This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Bertaux J, Schmid M, Prevost-Boure NC, Churin JL, Hartmann A, Garbaye J, Frey-Klett P. In situ identification of intracellular bacteria related to Paenibacillus spp. in the mycelium of the ectomycorrhizal fungus Laccaria bicolor S238N. Appl Environ Microbiol. 2003;69(7):4243–4248. doi:10.1128/AEM.69.7.4243–4248.2003 MedlineBertauxJSchmidMPrevost-BoureNCChurinJLHartmannAGarbayeJFrey-KlettPIn situ identification of intracellular bacteria related to Paenibacillus spp. in the mycelium of the ectomycorrhizal fungus Laccaria bicolor S238NAppl Environ Microbiol200369(7):4243–4248. doi:10.1128/AEM.69.7.4243–4248.2003MedlineOpen DOISearch in Google Scholar
Bianciotto V, Bandi C, Minerdi D, Sironi M, Tichy HV, Bonfante P. An obligately endosymbiotic mycorrhizal fungus itself harbors obligately intracellular bacteria. Appl Environ Microbiol. 1996;62(8):3005–3010. MedlineBianciottoVBandiCMinerdiDSironiMTichyHVBonfantePAn obligately endosymbiotic mycorrhizal fungus itself harbors obligately intracellular bacteriaAppl Environ Microbiol199662(8):3005–3010. Medline10.1128/aem.62.8.3005-3010.19961680878702293Search in Google Scholar
Bianciotto V, Lumini E, Lanfranco L, Minerdi D, Bonfante P, Perotto S. Detection and identification of bacterial endosymbionts in arbuscular mycorrhizal fungi belonging to the family Gigasporaceae. Appl Environ Microbiol. 2000;66(10):4503–4509. doi:10.1128/AEM.66.10.4503–4509.2000 MedlineBianciottoVLuminiELanfrancoLMinerdiDBonfantePPerottoSDetection and identification of bacterial endosymbionts in arbuscular mycorrhizal fungi belonging to the family GigasporaceaeAppl Environ Microbiol200066(10):4503–4509. doi:10.1128/AEM.66.10.4503–4509.2000MedlineOpen DOISearch in Google Scholar
Bianciotto V, Lumini E, Bonfante P, Vandamme P. ‘Candidatus Glomeribacter gigasporarum’ gen. nov., sp. nov., an endosymbiont of arbuscular mycorrhizal fungi. Int J Syst Evol Microbiol. 2003; 53(1): 121–124. doi:10.1099/ijs.0.02382–0 MedlineBianciottoVLuminiEBonfantePVandammeP‘Candidatus Glomeribacter gigasporarum’ gen. nov., sp. nov., an endosymbiont of arbuscular mycorrhizal fungiInt J Syst Evol Microbiol200353(1): 121–124. doi:10.1099/ijs.0.02382–0MedlineOpen DOISearch in Google Scholar
Bonfante P. Plants, mycorrhizal fungi and endobacteria: a dialog among cells and genomes. Biol Bull. 2003;204(2):215–220. doi:10.2307/1543562 MedlineBonfantePPlants, mycorrhizal fungi and endobacteria: a dialog among cells and genomesBiol Bull2003204(2):215–220. doi:10.2307/1543562Medline12700157Open DOISearch in Google Scholar
Cañizares R, Benitez E, Ogunseitan OA. Molecular analyses of β-glucosidase diversity and function in soil. Eur J Soil Biol. 2011; 47(1):1–8. doi:10.1016/j.ejsobi.2010.11.002CañizaresRBenitezEOgunseitanOAMolecular analyses of β-glucosidase diversity and function in soilEur J Soil Biol201147(1):1–8. doi:10.1016/j.ejsobi.2010.11.002Open DOISearch in Google Scholar
Chelius MK, Triplett EW. The diversity of archaea and bacteria in association with the roots of Zea mays L. Microb Ecol. 2001;41(3): 252–263. doi:10.1007/s002480000087 MedlineCheliusMKTriplettEWThe diversity of archaea and bacteria in association with the roots of Zea mays LMicrob Ecol200141(3): 252–263. doi:10.1007/s002480000087Medline11391463Open DOISearch in Google Scholar
