Abstract
Predatory insects play an important role in the regulation of arthropod’s numbers. When they counteract with the diseased prey, the entomopathogenic microorganisms may be disseminated mechanically or parasitize such secondary hosts. Microsporidia are wide-spread pathogens of insects with diverse host ranges, and infection of entomophagous hosts is not uncommon. In the present study, the spined soldier bug nymphs were fed with the adzuki bean borer larvae infected with Nosema pyrausta (A. Paillot) J. Weiser, 1961 or the silkworm larvae infected with N. bombycis Nägeli, 1857. Both pathogens were infective to the predator at the prevalence level of 15-30%. The former pathogen displayed a decrease of prevalence level in the filial generation to as low as 5 % and no infection in consequent generations. The latter could only be transmitted to bugs horizontally and no infections in the filial generation was found. This indicates low (or no) risk of vertical transmission of these two pathogens, making them suitable for combined application with the predatory bug in the integrated pest management programmes.
References
Abbas MST, Boucias DG (1984) Interaction between nuclear polyhedrosis virus-infected Anticarsia gemmatalis (Lepidoptera: Noctuidae) larvae and predator Podisus maculiventris (Say) (Hemiptera: Pentatomidae). Environmental Entomology 13(2): 599–602. https://doi.org/10.1093/ee/13.2.599
Aldrich JR, Cantelo WW (1999) Suppression of Colorado potato beetle infestation by pheromone‐mediated augmentation of the predatory spined soldier bug, Podisus maculiventris (Say) (Heteroptera: Pentatomidae). Agricultural and Forest Entomology 1: 209–217. https://doi.org/10.1046/j.1461-9563.1999.00026.x
Amarasekare KG, Edelson JV (2004) Effect of temperature on efficacy of insecticides to differential grasshopper (Orthoptera: Acrididae). Journal of Economic Entomology 97(5): 1595–1602. https://doi.org/10.1603/0022-0493-97.5.1595
Avery PB, George J, Markle L, Martini X, Rowley AL, Meagher RL, Barger RE, Duren EB, Dawson JS, Cave RD (2022) Choice behavior of the generalist pentatomid predator Podisus maculiventris when offered lepidopteran larvae infected with an entomopathogenic fungus. Biological Control 67: 201–211. https://doi.org/10.1007/s10526-021-10124-4
Babin A, Schurr F, Rivière MP, Chauzat MP, Dubois E (2022) Specific detection and quantification of three microsporidia infecting bees, Nosema apis, Nosema ceranae, and Nosema bombi, using probe-based real-time PCR. European Journal of Protistology 86: 125935. https://doi.org/10.1016/j.ejop.2022.125935
Becnel JJ, Andreadis TG (1999) Microsporidia in insects. In: Wittner M, Weiss LM (Eds) The Microsporidia and Microsporidiosis. American Society for Microbiology Press, Washington, DC, 447e501.
Biddinger DJ, Leslie TW, Joshi NK (2014) Reduced-risk pest management programs for Eastern US peach orchards: effects on arthropod predators, parasitoids, and select pests. Journal of Economic Entomology 107(3): 1084–1091. https://doi.org/10.1603/EC13441
Biever KD, Andrews PL, Andrews PA (1982) Use of a predator, Podisus maculiventris, to distribute virus and initiate epizootics. Journal of Economic Entomology 75(1): 150–152. https://doi.org/10.1093/jee/75.1.150
Bird AE, Hesketh H, Cross JV, Copland M (2004) The common black ant, Lasius niger (Hymenoptera: Formicidae), as a vector of the entomopathogen Lecanicillium longisporum to rosy apple aphid, Dysaphis plantaginea (Homoptera: Aphididae). Biocontrol Science and Technology 14: 757–767. https://doi.org/10.1080/09583150410001720716
Brooks WM (1988) Entomogenous protozoa. In: Ignoffo CM (Ed) Handbook of Natural Pesticides. Vol. V. Microbial Insecticides, Part A, Entomogenous Protozoa and Fungi. CRC Press, Inc., Boca Raton, 1–149.
