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Complete genome sequence of Bacillus thuringiensis BR145, a strain with insecticidal activity against Lepidoptera pests

Abstract

Bacillus thuringiensis BR145 isolated from a soybean field in Southern Brazil showed toxicity against two important insect pests from soybean crop, Helicoverpa armigera, and Chrysodeixis includens, with LC50 0.294 µg.cm-2 and 0.277 µg.cm-2, respectively. We analyzed the genome of this strain through sequences obtained by Next Generation DNA Sequencing and de novo assembly. The analysis of the genome revealed insecticidal genes cry1Aa, cry1Ab, cry1Ac, cry1Ia, cry2Ab, cyt1, and vip3Aa, suggesting the use of this strain in new strategies of biological control.

Keywords:
Bacillus thuringiensis ; insecticidal genes; virulence factors; Helicoverpa armigera ; Chrysodeixis includens

Bacillus thuringiensis is a Gram-positive bacterium with entomopathogenic activity associated with Cry, Cyt, and Vip proteins, synthesized in the sporulation phase and during vegetative growth. Besides these toxins, B. thuringiensis produces virulence factors, which potentiate their pathogenicity, including phospholipases, metalloproteases, hemolysins, enterotoxins, cytotoxins, and others factors (Vilas-Bôas et al., 2007Vilas-Bôas GT, Peruca APS and Arantes OMN (2007) Biology and taxonomy of Bacillus cereus, Bacillus anthracis, and Bacillus thuringiensis. Can J Microbiol 53:673-687. ; Palma et al., 2014Palma L, Muñoz D, Berry C, Murillo J, de Escudero I and Caballero P (2014) Molecular and insecticidal characterization of a novel Cry-related protein from Bacillus thuringiensis toxic against Myzus persicae. Toxins (Basel) 6:3144-3156. ). Several toxins produced by B. thuringiensis strains were described with toxicity to insect larvae of Lepidoptera, Coleoptera, Diptera, and against species of other phyla (Vilas-Bôas et al., 2012Vilas-Bôas GT, Alvarez RC, Santos CA and Vilas-Boas LA (2012) Fatores de Virulência de Bacillus thuringiensis Berliner: O que existe além das proteínas Cry? EntomoBrasilis 5:190-197.) and recently the classification of these toxins was revised (Crickmore et al., 2020Crickmore N, Berry C, Panneerselvam S, Mishra R, Connor TR and Bonning BC (2020) A structure-based nomenclature for Bacillus thuringiensis and other bacteria-derived pesticidal proteins. J Invertebr Pathol 186:107438. ). Therefore, B. thuringiensis-based biopesticides have been used as alternative insect pest control and represent about 98% of formulated sprayable bacterial microbial pesticides (Lacey et al., 2015Lacey LA, Grzywacz D, Shapiro-Ilan DI, Frutos R, Brownbridge M and Goettel MS (2015) Insect pathogens as biological control agents: Back to the future. J Invertebr Pathol 132:1-41. ).

Brazil has emerged as the largest producer and exporter of soybean. Therefore, key soybean pests such as soybean looper Chrysodeixis includensWalker, 1858 (Lepidoptera: NoctuidaeYano SA, Specht A, Moscardi F, Carvalho RA, Dourado PM, Martinelli S, Head GP and Sosa-Gómez DR (2016) High susceptibility and low resistance allele frequency of Chrysodeixis includens (Lepidoptera: Noctuidae) field populations to Cry1Ac in Brazil. Pest Manag Sci 72:1578-1584. ), one of the most important soybean pests in Brazil (Yano et al., 2016Yano SA, Specht A, Moscardi F, Carvalho RA, Dourado PM, Martinelli S, Head GP and Sosa-Gómez DR (2016) High susceptibility and low resistance allele frequency of Chrysodeixis includens (Lepidoptera: Noctuidae) field populations to Cry1Ac in Brazil. Pest Manag Sci 72:1578-1584. ), have a profound impact on insecticide use, as well as the polyphagous pest Helicoverpa armigera Hübner, 1805 (Lepidoptera: Noctuidae), which eventually can reach pest status and cause damage, also in cotton and corn (Bueno and Sosa-Gómez, 2014Bueno A and Sosa-Gómez DR (2014) The old world bollworm in the neotropical region: The experience of brazilian growers with Helicoverpa armigera. Outlooks Pest Manag 25:261-264. ; Pomari-Fernandes et al., 2015Pomari-Fernandes A, De Freitas Bueno A and Sosa-Gómez DR (2015) Helicoverpa armigera: current status and future perspectives in Brazil. CAST 21:1-7. ). Since the use of safe and more selective insecticides is increasing in the world and is an important demand of the public and farmers, alternative methods of control of these insect pests must be developed. For these reasons, in this study, we performed a characterization of B. thuringiensis BR145, a novel strain with toxicity against Lepidoptera pests.