Compant S, Clément C, Sessitsch A. Plant growth-promoting bacteria in the rhizo- and endosphere of plants: their role, colonization, mechanisms involved and prospects for utilization. Soil Biol Biochem. 2010;42(5): 669–678. doi:10.1016/j.soilbio.2009.11.024CompantSClémentCSessitschAPlant growth-promoting bacteria in the rhizo- and endosphere of plants: their role, colonization, mechanisms involved and prospects for utilizationSoil Biol Biochem201042(5): 669–678. doi:10.1016/j.soilbio.2009.11.024Open DOISearch in Google Scholar
Cruz AF, Horii S, Ochiai S, Yasuda A, Ishii T. Isolation and analysis of bacteria associated with spores of Gigaspora margarita. J Appl Microbiol. 2008;104(6):1711–1717. doi:10.1111/j.1365–2672.2007.03695.x MedlineCruzAFHoriiSOchiaiSYasudaAIshiiTIsolation and analysis of bacteria associated with spores of Gigaspora margaritaJ Appl Microbiol2008104(6):1711–1717. doi:10.1111/j.1365–2672.2007.03695.xMedlineOpen DOISearch in Google Scholar
Donlan RM, Costerton JW. Biofilms: survival mechanisms of clinically relevant microorganisms. Clin Microbiol Rev. 2002;15(2): 167–193. doi:10.1128/CMR.15.2.167–193.2002 MedlineDonlanRMCostertonJWBiofilms: survival mechanisms of clinically relevant microorganismsClin Microbiol Rev200215(2): 167–193. doi:10.1128/CMR.15.2.167–193.2002MedlineOpen DOISearch in Google Scholar
Fraune S, Anton-Erxleben F, Augustin R, Franzenburg S, Knop M, Schröder K, Willoweit-Ohl D, Bosch TCG. Bacteria-bacteria interactions within the microbiota of the ancestral metazoan Hydra contribute to fungal resistance. ISME J. 2015;9(7): 1543–1556. doi:10.1038/ismej.2014.239 MedlineFrauneSAnton-ErxlebenFAugustinRFranzenburgSKnopMSchröderKWilloweit-OhlDBoschTCGBacteria-bacteria interactions within the microbiota of the ancestral metazoan Hydra contribute to fungal resistanceISME J20159(7): 1543–1556. doi:10.1038/ismej.2014.239Medline447869525514534Open DOISearch in Google Scholar
Frey-Klett P, Burlinson P, Deveau A, Barret M, Tarkka M, Sarniguet A. Bacterial-fungal interactions: hyphens between agricultural, clinical, environmental, and food microbiologists. Microbiol Mol Biol Rev. 2011;75(4):583–609. doi:10.1128/MMBR.00020–11 MedlineFrey-KlettPBurlinsonPDeveauABarretMTarkkaMSarniguetABacterial-fungal interactions: hyphens between agricultural, clinical, environmental, and food microbiologistsMicrobiol Mol Biol Rev201175(4):583–609. doi:10.1128/MMBR.00020–11MedlineOpen DOISearch in Google Scholar
Gyaneshwar P, Hirsch AM, Moulin L, Chen WM, Elliott GN, Bontemps C, Estrada-de los Santos P, Gross E, dos Reis FB Jr, Sprent JI, et al. Legume-nodulating betaproteobacteria: diversity, host range, and future prospects. Mol Plant Microbe Interact. 2011;24(11):1276–1288. doi:10.1094/MPMI-06–11–0172 MedlineGyaneshwarPHirschAMMoulinLChenWMElliottGNBontempsCEstrada-de los SantosPGrossEdos ReisFBJrSprentJILegume-nodulating betaproteobacteria: diversity, host range, and future prospectsMol Plant Microbe Interact201124(11):1276–1288. doi:10.1094/MPMI-06–11–0172MedlineOpen DOISearch in Google Scholar
Hogan DA, Wargo MJ, Beck N. Bacterial biofilms on fungal surfaces, In: Kjelleberg S, Givskov M, editors. The biofilm mode of life: mechanisms and adaptations. Norfolk (United Kingdom): Horizon Scientific Press. 2007; p. 235–245.HoganDAWargoMJBeckNBacterial biofilms on fungal surfaces, In: KjellebergSGivskovM, editors. The biofilm mode of life: mechanisms and adaptationsNorfolk (United Kingdom)Horizon Scientific Press2007; p. 235–245Search in Google Scholar
