Abstract
The ambrosia beetles are farming insects that feed mainly on their cultivated fungi, which in some occasions are pathogens from forest and fruit trees. We used a culture-independent approach based on 16S and 18S rRNA gene metabarcoding analysis to investigate the diversity and composition of the bacterial and fungal communities associated with five ambrosia beetle species: four species native to America (Monarthrum dimidiatum, Dryocoetoides capucinus, Euwallacea discretus, Corthylus consimilis) and an introduced species (Xylosandrus morigerus). For the bacterial community, the beetle species hosted a broad diversity with 1,579 amplicon sequence variants (ASVs) and 66 genera, while for the fungal community they hosted 288 ASVs and 39 genera. Some microbial groups dominated the community within a host species or a body part (Wolbachia in the head-thorax of E. discretus; Ambrosiella in the head-thorax and abdomen of X. morigerus). The taxonomic composition and structure of the microbial communities appeared to differ between beetle species; this was supported by beta-diversity analysis, which indicated that bacterial and fungal communities were clustered mainly by host species. This study characterizes for the first time the microbial communities associated with unexplored ambrosia beetle species, as well as the factors that affect the composition and taxonomic diversity per se, contributing to the knowledge of the ambrosia beetle system.
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Data availability
The 16S and 18S amplicon sequence data are available on NCBI (PRJNA1049028) and can be accessed at https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1049028
References
Adams AS, Six DL, Adams SM, Holben WE (2008) In vitro interactions between yeasts and bacteria and the fungal symbionts of the mountain pine beetle (Dendroctonus ponderosae). Microb Ecol 56:460–466. https://doi.org/10.1007/s00248-008-9364-0
Amir A, Daniel M, Navas-Molina J, Kopylova E, Morton J, Xu ZZ, Eric K, Thompson L, Hyde E, Gonzalez A, Knight R (2017) Deblur Rapidly Resolves Single-Nucleotide Community Sequence Patterns. Am Soc Microbiol 2:1–7
Ángel-Restrepo M, Parra PP, Ochoa-Ascencio S, Fernández-Pavía S, Vázquez-Marrufo G, Equihua-Martínez A, Barrientos-Priego AF, Ploetz RC, Konkol JL, Saucedo-Carabez JR, Gazis R (2022) First look into the ambrosia beetle-fungus symbiosis present in commercial avocado orchards in Michoacán, Mexico. Environ Entomol. 2;51(2):385–396. https://doi.org/10.1093/ee/nvab142.
Araújo JPM, Li Y, Duong TA, Smith ME, Adams S, Hulcr J (2022) Four New Species of Harringtonia: Unravelling the Laurel Wilt Fungal Genus. J Fungi 8 8(6):613. https://doi.org/10.3390/jof8060613
Ayala-Silva T, Ledesma N (2014) Avocado History, Biodiversity and Production
Aylward FO, Suen G, Biedermann PHW, Adams AS, Scott JJ, Malfatti SA, del Rio T, Tringe SG, Poulsen M, Raffa KF, Klepzig KD, Currie CR (2014) Convergent bacterial microbiotas in the fungal agricultural systems of insects. MBio 5:e02077--14, /mbio/5/6/e02077--14.atom. https://doi.org/10.1128/mBio.02077-14
Bateman C, Huang YT, Simmons DR, Kasson MT, Stanley EL, Hulcr J (2017) Ambrosia beetle Premnobius cavipennis (Scolytinae: Ipini) carries highly divergent ascomycotan ambrosia fungus, Afroraffaelea ambrosiae gen. nov. et sp. nov. (Ophiostomatales). Fungal Ecol 25:41–49. https://doi.org/10.1016/j.funeco.2016.10.008
