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A comparison of the FMRFamide-like peptide proteolytic activities of preparations from two plant-parasitic nematodes (Heterodera glycines and Meloidogyne incognita): possible targets for novel control

Published online by Cambridge University Press:  06 February 2012

E.P. Masler*
Affiliation:
Nematology Laboratory, United States Department of Agriculture, Agricultural Research Service, 10300 Baltimore Avenue, BARC-West, Beltsville, MD20705-2350, USA
*
* Fax: 301-504-5062, E-mail: edward.masler@ars.usda.gov

Abstract

Proteolytic activities in extracts from the plant-parasitic nematodes Heterodera glycines and Meloidogyneincognita were examined for their abilities to digest three FRET-modified peptide substrates representing members of the large FMRFamide-like peptide (FLP) family in nematodes. Included were sequences distributed across all nematode species (KSAYMRFa and KHEYLRFa) and a sequence confined to a narrow range of plant-parasitic nematodes (KHEFVRFa). Species variations were observed among substrate affinities, reaction rates and effect of protease inhibitors. Km values for KHEYLRFa (1.48 ± 0.34 μm) and KSAYMRFa (2.13 ± 0.24 μm) in H. glycines were each lower (P< 0.05) than those for the same substrates in M. incognita (5.26 ± 1.30 μm and 3.90 ± 0.61 μm, respectively). The Km of KHEFVRFa was lower (P< 0.05) in M. incognita (5.83 ± 0.36 μm) than in H. glycines (11.01 ± 1.26 μm). Reaction rates (Vmax/min/μg) for KHEYLRFa were the same for both species, but KSAYMRFa and KHEFVRFa digestion rates were each nearly twofold higher (P< 0.05) in M. incognita than in H. glycines. Digestion of KSAYMRFa was strongly inhibited in both species by 4-(2-aminoethyl)-benzenesulfonyl-fluoride-HCl (AEBSF) and EDTA, but M. incognita was more sensitive (P< 0.05) to inhibition. AEBSF and EDTA (both at 1 mm) inhibited M. incognita activity 62.3% and 36.6% more, respectively, than H. glycines activity. Serine protease inhibition differed significantly (P< 0.05) between the two species. Maximum inhibition of M. incognita (76%) occurred at 1.85 mm AEBSF while maximum inhibition of H. glycines was 40% at 1.19 mm AEBSF.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2012. This is a work of the US Government and is not subject to copyright protection in the United States

