@ARTICLE{TreeBASE2Ref17756,
author = {Susumu Takamatsu and Mihoko Inagaki and Seiko Niinomi and Seyed Akbar Khodaparast and H. D. Shin and Banga Grigaliunaite and Mar?a Havrylenko},
title = {Molecular phylogeny and evolution of the genus Phyllactinia (Ascomycete: Erysiphales) and its allied genera},
year = {2007},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Mycological Research},
volume = {},
number = {},
pages = {},
abstract = {Phyllactinia is a unique genus within the Erysiphales (Ascomycota) having a partly endo-parasitic nature of the mycelium within the host plant tissues. We constructed phylogenetic trees for the genus Phyllactinia and its allied genera based on a total of120 nucleotide sequences of the 28S rDNA and ITS regions to discuss their phylogenetic relationships with special references to host plants, biogeography, evolutionary dating, and taxonomy. The analysis of the Erysiphales confirmed the monophyly of the endo-parasitic genera, i.e., Leveillula, Phyllactinia and Pleochaeta. Phyllactinia specimens used in this study were divided into six distinctive groups and three subgroups. Interestingly, Leveillula, an obligately endo-parasitic genus of the Erysiphales, grouped together with Phyllactinia, although this was not significantly supported by the Kishino-Hasegawa and Shimodaira-Hasegawa tests. This suggests that the evolution within this group of fungi occurred from partial endo-parasitism to obligate endo-parasitism. The host range of Phyllactinia is mostly confined to woody plants, especially deciduous trees. Betulaceae, Fagaceae, Ulmaceae, Moraceae, and Rosaceae may have a close connection to the divergence of the groups and subgroups of Phyllactinia concerned. Most of these plant families are known as major members of the boreotropical flora of the Tertiary, which suggests an early Tertiary origin of this genus. A comparison of the phylogenies of hosts and parasites revealed that host range expansion at higher taxonomic levels (higher than family level) is independent of the phylogeny of plants. On the other hand, host range expansions in lower taxonomic levels (infrafamilial or infrageneric) tend to occur within a single family or genus. An estimation of the evolutionary timing using a molecular clock suggested that Phyllactinia split from Pleochaeta about 60 million years ago (Mya) in the early Tertiary and divergence of the six major clades of Phyllactinia occurred between 5 and 40 Mya during Oligocene and Miocene. Divergence within the major clades and within Leveillula occurred maybe more than 5 Mya in Pliocene and Quaternary. This is the first comprehensive phylogenetic study of Phyllactinia and other endo-parasitic genera of the Erysiphales.}
}
Taxa for matrix 20984 of Study 1919

Citation title:
"Molecular phylogeny and evolution of the genus Phyllactinia (Ascomycete: Erysiphales) and its allied genera".

This study was previously identified under the legacy study ID S1896
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 1288973 |
Aporpium caryae Dai 3952 |
|
|
| 1288988 |
Aporpium caryae Dai 4549 |
|
|
| 1288969 |
Aporpium caryae WD2207 |
|
3175053
|
| 1288972 |
Aporpium caryae WD2274 |
|
3175053
|
| 1398121 |
Aporpium dimidiata O18238 |
|
|
| 1398124 |
Aporpium dimidiata O18261 |
|
|
| 1398129 |
Aporpium efibulata |
|
|
| 1288983 |
Aporpium hexagonoides ML297 |
|
|
| 1288995 |
Aporpium hexagonoides TFM_F_27498 |
|
|
| 1288981 |
Aporpium hexagonoides Wei5584 |
|
|
| 1288975 |
Aporpium hexagonoides Wei5680 |
|
|
| 1288989 |
Aporpium strigosum TFM_F_27651 |
|
|
| 1288977 |
Aporpium strigosum TUFC10589 |
|
|
| 1289004 |
Aporpium strigosum TUFC14542 |
|
|
| 1288976 |
Aporpium strigosum WD1710 |
|
|
| 1289000 |
Aporpium strigosum WD680 |
|
|
| 1288998 |
Aporpium strigosum Wei5621 |
|
|
| 1288985 |
Aporpium strigosum Wei5990 |
|
|
| 1409859 |
Auricularia mesenterica |
160862
|
1202771
|
| 1288999 |
Auricularia polytricha HN4076 |
29893
|
3066663
|
| 1288997 |
Auricularia polytricha TUFC12867 |
29893
|
3066663
|
| 1289001 |
Auricularia polytricha TUFC12920 |
29893
|
3066663
|
| 1398120 |
Basidiodendron eyrei |
160888
|
3205200
|
| 1398118 |
Exidia crenata |
228672
|
3113102
|
| 1288968 |
Exidia glandulosa TUFC34008 |
5219
|
3109140
|
| 1398123 |
Exidiopsis calcea |
160903
|
3208707
|
| 1289006 |
Exidiopsis grisea TUFC100049 |
160905
|
3146611
|
| 1398117 |
Exidiopsis sp. |
|
|
| 1398119 |
Heterochaete delicata |
|
3137228
|
| 1398130 |
Heterochaetella brachyspora |
160913
|
3209826
|
| 1398125 |
Protodaedalea foliace WD548 |
|
|
| 1288986 |
Protodaedalea foliacea E701 |
|
|
| 1289005 |
Protodaedalea foliacea Yuan5691 |
|
|
| 1398128 |
Protomerulius africanus |
160925
|
3354719
|
| 1398126 |
Protomerulius brasiliensis |
160926
|
3117989
|
| 1398122 |
Pseudohydnum gelatinosum |
29895
|
3035875
|
| 1398127 |
Tremella foliacea |
29897
|
3080850
|