Bateman C, Šigut M, Skelton J, Smith KE, Hulcr J (2016) Fungal associates of the Xylosandrus compactus (Coleoptera: Curculionidae, Scolytinae) Are Spatially Segregated on the Insect Body. Environ Entomol 45:883–890. https://doi.org/10.1093/ee/nvw070
Batra LR (1963) Ecology of ambrosia fungi and their dissemination by beetles. Trans Kans Acad Sci 66(2):213–236
Beaver RA (1989) Insect–fungus relationships in the bark and ambrosia beetles. In: Wilding N, Collins NM, Hammond PM, Webber JF (eds) Insect-fungus Interactions. Academic, San Diego, pp 121–143
Benjamin RK, Blackwell M, Chapela IH, Humber RA, Jones KG, Klepzing KD, Lichtwardt RW, Malloch D, Noda H, R.A. R, Spatafora JW, Weir A (2004) INSECT- AND OTHER ARTHROPOD-ASSOCIATED FUNGI. In: Mueller GM, Foster MS, Bills GF (eds) Biodiversity of fungi: inventory and monitoring methods. Elsevier Inc., pp 247–255
Bolyen E, Dillon M, Bokulich N, Abnet C, Al-Ghalith G, Alexander H, Alm E, Arumugam M, Asnicar F, Bai Y, Bisanz J, Bittinger K, Brejnrod A, Brislawn C, Brown T, Callahan B, Chase J, Cope E, Dorrestein P, Douglas G, Durall D, Duvallet C, Edwardson C, Ernst M, Estaki M, Fouquier J, Gauglitz J, Gibson D, Gonzalez A, Gorlick K, Guo J, Hillmann B, Holmes S, Holste H, Huttenhower C, Huttley G, Janssen S, Jarmusch A, Jiang L, Kaehler B, Keefe C, Keim P, Kelley S, Knights D, Koester I, Kosciolek T, Kreps J, Lee J, Ley R, Liu Y-X, Loftfield E, Lozupone C, Maher M, Marotz C, Martin B, McDonald D, McIver L, Melnik A, Metcalf J, Morgan S, Morton J, Navas-Molina J, Orchanian S, Pearson T, Peoples S, Petras D, Pruesse E, Rivers A, Robeson M, Rosenthal P, Segata N, Shaffer M, Shiffer A, Sinha R, Spear J, Swafford A, Thompson L, Torres P, Trinh P, Tripathi A, Turnbaugh P, Ul-Hasan S, Vargas F, Vogtmann E, Walters W, Wan Y, Wang M, Warren J, Weber K, Willis A, Zaneveld J, Zhang Y, Zhu Q, Knight R, Caporaso G (2018) QIIME 2: Reproducible, interactive, scalable, and extensible microbiome data science. PeerJ Prepr.https://doi.org/10.7287/peerj.preprints.27295
Bouchard P, Bousquet Y, Davies AE, Alonso-Zarazaga MA, Lawrence JF, Lyal CHC, Newton AF, Reid CAM, Schmitt M, Ślipiński SA, Smith ABT (2011) Family-group names in Coleoptera (Insecta). Zookeys 1–972. https://doi.org/10.3897/zookeys.88.807
Bray JR, Curtis JT (1957) An ordination of the upland forest communities of Southern Wisconsin. Ecol Monogr 27:325–349
Broderick NA, Raffa KF, Goodman RM, Handelsman J (2004) Census of the bacterial community of the gypsy moth larval midgut by using culturing and culture-independent methods. Appl Environ Microbiol 70:293–300. https://doi.org/10.1128/AEM.70.1.293-300.2004
Cambronero-Heinrichs JC, Battisti A, Biedermann PHW, Cavaletto G, Castro-Gutierrez V, Favaro L, Santoiemma G, Rassati D (2023) Erwiniaceae bacteria play defensive and nutritional roles in two widespread ambrosia beetles. FEMS Microbiol Ecol 99:1–11. https://doi.org/10.1093/femsec/fiad144
Cardoza YJ, Klepzig KD, Raffa KF (2006) Bacteria in oral secretions of an endophytic insect inhibit antagonistic fungi. Ecol Entomol 31:636–645. https://doi.org/10.1111/j.1365-2311.2006.00829.x
Carreras-Villaseñor N, Rodríguez-Haas JB, Martínez-Rodríguez LA, Pérez-Lira AJ, Ibarra-Laclette E, Villafán E, Castillo-Díaz AP, Ibarra-Juárez LA, Carrillo-Hernández ED, Sánchez-Rangel D (2022) Characterization of two fusarium solani species complex isolates from the ambrosia beetle Xylosandrus morigerus. J Fungi 8. https://doi.org/10.3390/jof8030231
