Seventeen plaque purified isolates of two viral preparations of Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMNPV), were analyzed in terms of the genomic changes after digestion of their DNAs with HindIII and PstI restriction enzymes. The 1979 AgMNPV wild type preparation (AgMNPV-’79) resulted in six different variants and the 1985 viral commercial preparation (AgMNPV-’85), in eleven. The genomic variation of all the isolates was mapped showing that those from 1985 presented more heterogeneity with changes mapped in additional sites in comparison to the AgMNPV-’79 variants. Their virulence was compared by infecting two Lepidopteran cell lines, Spodoptera frugiperda (IPLB-SF-21AE) and Anticarsia gemmatalis (UFL-AG-286). The results indicated that there was some difference in virulence within the AgMNPV-’85 variants. This commercial preparation had been applied in soybean fields in Brazil over several years to control the velvetbean caterpillar defoliation.

While melanization in insects is a well-documented physiological response to wounds, bacterial, fungal and viral infections, and parasites, the potential influence of the process on the wing color of Lepidoptera has not received as much attention. Here we report a case in which the response to melanization influenced the wing color of a subgroup of Heliconius charithonia (Nymphalidae) infected with baculovirus. The individuals that survived the infection had dark-orange rather than light yellow stripes. This observation may help to explain dusky-winged melanic variants in this and other species that are known to be occasionally collected in the wild. The next logical step will be to culture the virus and to conduct a set of controlled experiments infecting mature larvae at different stages of development, in order to document the precise moment at which the infection transitions from being lethal to becoming color-altering

La detección de Escherichia coli O157:H7 en las lecherías es importante para mejorar la seguridad de los productos lácteos, y se ha llevado a cabo principalmente mediante el aislamiento de las bacterias a partir de las muestras de estiércol. Sin embargo, los componentes biliares presentes en el estiércol complica la identificación genética utilizando la técnica del PCR, y el aislamiento microbiológico se dificulta por la presencia de bacterias competidoras que comparten características microbiológicas similares. El aislamiento de E. coli O157:H7 a partir de la mosca doméstica evita las dificultades asociadas con el estiércol del ganado. El aislamiento de patógenos a partir de las moscas domésticas proporciona información adicional sobre el potencial impacto epidemiológico de la dispersión de la mosca doméstica en la distribución de patógenos, ya que las moscas domésticas se dispersan desde las lecherías donde la E. coli O157:H7 existe en forma endémica en el ganado. En este estudio, se encontró que las moscas domésticas son 2,6 veces más sensibles para la detección de E. coli O157:H7 en las lecherías. Las moscas son más fáciles de capturar y manejar que el estiércol, y deberían ser utilizadas en cualquier ensayo para detectar E. coli O157:H7 en las lecherías y otros establecimientos.

Baculoviruses infect insects, producing two distinct phenotypes during the viral life cycle: the budded virus (BV) and the occlusion-derived virus (ODV) for intra- and inter-host spread, respectively. Since the 1980s, several countries have been using Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMNPV) as a biological control agent against the velvet bean caterpillar, A. gemmatalis . The genome of AgMNPV isolate 2D (AgMNPV-2D) carries at least 152 potential genes, with 24 that possibly code for structural proteins. Proteomic studies have been carried out on a few baculoviruses, with six ODV and two BV proteomes completed so far. Moreover, there are limited data on virion proteins carried by AgMNPV-2D. Therefore, structural proteins of AgMNPV-2D were analysed by MALDI- quadrupole-TOF and liquid chromatography MS/MS. A total of 44 proteins were associated with the ODV and 33 with the BV of AgMNPV-2D. Although 38 structural proteins were already known, we found six new proteins in the ODV and seven new proteins carried by the AgMNPV-2D BV. Eleven cellular proteins that were found on several other enveloped viruses were also identified, which are possibly carried with the virion. These findings may provide novel insights into baculovirus biology and their host interaction. Moreover, our data may be helpful in subsequent applied studies aiming to improve AgMNPV use as a biopesticide and a biotechnology tool for gene expression or delivery.

