2019
DOI: 10.3390/molecules24071200
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Alternative Molecular-Based Diagnostic Methods of Plant Pathogenic Fungi Affecting Berry Crops—A Review

Abstract: Increasing consumer awareness of potentially harmful pesticides used in conventional agriculture has prompted organic farming to become notably more prevalent in recent decades. Central European countries are some of the most important producers of blueberries, raspberries and strawberries in the world and organic cultivation methods for these fruits have a significant market share. Fungal pathogens are considered to be the most significant threat to organic crops of berries, causing serious economic losses an… Show more

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Cited by 17 publications
(19 citation statements)
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References 153 publications
(171 reference statements)
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“…The crucial plant pathogens are those from the fungal genera Colletotrichum, Botrytis as well as Verticillium and fungal-like Phytophthora. These pathogens may wreak havoc, especially in organic production [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
“…The crucial plant pathogens are those from the fungal genera Colletotrichum, Botrytis as well as Verticillium and fungal-like Phytophthora. These pathogens may wreak havoc, especially in organic production [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
“…They were transferred to fresh PDA to obtain pure cultures by the single conidium technique. A Phytophthora cinnamomi (CPO-PCU) was isolated on V8 juice agar medium amended with chloramphenicol at 20 µg mL −1 and then incubated in the dark at 28 °C for 72 h. The plates were examined, and they showed morphological characteristics (hyphal swellings, chlamydospore and sporangium) similar to P. cinnamomi [ 5 , 22 ].…”
Section: Methodsmentioning
confidence: 99%
“…The oomycete P. cinnamomi was incubated on PDA for 7 days. For the production of sporangia of P. cinnamomi , agar discs (5 mm in diameter) with mycelia were placed into 500-mL flasks with V8 juice liquid medium [ 5 ] and incubated at 28 °C for 8 days. Subsequently, the flasks were placed at 4 °C for 5 min; after that, the number of zoospores per milliliter was quantified with a hemocytometer.…”
Section: Methodsmentioning
confidence: 99%
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