2013
DOI: 10.5897/ajb12.2355
|View full text |Cite
|
Sign up to set email alerts
|

Molecular and morphological characterization of Phyllactinia cassiae-fistulae (Erysiphaceae; Ascomycota) from Thailand

Abstract: Phyllactinia cassiae-fistulae and its Ovulariopsis anamorph, a causal agent of powdery mildew on Cassia fistula, have been found in Thailand for the first time. Phylogenetic analysis using the 28S ribosomal DNA sequences clearly demonstrated that P. cassiae-fistulae distinctly formed a unique clade at the basal part of Phyllactinia with 100% bootstrap support. This phylogenetic analysis supports the unique morphology of P. cassiae-fistulae anamorph having cylindrical-ellipsoil conidia and short conidiophores s… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2016
2016
2021
2021

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 11 publications
(1 citation statement)
references
References 18 publications
0
1
0
Order By: Relevance
“…The 5’-end of the 28S rDNA (including D1 and D2 domains) and internal transcribed spacer (ITS) regions were amplified and sequenced. Primer sets Ph7 (TGTTGCTTTGGYAGGCCG; Monkhung, Takamatsu, & To-anun, 2013 )/NLP2 (GGTCCCAACAGCTATGCTCT; Mori, Sato, & Takamatsu, 2000 ) and ITS5 (GGAAGTAAAAGTCGTAACAAGG; White, Bruns, Lee, & Taylor, 1990 )/Ph8 (GCCCCAAGACCAAGCC; this study) were used for amplification of the 28S rDNA and ITS region, respectively. Ph8 was newly designed in this study based on the sequences of Phyllactinia spp.…”
Section: Methodsmentioning
confidence: 99%
“…The 5’-end of the 28S rDNA (including D1 and D2 domains) and internal transcribed spacer (ITS) regions were amplified and sequenced. Primer sets Ph7 (TGTTGCTTTGGYAGGCCG; Monkhung, Takamatsu, & To-anun, 2013 )/NLP2 (GGTCCCAACAGCTATGCTCT; Mori, Sato, & Takamatsu, 2000 ) and ITS5 (GGAAGTAAAAGTCGTAACAAGG; White, Bruns, Lee, & Taylor, 1990 )/Ph8 (GCCCCAAGACCAAGCC; this study) were used for amplification of the 28S rDNA and ITS region, respectively. Ph8 was newly designed in this study based on the sequences of Phyllactinia spp.…”
Section: Methodsmentioning
confidence: 99%