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Larvicidal Effects of Metabolites Extracted from Nocardia and Streptomyces Species against the Forth Larval Stage of Anopheles stephensi (Diptera: Culicidae).
Seratnahaei, Marjan; Eshraghi, Seyyed Saeed; Pakzad, Parviz; Zahraei-Ramazani, Alireza; Yaseri, Mehdi.
Afiliación
  • Seratnahaei M; Department of Microbiology, North Tehran Branch, Islamic Azad University, Tehran, Iran.
  • Eshraghi SS; Department of Microbiology, North Tehran Branch, Islamic Azad University, Tehran, Iran.
  • Pakzad P; Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  • Zahraei-Ramazani A; Department of Microbiology, faculty of Basic Sciences, North Tehran Branch, Islamic Azad University, Tehran, Iran.
  • Yaseri M; Department of Biology and Vector Control of Diseases, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
J Arthropod Borne Dis ; 17(2): 187-196, 2023 Jun.
Article en En | MEDLINE | ID: mdl-37822754
ABSTRACT

Background:

Larvicidal agents can be produced using microbial resources, which are environmentally friendly, biodegradable, and economical. The study's goal was to evaluate the larvicidal activity of metabolites isolated from Nocardia (N. fluminea, N. soli and N. pseudobrasiliensis) and Streptomyces (S. alboflavus) bacterial species against Anopheles stephensi.

Methods:

Four metabolites isolated from Nocardia and Streptomyces strains were exanimated for larvicidal activity. The experiments were performed for 24, 48, and 72 hours. 300, 350, 400, 450, 500, 550, and 600 µl of Actinobacteria metabolites were added to 100 cc of dechlorinated water. Fourth-stage larvae were placed in dechlorinated water as a control. LC50 and LC90 were calculated using toxicity data and analyzed.

Results:

All metabolites had a statistically significant influence on mosquito larvae (P< 0.05). At 24, 48, and 72 hours, the LC50 for N2 (N. fluminea) was 417, 386, and 370 ppm, respectively, and the LC90 was 650, 595, and 561 ppm. Moreover, LC50 for N4 (N. soli) was 389, 376, and 347 and LC90 were 591, 565, and 533 and LC50 for N5 (N. pseudobrasiliensis) was 390, 357, and 341 ppm and LC90 were 589, 532 ppm. In addition, LC50 for S921 (S. alboflavus) was 484, 416, and 382 ppm, and LC90 was 701, 612, and 574 ppm.

Conclusion:

The four bacterial metabolites tested in our study were found to have a notable effect on the mortality rate of Anopheles stephensi larvae, indicating their potential as natural larvicides. This is an effective technique for controlling Anopheles stephensi that has no detrimental environmental impact.
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