Carrillo D, Cruz LF, Kendra PE, Narvaez TI, Montgomery WS, Monterroso A, De Grave C, Cooperband MF (2016) Distribution, pest status and fungal associates of Euwallacea nr. fornicatus in Florida avocado groves. Insects 7:1–11. https://doi.org/10.3390/insects7040055
Carrillo D, Duncan RE, Peña JE (2012) Ambrosia beetles (Coleoptera: Curculionidae: Scolytinae) that breed in avocado wood in Florida. Florida Entomol 95:573–579. https://doi.org/10.1653/024.095.0306
Carrillo D, Duncan RE, Ploetz JN, Campbell AF, Ploetz RC, Peña JE (2014) Lateral transfer of a phytopathogenic symbiont among native and exotic ambrosia beetles. Plant Pathol 63:54–62. https://doi.org/10.1111/ppa.12073
Ceriani-Nakamurakare E, Mc Cargo P, Gonzalez-Audino P, Ramos S, Carmarán C (2020) New insights into fungal diversity associated with Megaplatypus mutatus: gut mycobiota. Symbiosis 81:127–137. https://doi.org/10.1007/s13199-020-00687-8
Chen H, Boutros PC (2011) VennDiagram: A package for the generation of highly-customizable Venn and Euler diagrams in R. BMC Bioinformatics 12. https://doi.org/10.1186/1471-2105-12-35
Cruz LF, Menocal O, Mantilla J, Ibarra-Juarez LA, Carrillo D (2019) Xyleborus volvulus (Coleoptera: Curculionidae): Biology and fungal associates. Appl Environ Microbiol 85. https://doi.org/10.1128/AEM.01190-19
Daehler CC, Dudley N (2002) Impact of the black twig borer, an introduced insect pest, on Acacia koa in the Hawaiian Islands. Micronesia Suppl 6:35–53
Darriba D, Taboada G, Doallo R, Posada D (2012) jModelTest 2: more models, new heuristics and parallel computing. Nat Methods 9:772. https://doi.org/10.1038/nmeth.2109
Davis TS, Hofstetter RW, Foster JT, Foote NE, Keim P (2011) Interactions Between the Yeast Ogataea pini and Filamentous Fungi Associated with the Western Pine Beetle. Microb Ecol 61:626–634. https://doi.org/10.1007/s00248-010-9773-8
Dreaden TJ, Davis JM, de Beer ZW, Ploetz RC, Soltis PS, Wingfield MJ, Smith JA (2014) Phylogeny of ambrosia beetle symbionts in the genus Raffaelea. Fungal Biol 118:970–978. https://doi.org/10.1016/j.funbio.2014.09.001
Foster ZSL, Sharpton TJ, Grunwald NJ (2017) Metacoder : An R package for visualization and manipulation of community taxonomic diversity data. PLoS Comput Biol 13:1–15. https://doi.org/10.5281/zenodo.158228
Fraedrich SW, Harrington TC, Rabaglia RJ, Ulyshen MD, Mayfield AE, Hanula JL, Eickwort JM, Miller DR (2008) A Fungal Symbiont of the Redbay Ambrosia Beetle Causes a Lethal Wilt in Redbay and Other Lauraceae in the Southeastern United States. Plant Dis 92:215–224. https://doi.org/10.1094/PDIS-92-2-0215
Francke-Grosmann H (1956) Hautdrüsen als Träger der Pilzsymbiose bei Ambrosiakäfern. Z Morphol Okol Tiere 45:275–308
Freeman S, Sharon M, Dori-Bachash M, Maymon M, Belausov E, Maoz Y, Margalit O, Protasov A, Mendel Z (2016) Symbiotic association of three fungal species throughout the life cycle of the ambrosia beetle Euwallacea nr. fornicatus. Symbiosis 68:115–128. https://doi.org/10.1007/s13199-015-0356-9
Freeman S, Sharon M, Maymon M, Mendel Z, Protasov A, Aoki T, Eskalen A, O’Donnell K (2013) Fusarium euwallaceae sp. nov.–a symbiotic fungus of Euwallacea sp., an invasive ambrosia beetle in Israel and California. Mycologia 105:1595–1606. https://doi.org/10.3852/13-066
Fukuda TTH, Helfrich EJN, Mevers E, Melo WGP, van Arnam EB, Andes DR, Currie CR, Pupo MT, Clardy J (2021) Specialized metabolites reveal evolutionary history and geographic dispersion of a multilateral symbiosis. ACS Cent Sci 7:292–299. https://doi.org/10.1021/acscentsci.0c00978