Campbell C, van Frankenhuyzen K, Smith S (2007) Incubation period, spore egestion and horizontal transmission of Nosema fumiferanae (Microsporidia: Nosematidae) in spruce budworm (Choristoneura sp., Lepidoptera: Tortricidae): The role of temperature and dose. Journal of Invertebrate Pathology 94(3): 204–210. https://doi.org/10.1016/j.jip.2006.11.005
Capinera JL, Barbosa P (1975) Transmission of nuclear-polyhedrosis virus to gypsy moth larvae by Calosoma sycophanta. Annals of the Entomological Society of America 68(3): 593–594. https://doi.org/10.1093/aesa/68.3.593
Carvalho VFP, Vacari AM, Pomari AF, De Bortoli CP, Ramalho DG, De Bortoli SA (2012) Interaction between the predator Podisus nigrispinus (Hemiptera: Pentatomidae) and the entomopathogenic bacteria Bacillus thuringiensis. Environmental Entomology 41(6): 1454–1461. https://doi.org/10.1603/EN12060
Chakrabarty S, Saha AK, Manna B, Kumar SN (2013) Secondary contamination is the main source for spread of Nosema bombycis resulting in outbreak of pebrine disease in Bombyx mori L. International Journal of Industrial Entomology 27(2): 282–288. https://doi.org/10.1002/9780470015902.a0022555
Cooper DJ (1981) The role of predatory Hemiptera in disseminating a nuclear polyhedrosis virus of Heliothis punctiger. Australian Journal of Entomology 20(2): 145–150. https://doi.org/10.1111/j.1440-6055.1981.tb01017.x
Cross P (2013) Pesticide hazard trends in orchard fruit production in Great Britain from 1992 to 2008: a time‐series analysis. Pest Management Science 69(6): 768–774. https://doi.org/10.1002/ps.3436
de Azeredo Morgado MG, Passos CJS, Garnier J, De Lima LA, de Alcântara Mendes R, Samson-Brais É, Lucotte M (2023) Large-scale agriculture and environmental pollution of ground and surface water and sediment by pesticides in the Brazilian Amazon: the case of the santarém region. Water, Air, & Soil Pollution 234(3): 150. https://doi.org/10.1007/s11270-023-06152-8
de Castro AA, Poderoso JCM, Ribeiro RC, Legaspi JC, Serrão JE, Zanuncio JC (2015) Demographic parameters of the insecticide-exposed predator Podisus nigrispinus: implications for IPM. Biological Control 60: 231–239. https://doi.org/10.1007/s10526-014-9639-y
De Clercq P (2000) Predaceous stinkbugs (Pentatomidae: Asopinae). In: Schaefer CW, Panizzi AR (Eds) Heteroptera of economic importance. CRC Press, Boca Raton, Florida, 759–812. https://doi.org/10.1201/9781420041859
De Clercq P, Degheele D (1992) A meat-based diet for rearing the predatory stink bugs Podisus maculiventris and Podisus sagitta [Heteroptera: Pentatomidae]. Entomophaga 37: 149–157.
