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International audience; We evaluated the use of fluorescent powders for tracking dispersal by the emerald ash borer, Agrilus planipennis Fairmaire (Coleoptera: Buprestidae), of Beauveria bassiana isolates from an autocontamination device. Neither of the two DayGlow powders tested (Arc Yellow and Aurora Pink) interfered with fungal germination or growth, nor did they affect survival of beetles in the laboratory, or affect virulence of the fungus. The powders persisted at least 10 days out-of-doors on dead beetles in sticky band traps, and at least 14 days on pouches inside autocontamination traps. During field trials of autocontamination traps with powder-dusted fungal pouches in southwestern Ontario, 8.0% of the 4010 beetles captured in green prism and sticky-band traps were positive for fluorescent powders. Only half (46.2–57.8%) of the powder-positive beetles actually carried viable fungal conidia, as determined by plating of beetle rinses, possibly as a result of patchy growth of fungal isolates and reduced conidia production on pouch surfaces during the 16-day trapping experiment. The presence of viable conidia (either one or both isolates) on about 10% of beetles that did not carry any visible powder particles may be an indication of horizontal transmission of the fungus by beetles that had visited the autocontamination traps.

A microsporidium Nosema disstriae (Thomson) is a parasite of the forest tent caterpillar Malacasoma disstria (Lepidoptera: Lasiocampidae), a notable defoliator of deciduous trees in North America. The goal of this paper was to demonstrate the ultrastructure of N . disstriae and to determine the position of this microsporidium within the N . bombycis clade (NBC) using comparative morphology and multiple molecular phylogenetic markers: RPB1, LSU-, ITS- and SSU-rDNA. As a part of this goal, the revision of the described members of the NBC has been performed. The ultrastructure of proliferating stages and spores of N . disstriae were similar to previously described Nosema spp. parasitizing lepidopteran species. Meronts produced tubular-like structures on their surfaces and exhibited a tight association with host mitochondria. All stages were diplokaryotic and developed without interfacial envelopes. Disporoblastic sporogony produced typical Nosema -type spores with 9–12 polar filament coils. A vesicle with immature spores was once recognized on sections, concordant with the previous record of octosporous sporogony in the N . disstriae life cycle. Rarely, spores with thinner envelopes and large posterior vacuoles were seen in the midgut. Tracheae were most heavily infected. Midgut, surrounding muscles, haemocytes and fat body also contained microsporidia. SSUrRNA-inferred phylogenies were consistent with previously published articles and did not resolve the relation within the NBC clade. The RPB1-inferred trees and concatenated RPB1 and LSU-ITS-SSUrDNA-based trees demonstrated clustering of N . disstriae with N . antheraeae as early divergent species within the NBC.

Entomopathogenic fungi of the genera Isaria and Purpureocillium were recovered from infestation sites of emerald ash borer (EAB) in Southern Ontario, Canada. Isolates were identified using morphological characters and by sequencing the ITS1-5.8S-ITS2 ribosomal DNA gene and partial β-tubulin gene. Phylogenetic analysis and constructed trees based on the ITS and β-tubulin gene explicitly confirm isolates L66B, SY17-a and LHY46-a as Isaria farinosa and B3A, B59A and SY45B-a as Purpureocillium lilacinum. Pathogenicity was tested in the laboratory against adult EAB using a single concentration (2.0×107 conidia/ml) applied topically to adults. Controls included three commercial isolates: Isaria fumosorosea LRC176, Metarhizium brunneum LRC187 and Beauveria bassiana strain GHA. The native isolates I. farinosa L66B and P. lilacinum SY45B-a killed 75 and 50% of the beetles 14 days post-inoculation. Although these indigenous entomogenous fungi were less virulent compared with the commercial isolates, yearly...

