Ahmed MZ, Li SJ, Xue X, Yin XJ, Ren SX, Jiggins FM et al. (2015) The Intracellular bacterium Wolbachia uses parasitoid wasps as phoretic vectors for efficient horizontal transmission. PLoS Pathog 11:1–19
Arai H, Hirano T, Akizuki N, Abe A, Nakai M, Kunimi Y et al. (2019) Multiple infection and reproductive manipulations of Wolbachia in Homona magnanima (Lepidoptera: Tortricidae). Microb Ecol 77:257–266
Google Scholar
Arai H, Lin SR, Nakai M, Kunimi Y, Inoue MN (2020) Closely related male-killing and nonmale-killing Wolbachia strains in the oriental tea tortrix Homona magnanima. Microb Ecol 79:1011–1020
Google Scholar
Bailey NW, Zuk M (2008) Changes in immune effort of male field crickets infested with mobile parasitoid larvae. J Insect Physiol 54:96–104
Google Scholar
Ballad JWO, Hatzidakis J, Karr TL, Kreitman M (1996) Reduced variation in Drosophila simulans mitochondrial DNA. Genetics 144:1519–1528
Birch LC (1948) The intrinsic rate of natural increase of an insect population. J Anim Ecol 17:15–26
Capobianco IIIF, Nandkumar S, Parker JD (2018) Wolbachia affects survival to different oxidative stressors dependent upon the genetic background in Drosophila melanogaster. Physiol Entomol 43:239–244
Danthanarayana W (1975) Factors determining variation in fecundity of the light brown apple moth, Epiphyas postvittana (Walker) (Tortricidae). Aust J Zool 23:309–319
Dean MD (2006) A Wolbachia-associated fitness benefit depends on genetic background in Drosophila simulans. Proc R Soc B 273:1415–1420
Google Scholar
Deseo KV (1971) Study of factors influencing the fecundity and fertility of codling moth (Laspeyresia pomonella L., Lepidoptera, Tortricidae). Acta Phytopathol Hun 6:243–252
Dobson SL, Rattanadechakul W, Marsland EJ (2004) Fitness advantage and cytoplasmic incompatibility in Wolbachia single-and superinfected Aedes albopictus. Heredity 93:135–142
Google Scholar
Duron O, Bouchon D, Boutin S, Bellamy L, Zhou L, Engelstädter J, Hurst GD (2008) The diversity of reproductive parasites among arthropods: Wolbachia do not walk alone. BMC Biol 6:1–12
Engelstädter J, Telschow A, Hammerstein P (2004) Infection dynamics of different Wolbachia-types within one host population. J Theor Biol 231:345–55
Google Scholar
Fleury F, Vavre F, Ris N, Fouillet P, Boulétreau M (2000) Physiological cost induced by the maternally-transmitted endosymbiont Wolbachia in the Drosophila parasitoid Leptopilina heterotoma. Parasitology 121:493–500
Google Scholar
Frank SA (1998) Dynamics of cytoplasmic incompatibility with multiple Wolbachia infections. J Theor Biol 192:213–18
Google Scholar
Frank SA, Hurst LD (1996) Mitochondria and male disease. Nature 383:224–224
Google Scholar
Fry AJ, Palmer MR, Rand DM (2004) Variable fitness effects of Wolbachia infection in Drosophila melanogaster. Heredity 93:379–389
Google Scholar
Gómez-Valero L, Soriano-Navarro M, Pérez-Brocal V, Heddi A, Moya A, García-Verdugo JM, Latorre A (2004) Coexistence of Wolbachia with Buchnera Aphidicola and a secondary symbiont in the aphid Cinara cedri. J Bacteriol 186:6626–33
Google Scholar
Hoffmann AA, Turelli M, Harshman LG (1990) Factors affecting the distribution of cytoplasmic incompatibility in Drosophila simulans. Genetics 126:933–948
Google Scholar