Funk A (1965) the Symbiotic Fungi of Certain Ambrosia Beetles in British Columbia. Can J Bot 43:929–932. https://doi.org/10.1139/b65-103
Galko J, Dzurenko M, Ranger CM, Kulfan J, Kula E, Nikolov C, Zúbrik M, Zach P (2019) Distribution, habitat preference, and management of the invasive ambrosia beetle xylosandrus germanus (Coleoptera: Curculionidae, Scolytinae) in European forests with an emphasis on the West Carpathians. Forests 10. https://doi.org/10.3390/f10010010
García-Avila CDJ, Trujillo-Arriaga FJ, López-Buenfil JA, González-Gómez R, Carrillo D, Cruz LF, Ruiz-Galván I, Quezada-Salinas A, Acevedo-Reyes N (2016) First Report of Euwallacea nr. fornicatus (Coleoptera: Curculionidae) in Mexico. Florida Entomol 99:555–556. https://doi.org/10.1653/024.099.0335
García-Fraile P (2018) Roles of bacteria in the bark beetle holobiont – how do they shape this forest pest? Ann Appl Biol 172:111–125. https://doi.org/10.1111/aab.12406
Gibson CM, Hunter MS (2010) Extraordinarily widespread and fantastically complex: Comparative biology of endosymbiotic bacterial and fungal mutualists of insects. Ecol Lett 13:223–234. https://doi.org/10.1111/j.1461-0248.2009.01416.x
Grubbs KJ, Surup F, Biedermann PHW, McDonald BR, Klassen JL, Carlson CM, Clardy J, Currie CR (2020) Cycloheximide-Producing Streptomyces Associated With Xyleborinus saxesenii and Xyleborus affinis Fungus-Farming Ambrosia Beetles. Front Microbiol 11:1–12. https://doi.org/10.3389/fmicb.2020.562140
Haeder S, Wirth R, Herz H, Spiteller D (2009) Candicidin-producing Streptomyces support leaf-cutting ants to protect their fungus garden against the pathogenic fungus Escovopsis. Proc Natl Acad Sci U S A 106:4742–4746. https://doi.org/10.1073/pnas.0812082106
Huelsenbeck JP, Ronquist F (2001) MrBayes: Bayesian inference of phylogenetic trees. Bioinformatics 17:754–755. https://doi.org/10.1093/bioinformatics/17.8.754
Hughes MA, Smith JA, Ploetz RC, Kendra PE, Mayfield AE, Hanula JL, Hulcr J, Stelinski LL, Cameron S, Riggins JJ, Carrillo D, Rabaglia R, Eickwort J, Pernas T (2015) Recovery Plan for Laurel Wilt on Redbay and Other Forest Species Caused by Raffaelea lauricola and Disseminated by Xyleborus glabratus. Plant Heal Prog 16:173–210. https://doi.org/10.1094/PHP-RP-15-0017
Hulcr J, Dunn RR (2011) The sudden emergence of pathogenicity in insect-fungus symbioses threatens naive forest ecosystems. Proc R Soc B Biol Sci 278:2866–2873. https://doi.org/10.1098/rspb.2011.1130
Hulcr J, Mann R, Stelinski LL (2011) The scent of a partner: ambrosia beetles are attracted to volatiles from their fungal symbionts. J Chem Ecol 37:1374–1377. https://doi.org/10.1007/s10886-011-0046-x
Hulcr J, Rountree NR, Diamond SE, Stelinski LL, Fierer N, Dunn RR (2012) Mycangia of ambrosia beetles host communities of bacteria. Microb Ecol 64:784–793. https://doi.org/10.1007/s00248-012-0055-5
Hulcr J, Stelinski LL (2017) The Ambrosia Symbiosis: From Evolutionary Ecology to Practical Management. Annu Rev Entomol 62:285–303. https://doi.org/10.1146/annurev-ento-031616-035105
Ibarra-Juarez L, Desgarennes D, Vázquez-Rosas-Landa M, Villafan E, Alonso-Sánchez A, Ferrera-Rodríguez O, Moya A, Carrillo D, Cruz L, Carrión G, López-Buenfil A, García-Avila C, Ibarra-Laclette E, Lamelas A (2018) Impact of rearing conditions on the ambrosia beetle’s microbiome. Life 8:63. https://doi.org/10.3390/life8040063
