2021
DOI: 10.1094/pdis-07-20-1486-pdn
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First Report of Bipolaris yamadae Leaf Spot Disease on Guinea Grass (Panicum maximum) in Florida

Abstract: Guinea grass is an invasive perennial C4 grass and is a common weed around agricultural crops in Louisiana, Texas, and Hawaii, USA (Overholt and Franck 2019). In November 2018, leaf spots were observed on Guinea grass occurring in an organic garden located in Gainesville, Florida, USA. Lesions were oblong to irregular, dark grey to brownish center with pale-yellow to brownish black margin. Lesions had coalesced, forming necrotic margins that spread from the leaf tip, resulting in leaf blight and collapse of th… Show more

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Cited by 5 publications
(1 citation statement)
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“…Genomic DNA was extracted from the isolated single strain using a TIANamp DNA Kit (Beijing Tiangen Biochemical Co., Ltd., China) according to the manufacturer's instruction. The V3–V4 region of bacterial 16S rRNA genes and the ITS region of fungal ribosomal RNA (rRNA) genes were the polymerase chain reaction (PCR) amplified using two universal primer sets, 27 forward (F) (5′‐AGAGTTTGATCCTGGCTCAG‐3′)/1492 reverse (R) (5′‐GGTTACCTTGTTACGACTT‐3′) (Adhikari et al., 2020 ; Zhang et al., 2019 ) and internal transcribed spacer 1 (ITS1) (5′‐TCCGTAGGTGAACCT GCGG‐3′)/internal transcribed spacer 4 (ITS4) (5′‐TCCTCCGCTTATTGATATGC‐3′) (Kim, Koh, et al, 2017 ). The PCR amplification products were detected using agarose gel electrophoresis and sequenced by the Chengdu Qingke Biotechnology Company.…”
Section: Methodsmentioning
confidence: 99%
“…Genomic DNA was extracted from the isolated single strain using a TIANamp DNA Kit (Beijing Tiangen Biochemical Co., Ltd., China) according to the manufacturer's instruction. The V3–V4 region of bacterial 16S rRNA genes and the ITS region of fungal ribosomal RNA (rRNA) genes were the polymerase chain reaction (PCR) amplified using two universal primer sets, 27 forward (F) (5′‐AGAGTTTGATCCTGGCTCAG‐3′)/1492 reverse (R) (5′‐GGTTACCTTGTTACGACTT‐3′) (Adhikari et al., 2020 ; Zhang et al., 2019 ) and internal transcribed spacer 1 (ITS1) (5′‐TCCGTAGGTGAACCT GCGG‐3′)/internal transcribed spacer 4 (ITS4) (5′‐TCCTCCGCTTATTGATATGC‐3′) (Kim, Koh, et al, 2017 ). The PCR amplification products were detected using agarose gel electrophoresis and sequenced by the Chengdu Qingke Biotechnology Company.…”
Section: Methodsmentioning
confidence: 99%