Journals / Uludağ Arıcılık Dergisi / 2026 / Volume: 25 Issue: 1

STRATEGIES AND MECHANISMS OF PLANT-MICROBIOME-POLLINATOR COADAPTATION

Bitki-Mikrobiyom-Polinatör Ko-adaptasyon Stratejileri ve Mekanizmaları

Rustem Ilyasov(Koltzov Institute of Developmental Biology, Russian Academy of Sciences)0000-0003-2445-4739
Alla Ilyasova(Koltsov Institute of Developmental Biology of Russian academy of Sciences)0000-0002-7505-6805
Valery Danilenko(Vavilov Institune of General Genetics, Russian Academy of Sciences)0000-0001-5780-0621
Meral Kekeçoğlu(DÜZCE ÜNİVERSİTESİ)0000-0002-2564-8343
Pham Hong Thaı(Vietnam national University of Agriculture, Research Center for Tropical Bees and Beekeeping)0000-0002-6441-1402
Svetlana Khrapova(Russian State Agrarian University named after K.A. Timiryazev)0000-0002-1808-2302
Alfir Mannapov(Russian State Agrarian University named after K.A. Timiryazev)0000-0002-5093-9740
Sofia Prokudina(Koltsov Institute of Developmental Biology of Russian academy of Sciences)0009-0003-2594-7663
Vener Sattarov(Bashkir State Pedagogical University named after M. Akmulla)0000-0001-6331-4398
Dmitry Boguslavsky(Koltsov Institute of Developmental Biology of Russian academy of Sciences)0000-0001-9601-640X
Pages
—
Publication Date
2025-05-30
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Understanding these interactions is vital for predicting how climate change and habitat loss threaten pollination, affecting agriculture and biodiversity.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Plant-pollinator interactions showcase mutualistic coevolution, but the role of microorganisms in these relationships is often overlooked.
📊
Key Findings & Data:Nectar-dwelling microorganisms, mainly yeasts and bacteria, significantly influence floral chemistry, pollinator behavior, and plant reproduction.
💡
Conclusion & Impact:Understanding these interactions is vital for predicting how climate change and habitat loss threaten pollination, affecting agriculture and biodiversity.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Honey bee · Pollinators · Microbiome

Abstract

Plant-pollinator interactions showcase mutualistic coevolution, but the role of microorganisms in these relationships is often overlooked. Nectar-dwelling microorganisms, mainly yeasts and bacteria, significantly influence floral chemistry, pollinator behavior, and plant reproduction. These microorganisms alter nectar’s sugar content, amino acid profiles, pH, and scent emissions, shaping pollinator preferences. For example, the yeast Metschnikowia reukaufii produces fruity esters that attract bumble bees, while some bacteria lower pH, repelling honey bees. Pollinators spread these microorganisms between flowers, creating a feedback loop that shapes microbial communities and drives coevolution. Beyond nectar, microorganisms' impact on thermal regulation through metabolic heat, pollen health, and pollinator gut microbiomes. Specialized bacteria like Rosenbergiella nectarea and Acinetobacter spp. thrive in nectar’s high-sugar environment, while pollinator microorganisms, such as Lactobacillus kunkeei, protect honey bees from pathogens. Microbial diversity varies by region, with tropical flowers hosting richer communities than temperate ones. This review highlights how microorganisms act as key players in plant-pollinator networks, boosting pollinator nutrition, immunity, and foraging efficiency. It explores microbial spread, competition, and chemical influence, calling for studies that blend microbiology, ecology, and evolution. Understanding these interactions is vital for predicting how climate change and habitat loss threaten pollination, affecting agriculture and biodiversity.

Özet

Bitki-polinatör etkileşimleri, karşılıklı faydaya dayalı ko-evrimi sergilemektedir; ancak mikroorganizmaların bu ilişkilerdeki rolü genellikle göz ardı edilmektedir. Başlıca mayalar ve bakterilerden oluşan nektarda yaşayan mikroorganizmalar, çiçek kimyasını, polinatör davranışını ve bitki üremesini önemli ölçüde etkilemektedir. Bu mikroorganizmalar, nektarın şeker içeriğini, amino asit profillerini, pH'ını ve koku emisyonlarını değiştirerek polinatör tercihlerini şekillendirmektedir. Örneğin, Metschnikowia reukaufii mayası, bombus arılarını cezbeden meyvemsi esterler üretirken, bazı bakteriler pH'ı düşürerek bal arılarını uzaklaştırmaktadır. Polinatörler, bu mikroorganizmaları çiçekler arasında yayarak, mikrobiyal toplulukları şekillendiren ve ko-evrimi yönlendiren bir geri bildirim döngüsü oluşturmaktadır. Nektarın ötesinde, mikroorganizmalar metabolik ısı yoluyla termal düzenlemeyi, polen sağlığını ve polinatör bağırsak mikrobiyomlarını etkilemektedir. Rosenbergiella nectarea ve Acinetobacter spp. gibi özelleşmiş bakteriler, nektarın yüksek şekerli ortamında gelişirken, Lactobacillus kunkeei gibi polinatör mikroorganizmaları, bal arılarını patojenlerden korumaktadır. Mikrobiyal çeşitlilik bölgeye göre değişmekte olup, tropikal çiçekler ılıman iklim çiçeklerine göre daha zengin topluluklara ev sahipliği yapmaktadır. Bu derleme, mikroorganizmaların polinatör beslenmesini, bağışıklığını ve besin arama verimliliğini artırarak bitki-polinatör ağlarında nasıl kilit oyuncular olarak rol oynadığını vurgulamaktadır. Mikrobiyal yayılımı, rekabeti ve kimyasal etkileri inceleyerek, mikrobiyoloji, ekoloji ve evrimi harmanlayan çalışmalara çağrı yapmaktadır. Bu etkileşimleri anlamak, iklim değişikliğinin ve habitat kaybının tozlaşmayı nasıl tehdit ettiğini tahmin etmek, tarımı ve biyoçeşitliliği etkilemek için hayati öneme sahiptir.

