疟原虫类群物种的季节动态和除虫菊酯抗药性发展的差异。

IF 3 2区 医学 Q1 PARASITOLOGY Parasites & Vectors Pub Date : 2024-10-05 DOI:10.1186/s13071-024-06462-8
Do Eun Lee, Jeong Heum Han, Gang Chan Lee, Junhyeong Choi, Wonyong Kwun, Si Hyeock Lee, Ju Hyeon Kim
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引用次数: 0

摘要

背景:在韩国,传播间日疟原虫的按蚊群由六个已确认的种类组成。一项流行病学研究显示,各物种的季节性发生模式存在差异。中华疟蚊对拟除虫菊酯的抗药性可追溯到 2000 年代初,而其他种类对拟除虫菊酯抗药性的信息则缺乏,尽管它们在疟疾流行病学中的重要性更大:方法:从韩国两个疟疾流行地区收集了两年的按蚊,并对它们的抗性基因敲除(kdr)突变进行了基因分型。比较了六种按蚊幼虫对λ-氯氰菊酯的敏感性,并研究了三种按蚊幼虫对氯氰菊酯的季节性变化。比较了六个物种的电压敏感钠通道(VSSC)全长序列,以评估潜在的靶位不敏感性。通过比较不同基因型的疟原虫种群对λ-氰戊菊酯的中位致死时间(LT50),证实了kdr突变对表型抗性的贡献:稀有物种(Anopheles kleini、Anopheles lestri和Anopheles sineroides)的组成和季节性出现差异很大,而中华按蚊(An. sinensis)则在整个季节持续出现。在贝氏按蚊、莱斯特按蚊、拉氏按蚊和中华按蚊中新发现了杂合等位基因形式的kdr突变。贝伦氏蚁对λ-氯氰菊酯的基线敏感性最高,其次是莱斯特氏蚁、窦氏蚁、克利尼氏蚁、拉氏蚁和中华蚁,中位致死浓度(LC50)值是贝伦氏蚁的6.0-73.5倍。An. sinensis 和 An. pullus 的易感性随季节而变化,而 An. belenrae 的易感性则保持稳定。kdr杂合种群的LT50是易感种群的5.1倍。在六个物种中观察到了物种特异性 VSSC 序列差异:结论:我们的研究结果表明,拟除虫菊酯抗性的状况和程度在疟原虫中存在差异。我们的研究结果表明,拟除虫菊酯类昆虫的抗性状况和程度在中华疟蚊属昆虫中存在差异。虽然中华疟蚊属昆虫中的主要物种通过kdr突变产生了相当程度的拟除虫菊酯抗性,但其他物种的抗性水平似乎并不明显。考虑到气候变化对其病媒能力的持续影响,大规模监测对于充分了解特定物种的季节性发生和抗药性状况以制定有效的管理策略至关重要。
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Differences in seasonal dynamics and pyrethroid resistance development among Anopheles Hyrcanus group species.

Background: The Anopheles Hyrcanus group, which transmits Plasmodium vivax, consists of six confirmed species in South Korea. An epidemiological study revealed differences in the seasonal occurrence patterns of each species. Pyrethroid resistance in An. sinensis dates back to the early 2000s, whereas information on pyrethroid resistance in other species is lacking despite their greater significance in malaria epidemiology.

Methods: Anopheles mosquitoes were collected from two malaria-endemic regions in South Korea for 2 years and their knockdown resistance (kdr) mutations were genotyped. The larval susceptibility to λ-cyhalothrin was compared in six Anopheles species and its seasonal changes in three species were investigated. The full-length sequences of the voltage-sensitive sodium channel (VSSC) were compared across six species to evaluate potential target-site insensitivity. The contribution of the kdr mutation to phenotypic resistance was confirmed by comparing median lethal time (LT50) to λ-cyhalothrin between populations of Anopheles belenrae with distinct genotypes.

Results: The composition and seasonal occurrence of rare species (Anopheles kleini, Anopheles lestri, and Anopheles sineroides) varied considerably, whereas An. sinensis occurs continuously throughout the season. A kdr mutation in the form of heterozygous allele was newly identified in An. belenrae, An. lesteri, An. pullus, and An. sineroides. The baseline susceptibility to λ-cyhalothrin was the highest in An. belenrae, followed by An. lesteri, An. sineroides, An. kleini, An. pullus, and An. sinensis, with median lethal concentration (LC50) values ranging from 6.0- to 73.5-fold higher than that of An. belenrae. The susceptibility of An. sinensis and An. pullus varied by season, whereas that of An. belenrae remained stable. The kdr-heterozygous An. belenare population exhibited 5.1 times higher LT50 than that of the susceptible population. Species-specific VSSC sequence differences were observed among the six species.

Conclusions: Our findings suggest that the status and extent of pyrethroid resistance vary among Anopheles Hyrcanus group species. While An. sinensis, the predominant species, developed a considerable level of pyrethroid resistance through kdr mutation, the resistance levels of other species appeared to be less pronounced. Large-scale monitoring is crucial to fully understand species-specific seasonal occurrence and resistance status for effective management strategies, considering the ongoing impact of climate change on their vectorial capacity.

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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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