Viral diseases, especially those caused by mixed infections, are among the economically most important diseases of sweetpotato. Real-time PCR assays were developed for the detection and quantification of the potyviruses Sweet potato feathery mottle virus (SPFMV), Sweet potato virus G (SPVG), Ipomoea vein mosaic virus (IVMV); the crinivirus Sweet potato chlorotic stunt virus (SPCSV), and the begomovirus Sweet potato leaf curl virus (SPLCV) directly from infected sweetpotato plants. Titers of SPFMV, IVMV, and SPVG were lower in singly-infected sweetpotato plants compared to singly-infected plants of the standard indicator host Brazilian morning-glory (Ipomoea setosa) and the standard propagation host I. nil cv. Scarlet O Hara plants. The effect of SPSCV on titers of potyviruses infecting sweetpotato in the U.S. was investigated in a separate study. Titers of all potyviruses evaluated were enhanced in the presence of SPCSV suggesting that a conserved mechanism may underlie the enhancement of different potyviruses. Although titers of the common strain of SPFMV (SPFMV-C) were enhanced similarly to the russet crack strain (SPFMV-RC), SPFMV-C did not cause typical sweet potato virus disease (SPVD) symptoms when co-infecting with SPCSV, whereas SPFMV-RC with SPCSV caused severe SPVD symptoms. Titers of SPCSV were lower when coinfecting with potyviruses compared to plants infected with SPCSV alone. Expression analysis using cDNA microarrays revealed that the number of differentially expressed genes in plants infected with either SPFMV or SPCSV alone compared to virus-tested plants was 3 and 14, respectively. These findings were in stark contrast with SPVD-affected plants where over 200 genes were differentially expressed. SPVD-responsive genes are involved in various cellular processes including several that were identified as pathogenesis- or stress-induced. Even though titers of the U.S. isolate of SPLCV (SPLCV-US) were greater in the presence of potyviruses compared to titers of SPLCV in single infections, they were statistically different only when co-infecting SPFMV-RC and IVMV. Quantification of SPLCV in sweetpotato cultivars revealed that titers were significantly lower in cultivars known to be tolerant of the effects of SPLCV on yield. Real-time PCR was a more sensitive and specific detection method for the viruses evaluated compared to conventional PCR or ELISA assays.
| Identifer | oai:union.ndltd.org:LSU/oai:etd.lsu.edu:etd-03092006-163704 |
| Date | 10 March 2006 |
| Creators | Kokkinos, Charalambos D. |
| Contributors | Eric P. Webster, Raymond W. Schneider, Ding S. Shih, Rodrigo A. Valverde, Christopher A. Clark |
| Publisher | LSU |
| Source Sets | Louisiana State University |
| Language | English |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.lsu.edu/docs/available/etd-03092006-163704/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached herein a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to LSU or its agents the non-exclusive license to archive and make accessible, under the conditions specified below and in appropriate University policies, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
Page generated in 0.002 seconds