🔖

Cite This Article

Ilyasov, R., Ilyasova, A., Danilenko, V., Kekeçoğlu, M., Slađan, R., Thaı, P. H., Khrapova, S., Mannapov, A., Prokudina, S., Sattarov, V., Boguslavsky, D. (2025). STRATEGIES AND MECHANISMS OF PLANT-MICROBIOME-POLLINATOR COADAPTATION. Uludağ Arıcılık Dergisi, Volume: 25 Issue: 1. https://doi.org/10.31467/uluaricilik.1675598

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (175)

  1. Adler L. S. Alkaloid Uptake Increases Fitness in a Hemiparasitic Plant via Reduced Herbivory and Increased Pollination. The American naturalist, 2000; 156(1): 92-99. https://doi.org/10.1086/303374
  2. Adler L. S., Irwin R. E., McArt S. H., & Vannette R. L. Floral traits affecting the transmission of beneficial and pathogenic pollinator–associated microbes. Curr Opin Insect Sci, 2020; 44: 1-7. https://doi.org/10.1016/j.cois.2020.08.006
  3. Aizenberg-Gershtein Y., Izhaki I., & Halpern M. Do Honey bees Shape the Bacterial Community Composition in Floral Nectar? Plos One, 2013; 8(7): e67556. https://doi.org/10.1371/journal.pone.0067556
  4. Aleklett K., Hart M., & Shade A. The microbial ecology of flowers: an emerging frontier in phyllosphere research. Botany, 2014; 92(4): 253-266. https://doi.org/10.1139/cjb-2013-0166
  5. Alexander H., & Antonovics J. Disease spread and population dynamics of anther‐smut infection of Silene alba caused by the fungus Ustilago violacea. Journal of Ecology, 1988; 76(1): 91-104. https://doi.org/10.2307/2260456
  6. Álvarez-Pérez S., & Herrera C. M. Composition, richness and non-concurrent fungal communities in floral nectar of Mediterranean plants. FEMS Microbiology Ecology, 2013; 83(3): 685-699. https://doi.org/10.1111/1574-6941.12027
  7. Álvarez-Pérez S., Herrera C. M., & de Vega C. Zooming-in on floral nectar: A first exploration of nectar-associated bacteria in wild plant communities. FEMS Microbiology Ecology, 2012; 80(3): 591-602. https://doi.org/10.1111/j.1574-6941.2012.01329.x
  8. Álvarez-Pérez S., Lievens B., & Fukami T. Yeast-bacterium interactions: the next frontier in nectar research. Trends in Plant Science, 2019; 24(5): 393-401. https://doi.org/10.1016/j.tplants.2019.01.012
  9. Álvarez-Pérez S., Lievens B., Jacquemyn H., & Herrera C. M. Acinetobacter nectaris sp. nov. and Acinetobacter boissieri sp. nov., isolated from floral nectar of wild Mediterranean insect-pollinated plants. International Journal of Systematic and Evolutionary Microbiology, 2013; 63(Pt 4): 1532-1539. https://doi.org/10.1099/ijs.0.043489-0
  10. Álvarez-Pérez S., Tsuji K., Donald M., Van Assche A., Vannette R. L., Herrera C. M., Jacquemyn H., Fukami T., & Lievens B. Nitrogen assimilation varies among clades of nectar- and insect-associated Acinetobacters. Microbial Ecology, 2021; 81(4): 990-1003. https://doi.org/10.1007/s00248-020-01671-x
  11. Amoo S. O., Aremu A. O., & Van Staden J. Unraveling the medicinal potential of South African Aloe species. Journal of Ethnopharmacology, 2014; 153(1): 19-41. https://doi.org/10.1016/j.jep.2014.01.036
  12. An S. Q., Potnis N., Dow M., Vorhölter F. J., He Y. Q., Becker A., Teper D., Li Y., Wang N., Bleris L., & Tang J. L. Mechanistic insights into host adaptation, virulence and epidemiology of the phytopathogen Xanthomonas. FEMS Microbiology Reviews, 2020; 44(1): 1-32. https://doi.org/10.1093/femsre/fuz024
  13. Anderson K. E., Sheehan T. H., Mott B. M., Maes P., Snyder L., Schwan M. R., Walton A., Jones B. M., & Corby-Harris V. Microbial Ecology of the Hive and Pollination Landscape: Bacterial Associates from Floral Nectar, the Alimentary Tract and Stored Food of Honey Bees (Apis mellifera). Plos One, 2013; 8(12): e83125. https://doi.org/10.1371/journal.pone.0083125
  14. Aremu A. O., & Van Staden J. The genus Tulbaghia (Alliaceae) – A review of its ethnobotany, pharmacology, phytochemistry and conservation needs. Journal of Ethnopharmacology, 2013; 149(2): 387-400. https://doi.org/10.1016/j.jep.2013.06.046
  15. Arredondo D., Castelli L., Porrini M. P., Garrido P. M., Eguaras M. J., Zunino P., & Antúnez K. Lactobacillus kunkeei strains decreased the infection by honey bee pathogens Paenibacillus larvae and Nosema ceranae. Benef Microbes, 2018; 9(2): 279-290. https://doi.org/10.3920/bm2017.0075
  16. Baker H. G., & Baker I. Floral nectar constituents in relation to pollinator type. Handbook of Experimental Pollination Biology, 1983: 117-141.
  17. Baker H. G., & Baker I. The predictive value of nectar chemistry to the recognition of pollinator types. Israel Journal of Plant Sciences, 1990; 39(1-2): 157-166. https://doi.org/10.1080/0021213X.1990.10677140
  18. Barnes K., Nicolson S. W., & van Wyk B. E. Nectar sugar composition in Erica. Biochemical Systematics and Ecology, 1995; 23(4): 419-423. https://doi.org/10.1016/0305-1978(95)00024-O
  19. Belisle M., Peay K. G., & Fukami T. Flowers as islands: spatial distribution of nectar-inhabiting microfungi among plants of Mimulus aurantiacus, a hummingbird-pollinated shrub. Microbial Ecology, 2012; 63(4): 711-718. https://doi.org/10.1007/s00248-011-9975-8
  20. Biere A., & Honders S. C. Coping with third parties in a nursery pollination mutualism: Hadena bicruris avoids oviposition on pathogen-infected, less rewarding Silene latifolia. New Phytologist, 2006; 169(4): 719-727. https://doi.org/10.1111/j.1469-8137.2005.01511.x
  21. Boutroux L. Conservation des ferments alcooliques dans la nature. Annales des Sci Naturelles, Série IV, Botanique, 1884; 17: 144-209.