Kellner H, Luis P, Buscot F. Diversity of laccase-like multicopper oxidase genes in Morchellaceae: identification of genes potentially involved in extracellular activities related to plant litter decay. FEMS Microbiol Ecol. 2007;61(1):153–163. doi:10.1111/j.1574–6941.2007.00322.x MedlineKellnerHLuisPBuscotFDiversity of laccase-like multicopper oxidase genes in Morchellaceae: identification of genes potentially involved in extracellular activities related to plant litter decayFEMS Microbiol Ecol200761(1):153–163. doi:10.1111/j.1574–6941.2007.00322.xMedlineOpen DOISearch in Google Scholar
Khandeparker R, Verma P, Deobagkar D. A novel halotolerant xylanase from marine isolate Bacillus subtilis cho40: gene cloning and sequencing. N Biotechnol. 2011;28(6):814–821. doi:10.1016/j.nbt.2011.08.001 MedlineKhandeparkerRVermaPDeobagkarDA novel halotolerant xylanase from marine isolate Bacillus subtilis cho40: gene cloning and sequencingN Biotechnol201128(6):814–821. doi:10.1016/j.nbt.2011.08.001Medline21890005Open DOISearch in Google Scholar
Król MJ, Perzynski A. [Utilization of benzene as the sole carbon source in fixation of free nitrogen by Azospirillum spp. and Pseudomonas stutzeri strains of bacteria]. (in Polish). Pam Pulaw (Poland). 2005;140:103–115.KrólMJPerzynskiA[Utilization of benzene as the sole carbon source in fixation of free nitrogen by Azospirillum spp. and Pseudomonas stutzeri strains of bacteria]. (in Polish)Pam Pulaw (Poland)2005140103–115Search in Google Scholar
LiPuma JJ. Update on the Burkholderia cepacia complex. Curr Opin Pulm Med. 2005;11(6):528–533. doi:10.1097/01.mcp.0000181475.85187.ed MedlineLiPumaJJUpdate on the Burkholderia cepacia complexCurr Opin Pulm Med200511(6):528–533. doi:10.1097/01.mcp.0000181475.85187.edMedline16217180Open DOISearch in Google Scholar
Lioussanne L, Perreault F, Jolicoeur M, St-Arnaud M. The bacterial community of tomato rhizosphere is modified by inoculation with arbuscular mycorrhizal fungi but unaffected by soil enrichment with mycorrhizal root exudates or inoculation with Phytophthora nicotianae. Soil Biol Biochem. 2010;42(3):473–483. doi:10.1016/j.soilbio.2009.11.034LioussanneLPerreaultFJolicoeurMSt-ArnaudMThe bacterial community of tomato rhizosphere is modified by inoculation with arbuscular mycorrhizal fungi but unaffected by soil enrichment with mycorrhizal root exudates or inoculation with Phytophthora nicotianaeSoil Biol Biochem201042(3):473–483. doi:10.1016/j.soilbio.2009.11.034Open DOISearch in Google Scholar
Otsuka S, Abe Y, Fukui R, Nishiyama M, Sendoo K. Presence of previously undescribed bacterial taxa in non-axenic Chlorella cultures. J Gen Appl Microbiol. 2008;54(4):187–193. doi:10.2323/jgam.54.187 MedlineOtsukaSAbeYFukuiRNishiyamaMSendooKPresence of previously undescribed bacterial taxa in non-axenic Chlorella culturesJ Gen Appl Microbiol200854(4):187–193. doi:10.2323/jgam.54.187Medline18802317Open DOISearch in Google Scholar
Partida-Martinez LP, Groth I, Schmitt I, Richter W, Roth M, Hertweck C. Burkholderia rhizoxinica sp. nov. and Burkholderia endofungorum sp. nov., bacterial endosymbionts of the plant-pathogenic fungus Rhizopus microsporus. Int J Syst Evol Microbiol. 2007a;57(11):2583–2590. doi:10.1099/ijs.0.64660–0 MedlinePartida-MartinezLPGrothISchmittIRichterWRothMHertweckCBurkholderia rhizoxinica sp. nov. and Burkholderia endofungorum sp. nov., bacterial endosymbionts of the plant-pathogenic fungus Rhizopus microsporusInt J Syst Evol Microbiol2007a57(11):2583–2590. doi:10.1099/ijs.0.64660–0MedlineOpen DOISearch in Google Scholar