Ibarra-Juarez LA, Burton MAJ, Biedermann PHW, Cruz L, Desgarennes D, Ibarra-Laclette E, Latorre A, Alonso-Sánchez A, Villafan E, Hanako-Rosas G, López L, Vázquez-Rosas-Landa M, Carrion G, Carrillo D, Moya A, Lamelas A (2020) Evidence for succession and putative metabolic roles of fungi and bacteria in the farming mutualism of the ambrosia beetle Xyleborus affinis. mSystems 5. https://doi.org/10.1128/msystems.00541-20
Ibarra-Laclette E, Sánchez-Rangel D, Hernández-Domínguez E, Pérez-Torres CA, Ortiz-Castro R, Villafán E, Alonso-Sánchez A, Rodríguez-Haas B, López-Buenfil A, García-Avila C, Ramírez-Pool JA (2017) Draft genome sequence of the phytopathogenic fungus Fusarium euwallaceae, the causal agent of Fusarium dieback. Genome Announc 5:349–351. https://doi.org/10.1128/genomeA.00881-17
Jiang ZR, Masuya H, Kajimura H (2021) Novel symbiotic association between Euwallacea Ambrosia Beetle and Fusarium Fungus on Fig Trees in Japan. Front Microbiol 12:1–10. https://doi.org/10.3389/fmicb.2021.725210
Jiang ZR, Masuya H, Kajimura H (2022) Fungal flora in adult females of the rearing population of ambrosia beetle Euwallacea interjectus (Blandford) (Coleoptera: Curculionidae: Scolytinae): Does It Differ from the Wild Population? Diversity 14. https://doi.org/10.3390/d14070535
Kajtoch Ł, Kotásková N (2018) Current state of knowledge on Wolbachia infection among Coleoptera: A systematic review. PeerJ 2018:1–31. https://doi.org/10.7717/peerj.4471
Kandasamy D, Gershenzon J, Andersson MN, Hammerbacher A (2019) Volatile organic compounds influence the interaction of the Eurasian spruce bark beetle (Ips typographus) with its fungal symbionts. ISME J 13:1788–1800. https://doi.org/10.1038/s41396-019-0390-3
Katoh K, Standley DM (2013) MAFFT multiple sequence alignment software version 7: Improvements in performance and usability. Mol Biol Evol 30:772–780. https://doi.org/10.1093/molbev/mst010
Kawasaki Y, Schuler H, Stauffer C, Lakatos F, Kajimura H (2016) Wolbachia endosymbionts in haplodiploid and diploid scolytine beetles (Coleoptera: Curculionidae: Scolytinae). Environ Microbiol Rep 8:680–688. https://doi.org/10.1111/1758-2229.12425
Kikuchi Y (2018) Detoxifying symbiosis: Microbe-mediated detoxification of phytotoxins and pesticides in insects. Nat Prod Rep 35:434–454
Klindworth A, Pruesse E, Schweer T, Peplies J, Quast C, Horn M, Glöckner FO (2013) Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res 41:e1. https://doi.org/10.1093/nar/gks808
KnÍŽek M, Beaver R (2007) Taxonomy and Systematics of Bark and Ambrosia Beetles.In: Lieutier F, Day KR, Battisti A, Grégoire JC, Evans HF (eds) Bark and Wood Boring Insects in Living Trees in Europe, a Synthesis. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-2241-8_5
Kolasa M, Ścibior R, Mazur MA, Kubisz D, Dudek K, Kajtoch Ł (2019) How hosts taxonomy, trophy, and endosymbionts shape microbiome diversity in beetles. Microb Ecol.https://doi.org/10.1007/s00248-019-01358-y
Kostovcik M, Bateman CC, Kolarik M, Stelinski LL, Jordal BH, Hulcr J (2015) The ambrosia symbiosis is specific in some species and promiscuous in others: evidence from community pyrosequencing. ISME J 9:126–138. https://doi.org/10.1038/ismej.2014.115
Letunic I, Bork P (2019) Interactive Tree of Life (iTOL) v4: Recent updates and new developments. Nucleic Acids Res 47:256–259. https://doi.org/10.1093/nar/gkz239
Lex A, Gehlenborg N, Strobelt H, Vuillemot R, Pfister H (2014) UpSet: Visualization of intersecting sets. IEEE Trans vis Comput Graph 20:1983–1992. https://doi.org/10.1109/TVCG.2014.2346248
Lorea-Hernández FG (2002) La familia Lauraceae en el sur de México: Diversidad, distribución y estado de conservación. Bot Sci 70:59–70. https://doi.org/10.17129/botsci.1663
