Abstract
The study of insects and their associated microbial communities is an important field in agriculture, primarily due to the role of insects as pests. Recent advances in next-generation sequencing technology have aided in improving our understanding of the microbial communities associated with insects, revealing wide diversity in their taxonomy and function. The resident microorganisms can contribute to insect fitness by providing certain amino acids, vitamin B, and sterols for fungal partners. Some organisms protect their insect host by either making toxins or modifying the immune system of insects. Though, Drosophila melanogaster has been used as a model framework system to generate new insights into gut immunity and physiology; however, to date, little is known about the microbiota of other most damaging agricultural pests worldwide. In this chapter, we have discussed the omics approaches applied to study the insect gut microbiome and the advances made in this field. We have then reviewed the role of gut microbiota and the current understanding of intestinal epithelial immune responses of insects.
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References
Aggarwal K, Silverman N (2008) Positive and negative regulation of the Drosophila immune response. BMB Rep 41(4):267–277
Ajlan AM, Abdulsalam K (2000) Efficiency of pheromone traps for controlling the red palm weevil Rhynchophorus ferrugineus Olivier (Coleoptera: Curculionidae), under Saudi Arabia conditions. Bull Entomol Soc Egypt (Econ Ser) 27:109–120
Al-Dosary NMN, Al-Dobai S, Faleiro JR (2016) Review on the management of red palm weevil Rhynchophorus ferrugineus Olivier in date palm Phoenix dactylifera L. Emirates J Food Agri 28(1):34
Ami E, Yuval B, Jurkevitch E (2010) Manipulation of the microbiota of mass-reared Mediterranean fruit flies Ceratitis capitata (Diptera: Tephritidae) improves sterile male sexual performance. ISME J 4(1):28–37. https://doi.org/10.1038/ismej.2009.82
Bae YS, Choi MK, Lee WJ (2010) Dual oxidase in mucosal immunity and host-microbe homeostasis. Trends Immunol 31(7):278–287. https://doi.org/10.1016/j.it.2010.05.003
Belda E, Pedrola L, Peretó J, Martínez-Blanch JF, Montagud A, Navarro E, Porcar M (2011) Microbial diversity in the midguts of field and lab-reared populations of the European corn borer Ostrinia nubilalis. PLoS One 6(6):e21751
Bischoff V, Vignal C, Duvic B, Boneca IG, Hoffmann JA, Royet J (2006) Downregulation of the Drosophila immune response by peptidoglycan-recognition proteins SC1 and SC2. PLoS Pathog 2(2):e14
Blatch SA, Meyer KW, Harrison JF (2010) Effects of dietary folic acid level and symbiotic folate production on fitness and development in the fruit fly Drosophila melanogaster. Fly (Austin) 4(4):312–319. https://doi.org/10.4161/fly.4.4.13258
Boush MG, Matsumura F (1967) Insecticidal degradation by Pseudomonas melophthora, the bacterial symbiote of the apple maggot. J Econ Entomol 60(4):918–920
Broderick NA, Lemaitre B (2012) Gut-associated microbes of Drosophila melanogaster. J Gut Microbes 3(4):307–321
Broderick NA, Raffa KF, Handelsman J (2006) Midgut bacteria required for Bacillus thuringiensis insecticidal activity. Proc Natl Acad Sci U S A 103(41):15196–15199. https://doi.org/10.1073/pnas.0604865103
