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Root-Knot and Reniform Nematode Infection of Cotton Hairy Roots. Martin J. E. Wubben and Franklin E. Callahan USDA-ARS Crop Science Research Laboratory Genetics and Precision Agriculture Research Unit Mississippi State, MS. Plant-parasitic nematodes of cotton. Sedentary root parasites
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Root-Knot and Reniform Nematode Infection of Cotton Hairy Roots Martin J. E. Wubben and Franklin E. Callahan USDA-ARS Crop Science Research Laboratory Genetics and Precision Agriculture Research Unit Mississippi State, MS
Plant-parasitic nematodes of cotton • Sedentary root parasites • Require living cells to siphon nutrients • from the host root • Inflict significant annual yield losses • Incorporation of genetic resistance into • elite cultivars is ongoing • Molecular aspects of their interaction • with cotton remain largely unstudied Root-Knot Nematode Meloidogyne incognita Reniform Nematode Rotylenchulus reniformis
Advantages of an in vitro system • Provide a controlled environment - limit abiotic stresses - eliminate secondary infections - requires a growth chamber and not a greenhouse (saves space) • Feeding reniform nematodes can more easily be collected for functional genomic studies • Candidate resistance gene screening • Increase throughput for testing alternative biotech-driven control methods (example: RNAi)
Cotton hairy roots • Established for soybean, tomato, tobacco, coffee and others in studying nematode parasitism • Arabidopsis lacks resistance to root-knot and reniform nematode • Cheaper and easier to generate transgenic hairy roots versus whole plant transformation Hairy root initiation on cotton cotyledons
Primary objectives • Optimize hairy root growth conditions for propagation and nematode inoculation • Optimize protocol for inoculum collection and surface-sterilization of infective nematode life-stages • Verify nematode life-cycle completion on the susceptible hairy root culture DP90
Root-knot nematode inoculations NaOCl extraction Sugar floatation Hatch chamber Surface sterilization Apply nematode / LMP suspension directly to the root tips Suspend in 1.5 % low-melting-point agarose
RKN infection of cotton hairy roots Galls 7 days after inoculation with infective RKN J2 10 days after inoculation with infective RKN J2
J3 J2 RKN infection of cotton hairy roots 17 days after inoculation roots stained with acid fuchsin
RKN infection of cotton hairy roots 17 days after inoculation roots stained with acid fuchsin
RKN fourth-stage juvenile RKN third-stage juvenile
Gelatinous matrix exuded by RKN female (45 dai) RKN egg production on cotton hairy root culture (45 dai)
Reniform nematode inoculations • Autoclaved sand • Growth chamber • Egg inoculum Baerman funnel Surface sterilization Apply nematode / LMP suspension directly to the root tips Suspend in 1.5 % low-melting-point agarose
Reniform nematode infection of cotton hairy roots 11 days after inoculation roots stained with acid fuchsin
Reniform nematode on cotton hairy roots 24 days after inoculation roots stained with acid fuchsin
live feeding nematodes 32 days after inoculation
complete egg mass mature female 32 days after inoculation
Research in progress • Hairy root lines from root-knot and reniform nematode resistant plants are being propagated • Determine best method for measuring nematode reproduction (galls, eggs, females, ….) • Histopathology of susceptible and resistant interactions • Candidate gene over-expression in susceptible root culture
USDA-ARS, MS State Dr. Russel Hayes Dr. Johnie Jenkins Mr. Kimber Gorley USDA-ARS, Lubbock Dr. Forest Robinson USDA-ARS, Stoneville Dr. Erik Sacks USDA-ARS, New Orleans Dr. Barbara Triplett Acknowledgements