Nosema isolates from five lepidopteran forest defoliators, Nosema fumiferanae from spruce budworm, Choristoneura fumiferana; a Nosema sp. from jack pine budworm, Choristoneura pinus pinus and western spruce budworm, Choristoneura occidentalis (Nosema sp. CPP and Nosema sp. CO, respectively); Nosema thomsoni from large aspen tortrix, Choristoneura conflictana; and Nosema disstriae, from the forest tent caterpillar, Malacosoma disstria were compared based on their small subunit (SSU) ribosomal RNA (rRNA) gene sequences. Four of the species sequenced, N. fumiferanae, Nosema sp. CPP, Nosema sp. CO, and N. disstriae have a high SSU rDNA sequence identity (0.6%-1.5%) and are members of the "true Nosema" clade. They all showed the reverse arrangement of the (large subunit [LSU]-internal transcribed spacer [ITS]-SSU) of the rRNA gene. The fifth species, N. thomsoni has the usual (SSU-ITS-LSU) arrangement and is not a member of this clade showing only an 82% sequence similarity. We speculate, therefore, that a genetic reversal may have occurred in the common ancestor to the "true Nosema" clade. Although, the mechanism for rearrangement of the rRNA gene subunits is not known we provide a possible explanation for the localization. N. fumiferanae, Nosema sp. CPP, and Nosema sp. CO clustered together on the inferred phylogenetic tree. The high sequence similarities, the reverse arrangement in the rRNA gene subunits, and the phylogenetic clustering suggest that these three species are closely related but separate species.

The house fly, Musca domestica L., and the stable fly, Stomoxys calcitrans (L.) (Diptera: Muscidae), are cosmopolitan pests parasitized by a guild of more than two dozen species of wasps. Several species of these wasps have been commercialized as biocontrol agents or are being studied for this purpose. Wolbachia bacteria are known to infect at least some of these wasps and are of interest because infections can dramatically affect insect reproduction. A survey in this parasitoid-fly system detected Wolbachia in 15 of 21 species of wasps and in three of nine species of flies parasitized by these wasps. Phylogenetic analyses using wsp gene sequences identified single isolate infections in most cases. Infections of two and four isolates were detected in Nasonia vitripennis (Walker) and Spalangia cameroni Perkins (Hymenoptera: Pteromalidae), respectively. Laboratory experiments showed infections in S. cameroni to cause an incomplete form of female-mortality (FM) type cytoplasmic incompatibility (CI). Crosses between uninfected female and infected male partners (♀ x ♂ w ) produced fewer progeny, which had a strong male-biased sex ratio. Crosses between 9 x ♂,♀ w x ♂ w , and ♀ w x ♂ produced more progeny, which had a female-biased sex ratio. Developmental times of progeny were increased when the paternal parent was infected with Wolbachia, regardless of whether the maternal parent was infected or whether offspring developed from fertilized eggs. This result may reflect the action of Wolbachia on components of the seminal fluid that then affect the development of offspring from inseminated females. It is hoped that future studies of Wolbachia in this guild will facilitate the rearing and application of these wasps as biocontrol agents of house fly and stable fly.

We provide molecular systematics of a microporidian species, Nosema fumiferanae, one of the most common natural enemies of spruce budworm, Choristoneura fumiferana. The uncharacterized flanking region upstream of the large subunit (LSU) rRNA and the complete rRNA cistron of N. fumiferanae was 4,769 bp long. The organization of the rRNA gene was 5′-LSU rRNA-ITS-SSU rRNA-IGS-5S-3′ and corresponded primarily to most insect (i.e. lepidopteran) Nosema species identified and classified to date. Phylogenetic analysis based on the complete rRNA cistron indicated that N. fumiferanae is closely related to Nosema plutellae and is correctly assigned to the “true” Nosema group. Suggestions were provided on a criterion to delineate the “true” Nosema from other microsporidian species.

A microsporidium was isolated from the bronze birch borer, Agrilus anxius Gory (Coleoptera: Buprestidae), collected near Sudbury and Sault Ste Marie, Canada. Light and electron microscopic investigations showed that gross pathology and ultrastructure of the investigated Cystosporogenes species was similar to those characterized and described for other Cystosporogenes species. Small subunit rRNA gene sequence data and comparative phylogenetic analysis confirmed that the microsporidian species from A. anxius is most closely related to the genus Cystosporogenes clade of microsporidia. Infection average in the Sudbury and Sault Ste Marie beetle populations was >80% and relatively stable in 2006-2007 but declined in 2008. Field prevalence of the A. anxius isolate, mechanisms that may potentially be involved in its horizontal (autoinfection) and vertical (transovarial) transmission, and disease dynamics are discussed. The congeneric relationship between Agrilus planipennis and A. anxius makes it imperative to study the virulence of this Cystosporogenes species in A. planipennis.