Broderick NA, Robinson CJ, McMahon MD, Holt J, Handelsman J, Raffa KF (2009) Contributions of gut bacteria to Bacillus thuringiensis-induced mortality vary across a range of Lepidoptera. BMC Biol 7(1):11
Buchon N, Broderick NA, Lemaitre B (2013) Gut homeostasis in a microbial world: insights from Drosophila melanogaster. Nat Rev Microbiol 11(9):615–626. https://doi.org/10.1038/nrmicro3074
Buchon N, Silverman N, Cherry S (2014) Immunity in Drosophila melanogaster from microbial recognition to whole-organism physiology. Nat Rev Immunol 14(12):796–810. https://doi.org/10.1038/nri3763
Cariveau DP, Powell JE, Koch H, Winfree R, Moran NA (2014) Variation in gut microbial communities and its association with pathogen infection in wild bumble bees (Bombus). ISME J 8(12):2369–2379
Casanova-Torres AM, Goodrich-Blair H (2013) Immune signaling and antimicrobial peptide expression in Lepidoptera. Insects 4(3):320–338. https://doi.org/10.3390/insects4030320
Ceja-Navarro JA, Karaoz U, Bill M, Hao Z, White RA, Arellano A, Conrad ME (2019) Gut anatomical properties and microbial functional assembly promote lignocellulose deconstruction and colony subsistence of a wood-feeding beetle. Nat Microbiol 4(5):864
Cerenius L, Soderhall K (2004) The prophenoloxidase-activating system in invertebrates. Immunol Rev 198:116–126. https://doi.org/10.1111/j.0105-2896.2004.00116.x
Chen XQ, Lee KA, Ren XT, Ryu JC, Kim G, Ryu JH, Yoon J (2016) Synthesis of a highly HOCl-selective fluorescent probe and its use for imaging HOCl in cells and organisms. Nat Protoc 11(7):1219–1228. https://doi.org/10.1038/nprot.2016.062
Cheng DF, Guo ZJ, Riegler M, ** ZY, Liang GW, Xu YJ (2017) Gut symbiont enhances insecticide resistance in a significant pest, the oriental fruit fly Bactrocera dorsalis (Hendel). Microbiome 5:13. https://doi.org/10.1186/s40168-017-0236-z
Colman DR, Toolson EC, Takacs-Vesbach C (2012) Do diet and taxonomy influence insect gut bacterial communities? Mol Ecol 21(20):5124–5137
Corby-Harris V, Maes P, Anderson KE (2014) The bacterial communities associated with honey bee (Apis mellifera) foragers. PLoS One 9(4):e95056
Dave M, Higgins PD, Middha S, Rioux KPJTR (2012) The human gut microbiome: current knowledge, challenges, and future directions. Transl Res 160(4):246–257
Dawadi B, Wang XH, **ao R, Muhammad A, Hou YM, Shi ZH (2018) PGRP-LB homolog acts as a negative modulator of immunity in maintaining the gut-microbe symbiosis of red palm weevil, Rhynchophorus ferrugineus Olivier. Dev Comp Immunol 86:65–77. https://doi.org/10.1016/j.dci.2018.04.021
De Mandal S, Panda A, Bisht S, Kumar N (2015) Microbial ecology in the era of next generation sequencing 1:2
Dillon RJ, Vennard CT, Buckling A, Charnley AK (2005) Diversity of locust gut bacteria protects against pathogen invasion. Ecol Lett 8(12):1291–1298. https://doi.org/10.1111/j.1461-0248.2005.00828.x
Douglas AE (2015) Multiorganismal insects: diversity and function of resident microorganisms. Annu Rev Entomol 60:17–34. https://doi.org/10.1146/annurev-ento-010814-020822
El-Mergawy R, Al-Ajlan A (2011) Red palm weevil, Rhynchophorus ferrugineus (Olivier): economic importance, biology, biogeography and integrated pest management. J Agric Sci Technol A 1:1–23