Hornett EA, Charlat S, Duplouy AMR, Davies N, Roderick GK, Wedell N et al. (2006) Evolution of male-killer suppression in a natural population. PLoS Biol 4:1643–1648
Google Scholar
Hough JA, Pimentel D (1978) Influence of host foliage on development, survival, and fecundity of the gypsy moth. Environ Entomol 7:97–102
Ikeda T, Ishikawa H, Sasaki T (2003) Infection density of Wolbachia and level of cytoplasmic incompatibility in the Mediterranean flour moth, Ephestia kuehniella. J Invertebr Pathol 84:1–5
Google Scholar
Ishii T, Nakai M, Okuno S, Takatsuka J, Kunimi Y (2003) Characterization of Adoxophyes honmai single-nucleocapsid nucleopolyhedrovirus: morphology, structure, and effects on larvae. J Invertebr Pathol 83:206–214
Google Scholar
Kondo N, Shimada M, Fukatsu T (2005) Infection density of Wolbachia endosymbiont affected by coinfection and host genotype. Biol Lett 1:488–491
Google Scholar
Lu P, Bian G, Pan X, Xi Z (2012) Wolbachia induces density-dependent inhibition to dengue virus in mosquito cells. PLoS Negl Trop D 6:1–8
Google Scholar
Maia AHN, Luiz AJB, Campanhola C (2000) Statistical inference on associated fertility life table parameters using jackknife technique: computational aspects. J Econ Entomol 93:511–518
Mazzetto F, Gonella E, Alma A (2015) Wolbachia infection affects female fecundity in Drosophila suzukii. Bull Insectol 68:153–157
Meyer JS, Ingersoll CG, McDonald LL, Boyce MS (1986) Estimating uncertainty in population growth rates: jackknife vs. bootstrap techniques. Ecology 67:1156–1166
Moreira LA, Iturbe-Ormaetxe I, Jeffery JA, Lu G, Pyke AT, Hedges LM et al. (2009) A Wolbachia symbiont in Aedes aegypti limits infection with dengue, Chikungunya, and Plasmodium. Cell 139:1268–1278
Google Scholar
Mouton L, Henri H, Bouletreau M, Vavre F (2006) Effect of temperature on Wolbachia density and impact on cytoplasmic incompatibility. Parasitology 132:49–56
Google Scholar
Narita S, Nomura M, Kageyama D (2007) Naturally occurring single and double infection with Wolbachia strains in the butterfly Eurema hecabe: transmission efficiencies and population density dynamics of each Wolbachia strain. FEMS Microb Ecol 61:235–245
Google Scholar
Pigeault R, Braquart-Varnier C, Marcadé I, Mappa G, Mottin E, Sicard M (2014) Modulation of host immunity and reproduction by horizontally acquired Wolbachia. J Insect Physiol 70:125–133
Google Scholar
Rancès E, Ye YH, Woolfit M, McGraw EA, O´Neill SL (2012) The relative importance of innate immune priming in Wolbachia-mediated dengue interference. PLoS Pathog 8:e1002548. https://doi.org/10.1371/journal.ppat.1002548
Google Scholar
R Core Team (2021) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/
Stevanovic AL, Arnold PA, Johnson KN (2015) Wolbachia -mediated antiviral protection in Drosophila larvae and adults following oral infection. Appl Environ Micro 81:8215–8223
Google Scholar
Takamatsu T, Arai H, Abe N, Nakai M, Kunimi Y, Inoue MN (2021) Coexistence of two male-killers and their impact on the development of oriental tea tortrix Homona magnanima. Microb Ecol 81:193–202
Google Scholar
Takehana A, Katsuyama T, Yano T, Oshima Y, Takada H, Aigaki T et al. (2002) Overexpression of a pattern-recognition receptor, peptidoglycan-recognition protein-LE, activates imd/relish-mediated antibacterial defense and the prophenoloxidase cascade in Drosophila larvae. Proc Natl Acad Sci USA 99:13705–13710
