A set of introgression lines (ILs), containing individual chromosome segments from the wild nightshade Solanum lycopersicoides bred into the genetic background of cultivated tomato (Lycopersicon esculentum), has been developed. A primary group of 56 lines was selected for maximum representation of the S. lycopersicoides genome (approximately 96% of the total map units), homozygosity, and a minimum number of introgressed segments per line. A secondary set of 34 lines provides increased map resolution in certain regions. Approximately 34% of the lines were sterile in the homozygous condition, but could be maintained by heterozygotes. To facilitate identification of segregating ILs, restriction fragment length polymorphism probes were converted to higher throughput cleaved amplified polymorphic sequence markers, which supplement allozyme and morphological loci. Strong segregation distortion was observed in F2 progeny of heterozygous ILs, with an excess of L. esculentum alleles in most regions. For introgressions on distal chromosome 1L, a preferential transmission of S. lycopersicoides alleles was observed in the male germ line. Homozygous ILs generally yielded less seed from self pollination than corresponding heterozygotes, indicating that sterility effects were recessive. This IL library provides a novel resource for genetic studies of traits found in S. lycopersicoides.

A library of ''introgression lines'' containing Solanum lycopersicoides chromosome segments in the genetic background of cultivated tomato (Lycopersicon esculentum) was used to study factors affecting homeologous recombination. Recombination rates were estimated in progeny of 43 heterozygous introgressions and whole-chromosome substitution lines, together representing 11 of the 12 tomato chromosomes. Recombination within homeologous segments was reduced to as little as 0-10% of expected frequencies. Relative recombination rates were positively correlated with the length of introgressed segments on the tomato map. The highest recombination (up to 40-50% of normal) was observed in long introgressions or substitution lines. Double-introgression lines containing two homeologous segments on opposite chromosome arms were synthesized to increase their combined length. Recombination was higher in the double than in the single segment lines, despite a preference for crossovers in the region of homology between segments. A greater increase in homeologous recombination was obtained by crossing the S. lycopersicoides introgression lines to L. pennellii-a phylogenetically intermediate species-or to L. esculentum lines containing single L. pennellii segments on the same chromosome. Recombination rates were highest in regions of overlap between S. lycopersicoides and L. pennellii segments. The potential application of these results to breeding with introgression lines is discussed.

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Nineteen interspecific hybrid breeding lines were tested for resistance to a TSWV isolate using enzyme-linked immunosorbent assay (ELISA) to check for presence of the virus after inoculation. These lines were all BC1F6 lines derived from L. esculentum crosses with seven L. chilense accessions. All of these lines had been selected for high tolerance/resistance to tomato mottle virus (ToMoV), a geminivirus [Scott et al., Bemisia 1995: Taxonomy, Biology, Damage Control and Management 30: 357–367 (1996)]. The initial TSWV screening indicated that eight of the 19 original lines had “possible” TSWV resistance. Seed from these selected eight lines were then planted and inoculated with TSWV ≈3 weeks after emergence. Three weeks later, ELISA results indicated that all plants from all lines were infected with TSWV. However, none of the plants from Y118 (derived from the LA 1938 cross) showed visual TSWV symptoms. The Y118-derived plants were allowed to grow for several months, and at no time developed significant visual symptoms of the virus. The consistent lack of TSWV symptoms prompted a second ELISA test on the Y118 plants, and the results indicated the plants were completely free of TSWV. Further tests were then initiated with F2 (L. esculentum × Y118) seed, and results indicate a single dominant gene is responsible for TSWV resistance. Data from this segregating population, including a molecular marker study which screened 800 randomly amplified polymorphic DNA (RAPD) primers, will be presented. Approximately two to five RAPD primers are possibly linked to TSWV resistance.