Engel P, Moran NA (2013) The gut microbiota of insects—diversity in structure and function. FEMS Microbiol Rev 37(5):699–735. https://doi.org/10.1111/1574-6976.12025
Engel P, Martinson VG, Moran NA (2012) Functional diversity within the simple gut microbiota of the honey bee. Proc Natl Acad Sci U S A 109(27):11002–11007. https://doi.org/10.1073/pnas.1202970109
Etebari K, Asgari S (2013) Conserved microRNA miR-8 blocks activation of the toll pathway by upregulating serpin 27 transcripts. RNA Biol 10(8):1356–1364. https://doi.org/10.4161/rna.25481
Faleiro J (2006) A review of the issues and management of the red palm weevil Rhynchophorus ferrugineus (Coleoptera: Rhynchophoridae) in coconut and date palm during the last one hundred years. Int J Trop Insect Sci 26(03):135–154
Furlong MJ, Wright DJ, Dosdall LM (2013) Diamondback moth ecology and management: problems, progress, and prospects. Annu Rev Entomol 58:517–541. https://doi.org/10.1146/annurev-ento-120811-153605
Gil R, Latorre A, Moya A (2004) Bacterial endosymbionts of insects: insights from comparative genomics. J Environ Microbiol 6(11):1109–1122
Gottar M, Gobert V, Michel T, Belvin M, Duyk G, Hoffmann JA, Royet J (2002) The Drosophila immune response against gram-negative bacteria is mediated by a peptidoglycan recognition protein. Nature 416(6881):640–644. https://doi.org/10.1038/nature734
Grau T, Vilcinskas A, Joop G (2017) Probiotic Enterococcus mundtii isolate protects the model insect Tribolium castaneum against Bacillus thuringiensis. Front Microbiol 8:1261. https://doi.org/10.3389/fmicb.2017.01261
Guntermann S, Primrose DA, Foley E (2009) Dnr1-dependent regulation of the Drosophila immune deficiency signaling pathway. Dev Comp Immunol 33(1):127–134
Guo L, Karpac J, Tran SL, Jasper H (2014) PGRP-SC2 promotes gut immune homeostasis to limit commensal dysbiosis and extend lifespan. Cell 156(1–2):109–122
Ha EM, Oh CT, Bae YS, Lee WJ (2005a) A direct role for dual oxidase in Drosophila gut immunity. Science 310(5749):847–850. https://doi.org/10.1126/science.1117311
Ha EM, Oh CT, Ryu JH, Bae YS, Kang SW, Jang IH, Lee WJ (2005b) An antioxidant system required for host protection against gut infection in Drosophila. Dev Cell 8(1):125–132. https://doi.org/10.1016/j.devcel.2004.11.007
Ha EM, Lee KA, Park SH, Kim SH, Nam HJ, Lee HY, Lee WJ (2009a) Regulation of DUOX by the Gαq-phospholipase Cβ-Ca2+ pathway in Drosophila gut immunity. Dev Cell 16(3):386–397
Ha EM, Lee KA, Seo YY, Kim SH, Lim JH, Oh BH, Lee WJ (2009b) Coordination of multiple dual oxidase–regulatory pathways in responses to commensal and infectious microbes in Drosophila gut. Nat Immunol 10(9):949
Habineza P, Muhammad A, Ji T, **ao R, Yin X, Hou Y, Shi Z (2019) The promoting effect of gut microbiota on growth and development of red palm weevil, Rhynchophorus ferrugineus (Olivier) (Coleoptera: Dryophthoridae) by modulating its nutritional metabolism. Front Microbiol 10:1212. https://doi.org/10.3389/fmicb.2019.01212
Hammer TJ, Janzen DH, Hallwachs W, Jaffe SP, Fierer N (2017) Caterpillars lack a resident gut microbiome. Proc Natl Acad Sci U S A 114(36):9641–9646
Hernandez-Martinez P, Naseri B, Navarro-Cerrillo G, Escriche B, Ferre J, Herrero S (2010) Increase in midgut microbiota load induces an apparent immune priming and increases tolerance to Bacillus thuringiensis. Environ Microbiol 12(10):2730–2737. https://doi.org/10.1111/j.1462-2920.2010.02241.x
