巨型虫卵菌Lagenidium giganteum和阿氏乳杆菌对按蚊幼虫的致病性评价

IF 1.6 Q2 ENTOMOLOGY
Mathew Mumo Sila, F. Musila, V. Wekesa, Imbahale Susan Sangilu
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引用次数: 0

摘要

疟疾是一种由蚊子传播的危及生命的人类寄生虫病,也是撒哈拉以南非洲地区死亡和发病的主要原因。尽管在疟疾控制方面作出了重大努力,但它面临着寄生虫对抗疟药物产生耐药性以及按蚊媒介对用于控制的杀虫剂产生耐药性的挑战。因此,有必要制定经济和环境友好的补充控制战略。利用昆虫病原真菌对未成熟的疟疾蚊媒进行生物防治是一个尚未开发的机会。本研究旨在从肯尼亚西部阿hero稻田野生按蚊幼虫中分离和鉴定昆虫病原卵菌Lagenidium giganteum和L. ajelloi,并测试它们对实验室饲养的冈比亚按蚊幼虫的致病性。将实验室饲养的3龄和4龄冈比亚单胞虫幼虫暴露于5种不同浓度的巨型乳杆菌和乳杆菌游动孢子;分别为1000、2000、3000、4000和5000个游动孢子/mL。分别在暴露后24、48、72和96小时记录幼虫死亡率,直至所有幼虫死亡。结果表明,在不同浓度下暴露24和48 h后,巨乳杆菌对冈比亚单胞虫幼虫均无致病性。在72小时和96小时记录幼虫死亡率。各治疗组的死亡率差异无统计学意义(p < 0.05)。在去离子水(阴性对照)中未观察到死亡率,而暴露于Bti(阳性对照)的幼虫死亡率为100%。Probit分析显示,72 h和96 h的LC50分别为2.32 × 104和3.51 × 103 zoo孢子/ml。24、48、72、96 h后,5种浓度下的幼虫均有死亡,LC50分别为1.18 × 105、1.43 × 104、6.05 × 102和27.08个zoo孢子/ml。本研究从野外采集的lagenidia幼虫中分离和试验了两种lagenidia。jellagenidium ajelloi对冈比亚按蚊幼虫的致病性高于L. giganteum,使其成为开发生物杀幼虫剂以控制按蚊幼虫的潜在候选物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Pathogenicity of Entomopathogenic Oomycetes Lagenidium giganteum and L. ajelloi against Anopheles Mosquito Larvae
Malaria is a mosquito-borne life-threatening parasitic disease of humans and the leading cause of mortality and morbidity in sub-Saharan Africa. Despite the major efforts made towards malaria control, it is facing challenges of development of parasite resistance towards antimalarial drugs coupled with Anopheles vector resistance towards insecticides being used in control. There is, therefore, a need to develop complementary control strategies that are economical and environmentally friendly. Biological control using entomopathogenic fungi against the immature malaria mosquito vectors presents an untapped opportunity. This study sought to isolate and characterize entomopathogenic oomycetes Lagenidium giganteum and L. ajelloi from wild Anopheles larvae from Ahero rice fields in western Kenya and test their pathogenicity against laboratory-reared Anopheles gambiae larvae. Laboratory-reared A. gambiae larvae (3rd and 4th instar) were exposed to five different concentrations of L. giganteum and L. ajelloi zoospores; 1000, 2000, 3000, 4000, and 5000 zoospores/mL, respectively. The larval mortality was recorded after 24, 48, 72, and 96 hours post-exposure, until all larvae were dead. The results obtained showed that L. giganteum was not pathogenic to A. gambiae larvae after 24 and 48 hours post-exposure to all concentrations. Larval mortality was recorded at 72 and 96 hours. There were no significant differences observed in the mortalities p > 0.05 from all treatments. No mortalities were observed in deionized water (negative control) whereas 100% mortality was recorded in larvae exposed to Bti (positive control). Probit analysis showed that LC50 after 72 hours and 96 hours was 2.32 × 104 and 3.51 × 103 zoospores/ml, respectively. L. ajelloi caused larval mortalities at all the 5 test concentrations after 24-, 48-, 72- and 96-hours post-exposure with LC50 values of 1.18 × 105, 1.43 × 104, and 6.05 × 102, and 27.08 zoospores/ml, respectively. This study isolated and tested two species of Lagenidium from field collected larvae. Lagenidium ajelloi recorded greater pathogenicity than that of L. giganteum against A. gambiae larvae, making them potential candidates for use in the development of bio-larvicide for the control of Anopheles larvae.
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来源期刊
CiteScore
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