Plant Protection (Scientific Journal of Agriculture)

Plant Protection (Scientific Journal of Agriculture)

Study of the culturable bacterial community in the digestive tract of Helicoverpa armigera larvae and the effect of the fungus Beauveria bassiana on the abundance of digestive tract bacteria

Document Type : Research paper-Persian

Authors
1 Ph.D. student, Department of Plant Protection, Faculty of Agriculture, University of Zabol, Zabol, Iran
2 Associate Professor, Department of Plant Protection, Faculty of Agriculture, University of Zabol, Zabol, Iran
3 Associate Professor, Department of Pathobiology, Faculty of Veterinary Medicine, University of Zabol, Zabol, Iran
Abstract
Background and Objectives
Bacteria are an important group of microorganisms that live within the insect guts. Bacteria inhabiting the gut of insects provide many benefits to their hosts, such as aiding in digestion, reproduction, immunity, tissue homeostasis, adaptation to environment and resistance to pathogen and pesticides. Insect microbial associates play important roles in the development of diseases caused by entomopathogens and toxicoses caused by insecticides. Different types of interactions may occur between bacterial symbionts and insect-pathogenic ascomycetes (e.g., B. bassiana). Helicoverpa armigera Hubner (Lepidoptera: Noctuidae) is a polyphagous and economically important pest of the order Lepidoptera, that infests important crops worldwide, including cotton, tomatoes, sunflowers, corn, peas, vegetables and agricultural crops. However, studies on the microbiota in the insect order are scarce. This study aimed to identify the symbiotic bacteria associated with H. armigera guts and to survey the effect of the pathogenic fungus, B. bassiana (concentration of 106 conidia/ml) on the abundance of bacterial flora.
Materials and Methods
Eggs and larvae were collected from the corn fields of Jiroft, Kerman, and reared in laboratory conditions at 27±2°C, 65±5% relative humidity and a 16L: 8D photoperiod. The fungus B. bassiana Isolate (IRAN 1395C) was obtained from the Iranian Plant Protection Research Institute and grown on Potato Dextrose Agar (PDA) at 25 °C until sporulation. Bacterial identification was performed based on phenotypic characteristics using standard bacteriological methods, as well as the 16S rRNA encoding gene sequence and its comparison with the NCBI database. The contents of the digestive tube of fifth instar larvae were cultured in enriched Nutrient Agar medium using the 16 linear methods. After colony formation and purification, Gram staining was performed, and individual isolates were transferred to specific culture media (blood agar for Gram-positive bacteria and Eosin Methylene Blue agar (EMB) and MacConkey agar for Gram-negative bacteria). After purification in specific culture media, biochemical and differential tests, including oxidase, urease, catalase, Simon citrate agar, mannitol fermentation, motility, methyl red, gas production in Triple sugar iron agar (TSI) and Wegas-Persquaer tests, were used to identify bacteria. The appearance of the colonies was examined based on certain characteristics, such as size, form, color, elevation, consistency and opacity. In addition, the study involved counting bacterial colonies in treated larvae inoculated with the fungus B. bassiana and in a control group, using a mixed-culture method.
Results
The results of biochemical and differential tests and phenotypic studies showed that the predominant commensal bacteria in the digestive tract of Helicoverpa armigera larvae were the Gram-positive bacteria genus, include Staphylococcus (Bacillales: Staphylococcaceae, are Gram-positive cocci 1μm in diameter that form clumps.), Streptococcus (Lactobacillales: Streptococcaceae, are Gram-positive, nonmotile, nonsporeforming, catalase-negative cocci that occur in pairs or chains.), Bacillus (Bacillales: Bacillaceae, are rod-shaped, endospore-forming, aerobic or facultative anaerobic), Enterococcus (Lactobacillales: Enterococcaceae, are Gram-positive cocci that often occur in pairs (diplococci) or short chains, and are difficult to distinguish from streptococci on physical characteristics alone) and Gram-negative bacteria genus contain Enterobacter (Enterobacterales: Enterobacteriaceae, is a genus of Gram-negative, facultatively anaerobic, rod-shaped or coliform bacilli, non-spore-forming bacteria) and Klebsiella (Enterobacterales: Enterobacteriaceae, is a genus of Gram-negative, oxidase-negative, rod-shaped bacteria with a prominent polysaccharide-based capsule). The accuracy of the results for biochemical and differential determination was verified by molecular analysis using DNA sequences of the 16S rRNA gene, compared with the NCBI sequences database. After identifying the culturable bacteria in biochemical media, the number of bacterial colonies in the digestive tract of larvae infected with the fungus B. bassiana in the bacterial culture medium was counted using a colony counter, and the numbers in the treated and control larvae were compared. The number of bacterial colonies in the growth medium decreased significantly in the digestive tracts of treated larvae infected with pathogenic fungi compared to control larvae.