De Clercq P, Degheele D (1994) Laboratory measurement of predation by Podisus maculiventris and P. sagitta (Hemiptera: Pentatomidae) on beet armyworm (Lepidoptera: Noctuidae). Journal of Economic Entomology 87(1): 76–83. https://doi.org/10.1093/jee/87.1.76
De Clercq P, Merlevede F, Tirry L (1998) Unnatural Prey and Artificial Diets for Rearing Podisus maculiventris (Heteroptera: Pentatomidae). Biological Control 12(2): 137–142. https://doi.org/10.1006/bcon.1998.0611
de Nardo EAB, Maia AHN, Watanabe MA (2001) Effect of a formulation of Anticarsia gemmatalis (Lepidoptera: Noctuidae) nuclear polyhedrosis virus on the predator Podisus nigrispinus (Heteroptera: Pentatomidae: Asopinae), using the fertility life table parameters. Environmental Entomology 30: 1164–1173. https://doi.org/10.1603/0046-225X-30.6.1164
Desurmont G, Weston PA (2008) Predation by Podisus maculiventris (Say) (Hemiptera: Pentatomidae) on viburnum leaf beetle, Pyrrhalta viburni (Paykull) (Coleoptera: Chrysomelidae), under laboratory and field conditions. Environmental Entomology 37(5): 1241–1251. https://doi.org/10.1093/ee/37.5.1241
Dolzhenko VI, Laptiev AB (2021) Modern range of plant protection means: biological efficiency and safety. Plodorodie 3(120): 71–75. https://doi.org/10.25680/S19948603.2021.120.13 [In Russian with English summary]
Down RE, Cuthbertson AG, Mathers JJ, Walters KF (2009) Dissemination of the entomopathogenic fungi, Lecanicillium longisporum and L. muscarium, by the predatory bug, Orius laevigatus, to provide concurrent control of Myzus persicae, Frankliniella occidentalis and Bemisia tabaci. Biological Control 50(2): 172–178. https://doi.org/10.1016/j.biocontrol.2009.03.010
Down RE, Bell HA, Matthews HJ, Kirkbride‐Smith AE, Edwards JP (2004) Dissemination of the biocontrol agent Vairimorpha necatrix by the spined soldier bug, Podisus maculiventris. Entomologia Experimentalis et Applicata 110(2): 103–114. https://doi.org/10.1111/j.0013-8703.2004.00122.x
Dwivedi SA, Sonawane VK, Pandit TR (2022) Review on the impact of insecticides utilization in crop ecosystem: Their prosperity and threats. In: Ranz RER (Ed.) Insecticides-Impact and Benefits of Its Use for Humanity. IntechOpen, London, UK. https://doi.org/10.5772/intechopen.100385
Fisher RA (1992) Statistical Methods for Research Workers. In: Kotz S, Johnson NL (Eds) Breakthroughs in Statistics. Springer Series in Statistics. Springer, New York, NY, USA, 66–70. https://doi.org/10.1007/978-1-4612-4380-9_6
Flick AJ, Acevedo MA, Elderd BD (2016) The negative effects of pathogen-infected prey on predators: a meta-analysis. Oikos 125: 1554–1560. https://doi.org/10.1111/oik.03458
Frolov AN, Berim MN, Grushevaya IV (2019) Rearing of trilobed male uncus Ostrinia species in laboratory for experimental purposes. Vestnik zashchity rasteniy 3(101): 58–62. https://doi.org/10.31993/2308-6459-2019-3(101)-58-62
Futerman PH, Layen SJ, Kotzen ML, Franzen C, Kraaijeveld AR, Godfray HCJ (2006) Fitness effects and transmission routes of a microsporidian parasite infecting Drosophila and its parasitoids. Parasitology 132(4): 479–492. https://doi.org/10.1017/S0031182005009339
Geiger F, Bengtsson J, Berendse F, Weisser WW, Emmerson M, Morales MB, Ceryngier P, Liira J, Tscharntke T, Winqvist C, Eggers S, Bommarco R, Pärt T, Bretagnolle V, Plantegenest M, Clement LW, Dennis C, Palmer C, Oñate JJ, Guerrero I, Inchausti P (2010) Persistent negative effects of pesticides on biodiversity and biological control potential on European farmland. Basic and Applied Ecology 11(2): 97–105. https://doi.org/10.1016/j.baae.2009.12.001
Godfray HCJ, Garnett T (2014) Food security and sustainable intensification. Philosophical transactions of the Royal Society B: biological sciences 369: 20120273. http://dx.doi.org/10.1098/rstb.2012.0273
Goertz D, Hoch G (2013) Influence of the forest caterpillar hunter Calosoma sycophanta on the transmission of microsporidia in larvae of the gypsy moth Lymantria dispar. Agricultural and Forest Entomology 15(2): 178. https://doi.org/10.1111/afe.12000
