Abstract
Bombyx mori densonucleosis (BmDV), infectious flacherie (BmIFV) and nuclear polyhedrosis (BmNPV) viruses inflict huge losses in sericulture. The study was envisaged to develop productive bivoltine silkworm hybrid, tolerant to these viruses, employing marker-assisted breeding. One hundred and twenty diverse bivoltine silkworm breeds, B. mori L. (Lepidoptera: Bombycidae) in India were screened against BmDV, BmIFV and BmNPV. Eight SSR markers were identified with distinct amplification profiles between virus-tolerant and susceptible populations. Two specific populations derived from the bivoltine silkworm breeds—HBM10 and PAM117—exhibited multi-viral tolerance (PAM117: 36–67%; HBM10: 24–65%) and these lines were designated as PAM117-MVT and HBM10-MVT. The resultant foundation cross (HBM10-MVT × PAM117-MVT) showed 37% enhanced survival (BmDV: 71–75%, BmIFV: 71–74% and BmNPV: 71–72%) over the parental stocks. A productive and multi-viral-tolerant bivoltine double hybrid (RDIN1) was developed by crossing with productive foundation cross (CSR52 × CSR27). The rearing and reeling performance of RDIN1 {(CSR52 × CSR27) × (HBM10-MVT × PAM117-MVT)} was on par with the popular bivoltine double hybrid {(CSR2 × CSR27) × (CSR6 × CSR26)} across the locations. The identified SSR markers could be utilized to develop robust and resilient silkworm hybrids for commercial exploitation.
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References
Abe H, Shimada T, Tsuji T, Yokoyama T, Oshiki T, Kobayashi M (1995) Identification of random amplified polymorphic DNA linked to the densonucleosis virus type–1 Susceptibility gene of the silkworm, Bombyx mori L. Seric Sci Jpn 64:262–264
Abe H, Harada T, Kanehara M, Shimada T, Ohbayashi F, Oshiki T (1998) Genetic mapping of RAPD markers linked to the densonucleosis refractoriness gene, nsd-1, in the silkworm, Bombyx mori. Genes Genet Syst 73:237–242. https://doi.org/10.1266/ggs.73.237
Awasthi AK, Pradeep AR, Srivatava PP, Vijayan K, Kumar V, Urs SR (2007) PCR detection of densonucleosis virus isolates in silkworm (Bombyx mori) from India and their nucleotide variability. Ind J Biotech 7:55–60
Fan F, Ping H, Keping C (2013) Progress of antiviral mechanisms in the mulberry silkworm: a review. Afr J Microbiol Res 7(14):1173–1178. https://doi.org/10.5897/AJMRx12.020
Fang SM, Hu BL, Zhou QZ, Yu QY, Zhang Z (2015) Comparative analysis of the silk gland transcriptomes between the domestic and wild silkworms. BMC Genomics 16:60. https://doi.org/10.1186/s12864-015-1287-9
He S, Tong X, Han M, Bai Y, Dai F (2018) Genome-wide identification and characterization of tyrosine kinases in the silkworm Bombyx mori. Int J Mol Sci 19(4):934. https://doi.org/10.3390/ijms19040934
Kamita SG, Nagasaka K, Chua JW, Shimada T, Mita K, Kobayashi M, Maeda S, Hammock BD (2005) A baculovirus-encoded protein tyrosine phosphatase gene induces enhanced locomotory activity in a lepidopteran host. PNAS 102(7):2584–2589. https://doi.org/10.1073/pnas.040945710
Kaneko Y, Furukawa S, Tanaka H, Yamakawa M (2007) Expression of antimicrobial peptide genes encoding enbocin and gloverin isoforms in the silkworm. Biosci Biotechnol Biochem. https://doi.org/10.1271/bbb.70212
Kang L, Shi H, Liu X, Zhang C, Yao Q, Wang Y, Chang C, Shi J, Cao J, Kong J, Chen K (2011) Arginine kinase is highly expressed in a resistant strain of silkworm (Bombyx mori, Lepidoptera): implication of its role in resistance to Bombyx mori nucleopolyhedrovirus. Compar Biochem Physiol 158:230–234. https://doi.org/10.1016/j.cbpb.2010.12.001
Kobayashi J, Edimura HE, Kobayashi N (1986) The effect of temperature on the diapauses eggs production in the tropical silkworm Bombyx mori L. J Seric Sci Jpn 55(4):345–348