Discussion
The findings deepened the understanding of the role of associated microbiota–pathogen interaction in maintaining microbiota stability. They may also contribute to the development of novel biological control agents and pest management strategies. However, this is an initial step on the study of gut microbe communities of cotton bollworm. Further functional analysis remains to be done, including isolation, identification, and metabolic analysis of gut microbial strains by culture-independent techniques, in addition to the impact of pathogens on the diversity and abundance of bacterial flora.
Keywords
Subjects

Abd El Aziz, A., Moussa, S., Yassin, M. T., El Husseiny, I., & El Kholy, S. (2024). Biochemical and molecular analysis of gut microbial changes in Spodoptera littoralis (Lepidoptera: Noctuidae) to counteract Cry1c toxicity. Microbiology Research, 15(2), 943-961. https://doi.org/10.3390/microbiolres15020062
Arai, T., Ito, T. & Koyama, Y. (1967). Antimicrobial activity of aflatoxins. Journal of Bacteriology, 93(1), 59–64. https://doi.org/10.1128/jb.93.1.59-64.1967
Bagheri, N., Mohammadi Sharif, M. & Golmohammadi, G. (2021). Comparing the efficacy of some chemical and non-chemical insecticides for control of cotton bollworm, Helicoverpa armigera (Hübner) under cotton field conditions. Plant Protection (Scientific Journal of Agriculture), 44(3), 135-141. https://doi.org/10.22055/ppr.2021.17132
Bai, J., Xu, Z., Li, L., Zhang, Y., Diao, J., Cao, J., Xu, L. & Ma, L. (2023). Gut bacterial microbiota of Lymantria dispar asiatica and its involvement in Beauveria bassiana infection. Journal of Invertebrate Pathology 197, 107897. https://doi.org/10.1016/j.jip.2023.107897
Basavand, F., Khani, A., Yaghubi, S., Najimi, M. & Sahebzadeh, N. (2024) Investigation on Gut Microbiota Diversity of Rhynchophorus ferrugineus Olivier (Coleoptera: Curculionidae) Larvae. Biology bulletin of the Russian Academy of Sciences 51(2), 294–301. https://doi.org/10.1134/S106235902360352X
Bennett, J. W. & Klich, M. (2003). Mycotoxins. Clinical Microbiology Reviews, 16(3), 497–516. https://doi.org/10.1128/cmr.16.3.497-516.2003
Boucias, D. G., Zhou, Y. H., Huang, S. S. & Keyhani, N. O. (2018). Microbiota in insect fungal pathology. Applied Microbiology and Biotechnology, 102, 5873–5888. https://doi.org/10.1007/s00253-018-9089-z
Breznak, J. A. & Switzer, J. M. (1986). Acetate synthesis from H2 plus CO2 by termite gut microbes. Applied and Environmental Microbiology, 52, 623–630. https://doi.org/10.1128/aem.52.4.623-630.1986
Broderick, N. A., Raffa, K. F., Goodman, R. M. & Handelsman, J. (2004). Census of the bacterial community of the gypsy moth larval midgut by using culturing and culture-independent methods. Applied and Environmental Microbiology, 70, 293–300. https://doi.org/10.1128/AEM.70.1.293-300.2004
Butt, T. M. & Goettel, M. S. (2000). Bioassays of entomogenous fungi. In: Navon, A. & Ascher, K. R. S., Eds., Bioassays of entomopathogenic microbes and nematodes, CAB International, Wallingford, UK, 141-195. http://doi.org/10.1079/9780851994222.0141
Chen, D. Q. & Purcell, A. H. (1997). Occurrence and transmission of facultative endosymbionts in aphids. Current Microbiology, 34, 220–225. http://doi.org/10.1007/s002849900172