Hu Y, Łukasik P, Moreau CS, Russell JA (2014) Correlates of gut community composition across an ant species (Cephalotes varians) elucidate causes and consequences of symbiotic variability. J Mol Ecol 23(6):1284–1300
Huang XF, Bakker MG, Judd TM, Reardon KF, Vivanco JM (2013) Variations in diversity and richness of gut bacterial communities of termites (Reticulitermes flavipes) fed with grassy and woody plant substrates. J Microb Ecol 65(3):531–536
Hultmark D (2003) Drosophila immunity: paths and patterns. Curr Opin Immunol 15(1):12–19. https://doi.org/10.1016/s0952-7915(02)00005-5
Jang S, Kikuchi Y (2020) Impact of the insect gut microbiota on ecology, evolution, and industry. J Curr Opin Insect Sci 41:33–39
Janssen AW, Kersten S (2015) The role of the gut microbiota in metabolic health. FASEB J 29(8):3111–3123. https://doi.org/10.1096/fj.14-269514
Jia S, Zhang X, Zhang G, Yin A, Zhang S, Li F, Yu J (2013) Seasonally variable intestinal metagenomes of the red palm weevil (Rhynchophorus ferrugineus). Environ Microbiol 15(11):3020–3029. https://doi.org/10.1111/1462-2920.12262
Johnston PR, Crickmore N (2009) Gut bacteria are not required for the insecticidal activity of Bacillus thuringiensis toward the tobacco hornworm, Manduca sexta. Appl Environ Microbiol 75(15):5094–5099. https://doi.org/10.1128/AEM.00966-09
Ju RT, Wang F, Wan FH, Li B (2011) Effect of host plants on development and reproduction of Rhynchophorus ferrugineus (Olivier)(Coleoptera: Curculionidae). J Pest Sci 84(1):33–39
Jung J, Heo A, Park YW, Kim YJ, Koh H, Park WJJMB (2014) Gut microbiota of Tenebrio molitor and their response to environmental change. J Microbiol Biotechnol 24(7):888–897
Kanost MR, Jiang H, Yu XQ (2004) Innate immune responses of a lepidopteran insect, Manduca sexta. Immunol Rev 198:97–105. https://doi.org/10.1111/j.0105-2896.2004.0121.x
Kikuchi Y, Hosokawa T, Fukatsu T (2011) An ancient but promiscuous host–symbiont association between Burkholderia gut symbionts and their heteropteran hosts. ISME J 5(3):446
Kikuchi Y, Hayatsu M, Hosokawa T, Nagayama A, Tago K, Fukatsu T (2012) Symbiont-mediated insecticide resistance. Proc Natl Acad Sci U S A 109(22):8618–8622
Kim M, Lee JH, Lee SY, Kim E, Chung J (2006) Caspar, a suppressor of antibacterial immunity in Drosophila. Proc Natl Acad Sci 103(44):16358–16363
Kim JK, Kim NH, Am Jang H, Kikuchi Y, Kim CH, Fukatsu T, Lee BL (2013) Specific midgut region controlling the symbiont population in an insect-microbe gut symbiotic association. J Appl Environ Microbiol 79(23):7229–7233
Kim JK, Lee JB, Huh YR, Jang HA, Kim CH, Yoo JW, Lee BL (2015) Burkholderia gut symbionts enhance the innate immunity of host Riptortus pedestris. Dev Comp Immunol 53(1):265–269. https://doi.org/10.1016/j.dci.2015.07.006
Köhler T, Dietrich C, Scheffrahn RH, Brune A (2012) High-resolution analysis of gut environment and bacterial microbiota reveals functional compartmentation of the gut in wood-feeding higher termites (Nasutitermes spp.). J Appl Environ Microbiol 78(13):4691–4701
Langille MG, Zaneveld J, Caporaso JG, McDonald D, Knights D, Reyes JA, Clemente JC, Burkepile DE, Thurber RL, Knight R, Beiko RG (2013) Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences. Nat Biotechnol 31(9):814–821
