Table 5.
Numbers of unique polymorphic positions, heterozygous positions and indels along a 11259 character multigene (LSU, ITS, βtub, hsp90, tigA, rpl10, tef-1α, enl, ras-ypt1, cox1, nadhl, rps10) sequence alignment for 21 described Phytophthora species and P. taxon boehmeriae-like from Clade 10.
Nonpapillate species | Airborne papillate species | Sister species and species complexes | |||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Primarily aquatic | Soil-borne | ||||||||||||||||||||||||||||||||
P. gallica | P. intercalaris | P. ludoviciana | P. procera | P. pseudogallica | P. subarctica | P. tenuimura | P. tonkinensis | P. ukrainensis | P. scandinavica | P. boehmeriae | P. taxon boehmeriae-likec | P. morindaec | P. gondwanensis | P. kernoviae | P. chilensis | P. pseudochilensis | P. pseudokernoviae | P. celebensis | P. javanensis | P. multiglobulosad | P. gallica + P. subarctica | P. ludoviciana + P. tenuimura | P. ludoviciana, P. procera + P. tenuimura | P. chilensis + P. pseudochilensis | P. chilensis + P. pseudokernoviae | P. pseudochilensis + P. pseudokernoviae | P. chilensis, P. pseudochilensis + P. pseudokernoviae | P. chilensis, P. pseudochilensis, P. pseudokernoviae + P. kernoviae | P. celebensis + P. javanensis | P. celebensis + P. multiglobulosa | P. javanensis + P. multiglobulosa | P. celebensis + P. javanensis + P. multiglobulosa | |
Total no. of unique polymorphic positions present in > 50 % of isolates | 33 | 78 | 56 | 73 | 82 | 53 | 46 | 125 | 64 | 100 | 65 | 39 | 77 | 64 | 44 | 11 | 23 | 20 | 28 | 15 | 8 | 50 | 48 | 251 | 10 | 3 | 2 | 16 | 73 | 4 | 0 | 8 | 116 |
No. of unique heterozygous positions present in > 50 % of isolates a | 11 | 17 | 39 | 8 | 23 | 45 | 11 | 6 | 21 | 1 | 0 | 12 | 0 | 4 | 2 | 3 | 3 | 5 | 4 | 7 | 2 | 10 | 9 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 1 | 0 |
No. of unique indel positions present in > 50 % of isolates a | 0 | 0 | 1 | 1 | 1 | 0 | 1 | 3 | 4 | 8 | 0 | 0 | 1 | 0 | 0 | 0 | 18e | 0 | 0 | 0 | 0 | 16 | 3 | 89 | 0 | 0 | 0 | 1 | 3 | 0 | 0 | 0 | 11 |
Total no. of additional unique polymorphic positions present in individual isolates | 27 | 30 | 1 | 18 | 1 | 0 | 19 | 0 | 1 | 0 | 4 | 0 | 0 | 10 | 7 | 0 | 0 | 1 | 0 | 0 | 0 | n.a. | n.a | n.a. | n.a | n.a | n.a | n.a | n.a. | n.a | n.a | n.a | n.a |
No. of additional unique heterozygous positions present in individual isolates b | 24 | 29 | 1 | 14 | 1 | 0 | 11 | 0 | 1 | 0 | 0 | 0 | 0 | 4 | 4 | 0 | 0 | 1 | 0 | 0 | 0 | n.a. | n.a | n.a. | n.a | n.a | n.a | n.a | n.a. | n.a | n.a | n.a | n.a |
Total no. of heterozygous positions present in > 50 % of isolates | 25 | 18 | 60 | 13 | 32 | 59 | 34 | 9 | 26 | 2 | 0 | 12 | 1 | 5 | 3 | 4 | 5 | 6 | 5 | 8 | 1 | n.a. | n.a | n.a. | n.a | n.a | n.a | n.a | n.a. | n.a | n.a | n.a | n.a |
No. of additional heterozygous positions present in individual isolates | 30 | 42 | 3 | 19 | 1 | 0 | 18 | 0 | 5 | 0 | 0 | 0 | 0 | 7 | 7 | 0 | 0 | 1 | 0 | 0 | 0 | n.a | n.a | n.a. | n.a | n.a | n.a | n.a | n.a. | n.a | n.a | n.a | n.a |
a The no. of unique heterozygous positions and the number of unique indels are included in the total no. of unique polymorphic positions present in the majority of isolates of a species.
b The no. of unique heterozygous positions is included in the total no. of unique polymorphic positions present in individual isolates of a species.
c For P. taxon boehmeriae-like and P. morindae ras-ypt1, nadhl and rps10 genes were not available; 9-gene alignment length 9 650 bp.
d Due to a shorter length of the cox1 sequence the length of the 12-gene alignment of P. multiglobulosa; was 11098 bp.
e all indels in hsp90.
f all indels in ras-ypt1.
Due to the occurrence of intraspecfic variation some unique polymorphisms were only present in individual isolates of a species.
Nucleotides missing from the terminal part(s) of partial sequences and undetermined bases (N) were not considered as polymorphisms.