Goertz D, Hoch G (2008) Horizontal transmission pathways of terrestrial microsporidia: A quantitative comparison of three pathogens infecting different organs in Lymantria dispar L. (Lep.: Lymantriidae) larvae. Biological Control 44(2): 196–206. https://doi.org/10.1016/j.biocontrol.2007.07.014
Goertz D, Hoch G (2011) Modeling horizontal transmission of microsporidia infecting gypsy moth, Lymantria dispar (L.), larvae. Biological Control 56(3): 263–270. https://doi.org/10.1016/j.biocontrol.2010.11.013
Grushevaya I, Ignatieva A, Tokarev Y (2020) Susceptibility of three species of the genus Ostrinia (Lepidoptera: Crambidae) to Nosema pyrausta (Microsporidia: Nosematida). BIO Web of Conf EDP Sciences 21: 00040. https://doi.org/10.1051/bioconf/20202100040
Grushevaya IV, Ignatieva AN, Malysh SM, Senderskiy IV, Zubarev IV, Kononchuk AG (2018) Spore dimorphism in Nosema pyrausta (Microsporidia, Nosematidae): From morphological evidence to molecular genetic verification. Acta Protozoologica 57: 49– 52. https://doi.org/10.1017/S0031182018001737
Grushevaya IV, Senderskiy IV, Zubarev IV, Tokarev YS (2021) Transovarial transmission of Nosema pyrausta in three generations of Ostrinia nubilalis in laboratory tests. Entomologia Experimentalis et Applicata 169(11): 1057–1060. https://doi.org/10.1111/eea.13100
Gupta RK, Gani M, Jasrotia P, Srivastava K (2013) Development of the predator Eocanthecona furcellata on different proportions of nucleopolyhedrovirus infected Spodoptera litura larvae and potential for predator dissemination of virus in the field. Biological Control 58: 543–552. https://doi.org/10.1007/s10526-013-9515-1
Haddi K, Turchen LM, Viteri Jumbo LO, Guedes RN, Pereira EJ, Aguiar RW, Oliveira EE (2020) Rethinking biorational insecticides for pest management: Unintended effects and consequences. Pest Management Science 76(7): 2286–2293. https://doi.org/10.1002/ps.5837
Hall TA (1999) BIOEDIT: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41: 95–98.
Han M-S, Watanabe H (1998) Transovarian transmission of two microsporidia in the silk-worm, Bombyx mori and disease occurrence in progeny population. Journal of Invertebrate Pathology 51(1): 41–45. https://doi.org/10.1016/0022-2011(88)90086-9
Hare JD (1990) Ecology and management of the Colorado potato beetle. Annual Review of Entomology 35: 81–100. https://doi.org/10.1146/annurev.en.35.010190.000501
Hatcher MJ, Dick JTA, Dunn AM (2014) Parasites that change predator or prey behavior can have keystone effects on community composition. Biology Letters 10: 20130879. https://doi.org/10.1098/rsbl.2013.0879
He X, Deng H, Hwang HM (2019) The current application of nanotechnology in food and agriculture. Journal of Food and Drug Analysis 27(1): 1–21. https://doi.org/10.1016/j.jfda.2018.12.002
Kaya HK (1979) Microsporidan spores: retention of infectivity after passage through the gut of the assassin bug, Zelus exsanguis (Stal). In: Proceedings of the Hawaiian Entomological Society 13(1): 91–94.
Kevan PG, Shipp L, Smagghe G (2020) Ecological intensification: Managing biocomplexity and biodiversity in agriculture through pollinators, pollination and deploying biocontrol agents against crop and pollinator diseases, pests and parasites. In: Smagghe G, Boecking O, Maccagnani B, Mänd M, Kevan PG (Eds) Entomovectoring for Precision Biocontrol and Enhanced Pollination of Crops. Springer Switzerland, 19–51. https://doi.org/10.1007/978-3-030-18917-4_2
Kudsk P, Jørgensen LN, Ørum JE (2018) Pesticide Load – A new Danish pesticide risk indicator with multiple applications. Land Use Policy 70: 384–393. https://doi.org/10.1016/j.landusepol.2017.11.010
Lewis LC, Sumerford DV, Bing LA, Gunnarson RD (2006) Dynamics of Nosema pyrausta in natural populations of the European corn borer, Ostrinia nubilalis: A six-year study. Biological Control 51: 627–642. https://doi.org/10.1007/s10526-005-2937-7