Lee KA, Kim SH, Kim EK, Ha EM, You H, Kim B, Lee WJ (2013) Bacterial-derived uracil as a modulator of mucosal immunity and gut-microbe homeostasis in Drosophila. Cell 153(4):797–811. https://doi.org/10.1016/j.cell.2013.04.009
Lee KA, Kim B, Bhin J, Kim DH, You H, Kim EK, Lee WJ (2015) Bacterial uracil modulates Drosophila DUOX-dependent gut immunity via Hedgehog-induced signaling endosomes. Cell Host Microbe 17(2):191–204
Lee JH, Lee KA, Lee WJ (2017) Microbiota, gut physiology, and insect immunity. In: Advances in insect physiology, vol 52. Elsevier, pp 111–138
Lemaitre B, Hoffmann J (2007) The host defense of Drosophila melanogaster Annu Rev Immunol, 25, 697–743. doi: https://doi.org/10.1146/annurev.immunol.25.022106.141615
Li WH, ** DC, Shi CH, Li FL (2017) Midgut bacteria in deltamethrin-resistant, deltamethrin-susceptible, and field-caught populations of Plutella xylostella, and phenomics of the predominant midgut bacterium Enterococcus mundtii. Sci Rep 7:1947. https://doi.org/10.1038/s41598-017-02138-9
Li S, Xu X, Zheng Z, Zheng J, Shakeel M, ** F (2019) MicroRNA expression profiling of Plutella xylostella after challenge with B. thuringiensis. Dev Comp Immunol 93:115–124. https://doi.org/10.1016/j.dci.2018.12.008
Li S, De Mandal S, Xu X, ** F (2020a) The tripartite interaction of host immunity-Bacillus thuringiensis infection-gut microbiota. Toxins 12(8). https://doi.org/10.3390/toxins12080514
Li S, Xu X, De Mandal S, Shakeel M, Hua Y, Shoukat RF, ** F (2020b) Gut microbiota mediate Plutella xylostella susceptibility to Bt Cry1Ac protoxin is associated with host immune response. Environ Pollut 271:116271. https://doi.org/10.1016/j.envpol.2020.116271
Lin XL, Pan QJ, Tian HG, Douglas AE, Liu TX (2015) Bacteria abundance and diversity of different life stages of Plutella xylostella (Lepidoptera: Plutellidae), revealed by bacteria culture-dependent and PCR-DGGE methods. Insect Sci 22(3):375–385. https://doi.org/10.1111/1744-7917.12079
Lin JH, **a XF, Yu XQ, Shen JH, Li Y, Lin HL, You MS (2018) Gene expression profiling provides insights into the immune mechanism of Plutella xylostella midgut to microbial infection. Gene 647:21–30. https://doi.org/10.1016/j.gene.2018.01.001
Lin J, Yu XQ, Wang Q, Tao X, Li J, Zhang S, You M (2020) Immune responses to Bacillus thuringiensis in the midgut of the diamondback moth, Plutella xylostella. Dev Comp Immunol 107:103661. https://doi.org/10.1016/j.dci.2020.103661
Ma ZG, Li CF, Pan GQ, Li ZH, Han B, Xu JS, Zhou ZY (2013) Genome-wide transcriptional response of silkworm (Bombyx mori) to infection by the microsporidian Nosema bombycis. PLoS One 8(12):e84137. https://doi.org/10.1371/journal.pone.0084137
Malacrinò A, Campolo O, Medina RF, Palmeri V (2018) Instar-and host-associated differentiation of bacterial communities in the Mediterranean fruit fly Ceratitis capitata. PLoS One 13(3):e0194131
Mason CJ, Ray S, Shikano I, Peiffer M, Jones AG, Luthe DS, Felton GW (2019) Plant defenses interact with insect enteric bacteria by initiating a leaky gut syndrome. Proc Natl Acad Sci U S A 201908748
Mogensen TH (2009) Pathogen recognition and inflammatory signaling in innate immune defenses. Clin Microbiol Rev 22(2):240–273, Table of contents. https://doi.org/10.1128/CMR.00046-08
