Author
MELCHER, U. - OKLAHOMA STATE UNIV. | |
MITCHELL, F. - TEXAS A&M UNIV. | |
Pair, Sammy | |
FLETCHER, J. - OKLAHOMA STATE UNIV. | |
Bruton, Benny |
Submitted to: American Phytopathological Society Abstracts
Publication Type: Abstract Only Publication Acceptance Date: 11/13/1998 Publication Date: N/A Citation: N/A Interpretive Summary: Technical Abstract: Cucurbit yellow vine (YV) disease is associated with a gamma-3 proteobacterium, the YV bacterium (YVB). A pair of 16S rDNA oligonucleotide primers, YV1/YV2, amplified by PCR a 640 bp fragment from diseased plants but not from healthy plants or tested bacteria (Avila et al., Phytopathology 88:428). In a search for YVB insect vectors, several field collected leafhoppers were PCR-positive with YV1/YV2. The sequence of amplified fragments differed from that of YVB in over 30 positions but from that of an endosymbiont (BEV) of Euscelidius variegatus in only a few positions, suggesting that these leafhoppers harbor BEV or a closely related bacterium. New primer pairs were designed to differentiate YVB and BEV. BEV1/BEV2 (BEV nt 170-186 and 471-452) amplified an expected 302 bp fragment from YV1/YV2-positive insects but not from YV plants. YV1/YV4 (YV4 is YVB nt 471-454) amplified an expected 409 bp fragment from YV plants but not from YV1/YV2-positive insects. Databank searches revealed no other 16S rDNA sequences that should be amplifiable with these primers. |