First Report of Gray Mold on Crepe Myrtle (Lagerstroemia indica ) Caused by Botrytis cinerea in Korea
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RNA polymerase subunit II (RPB2) that are comm<strong>on</strong>ly used for <strong>Botrytis</strong> species<br />
identificati<strong>on</strong>s (Staats et al. 2005), were also sequenced for isolate BR003. The G3PDH,<br />
HSP60, and RPB2 sequences <str<strong>on</strong>g>of</str<strong>on</strong>g> BR003 (KT728902, KT728903, and KT728904) had 99, 100<br />
and 99% identity with the published GenBank accessi<strong>on</strong>s KM016535, KM016534 and<br />
KM032181 respectively. For pathogenicity test<strong>in</strong>g, three detached <strong>in</strong>florescences were<br />
sprayed with a c<strong>on</strong>idial suspensi<strong>on</strong> (2 × 10 4 c<strong>on</strong>idia/ml) prepared from a PDA culture and<br />
were ma<strong>in</strong>ta<strong>in</strong>ed with petioles immersed <strong>in</strong> sterilized water. An analogous three<br />
<strong>in</strong>florescences, serv<strong>in</strong>g as c<strong>on</strong>trols, were sprayed with sterilized water. All <strong>in</strong>florescences were<br />
sealed <strong>in</strong> plastic bags and <strong>in</strong>cubated <strong>in</strong> humid chambers at 20 ± 2°C. After 5 days flower<br />
petals <str<strong>on</strong>g>of</str<strong>on</strong>g> the <strong>in</strong>oculated treatments had brownish blemishes and blackish gray mycelia with<br />
c<strong>on</strong>idia, whereas c<strong>on</strong>trol <strong>in</strong>florescences rema<strong>in</strong>ed symptomless. The pathogenicity test was<br />
repeated with similar results. The pathogen was successfully re-isolated from <strong>in</strong>oculated<br />
flowers, fulfill<strong>in</strong>g Koch’s postulates. <str<strong>on</strong>g>Gray</str<strong>on</strong>g> mold disease <str<strong>on</strong>g>of</str<strong>on</strong>g> L. <strong><strong>in</strong>dica</strong> caused <strong>by</strong> B. <strong>c<strong>in</strong>erea</strong> has<br />
been recorded <strong>in</strong> Ch<strong>in</strong>a and New Zealand (Farr and Rossman 2015). To our knowledge, this is<br />
the first report <str<strong>on</strong>g>of</str<strong>on</strong>g> gray mold <strong>on</strong> L. <strong><strong>in</strong>dica</strong> <strong>in</strong> <strong>Korea</strong>. Accord<strong>in</strong>g to our field observati<strong>on</strong>s, gray<br />
mold was active at low temperatures and lesi<strong>on</strong>s expanded rapidly <strong>in</strong> humid c<strong>on</strong>diti<strong>on</strong>s.<br />
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