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		<title>Publications by S. Johny</title>
		<link>http://cfs.nrcan.gc.ca/authors/read/23290</link>
		<description>Publications by S. Johny</description>
		<language>en-ca</language>
		<pubDate>2013-01-07 13:30:54 MST</pubDate>
		<lastBuildDate>2013-01-07 13:30:54 MST</lastBuildDate>
		<webMaster>webmaster@nofc.cfs.nrcan.gc.ca</webMaster>
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			<title>Towards the development of an autocontamination trap system to manage populations of emerald ash borer(Coleoptera: Buprestidae) with the native entomopathogenic fungus, Beauveria bassiana. </title>
			<link>http://cfs.nrcan.gc.ca/publications?id=34261</link>
			<description>Emerald ash borer, Agrilus planipennis Fairmaire (Coleoptera: Buprestidae) is an
invasive species from Asia that was discovered in North America Canada, in 2002. Herein, we describe studies to develop an autocontamination trapping system to disseminate Beauveria bassiana to control beetle populations. The standard trap for emerald ash borer in Canada is a light green prism trap covered in an insect adhesive and baited with (Z)-3-hexenol.Wecompared of green multifunnel traps,
green intercept panel traps (both with and without ßuon coating) and green prism traps for capturing emerald ash borer in a green ash plantation. The coated green multifunnel traps captured signiÞcantly more males and more females than any other trap design. We examined the efÞcacy of two native B. bassiana isolates, INRS-CFL and L49Ð1AA. In a Þeld experiment the INRS-CFL isolate attached to
multifunnel traps in autocontamination chambers retained its pathogenicity to emerald ash borer adults for up to 43 d of outdoor exposure. Conidia germination of the INRS-CFL isolate was &gt;69% after outdoor exposure in the traps for up to 57 d. The L49Ð1AA isolate was not pathogenic in simulated trap exposures and the germination rate was extremely low (&amp;lt;5.3%). Mean (±SEM) conidia loads on
ash borer adults after being autocontaminated in the laboratory using pouches that had been exposed in traps out of doors for 29 d were 579,200 (±86,181) and 2,400 (±681) for the INRS-CFL and the L49-1AA isolates, respectively. We also examined the fungal dissemination process under field conditions using the L49-1AA isolate in a green ash plantation. Beetles were lured to baited green
multifunnel traps with attached autocontamination chambers. Beetles acquired fungal conidia from cultures growing on pouches in the chambers and were recaptured on Pestick-coated traps. In total, 2,532 beetles were captured of which 165 (6.5%) had fungal growth that resembled B. bassiana. Of
these 25 beetles were positive for the L49-1AA isolate.</description>
			<pubDate>Mon, 07 Jan 2013</pubDate>
			<guid>http://cfs.nrcan.gc.ca/publications?id=34261</guid>
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			<title>Isolation and characterisation of Isaria farinosa and Purpureocillium lilacinum associated with emerald ash borer, Agrilus planipennis in Canada.</title>
			<link>http://cfs.nrcan.gc.ca/publications?id=33890</link>
			<description></description>
			<pubDate>Thu, 12 Jul 2012</pubDate>
			<guid>http://cfs.nrcan.gc.ca/publications?id=33890</guid>
		</item>
		        		<item>
			<title>Characterization and virulence of Beauveria spp. recovered from emerald ash borer in southwestern Ontario, Canada.</title>
			<link>http://cfs.nrcan.gc.ca/publications?id=33857</link>
			<description>The emerald ash borer (EAB), Agrilus planipennis (Coleoptera: Buprestidae), is an invasive wood boring beetle that is decimating North America’s ash trees (Fraxinus spp.). To find effective and safe indigenous biocontrol agents to manage EAB, we conducted a survey in 2008–2009 of entomopathogenic fungi (EPF) infecting EAB in five outbreak sites in southwestern Ontario, Canada. A total of 78 Beauveria spp. isolates were retrieved from dead and mycosed EAB cadavers residing in the phloem tissues of dead ash barks, larval frass extracted from feeding galleries under the bark of dead trees. Molecular characterization using sequences of the ITS, 5′ end of EF1-α and intergenic Bloc region fragments revealed that Beauveria bassiana and Beauveria pseudobassiana were commonly associated with EAB in the sampled sites. Based on phylogenetic analysis inferred from ITS sequences, 17 of these isolates clustered with B. bassiana, which further grouped into three different sub-clades. However, the combined EF1-α and Bloc sequences detected five genotypes among the three sub-clades. The remaining 61 isolates clustered with B. pseudobassiana, which had identical ITS sequences but were further subdivided into two genotypes by variation in the EF1-α and Bloc regions. Initial virulence screening against EAB adults of 23 isolates representing the different clades yielded 8 that produced more than 90% mortality in a single concentration assay. These isolates differed in virulence based on LC50 values estimated from multiple concentration bioassay and based on mean survival times at a conidia concentration of 2 × 106 conidia/ml. B. bassiana isolate L49-1AA was significantly more virulent and produced more conidia on EAB cadavers compared to the other indigenous isolates and the commercial strain B. bassiana GHA suggesting that L49-1AA may have potential as a microbiological control agent against EAB.</description>
			<pubDate>Wed, 11 Jul 2012</pubDate>
			<guid>http://cfs.nrcan.gc.ca/publications?id=33857</guid>
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