This strain was isolated in a Brazilian soybean field (Ricieto et al., 2013Ricieto APS, Fazion FAP, Carvalho Filho CD, Vilas-Boas LA and Vilas-Bôas GT (2013) Effect of vegetation on the presence and genetic diversity of Bacillus thuringiensis in soil. Can J Microbiol 59:28-33. ) and showed entomopathogenic activity in assays with larvae of Ecdytolopha aurantiana Lima, 1927 (Lepidoptera: Tortricidae) (Zorzetti et al., 2017aZorzetti J, Ricietto APS, Fazion FAP, Meneguim AM, Neves PMOJ, Vilas-Boas LA, Rodrigues RB and Vilas-Bôas GT (2017a) Selection and characterization of Bacillus thuringiensis (Berliner) (Eubacteriales: Bacillaceae) strains for Ecdytolopha aurantiana (Lima) (Lepidoptera: Tortricidae) control. Neotrop Entomol 46:86-92. ) and Elasmopalpus lignosellus Zeller, 1848 (Lepidoptera: Pyralidae) (Zorzetti et al., 2017bZorzetti J, Ricietto APS, Fazion FAP, Meneguim AM, Neves PMOJ and Vilas-Bôas GT (2017b) Isolation and characterization of Bacillus thuringiensis strains active against Elasmopalpus lignosellus (Zeller, 1848) (Lepidoptera, Pyralidae). Acta Sci Agron 39:417-425.). Bioassays were performed using lyophilized spores and crystal suspensions against larvae of H. armigera and soybean looper C. includens. Dilutions of lyophilized B. thuringiensis were applied uniformly to the diet surface and allowed to dry. Surface treatments provide doses ranging from 0.02 to 1.05 µg/cm2. One neonate larva was placed on the treated surface in each cell of a bioassay tray (128 cells). The trays were sealed with self-adhesive plastic sheets (BIO-CV-16;CD International Inc., Pitman, NJ) and held for at 25 ±1.5 °C. Mortality data were obtained after seven days of exposure. Lethal doses and parameters associated were calculated with Polo software (LeOra Software, 1987LeOra Software (1987) Polo-PC: A User’s Guide to Probit or Logit Analysis. LeOra Software, Berkeley.).

The strain showed insecticidal activity against H. armigera (LC50 of 0.294 µg.cm-2) and to C. includens from both origins, with LC50 0.277 µg.cm-2, and 0.398 µg.cm-2, respectively (Table 1). This LC50 of in both species is comparable to previous bioactive B. thuringiensis isolates with potential use in microbial control (Ignoffo et al., 1977Ignoffo CM, Hostetter DL, Pinnell RE and Garcia C (1977) Relative susceptibility of six soybean caterpillars to a standard preparation of Bacillus thuringiensis var. kurstaki. J Econ Entomol 70:60-63. ; Pinheiro and Valicente, 2021Pinheiro DH and Valicente FH (2021) Identification of Bacillus thuringiensis strains for the management of lepidopteran pests. Neotrop Entomol 50:804-811.).