Dar, M. A., Shaikh, A. F., Pawar, K. D., Xie, R., Sun, J., Kandasamy, S. & Pandit, R. S. (2021). Evaluation of cellulose degrading bacteria isolated from the gut-system of cotton bollworm, Helicoverpa armigera and their potential values in biomass conversion. PeerJ, 9: e11254. http://doi.org/10.7717/peerj.11254
Delalibera, I., Handelsman, J. & Raffa, K. F. (2005). Contrastsin cellulolytic activities of gut microorganisms between the wood borer, Saperda vestita (Coleoptera: Cerambycidae), and the bark beetles, Ips pini and Dendroctonus frontalis (Coleoptera: Curculionidae). Environmental Entomology, 34(3), 541-547. https://doi.org/10.1603/0046-225X-34.3.541
‏Dillon, R. & Charnley, K. (2002). Mutualism between the desert locust Schistocerca gregaria and its gut microbiota. Research in Microbiology, 153(8), 503-509. https://doi.org/10.1016/s0923-2508(02)01361-x
Ebrahimifar, J., Jamshidnia, A. & Sadeghi, R. (2017). Pathogenicity of Beauveria bassiana and Metarhizium anisopliae on elm leaf beetle, Xanthogaleruca luteola Muller (Col., Chrysomelidae). Plant Protection (Scientific Journal of Agriculture), 40(2), 23-32. https://doi.org/10.22055/ppr.2017.12833
Edgar, R. )2013(. UPARSE: highly accurate OTU sequences from microbial amplicon reads. Nature Methods, 10, 996–998. https://doi.org/10.1038/nmeth.2604
Holding, A. J. & Collee, J. G. (1971). Routine biochemical tests. In: Norris, J. R. & Ribbons, D. W., Eds., Methods in microbiology, Vol. 6, Cambridge, Massachusetts, Academic Press, p. 1–32. https://doi.org/10.1016/S0580-9517(08)70573
Gayatri Priya, N., Ojha, A., Kajla, M. K., Raj, A. & Rajagopal, R (2012). Host plant induced variation in gut bacteria of Helicoverpa armigera. PLoS ONE, 7(1): e30768 https://doi.org/10.1371/journal.pone.0030768
Gomes, A. F. F., Omoto, C. & Cônsoli, F. L. (2020). Gut bacteria of field-collected larvae of Spodoptera frugiperda undergo selection and are more diverse and active in metabolizing multiple insecticides than laboratory-selected resistant strains. Journal of Pest Science, 93, 833–851. https://doi.org/10.1007/s10340-020-01202-0
Guerre, P. (2020). Mycotoxin and gut microbiota interactions. Toxins, 12(12), 769. https://doi.org/10.3390/toxins12120769
Gupta, P., Samant, K. & Sahu, A. (2012). Isolation of cellulose-degrading bacteria and determination of their cellulolytic potential. International Journal of Microbiology, 2012, Article ID 578925, 5 pages. https://doi.org/10.1155/2012/578925
Indiragandhi, P., Anandha, R., Madhaiyan, M. & Sa, T. M. (2008). Characterization of plant growth-promoting traits of bacteria isolated from larval guts of diamondback moth Plutella xylostella (Lepidoptera: Plutellidae). Current Microbiology, 56(4), 327–333. https://doi.org/10.1007/s00284-007-9086-4
Kohlerschmidt, D. J., Mingle, L. A., Dumas, N. B. & Nattanmai, G. (2021). Identification of aerobic gram-negative bacteria. In: Green, L. H & Goldman, E., Eds., Practical handbook of microbiology, 4th Edition, Boca Raton, CRC Press, p. 59–70. https://doi.org/10.1201/9781003099277