  22. Brown M., Downs C. T., & Johnson S. D. Concentration-dependent sugar preferences of the malachite sunbird (Nectarinia famosa). Ornithology, 2010; 127(1): 151-155. https://doi.org/10.1525/auk.2009.09054
  23. Brudzynski K. Honey as an Ecological Reservoir of Antibacterial Compounds Produced by Antagonistic Microbial Interactions in Plant Nectars, Honey and Honey Bee. Antibiotics (Basel), 2021; 10(5). https://doi.org/10.3390/antibiotics10050551
  24. Brunner F. S., Schmid-Hempel P., & Barribeau S. M. Protein-poor diet reduces host-specific immune gene expression in Bombus terrestris. Proceedings of the Royal Society B: Biological Sciences, 2014; 281(1786): 20140128. https://doi.org/10.1098/rspb.2014.0128
  25. Brysch-Herzberg M. Ecology of yeasts in plant-bumble bee mutualism in Central Europe. FEMS Microbiology Ecology, 2004; 50(2): 87-100. https://doi.org/10.1016/j.femsec.2004.06.003
  26. Burdon R. C. F., Junker R. R., Scofield D. G., & Parachnowitsch A. L. Bacteria colonising Penstemon digitalis show volatile and tissue-specific responses to a natural concentration range of the floral volatile linalool. Chemoecology, 2018; 28(1): 11-19. https://doi.org/10.1007/s00049-018-0252-x
  27. Buwa L. V., & Van Staden J. Antibacterial and antifungal activity of traditional medicinal plants used against venereal diseases in South Africa. Journal of Ethnopharmacology, 2006; 103(1): 139-142. https://doi.org/10.1016/j.jep.2005.09.020
  28. Canto A., & Herrera C. M. Micro-organisms behind the pollination scenes: Microbial imprint on floral nectar sugar variation in a tropical plant community. Annals of Botany, 2012; 110(6): 1173-1183. https://doi.org/10.1093/aob/mcs183
  29. Canto A., Herrera C. M., & Rodriguez R. Nectar-living yeasts of a tropical host plant community: diversity and effects on community-wide floral nectar traits. PeerJ, 2017; 5: e3517. https://doi.org/10.7717/peerj.3517
  30. Canto A., Herrera C. M., García I. M., García M., & Bazaga P. Comparative effects of two species of floricolous Metschnikowia yeasts on nectar. Anales Del Jardín Botánico de Madrid, 2015; 72(1): e019. https://doi.org/10.3989/ajbm.2396
  31. Canto A., Herrera C. M., Medrano M., Pérez R., & García I. M. Pollinator foraging modifies nectar sugar composition in Helleborus foetidus (Ranunculaceae): An experimental test. American Journal of Botany, 2008; 95(3): 315-320. https://doi.org/10.3732/ajb.95.3.315
  32. Carter C., & Thornburg R. W. Is the nectar redox cycle a floral defense against microbial attack? Trends in Plant Science, 2004; 9(7): 320-324. https://doi.org/10.1016/j.tplants.2004.05.008
  33. Carter C., Graham R. A., & Thornburg R. W. Nectarin I is a novel, soluble germin-like protein expressed in the nectar of Nicotiana sp. Plant Molecular Biology, 1999; 41(2): 207-216. https://doi.org/10.1023/A:1006363508648
  34. Christensen S. M., Munkres I., & Vannette R. L. Nectar bacteria stimulate pollen germination and bursting to enhance microbial fitness. Current Biology, 2021; 31(19): 4373-4380.e4376. https://doi.org/10.1016/j.cub.2021.07.016
  35. Colda A., Bossaert S., Verreth C., Vanhoutte B., Honnay O., Keulemans W., & Lievens B. Inoculation of pear flowers with Metschnikowia reukaufii and Acinetobacter nectaris enhances attraction of honeybees and hoverflies, but does not increase fruit and seed set. Plos One, 2021; 16(4): e0250203. https://doi.org/10.1371/journal.pone.0250203
  36. Corbet S. A., Willmer P. G., Beament J. W. L., Unwin D. M., & Prŷs-Jones O. E. Post-secretory determinants of sugar concentration in nectar. Plant, Cell & Environment, 1979; 2(4): 293-308. https://doi.org/10.1111/j.1365-3040.1979.tb00084.x
  37. Corby-Harris V., Maes P., & Anderson K. E. The bacterial communities associatedforagers. Plos One, 2014; 9(4): e95056. https://doi.org/10.1371/journal.pone.0095056
  38. Crotti E., Rizzi A., Chouaia B., Ricci I., Favia G., Alma A., Sacchi L., Bourtzis K., Mandrioli M., Cherif A., Bandi C., & Daffonchio D. Acetic Acid Bacteria, Newly Emerging Symbionts of Insects. Applied and Environmental Microbiology, 2010; 76(21): 6963-6970. https://doi.org/10.1128/aem.01336-10
  39. Cullen N. P., Fetters A. M., & Ashman T. L. Integrating microbes into pollination. Curr Opin Insect Sci, 2021; 44: 48-54. https://doi.org/10.1016/j.cois.2020.11.002
  40. de Vega C., & Herrera C. M. Relationships among nectar-dwelling yeasts, flowers and ants: patterns and incidence on nectar traits. Oikos, 2012; 121(11): 1878-1888. https://doi.org/10.1111/j.1600-0706.2012.20295.x
  41. de Vega C., Albaladejo R. G., Guzmán B., Steenhuisen S., Johnson S. D., Herrera C. M., & Lachance M. Flowers as a reservoir of yeast diversity: description of Wickerhamiella nectarea f.a. sp. nov., and Wickerhamiella natalensis f.a. sp. nov. from South African flowers and pollinators, and transfer of related Candida species to the genus Wickerhamiella as new combinations. FEMS Yeast Research, 2017; 17(5). https://doi.org/10.1093/femsyr/fox054
  42. de Vega C., Álvarez-Pérez S., Albaladejo R. G., Steenhuisen S. L., Lachance M. A., Johnson S. D., & Herrera C. M. The role of plant-pollinator interactions in structuring nectar microbial communities. Journal of Ecology, 2021; 109(9): 3379-3395. https://doi.org/10.1111/1365-2745.13726
  43. de Vega C., Álvarez-Pérez S., Albaladejo R. G., Steenhuisen S., Lachance M., Johnson S. D., & Herrera C. M. The role of plant-pollinator interactions in structuring nectar microbial communities. Journal of Ecology, 2021; 109(9): 3379-3395. https://doi.org/10.1111/1365-2745.13726
  44. de Vega C., Guzman B., Steenhuisen S. L., Johnson S. D., Herrera C. M., & Lachance M. A. Metschnikowia drakensbergensis sp. nov. and Metschnikowia caudata sp. nov., endemic yeasts associated with Protea flowers in South Africa. International Journal of Systematic and Evolutionary Microbiology, 2014; 64(11): 3724-3732. https://doi.org/10.1099/ijs.0.068445-0
  45. de Vega C., Herrera C. M., & Johnson S. D. Yeasts in floral nectar of some South African plants: quantification and associations with pollinator type and sugar concentration. South African Journal of Botany, 2009; 75(4): 798-806. https://doi.org/10.1016/j.sajb.2009.07.016
  46. Dhami M. K., Hartwig T., & Fukami T. Genetic basis of priority effects: insights from nectar yeast. Proceedings of the Royal Society B: Biological Sciences, 2016; 283(1840): 20161455. https://doi.org/10.1098/rspb.2016.1455
  47. Dhami M. K., Hartwig T., Letten A. D., Banf M., & Fukami T. Genomic diversity of a nectar yeast clusters into metabolically, but not geographically, distinct lineages. Molecular Ecology, 2018; 27(8): 2067-2076. https://doi.org/10.1111/mec.14535
  48. Dolezal A. G., & Toth A. L. Feedbacks between nutrition and disease in honey bee health. Curr Opin Insect Sci, 2018; 26: 114-119. https://doi.org/10.1016/j.cois.2018.02.006
  49. Eisikowitch D., Lachance M. A., Kevan P. G., Willis S., & Collins-Thompson D. L. The effect of the natural assemblage of microorganisms and selected strains of the yeast Metschnikowia reukaufii in controlling the germination of pollen of the common milkweed Asclepias syriaca. Canadian Journal of Botany, 1990; 68(5): 1163-1165. https://doi.org/10.1139/b90-147
  50. Engel P., Martinson V. G., & Moran N. A. Functional diversity within the simple gut microbiota of the honey bee. Proceedings of the National Academy of Sciences of the United States of America, 2012; 109(27): 11002-11007. https://doi.org/10.1073/pnas.1202970109
  51. Farré-Armengol G., Filella I., Llusia J., & Peñuelas J. Bidirectional Interaction between Phyllospheric Microbiotas and Plant Volatile Emissions. Trends in Plant Science, 2016; 21(10): 854-860. https://doi.org/10.1016/j.tplants.2016.06.005
  52. Figueroa L. L., Blinder M., Grincavitch C., Jelinek A., Mann E. K., Merva L. A., Metz L. E., Zhao A. Y., Irwin R. E., McArt S. H., & Adler L. S. Bee pathogen transmission dynamics: deposition, persistence and acquisition on flowers. Proceedings of the Royal Society B: Biological Sciences, 2019; 286(1903): 20190603. https://doi.org/10.1098/rspb.2019.0603
  53. Fine J. D., Shpigler H. Y., Ray A. M., Beach N. J., Sankey A. L., Cash-Ahmed A., Huang Z. Y., Astrauskaite I., Chao R., Zhao H., & Robinson G. E. Quantifying the effects of pollen nutrition on honey bee queen egg laying with a new laboratory system. Plos One, 2018; 13(9): e0203444. https://doi.org/10.1371/journal.pone.0203444
  54. Folly A. J., Barton-Navarro M., & Brown M. Exposure to nectar-realistic sugar concentrations negatively impacts the ability of the trypanto infect its bumble bee host. Ecological Entomology, 2020; 45(6): 1495-1498. https://doi.org/10.1111/een.12901
  55. Fridman S., Izhaki I., Gerchman Y., & Halpern M. Bacterial communities in floral nectar. Environmental Microbiology Reports, 2012; 4(1): 97-104. https://doi.org/10.1111/j.1758-2229.2011.00309.x
  56. Fukami T. Historical contingency in community assembly: integrating niches, species pools, and priority effects. Annual Review of Ecology, Evolution, and Systematics, 2015; 46(1): 1-23. https://doi.org/10.1146/annurev-ecolsys-110411-160340
  57. Gegear R. J., & Thomson J. D. Does the flower constancy of bumble bees reflect foraging economics? Ethology, 2004; 110(10): 793-805. https://doi.org/10.1111/j.1439-0310.2004.01010.x
  58. Golonka A. M., Johnson B. O., Freeman J., & Hinson D. W. Impact of nectarivorous yeasts on Silene caroliniana's scent. Eastern Biologist, 2014; 3: 1-26.