Lynch SC, Twizeyimana M, Mayorquin JS, Wang DH, Na F, Kayim M, Kasson MT, Thu PQ, Bateman C, Rugman-Jones P, Hulcr J, Stouthamer R, Eskalen A (2016) Identification, pathogenicity and abundance of Paracremonium pembeum sp. nov. and Graphium euwallaceae sp. nov.-two newly discovered mycangial associates of the polyphagous shot hole borer (Euwallacea sp.) in California. Mycologia 108:313–329. https://doi.org/10.3852/15-063
Masuya H (2007) Note on the dieback of Cornus florida caused by Xylosandrus compactus. Bull For For Prod Res Institute, Ibaraki
Mayers CG, Bateman CC, Harrington TC (2018) New Meredithiella species from mycangia of Corthylus ambrosia beetles suggest genus-level coadaptation but not species-level coevolution. Mycologia 110:63–78. https://doi.org/10.1080/00275514.2017.1400353
Mayers CG, Harrington TC, Biedermann PHW (2022) Mycangia Define the Diverse Ambrosia Beetle-Fungus Symbioses. In: Schultz T, Peregrine P, Gawne R (eds) The Convergent Evolution of Agriculture in Humans and Insects. MIT Press, Cambridge
Miller KE, Inward DJ, Gomez-Rodriguez C, Baselga A, Vogler AP (2019) Predicting the unpredictable: How host specific is the mycobiota of bark and ambrosia beetles? Fungal Ecol 42:100854. https://doi.org/10.1016/j.funeco.2019.07.008
O’Donnell K, Libeskind-Hadas R, Hulcr J, Bateman C, Kasson MT, Ploetz RC, Konkol JL, Ploetz JN, Carrillo D, Campbell A, Duncan RE, Liyanage PNH, Eskalen A, Lynch SC, Geiser DM, Freeman S, Mendel Z, Sharon M, Aoki T, Cossé AA, Rooney AP (2016) Invasive Asian Fusarium – Euwallacea ambrosia beetle mutualists pose a serious threat to forests, urban landscapes and the avocado industry. Phytoparasitica 44:435–442. https://doi.org/10.1007/s12600-016-0543-0
Oksanen J, Blanchet FG, Friendly M, Kindt R, Legendre P, McGlinn D, Minchin PR, O’Hara RB, Simpson GL, Solymos P, Stevens MHH, Szoecs E, Wagner H (2018) Vegan: Community Ecology Package. R Package Version 2.5–1. https://CRANR-project.org/package=vegan
Ploetz RC, Konkol JL, Narvaez T, Duncan RE, Saucedo RJ, Campbell A, Mantilla J, Carrillo D, Kendra PE (2017) Presence and prevalence of Raffaelea lauricola, cause of laurel wilt, in different species of Ambrosia Beetle in Florida. USA J Econ Entomol 110:347–354. https://doi.org/10.1093/jee/tow292
Rassati D, Marini L, Malacrinò A (2019) Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion. PeerJ 7:e8103. https://doi.org/10.7717/peerj.8103
Rugman-Jones PF, Hoddle MS, Mound LA, Stouthamer R (2006) Molecular Identification Key for Pest Species of Scirtothrips (Thysanoptera: Thripidae). J Econ Entomol 99:7
Scarborough CL, Ferrari J, Godfray HC (2005) Aphid Protected from Pathogen. Science (80- ) 310:2005
Scott JJ, Oh D-C, Yuceer C, Klepzig KD, Clardy J, Currie CR (2008) Bacterial protection of beetle-fungus mutualism. Science 322(5898):63–63. https://doi.org/10.1126/science.1160423.Bacterial
Six DL (2013) The Bark Beetle Holobiont: Why Microbes Matter. J Chem Ecol 39:989–1002. https://doi.org/10.1007/s10886-013-0318-8
Six DL (2012) Ecological and Evolutionary Determinants of Bark Beetle —Fungus Symbioses. Insects 3:339–366. https://doi.org/10.3390/insects3010339
Six DL (2003) Bark Beetle-Fungus Symbioses. Insect Symbiosis Contemp Top Entomol Ser
Skelton J, Johnson AJ, Jusino MA, Bateman CC, Li Y, Hulcr J (2019) A selective fungal transport organ (mycangium) maintains coarse phylogenetic congruence between fungus-farming ambrosia beetles and their symbionts. Proc R Soc B Biol Sci 286:20182127. https://doi.org/10.1098/rspb.2018.2127
