2019
DOI: 10.5958/2249-4677.2019.00045.8
|View full text |Cite
|
Sign up to set email alerts
|

Use of 12p and 36p genes as molecular markers in support of subgroup identification of two 16SrXIII phytoplasmas associated with strawberry phyllody in Chile

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2020
2020
2021
2021

Publication Types

Select...
2

Relationship

2
0

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 0 publications
0
2
0
Order By: Relevance
“…On the other hand, the phytoplasma 16SrXIII-F was detected for the first time in Chile in strawberry orchards of the Region of Valparaíso, associated with symptoms of phyllody and virescence [36]. Subsequent studies showed that this phytoplasma was present in all the strawberry production regions in Chile, including the localities where positive citrus samples have been detected in this survey [21,37]. In addition, this phytoplasma has been reported in calafate (Berberis microphylla G.…”
Section: Discussionmentioning
confidence: 78%
“…On the other hand, the phytoplasma 16SrXIII-F was detected for the first time in Chile in strawberry orchards of the Region of Valparaíso, associated with symptoms of phyllody and virescence [36]. Subsequent studies showed that this phytoplasma was present in all the strawberry production regions in Chile, including the localities where positive citrus samples have been detected in this survey [21,37]. In addition, this phytoplasma has been reported in calafate (Berberis microphylla G.…”
Section: Discussionmentioning
confidence: 78%
“…Total nucleic acids were extracted from leaf midribs and insects using a CTAB method [31], dissolved in Tris-EDTA pH 8.0 buffer and maintained at 4 • C. PCR amplification was carried out using 20 ng µL −1 of nucleic acid. Direct and nested PCR assays on the 30 S ribosomal protein SSu12p gene were performed according to the protocol of Cui et al [32]. Further PCR with primer pair P1/P7 [33,34] and nested PCR with R16F2n/R2 primers amplifying the 16S rRNA gene [35] were performed as described by Schaff et al [36].…”
Section: Phytoplasma Detectionmentioning
confidence: 99%