{"title":"Coleopteran active cry gene profiling and insecticidal activity of indigenous Bacillus thuringiensis strains against Holotrichia serrata.","authors":"Lavanya Siddanahalli Manjunath, Muthuraju Ramaiah, Jagadeesh Patil, Kolla Sreedevi, Aditya Kukreti, Prasannakumar Mothukapalli Krishnareddy, Pramesh Devanna, Sivakumar Gopalsamy, Satya Nand Sushil, Manjunatha Channappa","doi":"10.1093/femsle/fnag126","DOIUrl":null,"url":null,"abstract":"<p><p>White grub (Holotrichia serrata F.) is a destructive soil-dwelling pest causing severe yield losses in several agricultural and horticultural crops. Owing to its subterranean habit, chemical control is often ineffective, necessitating sustainable biological alternatives. This study investigated the distribution of coleopteran-active cry genes among indigenous Bacillus thuringiensis strains and evaluated their insecticidal activity against H. serrata. A total of 100 indigenous B. thuringiensis strains isolated from the Western Ghats of India were screened using gene-specific PCR for 12 coleopteran-active cry genes. The most prevalent genes were cry7 (66%), cry26 (65%), cry1b (64%), and cry34 (63%), whereas cry8 and cry9 occurred in fewer than 10% of the isolates. Preliminary bioassays at 380 µg mL⁻¹ identified 20 strains causing > 50% larval mortality. Concentration-dependent bioassays showed that strain NBAIR Bt68 was the most virulent, causing 73% mortality with an LC₅₀ of 149.95 µg mL⁻¹. Highly toxic strains consistently possessed the cry7-cry26-cry34-cry35 gene combination, whereas the total number of cry genes did not correlate with high insecticidal activity. Molecular profiling combined with bioassay evaluation identified indigenous B. thuringiensis strains with promising biocontrol potential and provides insights into the association between cry gene combinations and insecticidal activity against H. serrata.</p>","PeriodicalId":12214,"journal":{"name":"Fems Microbiology Letters","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fems Microbiology Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/femsle/fnag126","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
White grub (Holotrichia serrata F.) is a destructive soil-dwelling pest causing severe yield losses in several agricultural and horticultural crops. Owing to its subterranean habit, chemical control is often ineffective, necessitating sustainable biological alternatives. This study investigated the distribution of coleopteran-active cry genes among indigenous Bacillus thuringiensis strains and evaluated their insecticidal activity against H. serrata. A total of 100 indigenous B. thuringiensis strains isolated from the Western Ghats of India were screened using gene-specific PCR for 12 coleopteran-active cry genes. The most prevalent genes were cry7 (66%), cry26 (65%), cry1b (64%), and cry34 (63%), whereas cry8 and cry9 occurred in fewer than 10% of the isolates. Preliminary bioassays at 380 µg mL⁻¹ identified 20 strains causing > 50% larval mortality. Concentration-dependent bioassays showed that strain NBAIR Bt68 was the most virulent, causing 73% mortality with an LC₅₀ of 149.95 µg mL⁻¹. Highly toxic strains consistently possessed the cry7-cry26-cry34-cry35 gene combination, whereas the total number of cry genes did not correlate with high insecticidal activity. Molecular profiling combined with bioassay evaluation identified indigenous B. thuringiensis strains with promising biocontrol potential and provides insights into the association between cry gene combinations and insecticidal activity against H. serrata.
期刊介绍:
FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered.
2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020)
Ranking: 98/135 (Microbiology)
The journal is divided into eight Sections:
Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies)
Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens)
Biotechnology and Synthetic Biology
Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses)
Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies)
Virology (viruses infecting any organism, including Bacteria and Archaea)
Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature)
Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology)
If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.