2009
DOI: 10.1002/jpln.200900081
|View full text |Cite
|
Sign up to set email alerts
|

In‐field detection and quantification of extracellular DNA

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2011
2011
2018
2018

Publication Types

Select...
3
3

Relationship

1
5

Authors

Journals

citations
Cited by 9 publications
(2 citation statements)
references
References 17 publications
0
2
0
Order By: Relevance
“…Plants may also employ PRR(s) to perceive extracellular DNA (eDNA), as eDNA induces PTI-like defenses and pathogen resistance (Wen et al, 2009;Heil, 2014, 2015;Mazzoleni et al, 2015;Gallucci and Maffei, 2017). Of note, substantial amounts of DNA are secreted from plant roots, and influence both plants and microbes in the soil (Ceccherini et al, 2009;Driouich et al, 2013). eDNA serves as a nutrient source (Paungfoo-Lonhienne et al, 2010), but also causes plant growth inhibition in a conspecific manner (Mazzoleni et al, 2015).…”
Section: Recognition Of Common Patterns Across Kingdomsmentioning
confidence: 99%
“…Plants may also employ PRR(s) to perceive extracellular DNA (eDNA), as eDNA induces PTI-like defenses and pathogen resistance (Wen et al, 2009;Heil, 2014, 2015;Mazzoleni et al, 2015;Gallucci and Maffei, 2017). Of note, substantial amounts of DNA are secreted from plant roots, and influence both plants and microbes in the soil (Ceccherini et al, 2009;Driouich et al, 2013). eDNA serves as a nutrient source (Paungfoo-Lonhienne et al, 2010), but also causes plant growth inhibition in a conspecific manner (Mazzoleni et al, 2015).…”
Section: Recognition Of Common Patterns Across Kingdomsmentioning
confidence: 99%
“…Although the detection of the pathogen in plant tissues is improved by using polymerase chain reaction (PCR) methods compared with the isolation on growing media, quantification is still uncertain (Li et al 1994). Alternatively, real time quantitative PCR (qPCR) allows a simpler quantification, in addition to an increased sensitivity compared with conventional PCR assays (Ceccherini et al 2009;Luchi et al 2006;Mercado-Blanco et al 2003b). Sequences of the internal transcribed spacer region (ITS) of the ribosomal DNA (rDNA) are often used to design PCR primers in order to detect different fungal pathogens in host tissue, i.e., in potatoes (Mahuku et al 1999;Atallah et al 2007) and olive tissues (Markakis et al 2009;López-Escudero and Mercado-Blanco 2011).…”
Section: Introductionmentioning
confidence: 99%