Skip to main content
Log in

Verification of serological relationship between two phylogenetically related peanut-infecting Tospovirus species

  • Published:
European Journal of Plant Pathology Aims and scope Submit manuscript

Abstract

Based on the serological relationships of nucleocapsid proteins (NPs), a tospovirus species can be classified as a member of a serogroup or a distinct serotype, which greatly helps virus identification and disease diagnosis. Recent studies reported that distinct tospovirus species sharing above 51.8 % amino acid (aa) identity in their NPs may be serologically related. Two phylogenetically related peanut-infecting tospovirus species, Peanut chlorotic fan-spot virus (PCFV) in Taiwan and Peanut yellow spot virus (PYSV) in India, were previously considered as distinct serotypes, since no serological relationship has been established. To verify the serological relationship of PCFV and PYSV, the NP of PCFV was purified from leaf tissues of the infected Chenopodium quinoa plants and used to produce polyclonal antiserum (RAs-PCFV NP) and a monoclonal antibody (MAb-PCFV NP). Polyclonal antiserum to the bacterially expressed NP of PYSV (RAs-PYSV NP) was also prepared. RAs-PCFV NP reacted with the homologous PCFV NP and the bacterial-expressed PYSV NP and tissue extracts of PYSV-infected plants. Reciprocally, RAs-PYSV NP reacted with the homologous bacterial-expressed PYSV NP and the tissue extracts of PYSV-infected or PCFV-infected plants. In addition, MAb-PCFV NP reacted only with the tissue extracts of PCFV-infected plants. Our results demonstrate that PCFV NP is serologically related to PYSV NP and they should be classified as members of a unique serogroup.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Chen, C. C., & Chiu, R. J. (1996). A tospovirus infecting peanut in Taiwan. Acta Horticulturae, 431, 57–67.

    Google Scholar 

  • Chen, C. C., Chen, T. C., Lin, Y. H., Yeh, S. D., & Hsu, H. T. (2005a). A chlorotic spot disease on calla lilies (Zantedeschia spp.) is caused by a tospovirus serologically but distantly related to Watermelon silver mottle virus. Plant Disease, 89, 440–445.

    Article  CAS  Google Scholar 

  • Chen, T. C., Hsu, H. T., Jain, R. K., Huang, C. W., Lin, C. H., Liu, F. L., et al. (2005b). Purification and serological analyses of tospoviral nucleocapsid proteins expressed by Zucchini yellow mosaic virus vector in squash. Journal of Virological Methods, 129, 113–124.

    Article  PubMed  CAS  Google Scholar 

  • Chen, T. C., Huang, C. W., Kuo, Y. W., Liu, F. L., Hsuan Yuan, C. H., Hsu, H. T., et al. (2006). Identification of common epitopes on a conserved region of NSs proteins among tospoviruses of Watermelon silver mottle virus serogroup. Phytopathology, 96, 1296–1304.

    Article  PubMed  CAS  Google Scholar 

  • Chen, T. C., Lu, Y. Y., Cheng, Y. H., Chang, C. A., & Yeh, S. D. (2008). Melon yellow spot virus in watermelon: a first record from Taiwan. Plant Pathology, 57, 765.

    Article  Google Scholar 

  • Chen, T. C., Lu, Y. Y., Cheng, Y. H., Li, J. T., Yeh, Y. C., Kang, Y. C., et al. (2010). Serological relationship between melon yellow spot virus and Watermelon silver mottle virus and differential detection of the two viruses in cucurbits. Archives of Virology, 155, 1085–1095.

    Article  PubMed  CAS  Google Scholar 

  • Chen, T. C., Lu, Y. Y., Kang, Y. C., Li, J. T., Yeh, Y. C., Kormelink, R., et al. (2011). Detection of eight different Tospovirus species by a monoclonal antibody against the common epitope of NSs protein. Acta Horticulturae, 901, 61–66.