Miao XX, Xu SJ, Li MH, Li MW, Huang JH, Dai FY et al (2005) Simple sequence repeat-based consensus linkage map of Bombyx mori. PNAS 102:16303–16308. https://doi.org/10.1073/pnas.0507794102
Nesa J, Sadat A, Buccini DF, Kati A, Mandal AK, Franco OL (2020) Antimicrobial peptides from Bombyx mori: a splendid immune defense response in silkworms. RSC Adv 10:512–523. https://doi.org/10.1039/C9RA06864C
Okuda KK, Ito K, Murthy GN, Sivaprasad V, Ponnuvel KM (2014) Molecular Mechanism of densovirus resistance in silkworm Bombyx Mori. Sericologia 54(1):1–10
Ponnuvel KM, Nakazawa H, Furukawa S, Asaoka A, Ishibashi J, Tanaka H, Yamakawa M (2003) A lipase isolated from the silkworm Bombyx mori shows antiviral activity against nucleopolyhedrovirus. J Virol 77:10725–10729. https://doi.org/10.1128/JVI.77.19.10725-10729.2003
Seki H (1984) Mode of inheritance of the resistance to the infection with the densonucleosis virus (Yamanashi isolate) in the silkworm Bombyx mori. J Seric Sci Jpn 53:472–475
Seki H, Iwashita Y (1983) Histopathological features and pathogenicity of a densonucleosis virus of the silkworm Bombyx mori isolated from sericultural farms in Yamanashi prefecture. J Seric Sci Jpn 52:400–405
Selot R, Kumar V, Shukla S, Chandrakuntal K, Brahmaraju M, Dandin SB, Laloraya M, Kumar PG (2007) Identification of a soluble NADPH oxidoreductase (BmNOX) with antiviral activities in the gut juice of Bombyx mori. Biosci Biotechnol Biochem 71(1):200–205. https://doi.org/10.1271/bbb.60450
Sivaprasad V, Chandrasekharaiah RC, Misra S, Kumar K, Rao Y (2003) Screening of silkworm breeds for tolerance to Bombyx mori nuclear polyhedron virus (BmNPV). Int J Indust Entomol. 2(2):123–127
Sivaprasad V, Rahul K, Makwana P (2021) Immunodiagnosis of silkworm diseases. Method Microbiol. https://doi.org/10.1016/bs.mim.2021.04.002
Subbaiah EV, Royer C, Kanginakudru S, Satyavathi VV, Babu AS, Sivaprasad V, Chavancy G, DaRocha M, Jalabert A et al (2013) Engineering silkworms for resistance to baculovirus through multigene RNA interference. Genetics 193:63–75. https://doi.org/10.1534/genetics.112.144402
Uzigawa K, Aruga (1966) On the selection of resistance strains of the infectious flacherie virus in silkworm Bombyx mori L. J Seric Sci Jpn 35(1):23–26
Wang XY, Yu HZ, Xu JP, Zhang SZ, Dong YuD, Liu MH, Wang LL (2017) Comparative subcellular proteomics analysis of susceptible and near-isogenic resistant Bombyx mori (Lepidoptera) larval midgut response to BmNPV infection. Sci Rep 7:45690. https://doi.org/10.1038/srep45690
Watanabe H (1986) Resistance to the silkworm, Bombyx mori to viral infection. Agr Ecosyst Environ 15:131–139
Yao Q, Li MW, Wang Y, Wang WB, Lu J, Dong Y, Chen KP (2003) Screening of molecular markers for NPV resistance in Bombyx mori L. (Lep., Bombycidae). J Appl Ent 127:134–136. https://doi.org/10.1046/j.1439-0418.2003.00741.x
Acknowledgements
The authors acknowledge the financial support of Central Silk Board, Ministry of Textiles, Government of India, Bengaluru, for the project “AIB-3596 Development of multi-viral disease-tolerant (NPV, IFV and DNV1) bivoltine silkworm breeds/hybrids of Bombyx mori L. through marker-assisted selection” at CSRTI-Mysuru.
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The work was funded by Central Silk Board (AIB-3596), Ministry of textiles, Government of India.
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Satish, L., Kusuma, L., Shery, A.V.M.J. et al. Development of productive multi-viral disease-tolerant bivoltine silkworm breeds of Bombyx mori (Lepidoptera: Bombycidae). Appl Entomol Zool 58, 61–71 (2023). https://doi.org/10.1007/s13355-022-00803-8
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DOI: https://doi.org/10.1007/s13355-022-00803-8