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References

Castagnone-Sereno, P., Deleury, E., Danchin, E.G.J., Perfus-Barbeoch, L. & Abad, P. (2011) Data-mining of the Meloidogyne incognita degradome and comparative analysis of proteases in nematodes. Genomics 97, 2936.CrossRefGoogle ScholarPubMed
Cohen, M., Reale, V., Olofsson, B., Knights, A., Evans, P. & de Bono, M. (2009) Coordinated regulation of foraging and metabolism in C. elegans by RFamide neuropeptide signaling. Cell Metabolism 9, 375385.CrossRefGoogle Scholar
Craig, H., Isaac, R.E. & Brooks, D.R. (2007) Unravelling the moulting degradome: new opportunities for chemotherapy? Trends in Parasitology 23, 248253.CrossRefGoogle ScholarPubMed
Greenwood, K., Williams, T. & Geary, T. (2005) Nematode neuropeptide receptors and their development as anthelmintic screens. Parasitology 131, S169S177.CrossRefGoogle ScholarPubMed
Holden-Dye, L. & Walker, R.J. (2011) Neurobiology of plant parasitic nematodes. Invertebrate Neuroscience 11, 919.CrossRefGoogle ScholarPubMed
Husson, S.J., Mertens, I., Janssen, T., Lindemans, M. & Schoofs, L. (2007) Neuropeptidergic signaling in the nematode Caenorhabditis elegans. Progress in Neurobiology 82, 3355.CrossRefGoogle ScholarPubMed
Johnston, M.J.G., McVeigh, P., McMaster, S., Fleming, C.C. & Maule, A.G. (2010) FMRFamide-like peptides in root knot nematodes and their potential role in nematode physiology. Journal of Helminthology 84, 253265.CrossRefGoogle ScholarPubMed
Kimber, M.J. & Fleming, C.C. (2005) Neuromuscular function in plant parasitic nematodes: a target for novel control strategies? Parasitology 131, S129S142.CrossRefGoogle ScholarPubMed
Kimber, M.J., Fleming, C.C., Prior, A., Jones, J.T., Halton, D.W. & Maule, A.G. (2002) Localisation of Globodera pallida FMRFamide-related peptide encoding genes using in situ hybridization. International Journal for Parasitology 32, 10951105.CrossRefGoogle Scholar
Kimber, M.J., McKinney, S., McMaster, S., Day, T.A., Fleming, C.C. & Maule, A.G. (2007) flp gene disruption in a parasitic nematode reveals motor dysfunction and unusual neuronal sensitivity to RNA interference. FASEB Journal 21, 12331243.CrossRefGoogle Scholar
Li, C. & Kim, K. (2010) Neuropeptide gene families in Caenorhabditis elegans. pp. 98137in Geary, T.G. & Maule, A.G. (Eds) Neuropeptide systems as targets for parasite and pest control, Advances in experimental medicine and biology 692. New York, Springer Science & Business Media.Google Scholar
Liu, T., Kim, K., Li, C. & Barr, M.M. (2007) FMRFamide-like peptides and mechanosensory touch receptor neurons regulate male sexual turning behavior in Caenorhabditis elegans. Journal of Neuroscience 27, 71747182.CrossRefGoogle ScholarPubMed
Masler, E.P. (2008) Digestion of invertebrate neuropeptides by preparations from the free-living nematode Panagrellus redivivus. Journal of Helminthology 82, 279285.CrossRefGoogle ScholarPubMed
Masler, E.P. (2012) In vitro proteolysis of nematode FMRFamide-like peptides (FLPs) by preparations from a free-living nematode (Panagrellus redivivus) and two plant-parasitic nematodes (Heterodera glycines and Meloidogyne incognita). Journal of Helminthology 86, 7784.CrossRefGoogle ScholarPubMed
Maule, A.G., Mousley, A., Marks, N.J., Day, T.A., Thompson, D.P., Geary, T.G. & Halton, D.W. (2002) Neuropeptide signaling systems – potential drug targets for parasite control. Current Topics in Medicinal Chemistry 2, 733758.CrossRefGoogle Scholar
McVeigh, P., Leech, S., Mair, G.R., Marks, N.J., Geary, T.G. & Maule, A.G. (2005) Analysis of FMRFamide-like peptide (FLP) diversity in phylum Nematoda. International Journal for Parasitology 35, 10431060.CrossRefGoogle ScholarPubMed
McVeigh, P., Geary, T.G., Marks, N.J. & Maule, A.G. (2006) The FLP-side of nematodes. Trends in Parasitology 22, 385396.CrossRefGoogle ScholarPubMed
Moffett, C.L., Beckett, A.M., Mousley, A., Geary, T.G., Marks, N.J., Halton, D.W., Thompson, D.P. & Maule, A.G. (2003) The ovijector of Ascaris suum: multiple response types revealed by Caenorhabditis elegans FMRFamide-related peptides. International Journal for Parasitology 33, 859876.CrossRefGoogle ScholarPubMed
Papaioannou, S., Marsden, D., Franks, C.J., Walker, R.J. & Holden-Dye, L. (2005) Role of a FMRFamide-like family of neuropeptides in the pharyngeal nervous system of Caenorhabditis elegans. Journal of Neurobiology 65, 304319.CrossRefGoogle ScholarPubMed
Rogers, C., Reale, V., Kim, K., Chatwin, H., Li, C., Evans, P. & de Bono, M. (2003) Inhibition of Caenorhabditis elegans social feeding by FMRFamide-related peptide activation of NPR-1. Nature Neuroscience 6, 11781185.CrossRefGoogle ScholarPubMed
Sardanelli, S. & Kenworthy, W.J. (1997) Soil moisture control and direct seeding for bioassay of Heterodera glycines on soybean. Journal of Nematology 29, 625634.Google ScholarPubMed