Table 1 -
Concentration/mortality responses of neonate larva to lyophilized Bacillus thuringiensis BR145 applied on artificial diet.

Genomic DNA was isolated from strain BR145 using Wizard® Genomic DNA Purification kit (Promega, Madison, Wisconsin, USA) following the manufacturer’s instructions and the DNA library was prepared with Illumina DNA Prep. Whole-genome sequencing was performed by Illumina Hiseq sequencing and the paired-end sequence strategy was chosen, which generated a total of 3,042,174 reads of high quality. The analysis methods were performed according to Zorzetti et al. (2015Zorzetti J, Ricietto APS, da Silva CRM, Wolf IR, Vilas-Bôas GT, Neves PMOJ, Meneguim AM and Vilas-Boas LA (2015) Genome Sequence of the mosquitocidal Bacillus thuringiensis strain BR58, a biopesticide product effective against the coffee berry borer (Hypothenemus hampei ). Genome Announc 3:e01232-15. ). The genome was assembled de novo with SPAdes version 3.9.0 (Gurevich et al., 2013Gurevich A, Saveliev V, Vyahhi N and Tesler G (2013) QUAST: A quality assessment tool for genome assemblies. Bioinformatics 29:1072-1075.). The final draft genome consisted of 235 contigs (length>1000 bp), with a total size of 6,350,733 bp, N50 value of 84,578, and a G+C content of 34.78%. The RAST server program (Aziz et al., 2008Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M et al. (2008) The RAST Server: Rapid annotations using subsystems technology. BMC Genomics 9:75. ) proposed that this strain contains 6,647 coding sequences and 224 RNA genes in 494 subsystems (Figure 1).

Figure 1 -
Subsystem coverage and category described by RAST server program in the genome sequence of B. thuringiensis BR145.

Sequences that indicate insecticidal genes were identified using Blast tools. Five cry genes were found: cry1Aa, cry1Ab, cry1Ac, cry1Ia, and cry2Ab, as well as cyt1 and vip3Aa genes. All cry genes and the vip3Aa gene were found in plasmid sequences. Genes associated with virulence factirs, such as phospholipases, hemolysins, metalloproteases, and enterotoxins were also located in this genome. The data can be found in genome annotation. Complete genome sequences of several B. thuringiensis strains are available on the NCBI Genome website (https://www.ncbi.nlm.nih.gov/genome/genomes/486/). Comparative analysis using BR145 contigs against the nonredundant database identified B. thuringiensis serovar kurstaki as the closest relative. The complete genome sequence of B. thuringiensis BR145 strain has been deposited at GenBank and is available on the NCBI website (https://www.ncbi.nlm.nih.gov/nuccore?term=NZ_PDVK01000001:NZ_PDVK01000235[PACC])

The analysis of the genome sequence and the bioassay results allowed the characterization of B. thuringiensis BR145 as a new alternative to be used against a wide range of lepidopteran pests with economic importance, including H. armigera and C. includens, two important pests causing damages in soybean culture in Brazil.

Acknowledgments

We thank Fabio Paro from Entomology Laboratory (EMBRAPA Soja, Brazil) for performing bioassays against H. armigera and C. includens. This work received support from the Coordenação de Aperfeiçoamento de Nível Superior (CAPES) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil. Ricietto, A.P.S., Gonçalves, K.C.B and Appel, R.J.C were supported by fellowships from CAPES and CNPq.