  59. Good A. P., Gauthier M. P. L., Vannette R. L., & Fukami T. Honey bees avoid nectar colonized by three bacterial species, but not by a yeast species, isolated from the bee gut. Plos One, 2014; 9(1): e86494. https://doi.org/10.1371/journal.pone.0086494
  60. Grund-Mueller N., Ruedenauer F. A., Spaethe J., & Leonhardt S. D. Adding amino acids to a sucrose diet is not sufficient to support longevity of adult bumble bees. Insects, 2020; 11(4): 247. https://doi.org/10.3390/insects11040247
  61. Hammer T. J., Le E., Martin A. N., & Moran N. A. The gut microbiota of bumble bees. Insectes Sociaux, 2021; 68(4): 287-301. https://doi.org/10.1007/s00040-021-00837-1
  62. Heiduk A., Brake I., Shuttleworth A., & Johnson S. D. 'Bleeding' flowers of Ceropegia gerrardii (Apocynaceae-asclepiadoideae) mimic wounded insects to attract kleptoparasitic fly pollinators. New Phytologist, 2023; 239(4): 1490-1504. https://doi.org/10.1111/nph.18888
  63. Herrera C. M. Scavengers that fit beneath a microscope lens. Ecology, 2017; 98(10): 2725-2726. https://doi.org/10.1002/ecy.1874
  64. Herrera C. M., & Pozo M. I. Nectar yeasts warm the flowers of a winter-blooming plant. Proceedings of the Royal Society B: Biological Sciences, 2010; 277(1689): 1827-1834. https://doi.org/10.1098/rspb.2009.2252
  65. Herrera C. M., Canto A., Pozo M. I., & Bazaga P. Inhospitable sweetness: Nectar filtering of pollinator-borne inocula leads to impoverished, phylogenetically clustered yeast communities. Proceedings of the Royal Society B: Biological Sciences, 2010; 277(1682): 747-754. https://doi.org/10.1098/rspb.2009.1485
  66. Herrera C. M., De Vega C., Canto A., & Pozo M. I. Yeasts in floral nectar: A quantitative survey. Annals of Botany, 2009; 103(9): 1415-1423. https://doi.org/10.1093/aob/mcp026
  67. Herrera C. M., García I. M., & Pérez R. Invisible floral larcenies: microbial communities degrade floral nectar of bumble bee-pollinated plants. Ecology, 2008; 89(9): 2369-2376. https://doi.org/10.1890/08-0241.1
  68. Herrera C. M., Pozo M. I., & Medrano M. Yeasts in nectar of an early-blooming herb: sought by bumble bees, detrimental to plant fecundity. Ecology, 2013; 94(2): 273-279. https://doi.org/10.1890/12-0595.1
  69. Hietaranta E., Juottonen H., & Kytöviita M. M. Honey bees affect floral microbiome composition in a central food source for wild pollinators in boreal ecosystems. Oecologia, 2022; 201(1): 59-72. https://doi.org/10.1007/s00442-022-05285-7
  70. Hinton D., & Bacon C. The distribution and ultrastructure of the endophyte of toxic tall fescue. Canadian Journal of Botany, 1985; 63(1): 36-42. https://doi.org/10.1139/b85-006
  71. Hodgson S., Cates C., Hodgson J., Morley N., Sutton B., & Gange A. Vertical transmission of fungal endophytes is widespread in forbs. Ecology and Evolution, 2014; 4(8): 1199-1208. https://doi.org/10.1002/ece3.953
  72. Hua S. S. T., Beck J. J., Sarreal S. B. L., & Gee W. The major volatile compound 2-phenylethanol from the biocontrol yeast, Pichia anomala, inhibits growth and expression of aflatoxin biosynthetic genes of Aspergillus flavus. Mycotoxin Res, 2014; 30(2): 71-78. https://doi.org/10.1007/s12550-014-0189-z
  73. Huang M., Sanchez-Moreiras A. M., Abel C., Sohrabi R., Lee S., Gershenzon J., & Tholl D. The major volatile organic compound emitted from Arabidopsis thaliana flowers, the sesquiterpene (e)-β-caryophyllene, is a defense against a bacterial pathogen. New Phytologist, 2012; 193(4): 997-1008. https://doi.org/10.1111/j.1469-8137.2011.04001.x
  74. lyasov R., Boguslavsky D., Ilyasova A., Sattarov V., & Danilenko V. A multifaceted bioactivity of honey: Interactions between bees, plants and microorganisms. Uludağ Arıcılık Dergisi, 2024; 24(2): 356-385. https://doi.org/10.31467/uluaricilik.1511847
  75. Jacquemyn H., Lenaerts M., Brys R., Willems K., Honnay O., & Lievens B. Among-population variation in microbial community structure in the floral nectar of the bee-pollinated forest herb Pulmonaria officinalis L. Plos One, 2013; 8(3): e56917. https://doi.org/10.1371/journal.pone.0056917
  76. Jersáková J., Johnson S. D., & Kindlmann P. Mechanisms and evolution of deceptive pollination in orchids. Biological Reviews of the Cambridge Philosophical Society, 2006; 81(2): 219-235. https://doi.org/10.1017/S1464793105006986
  77. Johnson S. D. Batesian mimicry in the non-rewarding orchid Disa pulchra, and its consequences for pollinator behavior. Biological Journal of the Linnean Society, 2000; 71(1): 119-132. https://doi.org/10.1111/j.1095-8312.2000.tb01246.x
  78. Junker R. R., Romeike T., Keller A., & Langen D. Density-dependent negative responses by bumble bees to bacteria isolated from flowers. Apidologie, 2014; 45(4): 467-477. https://doi.org/10.1007/s13592-013-0262-1
  79. Keller A., McFrederick Q. S., Dharampal P., Steffan S., Danforth B. N., & Leonhardt S. D. (More than) Hitchhikers through the network: The shared microbiome of bees and flowers. Curr Opin Insect Sci, 2021; 44: 8-15. https://doi.org/10.1016/j.cois.2020.09.007
  80. Khan A., Zhao Y., & Korban S. Molecular Mechanisms of Pathogenesis and Resistance to the Bacterial Pathogen Erwinia amylovora, Causal Agent of Fire Blight Disease in Rosaceae. Plant Molecular Biology Reporter, 2012; 30(2): 1-14. https://doi.org/10.1007/s11105-011-0334-1.