    CAS  Google Scholar 

  • Chu, F. H., Chao, C. H., Peng, Y. C., Lin, S. S., Chen, C. C., & Yeh, S. D. (2001). Serological and molecular characterization of Peanut chlorotic fan-spot virus, a new species of the genus Tospovirus. Phytopathology, 91, 856–863.

    Article  PubMed  CAS  Google Scholar 

  • Ciuffo, M., Tavella, L., Pacifico, D., Masenga, V., & Turina, M. (2008). A member of a new Tospovirus species isolated in Italy from wild buckwheat (Polygonum convolvulus). Archives of Virology, 153, 2059–2068.

    Article  PubMed  CAS  Google Scholar 

  • Ciuffo, M., Kurowski, C., Vivoda, E., Copes, B., Masenga, V., Falk, B. W., et al. (2009). A new Tospovirus sp. in cucurbit crops in Mexico. Plant Disease, 93, 467–474.

    Article  CAS  Google Scholar 

  • Cortes, I., Livieratos, I. C., Derks, A., Peters, D., & Kormelink, R. (1998). Molecular and serological characterization of Iris yellow spot virus, a new and distinct tospovirus species. Phytopathology, 88, 1276–1282.

    Article  PubMed  CAS  Google Scholar 

  • Dayhoff, M. O., Schwartz, R. M., & Orcutt, B. C. (1979). In Atlas of protein sequence and structure, Vol. 5, pp. 345–352. Ed M.O. Dayhoff. National Biomedical Research Foundation: Silver Spring.

  • de Ávila, A. C., Huguenot, C., Resende, R. O., Kitajima, E. W., Goldbach, R. W., & Peters, D. (1990). Serological differentiation of 20 isolates of tomato spotted wilt virus. Journal of General Virology, 71, 2801–2807.

    Article  PubMed  Google Scholar 

  • de Avila, A. C., de Haan, P., Kormelink, R., Resende, R. O., Goldbach, R. W., & Peters, D. (1993). Classification of tospoviruses based on phylogeny of nucleoprotein gene sequences. Journal of General Virology, 74, 153–159.

    Article  PubMed  Google Scholar 

  • de Haan, P., Wagemakers, L., Peters, D., & Goldbach, R. (1990). The S RNA segment of tomato spotted wilt virus has an ambisense character. Journal of General Virology, 71, 1001–1007.

    Article  PubMed  Google Scholar 

  • de Haan, P., Kormelink, R., de Oliveira Resende, R., van Poelwijk, F., Peters, D., & Goldbach, R. (1991). Tomato spotted wilt virus L RNA encodes a putative RNA polymerase. Journal of General Virology, 72, 2207–2216.

    Article  PubMed  Google Scholar 

  • de Oliveira, A. S., Bertran, A. G., Inoue-Nagata, A. K., Nagata, T., Kitajima, E. W., & Oliveira Resende, R. (2011). An RNA-dependent RNA polymerase gene of a distinct Brazilian tospovirus. Virus Genes, 43, 385–389.

    Article  PubMed  CAS  Google Scholar 

  • de Oliveira, A. S., Melo, F. L., Inoue-Nagata, A. K., Nagata, T., Kitajima, E. W., & Oliveira Resende, R. (2012). Characterization of Bean necrotic mosaic virus: A member of a novel evolutionary lineage within the genus Tospovirus. PLoS ONE, 7, e38634.

    Article  PubMed  PubMed Central  Google Scholar 

  • Felsenstein, J. (1989). PHYLIP – Phylogeny Inference Package (Version 3.2). Cladistics, 5, 164–166.

  • Goldbach, R., & Kuo, G. (1996). Introduction. Acta Horticulturae, 431, 21–26.

    Google Scholar 

  • Goldbach, R., & Peters, D. (1996). Molecular and biological aspects of tospoviruses. In The Bunyaviridae, pp. 129–157. Ed R.M. Elliott. New York, NY: Plenum Press.

  • Hassani-Mehraban, A., Saaijer, J., Peters, D., Goldbach, R., & Kormelink, R. (2005). A new tomato-infecting tospovirus from Iran. Phytopathology, 95, 852–858.

