Exoparasitic Mites – Vectors of Bacterial Symbionts Among Insects

Мұқаба

Дәйексөз келтіру

Толық мәтін

Аннотация

Inherited endosymbiotic bacteria from the genera Rickettsia, Wolbachia and Spiroplasma cause the death of male offspring in ladybirds (Coleoptera, Coccinellidae). As a rule, bacteria are transmitted through the cytoplasm of the mother’s egg to offspring – vertically. In addition to vertical transfer, there is increasing evidence of horizontal transfer of symbionts between unrelated insect taxa. Insect parasites such as mites can be potential vectors of endosymbiotic bacteria. The parasitic mite Coccipolipus hippodamiae (McDaniel & Morrill, 1969) (Acarina: Podapolipidae) occurs in natural populations of Coccinellidae. In this work, the ability of C. hippodamiae to become infected with Wolbachia and Spiroplasma from hosts and to spread bacteria among coccinellid beetles was proven for the first time.

Авторлар туралы

E. Shaikevich

Vavilov Institute of General Genetics, Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: elenashaikevich@mail.ru
Russia, 119333 , Moscow, Gubkina str., 3

A. Gorbacheva

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: elenashaikevich@mail.ru
Russia, 119333 , Moscow, Gubkina str., 3

D. Romanov

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: elenashaikevich@mail.ru
Russia, 119333 , Moscow, Gubkina str., 3

