药类别,因此了解目前使用驱虫药的危险因素以避免进一步的耐药性至关重要。目的:综述影响马抗虫药耐药性水平的因素,对马抗虫药的种类、使用方式、用量、线虫种类、使用地点等进行评价和总结。设计/程序:根据PRISMA框架进行系统回顾和荟萃分析,以识别、评估和综合报道驱虫药物对马的疗效的主要文献。收集文献资料、驱虫药、动物、大陆、寄生虫属、驱虫药种类、剂量等信息。在SPSS (v.27)中使用非参数检验(Kruskal-Wallis和Mann-Whitney)来调查变量之间的关联。对疗效有显著影响的因素进行了二元逻辑回归。在Microsoft Excel(2021)中进行了六项荟萃分析,以确定目前三种主要驱虫药类的耐药性问题。结果:最终数据库由1994 - 2022年间发表的60篇文章组成,共11835只动物。驱虫药的种类和活性成分的选择对耐药有显著影响(P < 0.01),而驱虫药的种类、使用方式和用量与药效无相关性。蛔虫的抗药性显著高于圆线虫(P < 0.01)。大环内酯(ML)类和苯并咪唑和丙苯咪唑(BP)类对蛔虫和蛔虫的药效最低,分别为67.83%和69.85%。地理位置(按洲)对ML类的抗性也有显著影响(P < 0.01)。在所有六大洲都证明了最普遍使用的BP类的抗性。二元logistic回归分析显示,寄生虫属和药物类别独立影响耐药的存在。本研究中包括的森林样地没有显示出随时间的显著差异。结论:目前有证据表明,ML和BP类抗药在蛔虫和圆线虫中普遍存在。联合使用驱虫药可能会减少对驱虫药的耐药性,但多药耐药性可能是一个问题。量身定制的驱虫策略可能有助于减少耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A systematic review and meta-analysis on the current status of anthelmintic resistance in equine nematodes: A global perspective

Background

The intensive application of anthelmintics in equine has led to considerable resistance in cyathostomins and Parascaris equorum. It has been well documented that benzimidazole (BZ) and pyrantel resistance is widespread in cyathostomins and Parascaris equorum. Since no new classes of anthelmintic have been introduced in the last 40 years, it is critical to be aware of the current risk factors of anthelmintic application to avoid further resistance.

Objective

To review the factors affecting the level of anthelmintics resistance in equine around the world, type of anthelmintics, mode of application, dosage, nematode species, and location of anthelmintics application were evaluated and summarized.

Design/procedure

A systematic review and meta-analyses following the PRISMA Framework were conducted to identify, evaluate, and synthesize primary literature reporting the efficacy of anthelmintic drugs in equines. Information on the bibliographic data, anthelmintic drugs, animals, continents, parasite genera, type of anthelmintics, and dosage was collected. Nonparametric tests (Kruskal-Wallis and Mann-Whitney) were used in SPSS (v.27) to investigate the association between variables. Factors that have a significant impact on efficacy have been subjected to binary logistic regression. Six meta-analyses were conducted in Microsoft Excel (2021) to qualify current resistance issues of the three major anthelmintics classes.

Results

The final database was composed of 60 articles published between 1994 and 2022 with a total of 11835 animals. Anthelmintic class as well as anthelmintic active principle selection did have a significant effect on resistance (P < 0.01), whilst no correlation of the type of anthelmintics, mode of application, and dosage with efficacy were found. Anthelmintics resistance in ascarid was significantly more severe than in strongyle (P < 0.01). Macrocyclic lactone (ML) class and the benzimidazole and probenzimidazole (BP) class have the lowest efficacy against ascarid and strongyle, respectively (67.83% and 69.85%). The effect of location (by continent) also had a significant influence on the resistance of the ML class (P < 0.01). The resistance of the BP class which is the most prevalently applied was demonstrated in all six continents. Binary logistic regression revealed that parasite genera and drug class independently influenced the presence of drug resistance. The forest plots included in this study did not show a significant difference over time.

Conclusion

Current evidence indicated that anthelmintics resistance of ML and BP class were common in ascarid and strongyle. A combination of anthelmintics may reduce anthelmintics resistance, but multi-drug resistance may be a concern. Customerised anthelmintics strategy could help reduce resistance.

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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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