Suárez-Moo P, Cruz-Rosales M, Ibarra-Laclette E, Desgarennes D, Huerta C, Lamelas A (2020) Diversity and Composition of the Gut Microbiota in the Developmental Stages of the Dung Beetle Copris incertus Say (Coleoptera, Scarabaeidae). Front Microbiol 11:1–12. https://doi.org/10.3389/fmicb.2020.01698
Team Rs (2015) RStudio: Integrated Development for R
Therrien J, Mason CJ, Cale JA, Adams A, Aukema BH, Currie CR, Raffa KF, Erbilgin N (2015) Bacteria influence mountain pine beetle brood development through interactions with symbiotic and antagonistic fungi: implications for climate-driven host range expansion. Oecologia 179:467–485. https://doi.org/10.1007/s00442-015-3356-9
Tsuchida T, Koga R, Horikawa M, Tsunoda T, Maoka T, Matsumoto S, Simon JC, Fukatsu T (2010) Symbiotic bacterium modifies aphid body color. Science (80- ) 330:1102–1104. https://doi.org/10.1126/science.1195463
Weiss B, Aksoy S (2011) Microbiome influences on insect host vector competence. Trends Parasitol 27:514–522. https://doi.org/10.1016/j.pt.2011.05.001
Wood SL (1986) A reclassification of the genera of Scolytidae (Coleoptera), 10th ed
Wood SL (1982) The bark and ambrosia beetles of North and Central America (Coleoptera: Scolytidae), a taxonomic monograph, 6th ed. Great Basin Naturalist Memoirs
Yuceer C, Hsu CY, Erbilgin N, Klepzig KD (2011) Ultrastructure of the mycangium of the southern pine beetle, Dendroctonus frontalis (Coleoptera: Curculionidae, Scolytinae): complex morphology for complex interactions. Acta Zool 92:216–224. https://doi.org/10.1111/j.1463-6395.2011.00500.x
Yun JH, Roh SW, Whon TW, Jung MJ, Kim MS, Park DS, Yoon C, Do NY, Kim YJ, Choi JH, Kim JY, Shin NR, Kim SH, Lee WJ, Bae JW (2014) Insect gut bacterial diversity determined by environmental habitat, diet, developmental stage, and phylogeny of host. Appl Environ Microbiol 80:5254–5264. https://doi.org/10.1128/AEM.01226-14
Acknowledgements
We would like to thank Ann Grant and Sean Rovito for her helpful discussions and suggestions. We also thank Guadalupe Hernández Cervantes for the processing of the biological samples and T. H. Atkinson for the photographs of the beetle specimens. We are grateful for the support of Consejo Nacional de Humanidades, Ciencias y Tecnologías (CONAHCyT) for a postdoctoral Fellowship to PSM (362331) and the Fondo Institucional de Fomento Regional para el Desarrollo Científico Tecnológico y de Innovación (FORDECyT), Grant No. 292399
Funding
This work was supported by Fondo Institucional de Fomento Regional para el Desarrollo Científico Tecnológico y de Innovación (FORDECyT) from Consejo Nacional de Ciencia y Tecnología (CONACyT), grant No. 292399.
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Araceli Lamelas and Arturo Ibarra Juarez designed the research. Arturo Ibarra-Juarez and Paulette Calleros-González contributed to experimental work. Paulette Calleros-González and Pablo Suárez-Moo performed the data analysis and wrote the manuscript. Pablo Suárez-Moo and Araceli Lamelas revised the manuscript. All authors reviewed and approved the manuscript.
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Calleros-González, P., Ibarra-Juarez, A., Lamelas, A. et al. How host species and body part determine the microbial communities of five ambrosia beetle species. Int Microbiol (2024). https://doi.org/10.1007/s10123-024-00502-0
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DOI: https://doi.org/10.1007/s10123-024-00502-0