^ШХР: *https://onlinelibrary.wiley.com/loi/14390434
(https://onlinelibrary.wiley.com/loi/14390434)
^АВТ: Ramiro J.; Ciampi-Guillardi M. ; Caldas D.G.G.; Duarte de Moraes M.H.; Goldoni Barbieri M.C.; Pereira W.V. ; Massola N.S.Jr.
^ЗГЛ: Quick and accurate detection of Sclerotinia sclerotiorum
and Phomopsis spp. in soybean seeds using qPCR and
seed-soaking method [Технология быстрого и точного
определения зараженности семян сои грибами Sclerotinia
sclerotiorum и Phomopsis spp. с использованием количественной
ПЦР и метода замачивания семян. (Бразилия)]
^ВЫХ: Journal of Phytopathology, 2019; Vol.167,N 5. - P.
273-282
^ДАТ: 2019
^ПРМ: Bibliogr.:p.281-282
+Реферат:
^РЕФ: Seed-borne pathogenic fungi can cause serious damage to soybean crops by reducing the germination, vigour and emergence of the seeds. Special attention should be paid to pathogen detection in seeds to prevent its introduction in disease-free areas. Considering the importance of rapid and successful diagnosis of seed-borne pathogenic fungi in soybeans, this study evaluated a method to detect Sclerotinia sclerotiorum and Phomopsis spp. in seeds using quantitative polymerase chain reaction (qPCR). Naturally infested samples were subjected to detection using qPCR and blotter test, and the findings were compared. Using soybean seeds soaked in water, both pathogens were detected at an infestation level up a 0.0625% (one infected seed out of 1,599 healthy seeds) by qPCR. This technique allowed the detection of 300 fg of S. sclerotiorum and 30 fg of Phomopsis spp. DNA in the seed samples. Phomopsis spp. was detected in 40.7% of the evaluated seed batches (81 batches) and S. sclerotiorum was detected in 32.1% of the evaluated batches, although most of the seeds had low infestation levels. It was up to 28.5 times more efficient to use qPCR rather than blotter test to detect pathogens with a low incidence of occurrence in soybean seeds. If routinely used to test healthy seeds, qPCR would contribute to reducing soybean losses due to diseases as well as decreasing the costs required to control those diseases.
aref1
^TRN: 1912639
^ВИД: Статья из книги
^ЯЗК: Английский
+Индексирование:
^РУБ: 68_37_31_31_19
^УДК: 635.655:631.531.011.5; 632.482.16; 632.488
^ТЕР: СОЯ. GLYCINE MAX [СОЯ КУЛЬТУРНАЯ]. СЕМЕНА (Seed)
[ПОСЕВНОЙ МАТЕРИАЛ; СЕМЕННОЙ МАТЕРИАЛ]. ЗАРАЖЕННОСТЬ.
SCLEROTINIA SCLEROTIORUM [SCLEROTINIA LIBERTIANA;
WHETZELINIA SCLEROTIORUM]. PHOMOPSIS. ОПРЕДЕЛЕНИЕ
ЗАРАЖЕННОСТИ. КОЛИЧЕСТВЕННАЯ ОЦЕНКА. PCR [АМПЛИФИКАЦИЯ IN
VITRO; ПОЛИМЕРАЗНАЯ ЦЕПНАЯ РЕАКЦИЯ; ПЦР; РЕАКЦИЯ ЦЕПНОЙ
ПОЛИМЕРИЗАЦИИ]. ЗАМАЧИВАНИЕ (Soaking). БРАЗИЛИЯ (Brazil).
^РТЗ: ASCOMYCOTINA [ASCOMYCETES; АСКОМИЦЕТЫ]. DEUTEROMYCOTINA
[FUNGI IMPERFECTI]. EUMYCOTA. FABACEAE [LEGUMINOSAE;
БОБОВЫЕ]. FABALES. GLYCINE (Glycine (genus)). HELOTIALES.
PAPILIONOIDEAE [FABOIDEAE; МОТЫЛЬКОВЫЕ]. SCLEROTINIA
[WHETZELINIA]. АМЕРИКА (Americas). ЗЕРНОБОБОВЫЕ КУЛЬТУРЫ.
ЛАТИНСКАЯ АМЕРИКА (Latin America). МАСЛИЧНЫЕ КУЛЬТУРЫ
(Oil crops). МЕТОДЫ (Methods). МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЕ
МЕТОДЫ. С-Х КУЛЬТУРЫ. СТРАНЫ БРИКС. СТРАНЫ МИРА.
ТЕХНИЧЕСКИЕ КУЛЬТУРЫ (Industrial crops). ТЕХНОЛОГИЧЕСКИЕ
ПРОЦЕССЫ (Operational processes). ЮЖНАЯ АМЕРИКА (South
America).