  81. Kim D. R., Cho G., Jeon C. W., Weller D. M., Thomashow L. S., Paulitz T. C., & Kwak Y. S. A mutualistic interaction between Streptomyces bacteria, strawberry plants and pollinating bees. Nat Commun, 2019; 10(1): 4802. https://doi.org/10.1038/s41467-019-12785-3.
  82. Kim P. S., Shin N. R., Kim J. Y., Yun J. H., Hyun D. W., & Bae J. W. Acinetobacter apis sp. nov., isolated from the intestinal tract of a honey bee, Apis mellifera. Journal of Microbiology, 2014; 52(8): 639-645. https://doi.org/10.1007/s12275-014-4078-0.
  83. Klaps J. Analysis of yeast diversity in floral microhabitats from Metrosideros polymorpha Gaud. KU Leuven. Leuven, 2019, Pages. Retrieved from URL| Available rom Database Provider Name of Database database.| (Document Number)
  84. Klaps J., Lievens B., & Álvarez-Pérez S. Towards a better understanding of the role of nectar-inhabiting yeasts in plant-animal interactions. Fungal Biology and Biotechnology, 2020; 7: 1. https://doi.org/10.1186/s40694-019-0091-8
  85. Koch H., Woodward J., Langat M. K., Brown M. J. F., & Stevenson P. C. Flagellum Removal by a Nectar Metabolite Inhibits Infectivity of a Bumble bee Parasite. Current Biology, 2019; 29(20): 3494-3500.e3495. https://doi.org/10.1016/j.cub.2019.08.037.
  86. Lachance M. A., Ewing C. P., Bowles J. M., & Starmer W. T. Metschnikowia hamakuensis sp. nov., Metschnikowia kamakouana sp. nov. and Metschnikowia mauinuiana sp. nov., three endemic yeasts from Hawaiian nitidulid beetles. International Journal of Systematic and Evolutionary Microbiology, 2005; 55(3): 1369-1377. https://doi.org/10.1099/ijs.0.63615-0.
  87. Lachance M. A., Vale H. M. M., Sperandio E. M., Carvalho A. O. S., Santos A. R. O., Grondin C., Jacques N., Casaregola S., & Rosa C. A. Wickerhamiella dianesei f.a., sp. nov. and Wickerhamiella kurtzmanii f.a., sp. nov., two yeast species isolated from plants and insects. International Journal of Systematic and Evolutionary Microbiology, 2018; 68(10): 3351-3355. https://doi.org/10.1099/ijsem.0.003000.
  88. Lachance M., Starmer W., Rosa C., Bowles J., Barker J., & Janzen D. Biogeography of the yeasts of ephemeral flowers and their insects. FEMS Yeast Research, 2001; 1(1): 1-8. https://doi.org/10.1016/s1567-1356(00)00003-9.
  89. Lara C., & Ornelas J. F. Hummingbirds as vectors of fungal spores in Moussonia deppeana (Gesneriaceae): Taking advantage of a mutualism? American Journal of Botany, 2003; 90(2): 260-267. https://doi.org/10.3732/ajb.90.2.262
  90. Lee F. J., Rusch D. B., Stewart F. J., Mattila H. R., & Newton I. L. G. Saccharide breakdown and fermentation by the honey bee gut microbiome. Environmental Microbiology, 2014; 17(3): 796-815. https://doi.org/10.1111/1462-2920.12526
  91. Lenaerts M., Álvarez-Pérez S., De Vega C., Van Assche A., Johnson S. D., Willems K. A., Herrera C. M., Jacquemyn H., & Lievens B. Rosenbergiella australoborealis sp. nov., Rosenbergiella collisarenosi sp. nov. and Rosenbergiella epipactidis sp. nov., three novel bacterial species isolated from floral nectar. Systematic and Applied Microbiology, 2014; 37(6): 402-411. https://doi.org/10.1016/j.syapm.2014.03.002
  92. Lenaerts M., Goelen T., Paulussen C., Herrera-Malaver B., Steensels J., Van Den Ende W., Verstrepen K. J., Wäckers F., Jacquemyn H., Lievens B., & Manson J. Nectar bacteria affect life history of a generalist aphid parasitoid by altering nectar chemistry. Functional Ecology, 2017; 31(11): 2061-2069. https://doi.org/10.1111/1365-2435.12933
  93. Lignon V. A., Mas F., Jones E. E., Kaiser C., & Dhami M. K. The floral interface: a playground for interactions between insect pollinators, microbes, and plants. New Zealand Journal of Zoology, 2024; 52(2): 218-237. https://doi.org/10.1080/03014223.2024.2353285
  94. Lin H., & Winston M. L. The role of nutrition and temperature in the ovarian development of the worker honey bee (Apis mellifera). The Canadian Entomologist, 1998; 130(6): 883-891. https://doi.org/10.4039/Ent130883-6
  95. Mallinger R. E., & Prasifka J. R. Bee visitation rates to cultivated sunflowers increase with the amount and accessibility of nectar sugars. Journal of Applied Entomology, 2017; 141(7): 561-573. https://doi.org/10.1111/jen.12375
  96. Manirajan B. A., Ratering S., Rusch V., Schwiertz A., Geissler-Plaum R., Cardinale M., & Schnell S. Bacterial microbiota associated with flower pollen is influenced by pollination type, and shows a high degree of diversity and species-specificity. Environmental Microbiology, 2016; 18(12): 5161-5174. https://doi.org/10.1111/1462-2920.13524
  97. Martin V. N., Schaeffer R. N., & Fukami T. Potential effects of nectar microbes on pollinator health. Philosophical Transactions of the Royal Society B: Biological Sciences, 2022; 377(1853): 20210155. https://doi.org/10.1098/rstb.2021.0155
  98. Massoni J., Bortfeld-Miller M., Jardillier L., Salazar G., Sunagawa S., & Vorholt J. A. Consistent host and organ occupancy of phyllosphere bacteria in a community of wild herbaceous plant species. ISME J, 2019; 14(1): 245-258. https://doi.org/10.1038/s41396-019-0531-8
  99. McCormack P. J., Wildman H. G., & Jeffries P. Production of antibacterial compounds by phylloplane-inhabiting yeasts and yeast-like fungi. Applied and Environmental Microbiology, 1994; 60(3): 927-931. https://doi.org/10.1128/aem.60.3.927-931.1994
  100. McFrederick Q. S., Thomas J. M., Neff J. L., Vuong H. Q., Russell K. A., Hale A. R., & Mueller U. G. Flowers and Wild Megachilid Bees Share Microbes. Microbial Ecology, 2016; 73(1): 188-200. https://doi.org/10.1007/s00248-016-0838-1
  101. McFrederick Q. S., Wcislo W. T., Taylor D. R., Ishak H. D., Dowd S. E., & Mueller U. G. Environment or kin: whence do bees obtain acidophilic bacteria? Molecular Ecology, 2012; 21(7): 1754-1768. https://doi.org/10.1111/j.1365-294x.2012.05496.x
  102. Miller R., Owens S. J., & Rørslett B. Plants and colour: flowers and pollination. Optics & Laser Technology, 2011; 43(2): 282-294. https://doi.org/10.1016/j.optlastec.2008.12.018