Kryukov, V. Y., Rotskaya, U, Yaroslavtseva, O., Polenogova, O., Kryukova, N., Akhanaev, Y., Krivopalov, A., Alikina, T., Vorontsova, Y. L., Slepneva, I., Kabilov, M. & Glupov, V. V. (2021). Fungus Metarhizium robertsii and neurotoxic insecticide affect gut immunity and microbiota in Colorado potato beetles. Scientific Reports, 11(1), Article number 1299. https://doi.org/10.1038/s41598-020-80565-x
Kuhnigk, T. & König, H. (1997). Degradation of dimeric lignin model compounds by aerobic bacteria isolated from the hindgut of xylophagous termites. Journal of Basic Microbiology, 37(3), 205-211. https://doi.org/10.1002/jobm.3620370309
Madhusudan, S., Jalali, S. K. & Sibi, G. (2021). Molecular identification of insecticide degradation by gut bacteria isolated from Helicoverpa armigera of Cotton plants. Journal of Applied and Natural Science, 13(2), 641-653. https://doi.org/10.31018/jans.v13i2.2678
Moghassem, M., Jamshidi, M., Khakvar, R. & Nematollahi, S. (2023). Assessing the Virulence of Iranian entomopathogenic fungi isolates in control of Ephestia kuehniella (Lep: Pyralidae) (Zeller). Plant Protection (Scientific Journal of Agriculture), 46(2), 73-86. https://doi.org/10.22055/ppr.2023.42895.1676
Mondal, S., Somani, J., Roy, S., Babu, A. & Pandey, A. K. (2023). Insect microbial symbionts: Ecology, interactions, and biological significance. Microorganisms, 11(11), 2665. https://doi.org/10.3390/microorganisms11112665
Pardo, S. S. & Almeida, R. P. P. (2009). Role of symbiotic gut bacteria in the development of Acrosternum hilare and Murgantia histrionica (Hemiptera: Pentatomidae). Entomological Experimental et Applica, 132(1), 21–29. https://doi.org/10.1111/j.1570-7458.2009.00863.x
Powers, E. M. & Latt, T. G. (1977). Simplified 48-hour IMVic test: an agar plate method. Applied and environmental microbiology, 34(3), 274–279. https://doi.org/10.1128/aem.34.3.274-279.1977
Quinn, P. J., Carter, M. E., Markey, B. & Carter, G. R. (1994). Clinical, Veterinary, Microbiology. Wolf Press, Spain. 648pp.
Reeson, A. F., Jankovic, T., Kasper, M. L., Rogers, S. & Austin, A. D. (2003). Application of 16S rDNA-DGGE to examine the microbial ecology associated with a social wasp Vespula germanica. Insect. Molecular Biology, 12(1), 85–91. https://doi.org/10.1046/j.1365-2583.2003.00390.x
Ren, L., Ma, Y., Xie, M., Lu, Y. & Cheng, D. (2021). Rectal bacteria produce sex pheromones in the male oriental fruit fly. Current Biology, 31(10), 2220-2226. https://doi.org/10.1016/j.cub.2021.02.046
Ryan, K. J. & Ray, C. G. (2004). Sherris Medical Microbiology. 4th Edition, McGraw-Hill, New York.
‏Shao, Y., Chen, B., Sun, C., Ishida, K., Hertweck, C. & Boland, W. (2017). Symbiont-derived antimicrobials contribute to the control of the lepidopteran gut microbiota. Cell Chemical Biology, 24(1), 66-75. https://doi.org/10.1016/j.chembiol.2016.11.015
Sharma, H. C., Pampapathy, G., Dhillon, M. K. & Ridsdill-Smith, J. T. (2005). Detached leaf assay to screen for host plant resistance to Helicoverpa armigera. Journal of Economic Entomology, 98(2), 568-576. https://doi.org/ 10.1093/jee/98.2.568
Shields, P. & Tsang, A. Y. (2006). Mannitol salt agar plates protocols. Available from MicrobeLibrary website http//www.microbelibrary.org/library/laboratory-test/3034-mannitol-salt-agar-plates-protocols.
