{"title":"Assessment of Lethal, Sublethal, Transgenerational, and Biochemical Effects of Isaria fumosorosea on Mythimna separata.","authors":"Mudasar Raza, Shoaib Freed, Rizwan Ahmed, Afifa Naeem","doi":"10.1002/jobm.202400548","DOIUrl":null,"url":null,"abstract":"<p><p>Mythimna separata is a destructive polyphagous pest of field crops. Insecticides are generally applied for its control which not only negatively affect natural enemies and the environment and cause resistance in the insect pests. There is a need for the friendly method which is safe for the environment and life. Currently, entomopathogenic fungi are being used as biological control agents for different insects. The influence of Isaria fumosorosea on survival, life table parameters, and enzymatic activities of M. separata were assessed. On the seventh day post-treatment, the highest concentration 3 × 10<sup>8</sup> spores/mL<sup>-1</sup> caused the 92.5% larval mortality. The effect of LC<sub>15</sub> and LC<sub>50</sub> of I. fumosorosea were recorded on parental generation (F<sub>0</sub>) and first filial generation (F<sub>1</sub>) of M. separata. The life table parameters of F<sub>1</sub> showed a decreasing trend in the intrinsic rate (r), net reproductive rate (R<sub>o</sub>), mean generational time (T), total larval duration, and fecundity ratio in treated groups. In LC<sub>15</sub> and LC<sub>50</sub>, groups the average fecundity ratio was 319.2 and 191.18 eggs/female, respectively. The activities of detoxifying enzymes were concentration-dependent and highest activities were recorded on the third day. I. fumosorosea negatively affected the growth parameters of M. separata and can be included in M. separata management program.</p>","PeriodicalId":15101,"journal":{"name":"Journal of Basic Microbiology","volume":null,"pages":null},"PeriodicalIF":3.5000,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Basic Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/jobm.202400548","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Mythimna separata is a destructive polyphagous pest of field crops. Insecticides are generally applied for its control which not only negatively affect natural enemies and the environment and cause resistance in the insect pests. There is a need for the friendly method which is safe for the environment and life. Currently, entomopathogenic fungi are being used as biological control agents for different insects. The influence of Isaria fumosorosea on survival, life table parameters, and enzymatic activities of M. separata were assessed. On the seventh day post-treatment, the highest concentration 3 × 108 spores/mL-1 caused the 92.5% larval mortality. The effect of LC15 and LC50 of I. fumosorosea were recorded on parental generation (F0) and first filial generation (F1) of M. separata. The life table parameters of F1 showed a decreasing trend in the intrinsic rate (r), net reproductive rate (Ro), mean generational time (T), total larval duration, and fecundity ratio in treated groups. In LC15 and LC50, groups the average fecundity ratio was 319.2 and 191.18 eggs/female, respectively. The activities of detoxifying enzymes were concentration-dependent and highest activities were recorded on the third day. I. fumosorosea negatively affected the growth parameters of M. separata and can be included in M. separata management program.
期刊介绍:
The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions.
Papers published deal with:
microbial interactions (pathogenic, mutualistic, environmental),
ecology,
physiology,
genetics and cell biology/development,
new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications)
novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).