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Optimisation of culture conditions for in vitro infection of tomato with the root-knot nematode Meloidogyne javanica

Hutangura, P., Jones, M.G.K.ORCID: 0000-0001-5002-0227 and Heinrich, T. (1998) Optimisation of culture conditions for in vitro infection of tomato with the root-knot nematode Meloidogyne javanica. Australasian Plant Pathology, 27 (2). pp. 84-89.

Link to Published Version: http://dx.doi.org/10.1071/AP98010
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Abstract

Conditions for in vitro culture of tomato seedlings (Lycopersicon esculentum) were optimised to yield high in vitro rates of infection by the root-knot nematode Meloidogyne javanica. The influence of nutrient salts, gelling agents, sucrose concentration and pH on the development of nematode-induced root galis was investigated. A quarter-strength Murashige and Skoog medium supplemented by 0.5% sucrose and solidified with 0.6% phytagel at pH 6.4 gave most galis on tomato roots. Eggs were sterilised in 2.5% sodium hypochlorite for 4 min followed by 0.2% mercuric chloride for 4 min. Surface-sterilised eggs showed a 16% cumulative hatching rate within 10 days. Tomato seedlings cultivated in vitro for 1 week were inoculated with sterile eggs and the infection process was monitored weekly. After 5 to 7 weeks, sterile egg masses were harvested, second-stage juveniles were hatched in sterile distilled water and used to re-inoculate tomato seedlings without further sterilisation. The culture conditions described gave similar infection results for the related root-knot nematodes M. incognita, M. arenaria and M. hapla.

Item Type: Journal Article
Murdoch Affiliation: Western Australian State Agricultural Biotechnology Centre
Publisher: CSIRO Publishing
Copyright: © Australasian Plant Pathology Society 1998
URI: http://researchrepository.murdoch.edu.au/id/eprint/18247
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