Previous View
 
APSnet Home
 
Phytopathology Home


VIEW ARTICLE

Physiology and Biochemistry

Concentration and Distribution of Mild and Severe Strains of Potato Spindle Tuber Viroid in Cross-Protected Tomato Plants. Josiane Khoury, Graduate student, Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 5A3; R. P. Singh(2), A. Boucher(3), and D. H. Coombs(4). (2)(3)Senior research scientist and virology technician, Agriculture Canada, Research Station, P.O. Box 20280, Fredericton, New Brunswick, Canada E3B 4Z7; (4)Associate professor, Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 5A3. Phytopathology 78:1331-1336. Accepted for publication 9 May 1988. Copyright 1988 The American Phytopathological Society. DOI: 10.1094/Phyto-78-1331.

Analysis by return polyacrylamide gel electrophoresis (R-PAGE) of a mild strain of potato spindle tuber viroid (MA-PSTV) and a severe strain (S-PSTV) showed that both strains replicated in the plant at a similar rate and could be distinguished from each other by different electrophoretic mobilities. In singly infected plants, both strains were detected 10 days after inoculation; in doubly infected plants they were detected 8 days after inoculation. MA-PSTV was detected in all the leaflets of tomato plants 14 days postinoculation, a duration often used before challenge inoculation. In MA-PSTV-protected plants, the challenge strain (S-PSTV) was first detected 21 days after inoculation, and its concentration increased with time. Symptoms of S-PSTV appeared 48 days after challenge inoculation. In unprotected plants, S-PSTV was detected 10 days and the symptoms appeared 2128 days after inoculation. In the top leaves of the MA-PSTV-protected plants, S-PSTV totally replaced the protecting strain in the later stages of infection. Both strains multiplied in the middle and bottom leaves of MA-PSTV-protected plants. In S-PSTV-protected plants, MA-PSTV as a challenge strain was detected only in the later stages of infection but was present in top, middle, and bottom leaves of doubly infected plants. Both strains were found to be present in sepals, petals, anthers, and pistils in MA-PSTV-protected and S-PSTV-challenged plants. Fruit pulp contained only S-PSTV in MA-PSTV-protected and S-PSTV-challenged plants but contained both strains in S-PSTV-protected and MA-PSTV-challenged plants. Only low percentages of seeds were infected with MA-PSTV, and none were infected with S-PSTV.

Additional keywords: breakdown of cross-protection, diagnosis, electrophoresis, replication.