Li Z, Wang Y, Wang L, Zhou Z (2018) Molecular and biochemical responses in the midgut of the silkworm, Bombyx mori, infected with Nosema bombycis. Parasites & Vectors 11: 1–10. https://doi.org/10.1186/s13071-018-2755-2
Lin T, Zeng Z, Chen Y, You Y, Hu J, Yang F, Wei H (2021) Compatibility of six reduced-risk insecticides with Orius strigicollis (Heteroptera: Anthocoridae) predators for controlling Thrips hawaiiensis (Thysanoptera: Thripidae) pests. Ecotoxicology and Environmental Safety 226: 112812. https://doi.org/10.1016/j.ecoenv.2021.112812
Litwin A, Nowak M, Różalska S (2020) Entomopathogenic fungi: unconventional applications. Reviews in Environmental Science and Bio/Technology 19(1): 23–42. https://doi.org/10.1007/s11157-020-09525-1
López Jr JD, Ridgway RL, Pinnell RE (1976) Comparative efficacy of four insect predators of the bollworm and tobacco budworm. Environmental Entomology 5(6): 1160–1164. https://doi.org/10.1093/ee/5.6.1160
Ma Z, Li C, Pan G, Li Z, Han B, Xu J, Lan X, Chen J, Yang D, Chen Q, Sang Q, Ji X, Li T, Long M, Zhou Z (2013) Genome-Wide Transcriptional Response of Silkworm (Bombyx mori) to Infection by the Microsporidian Nosema bombycis. PLoS ONE 8(12): e84137. https://doi.org/10.1371/journal.pone.0084137
Malysh JM, Ignatieva AN, Artokhin KS, Frolov AN, Tokarev YS (2018) Natural infection of the beet webworm Loxostege sticticalis L. (Lepidoptera: Crambidae) with three Microsporidia and host switching in Nosema ceranae. Parasitology Research 117(9): 3039–3044. https://doi.org/10.1007/s00436-018-5987-3
Malysh YuM, Tokarev YuS, Sitnikova NV, Kononchuk AG, Grushetskaya TA, Frolov AN (2011) Incidence of microsporidian infection of stem borers of the genus Ostrinia (Lepidoptera: Crambidae) in the Krasnodar territory. Parazitologiya 45(3): 234–244. [In Russian with English summary]
Mansour R, Biondi A (2021) Releasing natural enemies and applying microbial and botanical pesticides for managing Tuta absoluta in the MENA region. Phytoparasitica 49(2): 179–194. https://doi.org/10.1007/s12600-020-00849-w
Marti Jr OG, Hamm JJ (1985) Effect of Vairimorpha sp. on survival of Geocoris punctipes in the laboratory. Journal of Entomological Science 20(3): 354–358. https://doi.org/10.18474/0749-8004-20.3.354
Möhring N, Ingold K, Kudsk P, Martin-Laurent F, Niggli U, Siegrist M, Studer B, Walter A, Finger R (2020) Pathways for advancing pesticide policies. Nature food 1(9): 535–540. https://doi.org/10.1038/s43016-020-00141-4
Pell JK, Vandenberg JD (2002) Interactions among the aphid Diuraphis noxia, the entomopathogenic fungus Paecilomyces fumosoroseus and the coccinellid Hippodamia convergens. Biocontrol Science and Technology 12(2): 217–224. https://doi.org/10.1080/09583150120124478
Roy HE, Pell JK, Alderson PG (2001) Targeted dispersal of the aphid pathogenic fungus Erynia neoaphidis by the aphid predator Coccinella septempunctata. Biocontrol Science and Technology 11(1): 99–110. https://doi.org/10.1080/09583150020029781
Saito T, Bjørnson S (2006) Horizontal transmission of a microsporidium from the convergent lady beetle, Hippodamia convergens Guérin-Méneville (Coleoptera: Coccinellidae), to three coccinellid species of Nova Scotia. Biological Control 39(3): 427–433. https://doi.org/10.1016/j.biocontrol.2006.06.012
Saito T, Bjørnson S (2013) The convergent lady beetle, Hippodamia convergens Guérin-Méneville and its endoparasitoid Dinocampus coccinellae (Schrank): the effect of a microsporidium on parasitoid development and host preference. Journal of Invertebrate Pathology 113(1): 18–25. https://doi.org/10.1016/j.jip.2013.01.003
Sajap AS, Lewis LC (1989) Impact of Nosema pyrausta (Microsporida: Nosematidae) on a predator, Chrysoperla carnea (Neuroptera: Chrysopidae). Environmental Entomology 18(1): 172–176. https://doi.org/10.1093/ee/18.1.172
Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.
Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proceedings of the National Academy of Sciences 74(12): 5463–5467.
Schuld M, Madel G, Schmuck R (1999) Impact of Vairimorpha sp. (Microsporidia: Burnellidae) on Trichogramma chilonis (Hymenoptera, Trichogrammatidae), a hymenopteran parasitoid of the cabbage moth, Plutella xylostella (Lepidoptera, Yponomeutidae). Journal of Invertebrate Pathology 74(2): 120–126. https://doi.org/10.1006/jipa.1999.4865
Sedaratian A, Fathipour Y, Talaei-Hassanloui R (2014) Deleterious effects of Bacillus thuringiensis on biological parameters of Habrobracon hebetor parasitizing Helicoverpa armigera. Biological Control 59: 89–98. https://doi.org/10.1007/s10526-013-9531-1
Sedaratian-Jahromi A (2021) Effects of entomopathogens on insect predators and parasitoids. In: Khan MA, Ahmad W (Eds) Microbes for Sustainable Insect Pest Management: Hydrolytic Enzyme & Secondary Metabolite. Springer, Cham, Switzerland, 183–231. https://doi.org/10.1007/978-3-030-67231-7_9
Siegel JP, Maddox JV, Ruesink WG (1988) Seasonal progress of Nosema pyrausta in the European corn borer, Ostrinia nubilalis. Journal of Invertebrate Pathology 52: 130–136. https://doi.org/10.1016/0022-2011(88)90111-5
Simões RA, Feliciano JR, Solter LF, Delalibera JrI (2015) Impacts of Nosema sp. (Microsporidia: Nosematidae) on the sugarcane borer, Diatraea saccharalis (Lepidoptera: Crambidae). Journal of Invertebrate Pathology 129: 7–12. https://doi.org/10.1016/j.jip.2015.05.006
Smirnoff WA, Eichhorn O (1970) Diseases affecting predators of Adelges spp. on fir trees in Germany, Switzerland, and Turkey. Journal of Invertebrate Pathology 15(1): 6–9. https://doi.org/10.1016/0022-2011(70)90091-1
Solter LF, Becnel JJ, Vávra J (2012) Research methods for entomopathogenic microsporidia and other protists. In: Lacey LA (Ed) Manual of Techniques in Invertebrate Pathology 12: 329–371. https://doi.org/10.1016/B978-0-12-386899-2.00011-7
Sparks TC, Nauen R (2015) IRAC: Mode of action classification and insecticide resistance management. Pesticide Biochemistry and Physiology 121: 122–128. https://doi.org/10.1016/j.pestbp.2014.11.014
Sreelakshmi B, Induja S, Adarsh PP, Rahul HL, Arya SM, Aswana S, Haripriya R, Aswathy BR, Manoj PK, Vishnudasan D (2021) Drought stress amelioration in plants using green synthesised iron oxide nanoparticles. Materials Today: Proceedings 41: 723–727. https://doi.org/10.1016/j.matpr.2020.05.801
Stamopoulos DC, Chloridis A (1994) Predation rates, survivorship and development of Podisus maculiventris (Het.: Pentatomidae) on larvae of Leptinotarsa decemlineata (Col.: Chrysomelidae) and Pieris brassicae (Lep.: Pieridae), under field conditions. Entomophaga 39: 3–9. https://doi.org/10.1007/BF02373489
Stejskal V, Vendl T, Aulicky R, Athanassiou C (2021) Synthetic and natural insecticides: Gas, liquid, gel and solid formulations for stored-product and food-industry pest control. Insects 12(7): 590. https://doi.org/10.3390/insects12070590
Suraporn S, Terenius O (2021) Supplementation of Lactobacillus casei reduces the mortality of Bombyx mori larvae challenged by Nosema bombycis. BMC Research Notes 14: 398. https://doi.org/10.1186/s13104-021-05807-1
Tang FHM, Lenzen M, McBratney A, Maggi F (2021) Risk of pesticide pollution at the global scale. Nature Geoscience 14: 206–210. https://doi.org/10.1038/s41561-021-00712-5
