@ARTICLE{TreeBASE2Ref15936,
author = {Mitsuro Hyakumachi and Achmadi Priyatmojo and Mayumi Kubota and Hirokazu Fukui},
title = {New Anastomosis Groups, AG-T and AG-U, of Binucleate Rhizoctonia spp. Causing Root and Stem Rot of Cut-Flower and Miniature Roses},
year = {2005},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Phytopathology},
volume = {95},
number = {},
pages = {},
abstract = {Root and stem rot of cut-flower roses (Rosa spp.) was observed in commercial glasshouse-grown roses in 10 prefectures of Japan from 1998 through 2001. Binucleate-like Rhizoctonia were mainly isolated from the disease plants. In total, 670 isolates were divided into two types based on cultural appearance; 168 isolates of light brown to brown type and 502 isolates of whitish type. Hyphal anastomosis reaction using representative isolates from each type revealed that light brown to brown type belonged to anastomosis group G (AG-G), while whitish type (here after called AG-CUT) failed to anastomose with tester strains of binucleate Rhizoctonia AG-A through AG-S. Neither isolates of AG-G nor AG-CUT anastomosed with tester strains of a previously reported unknown AG of binucleate Rhizoctonia collected from miniature roses (AG-MIN). In pathogenicity tests, randomly selected isolates of the 3 groups caused root and stem rot on cut-flower and miniature roses. To differentiate AG-CUT and AG-MIN from known AGs of binucleate Rhizoctonia, RFLP and sequence analyses of rDNA-ITS region were conducted. Among the 8 restriction enzymes used, HaeIII produced DNA banding patterns for AG-CUT that differed from those of tester strains and AG-MIN. Additionally, restriction profiles of AG-MIN differed from those of all tester strains. AG-G isolates from cut-flower roses had the same RFLP pattern as the tester strains of AG-G. Based on the results of hyphal anastomosis and RFLP and sequence analysis of rDNA-ITS region, we propose AG-CUT be designated AG-T and AG-MIN be designated AG-U, two new AG of binucleate Rhizoctonia. The phylogenetic tree based on the sequence data of rDNA-ITS region showed that isolates of AG-MIN were in a distinct clade from other AGs while isolates of AG-CUT were in the same clade as those of AG-A. More detailed phylogenetic analysis besides rDNA-ITS region might be necessary for AG classification of binucleate Rhizoctonia.}
}
Taxa for Study 1365
Citation title:
"New Anastomosis Groups, AG-T and AG-U, of Binucleate Rhizoctonia spp. Causing Root and Stem Rot of Cut-Flower and Miniature Roses".
This study was previously identified under the legacy study ID S1294
(Status: Published).
Taxa
ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
38569 |
Ceratobasidium sp. AGA AF354092 |
5251
|
238566
|
38565 |
Ceratobasidium sp. AGA AH-1 AB196639 |
5251
|
238566
|
38552 |
Ceratobasidium sp. AGA C-538 AB196640 |
5251
|
238566
|
38568 |
Ceratobasidium sp. AGBa AF354088 |
5251
|
238566
|
38561 |
Ceratobasidium sp. AGBa C-484 AB196641 |
5251
|
238566
|
38557 |
Ceratobasidium sp. AGBb AB122144 |
63189
|
3043641
|
38543 |
Ceratobasidium sp. AGC Ka-1-1 AB196642 |
5251
|
238566
|
38546 |
Ceratobasidium sp. AGDI AF354090 |
5251
|
238566
|
38545 |
Ceratobasidium sp. AGDI ST-SDS-1 AB196643 |
5251
|
238566
|
38560 |
Ceratobasidium sp. AGDI W-12 AB196644 |
5251
|
238566
|
38548 |
Ceratobasidium sp. AGF AF354085 |
5251
|
238566
|
38541 |
Ceratobasidium sp. AGF AH-6 AB196645 |
5251
|
238566
|
38567 |
Ceratobasidium sp. AGG 1Shi-1299 |
5251
|
238566
|
38539 |
Ceratobasidium sp. AGG 4Wak-600 |
5251
|
238566
|
38563 |
Ceratobasidium sp. AGG AH-9 AB196646 |
5251
|
238566
|
38549 |
Ceratobasidium sp. AGG Su-1 AB196647 |
5251
|
238566
|
38554 |
Ceratobasidium sp. AGH AF354089 |
5251
|
238566
|
38544 |
Ceratobasidium sp. AGH STC-10 AB196648 |
5251
|
238566
|
38550 |
Ceratobasidium sp. AGH STC-11 AB196649 |
5251
|
238566
|
38555 |
Ceratobasidium sp. AGI AJ242898 |
5573
|
233441
|
38574 |
Ceratobasidium sp. AGI AJ419932 |
5251
|
238566
|
38566 |
Ceratobasidium sp. AGI AV-2 AB196650 |
5251
|
238566
|
38564 |
Ceratobasidium sp. AGI FKO-1-17 AB196651 |
5251
|
238566
|
38540 |
Ceratobasidium sp. AGK AB122145 |
5251
|
238566
|
38558 |
Ceratobasidium sp. AGK SH-10 AB196652 |
5251
|
238566
|
38547 |
Ceratobasidium sp. AGL AF354093 |
5251
|
238566
|
38559 |
Ceratobasidium sp. AGL FKO-2-26 AB196665 |
5251
|
238566
|
38551 |
Ceratobasidium sp. AGO AF354094 |
5251
|
238566
|
38537 |
Ceratobasidium sp. AGP C-578 AB196654 |
5251
|
238566
|
38533 |
Ceratobasidium sp. AGP C-579 AB196655 |
5251
|
238566
|
38536 |
Ceratobasidium sp. AGR AJ427407 |
5251
|
238566
|
38556 |
Ceratobasidium sp. AGS AJ427400 |
5251
|
238566
|
38535 |
Ceratobasidium sp. AGS S5 AB196656 |
5251
|
238566
|
38553 |
Ceratobasidium sp. AGT 1Fuk-600 |
5251
|
238566
|
38572 |
Ceratobasidium sp. AGT 2Shi-1999 |
5251
|
238566
|
38534 |
Ceratobasidium sp. AGT 3Iba-1000 |
5251
|
238566
|
38570 |
Ceratobasidium sp. AGT 4OIT-800 |
5251
|
238566
|
38538 |
Ceratobasidium sp. AGT Aic-400 AB196660 |
5251
|
238566
|
38571 |
Ceratobasidium sp. AGU MWR-20 AB196664 |
5251
|
238566
|
38542 |
Ceratobasidium sp. AGU MWR-22 AB196666 |
5251
|
238566
|
38562 |
Ceratobasidium sp. AGU MWR-24 AB196665 |
5251
|
238566
|
38573 |
Thanatephorus cucumeris |
107832
|
3187105
|