Әдебиет тізімі

  1. Горячева И.И., Блехман А.В., Андрианов Б.В., Горелова Т.В., Захаров И.А. Генотипическое разнообразие Wolbachia pipientis в нативных и инвазивных популяциях Harmonia axyridis Pall., 1773 (Coleoptera, Coccinellidae) // Генетика. 2015. Т. 51. № 8. С. 857–863.
  2. Захаров И.А., Эйдельберг М.М. Паразитический клещ Coccipolipus hyppodamia McDaniel et Morrill (Tarsonemina, Podapolipidae) в популяциях двухточечной коровки Adalia bipunctata L. (Coleoptera, Coccinellidae) // Энтомологическое обозрение. 1997. Т. 76. № 3. С. 680–683.
  3. Захаров И.А., Шайкевич Е.В. Полиморфизм мтДНК в петербургской популяции Adalia bipunctata и его связь с зараженностью симбиотической бактерией Spiroplasma // Экологическая генетика. 2011. Т. 9. № 1. С. 27–31.
  4. Романов Д.А., Матвейкина Е.А. Harmonia axyridis (Pallas, 1773) (Coleoptera: Coccinellidae) в г. Москве и г. Ялте: ее конкуренция с нативными видами кокцинеллид и влияние паразитоидов на ее численность // Российский журн. биологических инвазий. 2021. № 4. С. 114–133.
  5. Шайкевич Е.В., Захаров И.А., Хонек А. Экологическая генетика жуков рода Adalia: изменчивость и симбиотические бактерии в европейских популяциях десятиточечной божьей коровки Adalia decempunctata // Экологическая генетика. 2019. Т. 17. № 4. С. 37–45.
  6. Шайкевич Е.В., Ившина Е.В., Захаров И.А. Полиморфизм митохондриальной ДНК и распространение цитоплазматических симбионтов в популяциях двуточечной божьей коровки Adalia bipunctata // Генетика. 2012. Т. 48. № 5. С. 666–671.
  7. Эйдельберг М.М. Клещи семейства Podapolipidae (Heterostigmata, Tarsonemina) Украины и сопредельных территорий с описанием нового вида // Вестн. зоологии. 1994. № 1. С. 37–42.
  8. Ahmed M.Z., Breinholt J.W., Kawahara A.Y. Evidence for common horizontal transmission of Wolbachia among butterflies and moths // BMC Evol. Biol. 2016. V. 16. P. 118.
  9. Baldo L., Ayoub N.A., Hayashi C.Y., Russell J.A., Stahlhut J.K., Werren J.H. Insight into the routes of Wolbachia invasion: high levels of horizontal transfer in the spider genus Agelenopsis revealed by Wolbachia strain and mitochondrial DNA diversity // Mol Ecol. 2008. V. 17(2). P. 557–569.
  10. Brown A.N., Lloyd V.K. Evidence for horizontal transfer of Wolbachia by a Drosophila mite // Exp. Appl. Acarol. 2015. V. 63(3). P. 301–311.
  11. Ceryngier P., Roy H.E., Poland R.L. Natural enemies of ladybird beetles // In: Ecology and behaviour of the ladybird beetles (Coccinellidae) / Ed. by Hodek I., van Emden H.F., Honek A. Chichester: Wiley-Blackwell, 2012. P. 375–443.
  12. Folmer O., Black M., Hoeh W., Lutz R., Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates // Mol. Mar. Biol. Biotechnol. 1994. V. 3. P. 294–299.
  13. Gerth M., Röthe J., Bleidorn C. Tracing horizontal Wolbachia movements among bees (Anthophila): A combined approach using multilocus sequence typing data and host phylogeny // Molecular ecology. 2013. V. 22. https://doi.org/10.1111/mec.12549
  14. Goryacheva I., Blekhman A., Andrianov B., Zakharov I. Heritable bacterial endosymbionts in native and invasive populations of Harmonia axyridis // Biol. Invasions. 2017. V. 19. P. 493–502.
  15. Goryacheva I., Blekhman A., Andrianov B., Romanov D., Zakharov I. Spiroplasma infection in Harmonia axyridis – diversity and multiple infection // PLoS One. 2018. V. 13(5). e0198190.
  16. Hurst G.D.D., Sharpe R.G., Broomfield A.H., Walker L.E., Majerus T.M.O., Zakharov I.A., Majerus M.E.N. Sexually transmitted disease in a promiscuous insect, Adalia bipunctata // Ecological Entomology. 1995. V. 20(3). P. 230–236.
  17. Ilinsky Y., Kosterin O.E. Molecular diversity of Wolbachia in Lepidoptera: prevalent allelic content and high recombination of MLST genes // Mol Phylogenet Evol. 2017. V. 109. P.164–179.
  18. Jaenike J., Polak M., Fiskin A., Helou M., Minhas M. Interspecific transmission of endosymbiotic Spiroplasma by mites // Biol. Lett. 2007. V. 3(1). P. 23–25.
  19. Knell R.J., Webberley K.M. Sexually transmitted diseases of insects: distribution, evolution, ecology and host behaviour // Biological Reviews. 2004. V. 79(3). P. 557–581.
  20. Li H., Shu X., Meng L., Zhou X., Obrycki J.J., Li B. Prevalence in maternally-inherited bacteria in native and invasive populations of the harlequin ladybird beetle Harmonia axyridis // Biol. Invasions. 2021. V. 23. P. 1461–1471.
  21. O’Neill S.L., Giordano R., Colbert A.M., Karr T.L., Robertson H.M. 16S rRNA phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic incompatibility in insects // Proc. Natl. Acad. Sci. USA. 1992. V. 89(7). P. 2699–2702.
  22. Osaka R., Watada M., Kageyama D., Nomura M. Detection of Spiroplasma from the mite Macrocheles sp. (Acari: Macrochelidae) ectoparasitic to the fly Drosophila hydei (Diptera; Drosophilidae): a possible route of horizontal transmission // Symbiosis. 2013. V. 60(2). P. 79–84.
  23. Pietri J.E., DeBruhl H., Sullivan W. The rich somatic life of Wolbachia // MicrobiologyOpen. 2016. V. 5(6). P. 923–936.
  24. Raak-van den Berg C.L., van Wielink P.S., de Jong P.W., Gort G., Haelewaters D., Helder J., van Lenteren J.C. Invasive alien species under attack: natural enemies of Harmonia axyridis in the Netherlands // BioControl. 2014. V. 59(2). P. 229–240.
  25. Rhule E.L., Majerus M.E.N., Jiggins F.M., Ware R.L. Potential role of the sexually transmitted mite Coccipolipus hippodamiae in controlling populations of the invasive ladybird Harmonia axyridis // Biological Control. 2010. V. 53(2). P. 243–247.
  26. Riddick E.W. Ectoparasitic mite and fungus on an invasive lady beetle: parasite coexistence and influence on host survival // Bulletin of Insectology. 2010. V. 63(1). P. 13–20.
  27. Schulenburg J.H., Hurst G.D., Tetzlaff D., Booth G.E., Zakharov I.A., Majerus M.E. History of infection with different male-killing bacteria in the two-spot ladybird beetle Adalia bipunctata revealed through mitochondrial DNA sequence analysis // Genetics. 2002. V. 160. P. 1075–1086.
  28. Shaikevich E.V., Romanov D.A., Zakharov I.A. The diversity of Wolbachia in a single Adalia bipunctata (Coleoptera: Coccinellidae) population: correlations with host phylogeny and male-killing // Symbiosis. 2021. V. 85(2). P. 249–257.
  29. Shaikevich E.V., Zakharov I.A. Biodiversity in geographically remote natural populations of Adalia ladybirds (Coleoptera: Coccinellidae) // In: Beetles: Biodiversity, Ecology and Role in the Environment / Ed. by Stack C. Nova Science Publishers, Inc., 2015. P. 205–226.
  30. Tamura K., Stecher G., Peterson D. et al. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0 // Molecular Biology and Evolution. 2013. V. 30. P. 2725–2729.
  31. Webberley K.M., Hurst G.D.D. The effect of aggregative overwintering on an insect sexually transmitted parasite system // J. Parasitology. 2002. V. 88(4). P. 707–712.
  32. Webberley K.M., Hurst G.D.D., Husband R.W., Schulenburg J.H.G.V.D., Sloggett J.J., Isham V., Buszko J., Majerus M.E.N. Host reproduction and a sexually transmitted disease: causes and consequences of Coccipolipus hippodamiae distribution on coccinellid beetles // J. Animal Ecology. 2004. V. 73(1). P. 1–10.
  33. Webberley K.M., Tinsley M.C., Sloggett J.J., Majerus M.E.N., Hurst G.D.D. Spatial variation in the incidence of a sexually transmitted parasite of the ladybird beetle Adalia bipunctata (Coleoptera: Coccinellidae) // European J. Entomology. 2006. V. 103(4). P. 793–797.
  34. Werren J.H., Zhang W., Guo L.R. Evolution and phylogeny of Wolbachia: reproductive parasites of arthropods // Proc. Biol. Sci. 1995. V. 261(1360). P. 55–63.

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© Е.В. Шайкевич, А.А. Горбачева, Д.А. Романов, 2023

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