2018
DOI: 10.1016/j.cropro.2018.02.019
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Identification and pathogenicity of Fusarium spp. in row crops in Nebraska

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Cited by 46 publications
(39 citation statements)
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“…In this study, no introgressions affected resistance to either SCN or F. graminearum. Fusarium graminearum is a necrotophic ascomycete that infects soybean seed and seedlings (Broders et al, 2007;Parikh et al, 2018). Lack of pleiotropy in these interactions is not unexpected due to differences in pathogen biology and infection type between P. sojae and both SCN and F. graminearum.…”
Section: Discussionmentioning
confidence: 99%
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“…In this study, no introgressions affected resistance to either SCN or F. graminearum. Fusarium graminearum is a necrotophic ascomycete that infects soybean seed and seedlings (Broders et al, 2007;Parikh et al, 2018). Lack of pleiotropy in these interactions is not unexpected due to differences in pathogen biology and infection type between P. sojae and both SCN and F. graminearum.…”
Section: Discussionmentioning
confidence: 99%
“…For example, the wheat (Triticum aestivum L.) gene Lr34 encodes an ATP-binding cassette transporter and provides partial resistance to three leaf pathogens: leaf rust (Puccinia triticina Erikss. in Ohio (Broders et al, 2007;Parikh et al, 2018). ), and powdery mildew [Blumeria graminis (DC) Speer] (Krattinger et al, 2009).…”
mentioning
confidence: 99%
“…Fusarium fujikuroi W343 (henceforth referred to as Ffuji) was originally isolated and identified from roots of infected wheat samples collected in Nebraska and maintained long term at −80 °C as agar plugs kept in 2 mL Nalgene cryogenic vials containing 1 mL potato dextrose broth (PDB) with 20% glycerol by Parikh et al (). In that study, DNA extraction and PCR amplification were conducted and the internal transcribed spacer (ITS) and β‐tubulin (BT) regions were sequenced.…”
Section: Methodsmentioning
confidence: 99%
“…In that study, DNA extraction and PCR amplification were conducted and the internal transcribed spacer (ITS) and β‐tubulin (BT) regions were sequenced. The sequences were accessioned (accession numbers for ITS and for BT) and details of the PCR amplification protocol and sequence analysis were reported by Parikh et al (). The strain was grown from agar plug cultures stored at −80 °C and used for the present study.…”
Section: Methodsmentioning
confidence: 99%
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