Thieltges DW, Amundsen PA, Hechinger RF, Johnson PT, Lafferty KD, Mouritsen KN, Preston DL, Reise K, Zander CD, Poulin R (2013) Parasites as prey in aquatic food webs: implications for predator infection and parasite transmission. Oikos 122(10): 1473–1482. https://doi.org/10.1111/j.1600-0706.2013.00243.x
Tokarev YS, Simakova AV, Timofeev SA, Malysh JM, Sokolova ОI, Issi IV (2016) Host specificity in microsporidia. Parasitologia 50(6): 446–459. [In Russian with English summary]
Tokarev YS, Huang WF, Solter LF, Malysh JM, Becnel JJ, Vossbrinck CR (2020) A formal redefinition of the genera Nosema and Vairimorpha (Microsporidia: Nosematidae) and reassignment of species based on molecular phylogenetics. Journal of Invertebrate Pathology 169: 107279. https://doi.org/10.1016/j.jip.2019.107279
Valera F, Martín-Hernandez R, Higes M (2011) Evaluation of large-scale dissemination of Nosema ceranae spores by European beeeaters Merops apiaster. Environmental Microbiology Reports 3: 47–53. https://doi.org/10.1111/j.1758-2229.2010.00186.x
van Frankenhuyzen K, Ebling P, McCron B, Ladd T, Gauthier D, Vossbrinck C (2004) Occurrence of Cystosporogenes sp. (Protozoa, Microsporidia) in a multi-species insect production facility and its elimination from a colony of the eastern spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae). Journal of Invertebrate Pathology 87(1): 16–28. https://doi.org/10.1016/j.jip.2004.06.001
van Frankenhuyzen K, Nystrom C, Liu Y (2007) Vertical transmission of Nosema fumiferanae (Microsporidia: Nosematidae) and consequences for distribution, post-diapause emergence and dispersal of second-instar larvae of the spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae). Journal of Invertebrate Pathology 96(2): 173–182. https://doi.org/10.1016/j.jip.2007.03.017
Vivan LM, Torres JB, Fernandes PLS (2017) Activity of selected formulated biorational and synthetic insecticides against larvae of Helicoverpa armigera (Lepidoptera: Noctuidae). Journal of Economic Entomology 110(1): 118–126. https://doi.org/10.1093/jee/tow244
Vogelstein B, Gillespie D (1979) Preparative and analytical purification of DNA from agarose. The Proceedings of the National Academy of Sciences 76(2): 615–619.
Wang-Peng S, Zheng X, Jia WT, Li AM, Camara I, Chen HX, Tan SQ, Liu YQ, Ji R (2018) Horizontal transmission of Paranosema locustae (Microsporidia) in grasshopper populations via predatory natural enemies. Pest Management Science 74(11): 2589–2593. https://doi.org/10.1002/ps.5047
Young OP, Hamm JJ (1985) Compatibility of two fall armyworm pathogens with the predaceous beetle, Calosoma sayi (Coleoptera: Carabidae). Journal of Entomological Science 20(2): 212–218. https://doi.org/10.18474/0749-8004-20.2.212
Zhang X, Feng H, He J, Liang X, Zhang N, Shao Y, Zhang F, Lu X (2022) The gut commensal bacterium Enterococcus faecalis LX10 contributes to defending against Nosema bombycis infection in Bombyx mori. Pest Management Science 78(6): 2215–2227. https://doi.org/10.1002/ps.6846
Zhu H, Kim JJ (2012) Target-oriented dissemination of Beauveria bassiana conidia by the predators, Harmonia axyridis (Coleoptera: Coccinellidae) and Chrysoperla carnea (Neuroptera: Chrysopidae) for biocontrol of Myzus persicae. Biocontrol Science and Technology 22(4): 393–406. https://doi.org/10.1080/09583157.2012.661843
Zimmermann G, Huger AM, Langenbruch GA, Kleespies RG (2016) Pathogens of the European corn borer, Ostrinia nubilalis, with special regard to the microsporidium Nosema pyrausta. Journal of Pest Science 89(2): 329–346. https://doi.org/10.1007/s10340-016-0749-4
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