    Article  PubMed  CAS  Google Scholar 

  • Heinze, C., Roggero, P., Sohn, M., Vaira, A. M., Masenga, V., & Adam, G. (2000). Peptide-derived broad-reacting antisera against tospovirus NSs-protein. Journal of Virological Methods, 89, 137–146.

    Article  PubMed  CAS  Google Scholar 

  • Hsu, H. T., Aebig, J., & Rochow, W. F. (1984). Differences among monoclonal antibodies to Barley yellow dwarf viruses. Phytopathology, 74, 600–605.

    Article  Google Scholar 

  • Hsu, H. T., Ueng, P. P., Chu, F. H., Ye, Z., & Yeh, S. D. (2000). Serological and molecular characterization of a high temperature-recovered virus belonging to Tospovirus serogroup IV. Journal of General Plant Pathology, 66, 167–175.

    Article  CAS  Google Scholar 

  • Jan, F. J., Chen, T. C., & Yeh, S. D. (2003). Occurrence, importance, taxonomy, and control of thrips-borne tospoviruses. In Advances in Plant disease Management, pp. 399–421. Eds H.C. Huang and S.N. Acharya. Trivandrum, India: ResearchSignpost.

  • Kato, K., Hanada, K., & Kameya-Iwaki, M. (2000). Melon yellow spot virus: a distinct species of the genus tospovirus isolated from melon. Phytopathology, 90, 422–426.

    Article  PubMed  CAS  Google Scholar 

  • King, A. M. Q., Adams, M. J., Carstens, E. B., & Lefkowitz, E. J. (2011). Virus taxonomy: ninth report of the international committeeon taxonomy of viruses. Amsterdam: Elsevier Academic Press.

    Google Scholar 

  • Kormelink, R., de Haan, P., Meurs, C., Peters, D., & Goldbach, R. (1992). The nucleotide sequencw of the M RNA segments of tomato spotted wilt virus, a bunyavirus with two ambisense RNA segments. Journal of General Virology, 73, 2795–2804.

    Article  PubMed  CAS  Google Scholar 

  • Law, M. D., & Moyer, J. W. (1990). A tomato spotted wilt-like virus with a serologically distinct N protein. Journal of General Virology, 71, 933–938.

    Article  CAS  Google Scholar 

  • Law, M. D., Speck, J., & Moyer, J. W. (1992). The M RNA of impatiens necrotic spot tospovirus (Bunyaviridae) has an ambisense genomic organization. Virology, 188, 732–741.

    Article  PubMed  CAS  Google Scholar 

  • Li, J. T., Yeh, Y. C., Yeh, S. D., Raja, J. A. J., Rajagopalan, P. A., Liu, L. Y., et al. (2011). Complete genomic sequence of watermelon bud necrosis virus. Archives of Virology, 156, 359–362.

    Article  PubMed  CAS  Google Scholar 

  • Lin, Y. H., Chen, T. C., Hsu, H. T., Liu, F. L., Chu, F. H., Chen, C. C., et al. (2005). Serological comparison and molecular characterization for verification of Calla lily chlorotic spot virus as a new tospovirus species belonging to Watermelon silver mottle virus serogroup. Phytopathology, 95, 1482–1488.

    Article  PubMed  CAS  Google Scholar 

  • Mohamed, N. A. (1981). Isolation and characterization of subviral structures from tomato spotted wilt virus. Journal of General Virology, 53, 197–208.

    Article  CAS  Google Scholar 

  • Mohamed, N. A., Randles, J. W., & Francki, R. I. B. (1973). Protein composition of tomato spotted wilt virus. Virology, 56, 12–21.

    Article  PubMed  CAS  Google Scholar 

  • Pang, S. Z., Slightom, J. L., & Gonsalves, D. (1993). The biological properties of a distinct tospovirus and sequence analysis of its S RNA. Phytopathology, 83, 728–733.