Partida-Martinez LP, Monajembashi S, Greulich KO, Hertweck C. Endosymbiont-dependent host reproduction maintains bacterial-fungal mutualism. Curr Biol. 2007b;17(9):773–777. doi:10.1016/j.cub.2007.03.039 MedlinePartida-MartinezLPMonajembashiSGreulichKOHertweckCEndosymbiont-dependent host reproduction maintains bacterial-fungal mutualismCurr Biol2007b17(9):773–777. doi:10.1016/j.cub.2007.03.039Medline17412585Open DOISearch in Google Scholar
Pisarska K, Pietr SJ. Biodiversity of dominant cultivable endophytic bacteria inhabiting tissues of six different cultivars of maize (Zea mays L. ssp. mays) cropped under field conditions. Pol J Microbiol. 2015;64(2):163–170. MedlinePisarskaKPietrSJBiodiversity of dominant cultivable endophytic bacteria inhabiting tissues of six different cultivars of maize (Zea mays L. ssp. mays) cropped under field conditionsPol J Microbiol201564(2):163–170. Medline10.33073/pjm-2015-024Search in Google Scholar
Pierce GE. Pseudomonas aeruginosa, Candida albicans, and device-related nosocomial infections: implications, trends, and potential approaches for control. J Ind Microbiol Biotechnol. 2005;32(7): 309–318. doi:10.1007/s10295–005–0225–2 MedlinePierceGEPseudomonas aeruginosa, Candida albicans, and device-related nosocomial infections: implications, trends, and potential approaches for controlJ Ind Microbiol Biotechnol200532(7): 309–318. doi:10.1007/s10295–005–0225–2MedlineOpen DOISearch in Google Scholar
Rekuc A, Kruczkiewicz P, Kielczynski R, Jastrzembska B, Bryjak J. [Laccase production and its immobilation on selcted media]. (in Polish). Acta Sci Pol Biotechnol. 2006;1(05):3–15.RekucAKruczkiewiczPKielczynskiRJastrzembskaBBryjakJ[Laccase production and its immobilation on selcted media]. (in Polish)Acta Sci Pol Biotechnol20061(05):3–15Search in Google Scholar
Sarand I, Timonen S, Nurmiaho-Lassila EL, Koivula T, Haahtela K, Romantschuk M, Sen R. Microbial biofilms and catabolic plasmid harbouring degradative fluorescent pseudomonads in Scots pine mycorrhizospheres developed on petroleum contaminated soil. FEMS Microbiol Ecol. 1998 Oct;27(2):115–126. doi:10.1111/j.1574–6941.1998.tb00529.xSarandITimonenSNurmiaho-LassilaELKoivulaTHaahtelaKRomantschukMSenRMicrobial biofilms and catabolic plasmid harbouring degradative fluorescent pseudomonads in Scots pine mycorrhizospheres developed on petroleum contaminated soilFEMS Microbiol Ecol1998 Oct;27(2):115–126. doi:10.1111/j.1574–6941.1998.tb00529.xOpen DOISearch in Google Scholar
Singh RK, Mishra RPN, Jaiswal HK, Kumar V, Pandey SP, Rao SB, Annapurna K. Isolation and identification of natural endophytic rhizobia from rice (Oryza sativa L.) through rDNA PCR-RFLP and sequence analysis. Curr Microbiol. 2006;52(2):117–122. doi:10.1007/s00284–005–0136–5 MedlineSinghRKMishraRPNJaiswalHKKumarVPandeySPRaoSBAnnapurnaKIsolation and identification of natural endophytic rhizobia from rice (Oryza sativa L.) through rDNA PCR-RFLP and sequence analysisCurr Microbiol200652(2):117–122. doi:10.1007/s00284–005–0136–5MedlineOpen DOISearch in Google Scholar
Yara R, Azevedo JL, Maccheroni W, Kitajima EW, Leite B. Mycoplasma associated with cultures of the ligno-cellulolytic fungus Pleurotus sp. Acta Microsc. 1999;8:851–852.YaraRAzevedoJLMaccheroniWKitajimaEWLeiteBMycoplasma associated with cultures of the ligno-cellulolytic fungus Pleurotus spActa Microsc19998851–852Search in Google Scholar
Yara R, Maccheroni W Jr, Horii J, Azevedo JL. A bacterium belonging to the Burkholderia cepacia complex associated with Pleurotus ostreatus. J Microbiol. 2006;44(3):263–268. MedlinYaraRMaccheroniWJrHoriiJAzevedoJLA bacterium belonging to the Burkholderia cepacia complex associated with Pleurotus ostreatusJ Microbiol200644(3):263–268. MedlinSearch in Google Scholar