  103. Mittelbach M., Yurkov A. M., Nocentini D., Nepi M., Weigend M., & Begerow D. Nectar sugars and bird visitation define a floral niche for basidiomycetous yeast on the Canary Islands. BMC Ecology, 2015; 15(1): 2-2. https://doi.org/10.1186/s12898-015-0036-x
  104. Mommaerts V., Wäckers F., & Smagghe G. Assessment of gustatory responses to different sugars in harnessed and free-moving bumble bee workers (Bombus terrestris). Chemical Senses, 2013; 38(5): 399-407. https://doi.org/10.1093/chemse/bjt014
  105. Morris M. M., Frixione N. J., Burkert A. C., Dinsdale E. A., & Vannette R. L. Microbial abundance, composition, and function in nectar are shaped by flower visitor identity. FEMS Microbiology Ecology, 2020; 96(3). https://doi.org/10.1093/femsec/fiaa003
  106. Ncube B., Nair J. J., Rárová L., Strnad M., Finnie J. F., & Van Staden J. Seasonal pharmacological properties and alkaloid content in Cyrtanthus contractus N.E. Br. South African Journal of Botany, 2015; 97: 69-76. https://doi.org/10.1016/j.sajb.2014.12.005
  107. Nicolson S. W., & Thornburg R. W. Nectar chemistry. In Ed.^Eds. Springer Netherlands, Dordrecht, 2007, p. 215-264. https://doi.org/10.1007/978-1-4020-5937-7_5
  108. Nowak A., Szczuka D., Górczyńska A., Motyl I., & Kręgiel D. Characterization of Apis mellifera Gastrointestinal Microbiota and Lactic Acid Bacteria for Honeybee Protection-A Review. Cells, 2021; 10(3): 701-701. https://doi.org/10.3390/cells10030701
  109. O'Garro L., & Charlemange E. Comparison of bacterial growth and activity of glucanase and chitinase in pepper leaf and flower tissue infected with Xanthomonas campestris pv. vesicatoria. Physiological and Molecular Plant Pathology, 1994; 45(3): 181-188. https://doi.org/10.1016/S0885-5765(05)80075-X
  110. Oldroyd B. P., Rinderer T. E., & Buco S. M. Intracolonial variance in honey bee foraging behaviour: the effects of sucrose concentration. Journal of Apicultural Research, 1991; 30(3-4): 137-145. https://doi.org/10.1080/00218839.1991.11101248
  111. Palmer-Young E. C., Raffel T. R., & McFrederick Q. S. pH-mediated inhibition of a bumble bee parasite by an intestinal symbiont. Parasitology, 2019; 146(3): 380-388. https://doi.org/10.1017/S0031182018001555
  112. Parret A., & De Mot R. Bacteria killing their own kind: novel bacteriocins of Pseudomonas and other γ-proteobacteria. Trends in Microbiology, 2002; 10(3): 107-112. https://doi.org/10.1016/S0966-842X(02)02307-7
  113. Peakall R., Ebert D., Poldy J., Barrow R. A., Francke W., Bower C. C., & Schiestl F. P. Pollinator specificity, floral odour chemistry and the phylogeny of Australian sexually deceptive Chiloglottis orchids: implications for pollinator-driven speciation. New Phytologist, 2010; 188(2): 437-450. https://doi.org/10.1111/j.1469-8137.2010.03308.x
  114. Peay K. G., Belisle M., & Fukami T. Phylogenetic relatedness predicts priority effects in nectar yeast communities. Proceedings of the Royal Society B: Biological Sciences, 2011; 279(1729): 749-758. https://doi.org/10.1098/rspb.2011.1230
  115. Peshev D., & Van den Ende W. Fructans: prebiotics and immunomodulators. Journal of Functional Foods, 2014; 8: 348-357. https://doi.org/10.1016/j.jff.2014.04.005
  116. Pozo M. I., & Jacquemyn H. Addition of pollen increases growth of nectar-living yeasts. FEMS Microbiology Letters, 2019; 366(15): fnz191. https://doi.org/10.1093/femsle/fnz191
  117. Pozo M. I., Herrera C. M., & Bazaga P. Species richness of yeast communities in floral nectar of southern Spanish plants. Microbial Ecology, 2011; 61(1): 82-91. https://doi.org/10.1007/s00248-010-9682-x
  118. Pozo M. I., Lachance M. A., & Herrera C. M. Nectar yeasts of two southern Spanish plants: the roles of immigration and physiological traits in community assembly. FEMS Microbiology Ecology, 2012; 80: 281-293. https://doi.org/10.1111/j.1574-6941.2011.01286.x
  119. Pozo M. I., Mariën T., Van Kemenade G., Wäckers F., & Jacquemyn H. Effects of pollen and nectar inoculation by yeasts, bacteria or both on bumble bee colony development. Oecologia, 2021; 195: 689-703. https://doi.org/10.1007/s00442-021-04872-4
  120. Pozo M. I., Van Kemenade G., Van Oystaeyen A., Aledón-Catalá T., Benavente A., Van Den Ende W., Wäckers F., & Jacquemyn H. The impact of yeast presence in nectar on bumble bee behavior and fitness. Ecological Monographs, 2019; 90(1): 1-10. https://doi.org/10.1002/ecm.1393
  121. Pusey P. L., Stockwell V. O., & Mazzola M. Epiphytic bacteria and yeasts on apple blossoms and their potential as antagonists of Erwinia amylovora. Phytopathology, 2009; 99: 571–581. https://doi.org/10.1094/PHYTO-99-5-0571
  122. Pyke G. H. Floral Nectar: Pollinator Attraction or Manipulation? Trends in ecology & evolution, 2016; 31: 339-341. https://doi.org/10.1016/j.tree.2016.02.013
  123. Ramanovich N., Savelieva T., Biruk А., & Shukshyna M. Investigation of the Possibility of Using Bee Microbiotes and Bee Products for Isolation of Lactic Acids and Bifidobacteria. Topical issues of processing of meat and milk raw materials, 2021; 1(15) (15): 55-64. https://doi.org/10.47612/2220-8755-2020-15-55-64
  124. Rands S. A., & Whitney H. M. Floral temperature and optimal foraging: is heat a feasible floral reward for pollinators? Plos One, 2008; 3: e2007. https://doi.org/10.1371/journal.pone.0002007
  125. Rering C. C., Beck J. J., Hall G. W., McCartney M. M., & Vannette R. L. Nectar‐inhabiting microorganisms influence nectar volatile composition and attractiveness to a generalist pollinator. New Phytologist, 2017; 220: 750-759. https://doi.org/10.1111/nph.14809
  126. Richardson L. L., Adler L. S., Leonard A. S., Andicoechea J., Regan K. H., Anthony W. E., Manson J. S., & Irwin R. E. Secondary metabolites in floral nectar reduce parasite infections in bumble bees. Proceedings of the Royal Society B: Biological Sciences, 2015; 282: 20142471. https://doi.org/10.1098/rspb.2014.2471
  127. Ricigliano V., & Anderson K. Probing the Honey Bee Diet-Microbiota-Host Axis Using Pollen Restriction and Organic Acid Feeding. Insects, 2020; 11(5): 1-10. https://doi.org/10.3390/insects11050291