Google Scholar
Takatsuka J, Okuno S, Ishii T, Nakai M, Kunimi Y (2010) Fitness-related traits of entomopoxviruses isolated from Adoxophyes honmai (Lepidoptera: Tortricidae) at three localities in Japan. J Invertebr Pathol 105:121–131
Google Scholar
Teixeira L, Ferreira Á, Ashburner M (2008) The Bacterial symbiont Wolbachia induces resistance to RNA viral infections in Drosophila melanogaster. PLoS Biol 6:e1000002. https://doi.org/10.1371/journal.pbio.1000002
Google Scholar
Thomas P, Kenny N, Eyles D, Moreira LA, O´Neill SL, Asgari S (2011) Infection with the wMel and wMelPop strains of Wolbachia leads to higher levels of melanization in the hemolymph of Drosophila melanogaster, Drosophila simulans and Aedes aegypti. Dev Comp Immunol 35:360–365
Google Scholar
Tsuruta K, Wennmann JT, Kunimi Y, Inoue MN, Nakai M (2018) Morphological properties of the occlusion body of Adoxophyes orana granulovirus. J Invertebr Pathol 154:58–64
Google Scholar
Turelli M, Hoffmann AA (1991) Rapid spread of an inherited incompatibility factor in California Drosophila. Nature 353:440–442
Google Scholar
Vautrin E, Vavre F (2009) Interactions between vertically transmitted symbionts: cooperation or conflict? Trends Microbiol 17:95–99
Google Scholar
Vavre F, Fleury F, Lepetit D, Fouillet P, Boulétreau M (1999) Phylogenetic evidence for horizontal transmission of Wolbachia in host- parasitoid associations. Mol Biol Evol 16:1711–1723
Google Scholar
Vollmer J, Schiefer A, Schneider T, Jülicher K, Johnston KL, Taylor MJ et al. (2013) Requirement of lipid II biosynthesis for cell division in cell wall-less Wolbachia, endobacteria of arthropods and filarial nematodes. Int J Med Microbiol 303:140–149
Google Scholar
Voronin D, Guimarães AF, Molyneux GR, Johnston KL, Ford L, Taylor MJ (2014) Wolbachia lipoproteins: abundance, localization and serology of Wolbachia peptidoglycan associated lipoprotein and the Type IV Secretion System component, VirB6 from Brugia malayi and Aedes albopictus. Parasite Vector 7:462
Watanabe M, Miura K, Hunter MS, Wajnberg E (2011) Superinfection of cytoplasmic incompatibility-inducing Wolbachia is not additive in Orius strigicollis (Hemiptera: Anthocoridae). Heredity 106:642–648
Google Scholar
Weeks AR, Turelli M, Harcombe WR, Reynolds KT, Hoffmann AA (2007) From parasite to mutualist: rapid evolution of Wolbachia in natural populations of Drosophila. PLoS Biol 5:0997–1005
Google Scholar
Werren JH, Baldo L, Clark ME (2008) Wolbachia: Master manipulators of invertebrate biology. Nat Rev Microbiol 6:741–751
Google Scholar
Xue X, Li S, Ahmed MZ, Barro PJ, Ren S, Qiu B (2012) Inactivation of Wolbachia reveals its biological roles in whitefly host. PLoS One 7:e48148. https://doi.org/10.1371/journal.pone.0048148
Google Scholar
Zug R, Hammerstein P (2012) Still a host of hosts for Wolbachia: analysis of recent data suggests that 40% of terrestrial arthropod species are infected. PLoS One 7:e38544. https://doi.org/10.1371/journal.pone.0038544
Google Scholar
Zug R, Hammerstein P (2015) Wolbachia and the insect immune system: what reactive oxygen species can tell us about the mechanisms of Wolbachia-host interactions. Front Microbiol 6:1–16
Source: Ecology - nature.com