Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniv., 2001. / Härtill 3 uppsatser.

Thesis (Ph. D.)--Swedish University of Agricultural Sciences, 2001. / Includes bibliographical references.

Thesis (doctoral)--Swedish University of Agricultural Sciences, 2001. / Includes bibliographical references.

No description available.

Polyclonal antisera were raised against isolates of bean common mosaic virus (BCMV) and bean common mosaic necrosis virus (BCMNV) using conventional serological methods. Infected tissues containing, respectively, 22 recognized BCMV and BCMNV isolates were tested against the two antisera by antigen-coated plate (ACP) ELISA and double antibody sandwich (DAS) ELISA. Results indicated that each immunoglobulin was virus-specific by DAS-ELISA, providing clear distinction between BCMV and BCMNV. A reverse transcription, polymerase chain reaction (RT-PCR)-based assay in combination with restriction endonuclease analyses, was developed for molecular detection of BCMV, BCMNV and their pathogroups. Specific detection of the two viruses was accomplished by constructing two virus-specific primer pairs that amplified a PCR product specific for each virus. Distinction of two BCMNV pathogroups (PG-III and PG-VI) was achieved by restriction enzyme XbaI digestion of BCMNV PCR products. However, none of the tested restriction enzymes clearly differentiated the five recognized BCMV pathogroups. A primer pair Dts/Uny15 specific for BCMV pathogroup V was also developed. By its RT-PCR application, four BCMV-PG-V isolates were differentiated from the other known variants of BCMV pathogroup I, II, IV and VII. Thus, by a combination of RT-PCR and restriction enzyme analyses, it was possible to differentiate both viruses, and two pathogroups of BCMNV, and one pathogroup of BCMV. / Graduation date: 1996

Little is known about the mechanism of virus disease resistance in plants. The aim of the work presented here was to answer whether disease resistance is offered within the cell or at the level of intercellular movement of the virus. The protoplast system was used for this purpose. Conditions were optimized to isolate viable protoplasts from the leaves of Lactuca sativa cultivars. Protoplasts and leaves from resistant and susceptible Lactuca sativa cultivars were inoculated separately with turnip mosaic virus (TuMV) and lettuce mosaic virus (LMV), Virus multiplication was examined over time using enzyme-linked immunosorbent assay. Resistant cv. Kordaat did not support TuMV multiplication in protoplasts as well as in leaves. The results indicated that resistance to TuMV is available within the cell. The results ruled out the possibility of involvement of cell to cell movement and resistance to TuMV seems to be constitutive. On the other hand, protoplasts and leaves from both resistant and susceptible lettuce cultivars supported LMV multiplication. This suggested that resistance to LMV may not be offered within the cell. The results also indicated that the resistance to LMV was partly due to a hypersensitive response though virus was still able to spread systemically. To contribute towards mapping of the Tu resistance gene, the genotype of F$ sb2$ individuals was determined by screening an F$ sb3$ population from 71 F$ sb2$ individuals of a cross between cv. Calmar and cv. Kordaat for TuMV-infection. These data were useful for the production of bulks around the Tu locus to facilitate the search for new molecular markers linked to the Tu gene.

Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniv., 2003. / Härtill 4 uppsatser.

Graduation date: 1994

Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniv., 2007. / Härtill 3 uppsatser.

Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniversitet, 2006. / Härtill 4 uppsatser.