1992
DOI: 10.1094/phyto-82-881
|View full text |Cite
|
Sign up to set email alerts
|

Analysis of Repetitive DNA Sequences from Potato Cyst Nematodes and Their Use as Diagnostic Probes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
11
0

Year Published

1993
1993
2017
2017

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 21 publications
(11 citation statements)
references
References 0 publications
0
11
0
Order By: Relevance
“…citri (61). Other potential targets for specific amplification include the short, interspersed repetitive elements present in bacteria (35,94), and the species-specific tandem DNA repeats in many eukaryotes, including potato cyst nematodes (139). A strain or isolate can also be marked, or transformed, with a known gene and primers specific for the reporter gene used to detect the isolate.…”
Section: < Zmentioning
confidence: 99%
“…citri (61). Other potential targets for specific amplification include the short, interspersed repetitive elements present in bacteria (35,94), and the species-specific tandem DNA repeats in many eukaryotes, including potato cyst nematodes (139). A strain or isolate can also be marked, or transformed, with a known gene and primers specific for the reporter gene used to detect the isolate.…”
Section: < Zmentioning
confidence: 99%
“…18 Each of these methods has problems for use in routine identification13 and none of them has been fully tested and validated against the range of field populations found in the UK, as most of the work has been done only on known species from glasshouse cultures. The PCR technique offers the prospect of a simple, rapid and reliable diagnostic tool for plant parasitic nematodes that will enable advisers to identify and quantify populations of PCN from field samples,16, 19, 20 as do ELISA‐based procedures 21…”
Section: Introductionmentioning
confidence: 99%
“…Physical detection methods, such as fork sampling, are slow and often ineffective. Molecular biology tools have been applied to the separation of PCN species and pathotypes (e.g., Schnick et al 1990;Stratford et al 1992;Folkertsma et al 1994). Marshall (1993) applied molecular dot-blot hybridisation to define the distribution of PCN species throughout New Zealand.…”
Section: Introductionmentioning
confidence: 99%