Shin, S. C., Kim, S. H., You, H., Kim, B., Kim, A. C., Lee, K. A., Yoon, J. H., Ryu, J. H. & Lee, W. J. (2011). Drosophila microbiome modulates host developmental and metabolic homeostasis via insulin signaling. Science, 334(6065), 670–674. https://doi.org/10.1126/science.1212782
Sudakaran, S., Salem, H., Kost, C. & Kaltenpoth, M. (2012). Geographical and ecological stability of the symbiotic mid-gut microbiota in European firebugs, Pyrrhocoris apterus (Hemiptera, Pyrrhocoridae). Molecular Ecology, 21(24), 6134–6151. https://doi.org/10.1111/mec.12027
Thibout, E., Guillot, J. F., Ferary, S., Limouzin, P. & Auger, J. (1995). Origin and identification of bacteria which produce kairomones in the frass of Acrolepiopsis assectella (Lep., Hyponomeutoidea). Experientia, 51(11), 1073–1075. https://doi.org/10.1007/BF01946919
Tittsler, R. P. & Sandholzer, L. A. (1936). The use of semi-solid agar for the detection of bacterial motility. Journal of Bacteriology, 31(6), 575-580. https://doi.org/10.1128/jb.31.6.575-580.1936
van den Bosch, T. J. M. & Welte, C. U. (2017). Detoxifying symbionts in agriculturally important pest insects. Microbial Biotechnology, 10(3), 531–540. https://doi.org/10.1111/1751-7915.12483
Vaughan, E. E., Schut, F., Heilig, H. G., Zoetendal, E. G., de Vos, W. M. & Akkermans, A. D. (2000). A molecular view of the intestinal ecosystem. Current Issues in Intestinal Microbiology, 1(1), 1–12. PMID: 11709849
Visotto, L. E., Oliveira, M. G. A., Guedes, R. N. C., Ribon, A. O. B. & Good-God, P. I. V. (2009). Contribution of gut bacteria to digestion and development of the velvetbean caterpillar, Anticarsia gemmatalis. Journal of Insect Physiology, 55(3), 185–191. https://doi.org/10.1016/j.jinsphys.2008.10.017
Warnecke, F., Luginbu, P., Ivanova, N., Ghassemian, M., Richardson, T. H., Stege, J. T. & et al. (2007). Metagenomic and functional analysis of hindgut microbiota of awood-feeding higher termite. Nature, 450, 560–565. https://doi.org/10.1038/nature06269
Wei, G., Lai, Y., Wang, G., Chen, H., Li, F. & Wang, S. (2017). Insect pathogenic fungus interacts with the gut microbiota to accelerate mosquito mortality. Proceedings of the National Academy of Sciences of the United States of America, 114(23), 5994-5999. https://doi.org/10.1073/pnas.1703546114
Wilkinson, T. L. (1998). The elimination of intracellular microorganisms from insects: an analysis of antibiotic-treatment in the pea aphid (Acyrthosiphon pisum). Comparative Biochemistry and Physiology Part A, 119, 871–881. https://doi.org/10.1016/S1095-6433(98)00013-0
Wilson, G. R. & Benoit, T. G. (1993). Alkaline pH activated Bacillus thuringiensis spores. Journal of Invertebrate Pathology, 62, 87–89. https://doi.org/10.1006/jipa.1993.1079
Xiang, H., Wei, G. F., Jia, S., Huang, J., Miao, X. X., Zhou, Z., Zhao, L. P., Huang, Y. P. (2006). Microbial communities in the larval midgut of laboratory and field populations of cotton bollworm (Helicoverpa armigera). Canadian Journal of Microbiology, 52(11), 1085-1092. https://doi.org/10.1139/w06-064
‏Wu, W., Shan, H. W., Li, J. M., Zhang, C. X., Chen, J. P. & Mao, Q. (2022). Roles of bacterial symbionts in transmission of plant virus by Hemipteran vectors. Frontiers in Microbiology, 13: 805352. https://doi.org/10.3389/fmicb.2022.805352
Zhao, M., Lin, X. & Guo, X. (2022). The role of insect symbiotic bacteria in metabolizing phytochemicals and agrochemicals. Insects, 13(7), 583. https://doi.org/10.3390/insects13070583
‏Zheng, H., Powell, J. E., Steele, M. I., Dietrich, C. & Moran, N. A. (2017). Honeybee gut microbiota promotes host weight gain via bacterial metabolism and hormonal signaling. Proceedings of the National Academy of Sciences, 114(18), 4775-4780. https://doi.org/10.1073/pnas.1701819114
Zhou, F., Gao, Y., Liu, M., Xu, L., Wu, X., Zhao, X., & Zhang, X. (2021). Bacterial inhibition on Beauveria bassiana contributes to microbiota stability in Delia antiqua. Frontiers in Microbiology, 12, 710800. https://doi.org/10.3389/fmicb.2021.710800
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