Characterization of new Bacillus thuringiensis strains from Iran, based on cytocidal and insecticidal activity, proteomic analysis and gene content

BioControl ◽  
2018 ◽  
Vol 63 (6) ◽  
pp. 807-818 ◽  
Author(s):  
Ayda Khorramnejad ◽  
Reza Talaei-Hassanloui ◽  
Vahid Hosseininaveh ◽  
Yolanda Bel ◽  
Baltasar Escriche
Toxins ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 642
Author(s):  
Changlong Shu ◽  
Guixin Yan ◽  
Shizhi Huang ◽  
Yongxin Geng ◽  
Mario Soberón ◽  
...  

Scarabaeoidea and Chrysomeloidea insects are agriculture-destructive coleopteran pests. Few effective Bacillus thuringiensis (Bt) insecticidal proteins against these species have been described. Bt isolate BtSU4 was found to be active against coleopteran insects. Genome sequencing revealed two new cry8 genes in BtSU4, designated as cry8Ha1 and cry8Ia1. Both genes expressed a 135 kDa protoxin forming irregular shape crystals. Bioassays performed with Cry8Ha1 protoxin showed that it was toxic to both larvae and adult stages of Holotrichia parallela, also to Holotrichia oblita adults and to Anoplophora glabripennis larvae, but was not toxic to larval stages of H. oblita or Colaphellus bowringi. The Cry8Ia1 protoxin only showed toxicity against H. parallela larvae. After activation with chymotrypsin, the Cry8Ha1 activated toxin lost its insecticidal activity against H. oblita adults and reduced its activity on H. parallela adults, but gained toxicity against C. bowringi larvae, a Chrysomeloidea insect pest that feeds on crucifer crops. The chymotrypsin activated Cry8Ia1 toxin did not show toxicity to any one of these insects. These data show that Cry8Ha1 and Cry8Ia1 protoxin and activated toxin proteins have differential toxicity to diverse coleopteran species, and that protoxin is a more robust protein for the control of coleopteran insects.


PLoS ONE ◽  
2018 ◽  
Vol 13 (11) ◽  
pp. e0206813 ◽  
Author(s):  
Burcu Şahin ◽  
Joaquín Gomis-Cebolla ◽  
Hatice Güneş ◽  
Juan Ferré

2019 ◽  
Vol 17 (1) ◽  
Author(s):  
PETER GITHAIGA KIMANI ◽  
HUDSON NYAMBAKA ◽  
MUO KASINA

Abstract. Kimani PG, Nyambaka H, Kasina M. 2018. Screening and partial characterization of d-endotoxins from some local Bacillus thuringiensis isolates for insecticidal activity against the spotted stem borer. Biofarmasi J Nat Prod Biochem 17: 21-38. Prolonged use of synthetic chemical pesticides is environmentally undesirable, causing the rapid development of resistance among insect pests. Kenya has unexplored potential in controlling lepidopteran pests by using proteinous delta-endotoxins sourced from local isolates of a naturally occurring bacterium, Bacillus thuringiensis Berliner (Bt). This study attempted to identify the insecticidal proteins in some Kenyan Bt isolates, characteristic of Cry1 and/or Cry2 proteins. It also aimed to test their efficacy as affected by different temperatures and their specificity on an invasive and prevalent lepidopteran stem borer, Chilo partellus (Swinhoe). Delta-endotoxin crystals were isolated and purified from cultures of twenty unidentified local Bt isolates using froth floatation and centrifugation. Total protein in the resulting suspensions was quantified using the Bradford assay method, and the approximate protein yield was 3.14 ±0.084 mg/mL of nutrient broth culture with a purity level of 54.8 % ±15.3 %. Leaf-dip bioassays used for testing the efficacy of the d-endotoxins against C. partellus. Among the isolates evaluated, Bt 44 and Bt 48 had the most potent d-endotoxin crystals towards the 1st instar larvae, leading to mortality of 62.6 % and 64.8 % respectively after 72 h. The effect of the d-endotoxins' concentration and temperature on larval mortality was examined for 72 hours at temperatures of 24°C, 27°C and 31°C and levels of 0.01 mg/mL, 0.1 mg/mL and 1.0 mg/mL. The resulting LC50 was 52.3 µg/mL and 42.0 µg/mL, while LT50 values were 76.7h and 60.9h for Bt 44 and Bt 48, respectively. Higher efficacy found at 24°C and 31°C than at 27°C, an indication that these d-endotoxins are tolerable for local conditions where temperatures are higher than in temperate regions. The relationship between concentration and temperature was significant for d-endotoxins of Bt 48 but not those of Bt 44. A major protein component of the d-endotoxins had a molecular weight Mr ~ 130 kDa, which generates a trypsin-resistant core of Mr ~ 70 kDa. Cry protein analysis detected more Cry1 in Bt 44 than Bt 48 ?-endotoxins and no Cry2 in either. However, cry gene analysis using PCR detected the presence of both cry1 and cry2 genes in the DNA of Bt 44 but none in Bt 51, a negative control from toxicity tests against the pest. The chromatographic analysis revealed some differences in the elution profiles of d-endotoxins of both Bt 44 and Bt 48, an indication that there may be different types and amounts of the Cry toxins in the crystals or even novel proteins. These findings indicate that the two local Bt isolates expressed Cry1, and probably Cry2 proteins can control C. partellus and may, therefore, become promising sources for ?-endotoxins for biopesticide development for controlling the pest.


2010 ◽  
Vol 0 (0) ◽  
Author(s):  
Aileen González ◽  
Raúl Díaz ◽  
Manuel Díaz ◽  
Yainais Borrero ◽  
Rosa Y. Bruzón ◽  
...  

2016 ◽  
pp. 1522-1536 ◽  
Author(s):  
Fernando Barnabe Cerqueira ◽  
Giselly Batista Alves ◽  
Roberto Franco Teixeira Corrêa ◽  
Érica Soares Martins ◽  
Luiz Carlos Bertucci Barbosa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document