Montagna M, Chouaia B, Mazza G, Prosdocimi EM, Crotti E, Mereghetti V, Daffonchio D (2015) Effects of the diet on the microbiota of the red palm weevil (Coleoptera: Dryophthoridae). PLoS One 10(1):e0117439. https://doi.org/10.1371/journal.pone.0117439
Muhammad A, Fang Y, Hou YM, Shi ZH (2017) The gut entomotype of red palm weevil Rhynchophorus ferrugineus Olivier (Coleoptera: Dryophthoridae) and their effect on host nutrition metabolism. Front Microbiol 8:2291. https://doi.org/10.3389/fmicb.2017.02291
Muhammad A, Habineza P, Hou YM, Shi ZH (2019a) Preparation of red palm weevil Rhynchophorus Ferrugineus (Olivier) (Coleoptera: Dryophthoridae) germ-free larvae for host-gut microbes interaction studies. Bio-protocol 9(24):e3456. https://doi.org/10.21769/BioProtoc.3456
Muhammad A, Habineza P, Ji T, Hou Y, Shi Z (2019b) Intestinal microbiota confer protection by priming the immune system of red palm weevil Rhynchophorus ferrugineus Olivier (Coleoptera: Dryophthoridae). Front Physiol 10:1303. https://doi.org/10.3389/fphys.2019.01303
Muhammad A, Habineza P, Wang XH, **ao R, Ji TL, Hou YM, Shi ZH (2020) Spatzle homolog-mediated toll-like pathway regulates innate immune responses to maintain the homeostasis of gut microbiota in the red palm weevil, Rhynchophorus ferrugineus Olivier (Coleoptera: Dryophthoridae). Front Microbiol 11:846. https://doi.org/10.3389/fmicb.2020.00846
Murphy S, Briscoe B (1999) The red palm weevil as an alien invasive: biology and the prospects for biological control as a component of IPM. Biocontrol News Information 20(1):35–46
Nehme NT, Liegeois S, Kele B, Giammarinaro P, Pradel E, Hoffmann JA, Ferrandon D (2007) A model of bacterial intestinal infections in Drosophila melanogaster. PLoS Pathog 3(11):1694–1709. https://doi.org/10.1371/journal.ppat.0030173
Paredes JC, Welchman DP, Poidevin M, Lemaitre B (2011) Negative regulation by amidase PGRPs shapes the Drosophila antibacterial response and protects the fly from innocuous infection. Immunity 35(5):770–779
Peng L, Miao Y, Hou Y (2016) Demographic comparison and population projection of Rhynchophorus ferrugineus (Coleoptera: Curculionidae) reared on sugarcane at different temperatures. Sci Rep 6:31659
Qiao H, Keesey IW, Hansson BS, Knaden M (2019) Gut microbiota affects development and olfactory behavior in Drosophila melanogaster. J Exp Biol 222(Pt 5):jeb192500. https://doi.org/10.1242/jeb.192500
Ryu JH, Kim SH, Lee HY, Bai JY, Nam YD, Bae JW, Lee WJ (2008) Innate immune homeostasis by the homeobox gene caudal and commensal-gut mutualism in Drosophila. Science 319(5864):777–782
Sajjadian SM, Kim Y (2020) Dual oxidase-derived reactive oxygen species against Bacillus thuringiensis and its suppression by eicosanoid biosynthesis inhibitors. Front Microbiol 11:528. https://doi.org/10.3389/fmicb.2020.00528
Shakeel M, Farooq M, Nasim W, Akram W, Khan FZA, Jaleel W, ** F (2017a) Environment polluting conventional chemical control compared to an environmentally friendly IPM approach for control of diamondback moth, Plutella xylostella (L.), in China: a review. Environ Sci Pollut Res Int 24(17):14537–14550. https://doi.org/10.1007/s11356-017-8996-3
Shakeel M, Xu XX, Xu J, Zhu X, Li SZ, Zhou XQ, ** FL (2017b) Identification of immunity-related genes in Plutella xylostella in response to fungal peptide destruxin A: RNA-Seq and DGE analysis. Sci Rep 7:10966. https://doi.org/10.1038/s41598-017-11298-7