  128. Rivest S., & Forrest J. R. K. Defence compounds in pollen: Why do they occur and how do they affect the ecology and evolution of bees? New Phytologist, 2019; 225: 1053-1064. https://doi.org/10.1111/nph.16230
  129. Rosa C. A., Lachance M. A., Silva J. O., Teixeira A. C., Marini M. M., Antonini Y., & Martins R. P. Yeast communities associated with stingless bees. FEMS Yeast Research, 2003; 4: 271-275. https://doi.org/10.1016/s1567-1356(03)00173-9
  130. Rothman J. A., Russell K. A., Leger L., McFrederick Q. S., & Graystock P. The direct and indirect effects of environmental toxicants on the health of bumble bees and their microbiomes. Proceedings of the Royal Society B: Biological Sciences, 2020; 287: 20200980. https://doi.org/10.1098/rspb.2020.0980
  131. Roulston T. A. H., & Cane J. H. Pollen nutritional content and digestibility for animals. Plant Systematics and Evolution, 2000; 222: 187-209. https://doi.org/10.1007/978-3-7091-6306-1_10
  132. Roy R., Schmitt A. J., Thomas J. B., & Carter C. J. Nectar biology: from molecules to ecosystems. Plant Science, 2017; 262: 148-164. https://doi.org/10.1016/j.plantsci.2017.04.012
  133. Russell A. L., Rebolleda‐Gómez M., Shaible T. M., & Ashman T. Movers and shakers: Bumble bee foraging behavior shapes the dispersal of microbes among and within flowers. Ecosphere, 2019; 10: e02714. https://doi.org/10.1002/ecs2.2714
  134. Samuni-Blank M., Izhaki I., Laviad S., Bar-Massada A., Gerchman Y., & Halpern M. The Role of Abiotic Environmental Conditions and Herbivory in Shaping Bacterial Community Composition in Floral Nectar. Plos One, 2014; 9(6): e99107. https://doi.org/10.1371/journal.pone.0099107
  135. Sandhu D. K., & Waraich M. K. Yeasts Associated with Pollinating Bees and Flower Nectar. Microbial Ecology, 1985; 11(1): 51–58. https://doi.org/10.1007/BF02015108
  136. Santorelli L. A., Wilkinson T., Abdulmalik R., Rai Y., Creevey C. J., Huws S., & Gutierrez-Merino J. Beehives possess their own distinct microbiomes. Environmental Microbiome, 2023; 18(1): 1. https://doi.org/10.1186/s40793-023-00460-6
  137. Santos A. R. O., Leon M. P., Barros K. O., Freitas L. F. D., Hughes A. F. S., Morais P. B., Lachance M. A., & Rosa C. A. Starmerella camargoi f.a., sp. nov., Starmerella ilheusensis f.a., sp. nov., Starmerella litoralis f.a., sp. nov., Starmerella opuntiae f.a., sp. nov., Starmerella roubikii f.a., sp. nov. and Starmerella vitae f.a., sp. nov., isolated from flowers and bees, and transfer of related Candida species to the genus Starmerella as new combinations. International Journal of Systematic and Evolutionary Microbiology, 2018; 68: 1333-1343. https://doi.org/10.1099/ijsem.0.002675
  138. Schaeffer R. N., & Irwin R. E. Yeasts in nectar enhance male fitness in a montane perennial herb. Ecology, 2014; 95: 1792-1798. https://doi.org/10.1890/13-1740.1
  139. Schaeffer R. N., Mei Y. Z., Andicoechea J., Manson J. S., Irwin R. E., & Kudo G. Consequences of a nectar yeast for pollinator preference and performance. Functional Ecology, 2016; 31: 613-621. https://doi.org/10.1111/1365-2435.12762
  140. Schaeffer R. N., Rering C. C., Maalouf I., Beck J. J., & Vannette R. L. Microbial metabolites elicit distinct olfactory and gustatory preferences in bumble bees. Biology Letters, 2019; 15: 20190132. https://doi.org/10.1098/rsbl.2019.0132
  141. Schmitt A. J., Sathoff A. E., Holl C., Bauer B., Samac D. A., & Carter C. J. The major nectar protein of Brassica rapa is a non-specific lipid transfer protein, BrLTP2.1, with strong antifungal activity. Journal of Experimental Botany, 2018; 69: 5587-5597. https://doi.org/10.1093/jxb/ery319
  142. Seeley T. D., Mikheyev A. S., & Pagano G. J. Dancing bees tune both duration and rate of waggle-run production in relation to nectar-source profitability. Journal of comparative physiology. A, Sensory, neural, and behavioral physiology, 2000; 186: 813-819. https://doi.org/10.1007/s003590000134
  143. Seymour R. S., & Schultze-Motel P. Physiological temperature regulation by flowers of the sacred lotus. Philos Trans R Soc Lon B, 1998; 353: 935-943. https://doi.org/10.1098/rstb.1998.0258
  144. Seymour R. S., White C. R., & Gibernau M. Environmental biology: heat reward for insect pollinators. Nature, 2003; 426: 243-244. https://doi.org/10.1038/426243a
  145. Shade A., McManus P. S., & Handelsman J. Unexpected diversity during community succession in the apple flower microbiome. mBio, 2013; 4: e00602-00612. https://doi.org/10.1128/mBio.00602-12
  146. Sharaby Y., Rodríguez-Martínez S., Lalzar M., Halpern M., & Izhaki I. Geographic partitioning or environmental selection: What governs the global distribution of bacterial communities inhabiting floral nectar? The Science of the total environment, 2020; 749: 142305. https://doi.org/10.1016/j.scitotenv.2020.142305
  147. Shi H., Ratering S., Schneider B., & Schnell S. Microbiome of honey bee corbicular pollen: Factors influencing its structure and potential for studying pathogen transmission. The Science of the total environment, 2025; 958: 178107. https://doi.org/10.1016/j.scitotenv.2024.178107
  148. Sobhy I. S., Baets D., Goelen T., Herrera-Malaver B., Bosmans L., Van Den Ende W., Verstrepen K. J., Wäckers F., Jacquemyn H., & Lievens B. Sweet Scents: Nectar Specialist Yeasts Enhance Nectar Attraction of a Generalist Aphid Parasitoid Without Affecting Survival. Frontiers in plant science, 2018; 9: 1009. https://doi.org/10.3389/fpls.2018.01009
  149. Sobral M., Veiga T., Domínguez P., Guitián J. A., Guitián P., & Guitián J. M. Selective Pressures Explain Differences in Flower Color among Gentiana lutea Populations. Plos One, 2015; 10(7): e0132522. https://doi.org/10.1371/journal.pone.0132522
  150. Stabler D., Paoli P. P., Nicolson S. W., & Wright G. A. Nutrient balancing of the adult worker bumble bee (Bombus terrestris) depends on the dietary source of essential amino acids. Journal of experimental Biology, 2015; 218(5): 793-802. https://doi.org/10.1242/jeb.114249
  151. Steffan S. A., Dharampal P. S., Danforth B. N., Gaines-Day H. R., Takizawa Y., & Chikaraishi Y. Omnivory in Bees: Elevated Trophic Positions among All Major Bee Families. The American naturalist, 2019; 194(3): 414-421. https://doi.org/10.1086/704281