References

  • Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M et al (2008) The RAST Server: Rapid annotations using subsystems technology. BMC Genomics 9:75.
  • Bueno A and Sosa-Gómez DR (2014) The old world bollworm in the neotropical region: The experience of brazilian growers with Helicoverpa armigera Outlooks Pest Manag 25:261-264.
  • Crickmore N, Berry C, Panneerselvam S, Mishra R, Connor TR and Bonning BC (2020) A structure-based nomenclature for Bacillus thuringiensis and other bacteria-derived pesticidal proteins. J Invertebr Pathol 186:107438.
  • Gurevich A, Saveliev V, Vyahhi N and Tesler G (2013) QUAST: A quality assessment tool for genome assemblies. Bioinformatics 29:1072-1075.
  • Ignoffo CM, Hostetter DL, Pinnell RE and Garcia C (1977) Relative susceptibility of six soybean caterpillars to a standard preparation of Bacillus thuringiensis var. kurstaki J Econ Entomol 70:60-63.
  • Lacey LA, Grzywacz D, Shapiro-Ilan DI, Frutos R, Brownbridge M and Goettel MS (2015) Insect pathogens as biological control agents: Back to the future. J Invertebr Pathol 132:1-41.
  • LeOra Software (1987) Polo-PC: A User’s Guide to Probit or Logit Analysis. LeOra Software, Berkeley.
  • Palma L, Muñoz D, Berry C, Murillo J, de Escudero I and Caballero P (2014) Molecular and insecticidal characterization of a novel Cry-related protein from Bacillus thuringiensis toxic against Myzus persicae Toxins (Basel) 6:3144-3156.
  • Pinheiro DH and Valicente FH (2021) Identification of Bacillus thuringiensis strains for the management of lepidopteran pests. Neotrop Entomol 50:804-811.
  • Pomari-Fernandes A, De Freitas Bueno A and Sosa-Gómez DR (2015) Helicoverpa armigera: current status and future perspectives in Brazil. CAST 21:1-7.
  • Ricieto APS, Fazion FAP, Carvalho Filho CD, Vilas-Boas LA and Vilas-Bôas GT (2013) Effect of vegetation on the presence and genetic diversity of Bacillus thuringiensis in soil. Can J Microbiol 59:28-33.
  • Vilas-Bôas GT, Peruca APS and Arantes OMN (2007) Biology and taxonomy of Bacillus cereus, Bacillus anthracis, and Bacillus thuringiensis Can J Microbiol 53:673-687.
  • Vilas-Bôas GT, Alvarez RC, Santos CA and Vilas-Boas LA (2012) Fatores de Virulência de Bacillus thuringiensis Berliner: O que existe além das proteínas Cry? EntomoBrasilis 5:190-197.
  • Yano SA, Specht A, Moscardi F, Carvalho RA, Dourado PM, Martinelli S, Head GP and Sosa-Gómez DR (2016) High susceptibility and low resistance allele frequency of Chrysodeixis includens (Lepidoptera: Noctuidae) field populations to Cry1Ac in Brazil. Pest Manag Sci 72:1578-1584.
  • Zorzetti J, Ricietto APS, da Silva CRM, Wolf IR, Vilas-Bôas GT, Neves PMOJ, Meneguim AM and Vilas-Boas LA (2015) Genome Sequence of the mosquitocidal Bacillus thuringiensis strain BR58, a biopesticide product effective against the coffee berry borer (Hypothenemus hampei ). Genome Announc 3:e01232-15.
  • Zorzetti J, Ricietto APS, Fazion FAP, Meneguim AM, Neves PMOJ, Vilas-Boas LA, Rodrigues RB and Vilas-Bôas GT (2017a) Selection and characterization of Bacillus thuringiensis (Berliner) (Eubacteriales: Bacillaceae) strains for Ecdytolopha aurantiana (Lima) (Lepidoptera: Tortricidae) control. Neotrop Entomol 46:86-92.
  • Zorzetti J, Ricietto APS, Fazion FAP, Meneguim AM, Neves PMOJ and Vilas-Bôas GT (2017b) Isolation and characterization of Bacillus thuringiensis strains active against Elasmopalpus lignosellus (Zeller, 1848) (Lepidoptera, Pyralidae). Acta Sci Agron 39:417-425.

Edited by

Associate Editor:

Rogerio Margis

Publication Dates

  • Publication in this collection
    16 Mar 2022
  • Date of issue
    2022

History

  • Received
    15 Sept 2021
  • Accepted
    03 Feb 2022
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