Shakeel M, Xu X, Xu J, Li S, Yu J, Zhou X, ** F (2018) Genome-wide identification of destruxin A-responsive immunity-related microRNAs in diamondback moth, Plutella xylostella. Front Immunol 9:185. https://doi.org/10.3389/fimmu.2018.00185
Shao YQ, Chen BS, Sun C, Ishida K, Hertweck C, Boland W (2017) Symbiont-derived antimicrobials contribute to the control of the lepidopteran gut microbiota. Cell Chem Biol 24(1):66–75. https://doi.org/10.1016/j.chembiol.2016.11.015
Shelomi M, Danchin EG, Heckel D, Wipfler B, Bradler S, Zhou X, Pauchet Y (2016) Horizontal gene transfer of pectinases from bacteria preceded the diversification of stick and leaf insects. Sci Rep 6:26388
Suen G, Scott JJ, Aylward FO, Adams SM, Tringe SG, Pinto-Tomás AA, Barry KW (2010) An insect herbivore microbiome with high plant biomass-degrading capacity. PLoS Genet 6(9):e1001129
Sun H, Towb P, Chiem DN, Foster BA, Wasserman SA (2004) Regulated assembly of the toll signaling complex drives Drosophila dorsoventral patterning. EMBO J 23(1):100–110. https://doi.org/10.1038/sj.emboj.7600033
Tagliavia M, Messina E, Manachini B, Cappello S, Quatrini P (2014) The gut microbiota of larvae of Rhynchophorus ferrugineus Oliver (Coleoptera: Curculionidae). BMC Microbiol 14:136. https://doi.org/10.1186/1471-2180-14-136
Tang X, Freitak D, Vogel H, ** L, Shao Y, Cordero EA, Boland W (2012) Complexity and variability of gut commensal microbiota in polyphagous lepidopteran larvae. PLoS One 7(7):e36978
Tanji T, Ip YT (2005) Regulators of the toll and Imd pathways in the Drosophila innate immune response. Trends Immunol 26(4):193–198. https://doi.org/10.1016/j.it.2005.02.006
Tzou P, Ohresser S, Ferrandon D, Capovilla M, Reichhart J-M, Lemaitre B, Imler J-L (2000) Tissue-specific inducible expression of antimicrobial peptide genes in Drosophila surface epithelia. Immunity 13(5):737–748
Tzou P, Reichhart JM, Lemaitre B (2002) Constitutive expression of a single antimicrobial peptide can restore wild-type resistance to infection in immunodeficient Drosophila mutants. Proc Natl Acad Sci U S A 99(4):2152–2157. https://doi.org/10.1073/pnas.042411999
Valanne S, Wang JH, Ramet M (2011) The Drosophila toll signaling pathway. J Immunol 186(2):649–656. https://doi.org/10.4049/jimmunol.1002302
Vodovar N, Vinals M, Liehl P, Basset A, Degrouard J, Spellman P, Lemaitre B (2005) Drosophila host defense after oral infection by an entomopathogenic Pseudomonas species. Proc Natl Acad Sci U S A 102(32):11414–11419. https://doi.org/10.1073/pnas.0502240102
Wan FH, Yang NW (2016) Invasion and management of agricultural alien insects in China. Annu Rev Entomol 61:77–98
Wong AC, Dobson AJ, Douglas AE (2014) Gut microbiota dictates the metabolic response of Drosophila to diet. J Exp Biol 217(Pt 11):1894–1901. https://doi.org/10.1242/jeb.101725
Wu S, Zhang XF, Chen XM, Cao PS, Beerntsen BT, Ling EJ (2010) BmToll9, an arthropod conservative toll, is likely involved in the local gut immune response in the silkworm, Bombyx mori. Dev Comp Immunol 34(2):93–96. https://doi.org/10.1016/j.dci.2009.08.010