    Article  CAS  Google Scholar 

  • Pappu, H. R., Jones, R. A. C., & Jain, R. K. (2009). Global status of tospovirus epidemics in diverse cropping systems: successes achieved and challenges ahead. Virus Research, 141, 219–236.

    Article  PubMed  CAS  Google Scholar 

  • Peng, J. C., Yeh, S. D., Huang, L. H., Li, J. T., Cheng, Y. F., & Chen, T. C. (2011). Emerging threat of thrips-borne Melon yellow spot virus on melon and watermelon in Taiwan. European Journal of Plant Pathology, 130, 205–214.

    Article  Google Scholar 

  • Reddy, D. V. R., Sudarshana, M. R., Ratna, A. S., Reddy, A. S., Amin, P. W., Kumar, I. K., & Murthy, A. K. (1991). The occurrence of yellow spot virus, a member of tomato spotted wilt virus group, on peanut (Arachis hypogaea L) in India. In Virus-Thrips-Plant interactions of tomato spotted wilt virus, pp. 77–88. Eds H.T. Hsu and R.H. Lawson. Proceedings of the USDA Agricultural Research Service, ARS-87.

  • Saitou, N., & Nei, M. (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees. Molecular Biology and Evolution, 4, 406–425.

    PubMed  CAS  Google Scholar 

  • Satyanarayana, T., Gowda, S., Reddy, K. L., Mitchell, S. E., Dawson, W. O., & Reddy, D. V. R. (1998). Peanut yellow spot virus is a member of a new serogroup of Tospovirus genus based on small (S) RNA sequence and organization. Archives of Virology, 143, 353–364.

    Article  PubMed  CAS  Google Scholar 

  • Seepiban, C., Gajanandana, O., Attathom, T., & Attathom, S. (2011). Tomato necrotic ringspot virus, a new tospovirus isolated in Thailand. Archives of Virology, 156, 263–274.

    Article  PubMed  CAS  Google Scholar 

  • van Knippenberg, I., Goldbach, R., & Peters, D. (2002). Purified Tomato spotted wilt virus particles support both genome replication and transcription in vitro. Virology, 303, 278–286.

    Article  PubMed  Google Scholar 

  • Yeh, S. D., & Gonsalves, D. (1984). Purification and immunological analysis of cylindrical-inclusion protein induced by Papaya ringspot virus and Watermelon mosaic virus I. Phytopathology, 74, 1273–1278.

    Article  CAS  Google Scholar 

  • Yeh, S. D., Cheng, Y. H., Jih, C. L., Chen, C. C., & Chen, M. J. (1988). Identification of tomato spotted infecting horn melon and watermelon. Plant Protection Bulletin, 30, 319–320.

    Google Scholar 

  • Yeh, S. D., Chao, C. H., Cheng, Y. H., & Chen, C. C. (1996). Serological comparison of four distinct tospoviruses by polyclonal antibodies to purified nucleocapsid proteins. Acta Horticulturae, 431, 122–134.

    CAS  Google Scholar 

  • Zhou, J., Kantartzi, S. K., Wen, R. H., Newman, M., Hajimorad, M. R., Rupe, J. C., et al. (2011). Molecular characterization of a new tospovirus infecting soybean. Virus Genes, 43, 289–295.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We thank the funding from the Bureau of Animal and Plant Health Inspection and Quarantine, Council of Agriculture, Executive Yuan [101AS-10.3.1-BQ-B1(3)], the National Science Council (NSC-101-2911-I-005-301 and NSC-102-2911-I-005-301), and the Ministry of Education, Taiwan, R.O.C. under the ATU plan.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tsung-Chi Chen.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kang, YC., Yeh, SD., Liao, CH. et al. Verification of serological relationship between two phylogenetically related peanut-infecting Tospovirus species. Eur J Plant Pathol 140, 815–828 (2014). https://doi.org/10.1007/s10658-014-0511-9

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10658-014-0511-9

Keywords

Navigation