  152. Stökl J., Strutz A., Dafni A., Svatos A., Doubsky J., Knaden M., Sachse S., Hansson B. S., & Stensmyr M. C. A Deceptive Pollination System Targeting Drosophilids through Olfactory Mimicry of Yeast. Current Biology, 2010; 20(20): 1846-1852. https://doi.org/10.1016/j.cub.2010.09.033
  153. Taniwaki M. H., Pitt J. I., Iamanaka B. T., Massi F. P., Fungaro M. H. P., & Frisvad J. C. Penicillium excelsum sp. nov from the Brazil Nut Tree Ecosystem in the Amazon Basin. Plos One, 2015; 10(12): e0143189. https://doi.org/10.1371/journal.pone.0143189
  154. Teixido A. L., Barrio M., & Valladares F. Size Matters: Understanding the Conflict Faced by Large Flowers in Mediterranean Environments. Botanical Review, 2016; 82: 204-228. https://doi.org/10.1007/s12229-016-9168-
  155. Tucker C. M., & Fukami T. Environmental variability counteracts priority effects to facilitate species coexistence: evidence from nectar microbes. Proceedings of the Royal Society B: Biological Sciences, 2014; 281(1778): 20132637. https://doi.org/10.1098/rspb.2013.2637
  156. Ushio M., Yamasaki E., Takasu H., Nagano A. J., Fujinaga S., Honjo M. N., Ikemoto M., Sakai S., & Kudoh H. Microbial communities on flower surfaces act as signatures of pollinator visitation. Scientific Reports, 2015; 5(1): 8695. https://doi.org/10.1038/srep08695
  157. Vanneste J. L. Fire Blight: The Disease and Its Causative Agent, Erwinia amylovora. CABI Publ, New York, 2000, p. https://doi.org/10.1079/9780851992945.0000
  158. Vannette R. L. The floral microbiome: plant, pollinator, and microbial perspectives. Annual Review of Ecology, Evolution, and Systematics, 2020; 51(1): 363-386. https://doi.org/10.1146/annurev-ecolsys-011720-013401
  159. Vannette R. L., & Fukami T. Contrasting effects of yeasts and bacteria on floral nectar traits. Annals of Botany, 2018; 121(7): 1343-1349. https://doi.org/10.1093/aob/mcy032
  160. Vannette R. L., & Fukami T. Dispersal enhances beta diversity in nectar microbes. Ecology Letters, 2017; 20(7): 901-910. https://doi.org/10.1111/ele.12787
  161. Vannette R. L., & Fukami T. Historical contingency in species interactions: towards niche-based predictions. Ecology Letters, 2014; 17(1): 115-124. https://doi.org/10.1111/ele.12204
  162. Vannette R. L., Gauthier M.-P. L., & Fukami T. Nectar bacteria, but not yeast, weaken a plant-pollinator mutualism. Proceedings of the Royal Society B: Biological Sciences, 2013; 280(1752): 20122601. https://doi.org/10.1098/rspb.2012.2601
  163. Vásquez A., Forsgren E., Fries I., Paxton R. J., Flaberg E., Szekely L., & Olofsson T. C. Symbionts as major modulators of insect health: lactic acid bacteria and honeybees. Plos One, 2012; 7(7): e33188. https://doi.org/10.1371/annotation/3ac2b867-c013-4504-9e06-bebf3fa039d1
  164. Von Arx M., Moore A., Davidowitz G., & Arnold A. E. Diversity and distribution of microbial communities in floral nectar of two night-blooming plants of the Sonoran Desert. Plos One, 2019; 14(12): e0225309. https://doi.org/10.1371/journal.pone.0225309
  165. Vuong H. Q., & McFrederick Q. S. Comparative genomics of wild bee and flower isolated Lactobacillus reveals potential adaptation to the bee host. Genome Biology and Evolution, 2019; 11(8): 2151-2161. https://doi.org/10.1093/gbe/evz136
  166. Wang H., Liu C., Liu Z., Wang Y., Ma L., & Xu B. The different dietary sugars modulate the composition of the gut microbiota in honeybee during overwintering. BMC Microbiology, 2020; 20(1): 61. https://doi.org/10.1186/s12866-020-01726-6
  167. Wei N., & Ashman T. L. The effects of host species and sexual dimorphism differ among root, leaf and flower microbiomes of wild strawberries in situ. Scientific Reports, 2018; 8(1): 5195. https://doi.org/10.1038/s41598-018-23518-9
  168. Wiens F., Zitzmann A., Lachance M. A., Yegles M., Pragst F., Wurst F. M., Von Holst D., Guan S. L., & Spanagel R. Chronic intake of fermented floral nectar by wild treeshrews. Proceedings of the National Academy of Sciences, 2008; 105(30): 10426-10431. https://doi.org/10.1073/pnas.0801628105
  169. Willmer P. The Effects of Insect Visitors on Nectar Constituents in Temperate Plants. Oecologia, 1980; 47(2): 270-277. https://doi.org/10.1007/BF00346832
  170. Yan J., Wang G., Sui Y., Wang M., & Zhang L. Pollinator responses to floral colour change, nectar and scent promote reproductive fitness in Quisqualis indica (Combretaceae). Scientific Reports, 2016; 6(1): 24408. https://doi.org/10.1038/srep24408
  171. Yang M., Deng G. C., Gong Y. B., & Huang S. Q. Nectar yeasts enhance the interaction between Clematis akebioides and its bumble bee pollinator. Plant Biology, 2019; 21(4): 732-737. https://doi.org/10.1111/plb.12957
  172. Zariman A., Omar N., & Nurul Huda A. Plant Attractants and Rewards for Pollinators: Their Significance to Successful Crop Pollination. International Journal of Life Sciences and Biotechnology, 2022; 5(2): 270-293. https://doi.org/10.38001/ijlsb.1069254
  173. Zarraonaindia I., Owens S. M., Weisenhorn P., West K., Hampton-Marcell J., Lax S., Bokulich N. A., Mills D. A., Martin G., Taghavi S., Van Der Lelie D., & Gilbert J. A. The Soil Microbiome Influences Grapevine-Associated Microbiota. mBio, 2015; 6(2). https://doi.org/10.1128/mbio.02527-14
  174. Zheng H., Perreau J., Powell J. E., Han B., Zhang Z., Kwong W. K., Tringe S. G., & Moran N. A. Division of labor in honey bee gut microbiota for plant polysaccharide digestion. Proceedings of the National Academy of Sciences, 2019; 116(51): 25909-25916. https://doi.org/10.1073/pnas.1916224116
  175. Zheng J., Wittouck S., Salvetti E., Franz C. M. a. P., Harris H. M. B., Mattarelli P., O'Toole P. W., Pot B., Vandamme P., Walter J., Watanabe K., Wuyts S., Felis G. E., Gänzle M. G., & Lebeer S. A taxonomic note on the genus Lactobacillus: Description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacillaceae and Leuconostocaceae. International Journal of Systematic and Evolutionary Microbiology, 2020; 70(4): 2782-2858. https://doi.org/10.1099/ijsem.0.004107