**a XF, Zheng DD, Zhong HZ, Qin BC, Gurr GM, Vasseur L, You MS (2013) DNA sequencing reveals the midgut microbiota of diamondback moth, Plutella xylostella (L.) and a possible relationship with insecticide resistance. PLoS One 8(7):e68852. https://doi.org/10.1371/journal.pone.0068852
**a X, Yu L, Xue M, Yu X, Vasseur L, Gurr GM, You M (2015) Genome-wide characterization and expression profiling of immune genes in the diamondback moth, Plutella xylostella (L.). Sci Rep 5:9877. https://doi.org/10.1038/srep09877
**a XF, Gurr GM, Vasseur L, Zheng DD, Zhong HZ, Qin BC, You MS (2017) Metagenomic sequencing of diamondback moth gut microbiome unveils key holobiont adaptations for herbivory. Front Microbiol 8:663. https://doi.org/10.3389/fmicb.2017.00663
**a X, Sun B, Gurr GM, Vasseur L, Xue M, You M (2018) Gut microbiota mediate insecticide resistance in the diamondback moth, Plutella xylostella (L.). Front Microbiol 9:25. https://doi.org/10.3389/fmicb.2018.00025
**ao R, Wang X, **e E, Ji T, Li X, Muhammad A, Shi Z (2019) An IMD-like pathway mediates the intestinal immunity to modulate the homeostasis of gut microbiota in Rhynchophorus ferrugineus Olivier (Coleoptera: Dryophthoridae). Dev Comp Immunol 97:20–27. https://doi.org/10.1016/j.dci.2019.03.013
Xu J, Xu X, Li S, Wang S, Xu X, Zhou X, ** F (2017a) Genome-wide profiling of Plutella xylostella immunity-related miRNAs after Isaria fumosorosea infection. Front Physiol 8:1054. https://doi.org/10.3389/fphys.2017.01054
Xu J, Xu XX, Shakeel M, Li SZ, Wang S, Zhou XQ, ** FL (2017b) The entomopathogenic fungi isaria fumosorosea plays a vital role in suppressing the immune system of Plutella xylostella: RNA-Seq and DGE analysis of immunity-related genes. Front Microbiol 8:1–14. https://doi.org/10.3389/fmicb.2017.01421
Yang FY, Saqib HSA, Chen JH, Ruan QQ, Vasseur L, He WY, You MS (2020) Differential profiles of gut microbiota and metabolites associated with host shift of Plutella xylostella. Int J Mol Sci 21(17):6283. https://doi.org/10.3390/ijms21176283
Yao ZC, Wang AL, Li YS, Cai ZH, Lemaitre B, Zhang HY (2016) The dual oxidase gene BdDuox regulates the intestinal bacterial community homeostasis of Bactrocera dorsalis. ISME J 10(5):1037–1050. https://doi.org/10.1038/ismej.2015.202
Yun J-H, Roh SW, Whon TW, Jung M-J, Kim M-S, Park D-S, Choi J-H (2014) Insect gut bacterial diversity determined by environmental habitat, diet, developmental stage, and phylogeny of host. J Appl Environ Microbiol 80(17):5254–5264
Zhang L, Wang YW, Lu ZQ (2015) Midgut immune responses induced by bacterial infection in the silkworm, Bombyx mori. J Zhejiang Univ Sci B 16(10):875–882. https://doi.org/10.1631/jzus.B1500060
Acknowledgments
This work was supported by grants from the National Natural Science Foundation of China (31972345), Natural Science Foundation of Guangdong, China (2018A030313402, 2019A1515011221) and the Key-Area Research and Development Program of Guangdong Province (2019B020218009).
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Shakeel, M., Muhammad, A., Li, S., De Mandal, S., Xu, X., **, F. (2022). Insect Microbiota and Host Immunity: An Emerging Target for Pest Control. In: Mandal, S.D., Ramkumar, G., Karthi, S., **, F. (eds) New and Future Development in Biopesticide Research: Biotechnological Exploration. Springer, Singapore. https://doi.org/10.1007/978-981-16-3989-0_11
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