z-logo
Premium
Screening, isolation and evaluation of a nematicidal compound from actinomycetes against the pine wood nematode, Bursaphelenchus xylophilus
Author(s) -
Liu MinJiao,
Hwang ByungSoon,
Jin ChunZhi,
Li WenJun,
Park DongJin,
Seo SangTae,
Kim ChangJin
Publication year - 2019
Publication title -
pest management science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.296
H-Index - 125
eISSN - 1526-4998
pISSN - 1526-498X
DOI - 10.1002/ps.5272
Subject(s) - bursaphelenchus xylophilus , xylophilus , wilt disease , biology , botany , pinus densiflora , nematode , biological pest control , ecology
BACKGROUND Bursaphelenchus xylophilus is a migratory endoparasitic nematode known to cause severe environmental damage and economic losses in pine forest ecosystems. This present study investigated the nematicidal metabolites of actinomycetes in vitro and evaluated the disease control efficacy of the active compound and metabolites under greenhouse and field conditions. RESULTS Five thousand types of actinobacteria from Korean forest soil samples were screened to identify novel nematicidal agents against the pine wood nematode. Streptomyces sp. AN091965 showed the strongest nematicidal activity. One active compound, spectinabilin, was obtained by nematicidal asssy‐directed fractionation, and it showed significant nematicidal activity against B. xylophilus , with an LC 50 value of 0.84 µg mL −1 . Spectinabilin effectively suppressed the development of pine wilt disease in 5‐year‐old Pinus densiflora trees, even at 0.9 mg per tree under greenhouse conditions. Moreover, the acetone extract of the active strain's mycelia efficiently suppressed the development of pine wilt disease under field conditions. CONCLUSION To the best of our knowledge, this the first report to describe the nematicidal activity of spectinabilin against B. xylophilus . The cell extracts described herein merit further field studies as potential nematicides against the pine wood nematode. © 2018 Society of Chemical Industry

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here