A bunyavirus surveillance was performed in 2,600 pools consisting of 45,728 mosquitoes collected in north-central Florida from May 2006 to April 2007. Fifteen mosquito pools were found to be virus-positive from the total 2,600 mosquito pools tested (0.6% infection rate), which resulted in a minimum infection rate of 0.33 per 1,000 mosquitoes. Sequence data identified the virus to be Tensaw virus, a member of the Bunyaviridae family. All the virus-positive samples were obtained from pools collected from May to October 2006, in 3 of the 4 major locations studied, revealing the presence of Tensaw virus in north-central Florida mosquito populations in 2006.

A certain level of genetic diversity and connectivity between populations is necessary to allow small populations to persist over time. In this study, we investigate the last two populations of the highly endangered Miami blue butterfly, one of which was extirpated in 2010. We investigate whether an erosion of genetic diversity was the cause for the extirpation of the Bahia Honda State Park (BHSP) population. As the level of existing molecular diversity within and gene flow between the last two populations of the endangered Miami blue butterfly was unknown, we present data from twelve polymorphic microsatellite loci as an assessment. We show that greater genetic diversity (allelic richness and observed heterozygosity) than originally predicted existed in the BHSP population prior to its extirpation and values were even greater in the Key West National Wildlife Refuge population. Allelic frequencies show short-range gene flow between neighboring habitat patches and underline the importance of habitat connectivity. It does not appear that loss of genetic diversity was the cause for the loss of the BHSP population. Greater consideration of habitat connectivity should be considered for short and long-term conservation and management of this taxon.

Dense populations of extracellular bacteria were detected in midgut crypts of the southern chinch bug, Blissus insularis Barber (Hemiptera: Blissidae). Examination by epifluorescent and transmission electron microscopy revealed that the bacteria covered the luminal surface of the crypts and filled the entire lumen. Attempts to culture the extracellular endosymbionts in various media failed. Sequencing and phylogenetic analyses of 16S rRNA gene clones obtained from insects of five Florida populations showed high nucleotide homology to either betaproteobacterial Burkholderia spp. (243 clones from five populations) or gammaproteobacterial Pseudomonas spp. (58 clones from one population). Using Burkholderia-specific primers, bacteria were detected in the egg, nymph, and adult stages. Fluorescent in situ hybridization with genus-specific oligonucleotide probes confirmed the localization of Burkholderia in the crypts. Quantitative real-time PCR showed that antibiotic treatments of nymphs significantly reduced the amount of Burkholderia 16S rRNA gene copies in chinch bugs sampled 11 days after the treatment. Furthermore, these treatments resulted in retarded development and high mortality of B. insularis, indicating a beneficial impact of Burkholderia on its host.

The chilli thrips, Scirtothrips dorsalis Hood (Thysanoptera: Thripidae) is an emerging pest of many economically important vegetable and ornamental crops grown in the United States. Accurate identification of this pest is a fundamental requirement in development of effective quarantine and management strategies. Using scanning electron microscopy, high resolution images of important taxonomic traits of this pest were produced, which will aid research, regulatory and extension personnel to identify this pest. High resolution images were obtained for identifying characters of S. dorsalis including tergites with antecostal ridges; head with 3 pairs of ocellar setae, metanotum presenting longitudinal striations with medially located pair of setae; veins of forewing presenting widely spaced setae; segment VIII with complete posteromarginal comb of microtrichia; and sternites lacking discal setae but covered with rows of microtrichia except in the antero-medial region. Further, a preliminary comparison of morphological traits of S. dorsalis populations from different geographical regions was conducted, which can help in understanding the phenotype of this pest. Specimens of S. dorsalis were obtained from 5 distinct geographical regions: New Delhi, India; Shizouka, Japan; Negev, Israel; St. Vincent and Florida in the United States. Fourteen morphological characters of each population of S. dorsalis were measured and compared among the 5 populations. No significant differences were observed between the body lengths of the various S. dorsalis populations, which ranged from 0.85 mm (Negev) to 0.98 mm (Florida). When comparing 12 morphological characters, we found no significant differences among New Delhi, St. Vincent, Negev and Florida populations. However, when S. dorsalis populations of these 4 regions were compared with Shizouka, significant differences were detected for either 2 or 5 morphological characters depending on the population, suggesting the Japan population is more robust i.e., longer and wider mesothorax and metathorax, and wider abdomens. Also, the mean lengths of body size among different populations did not vary directly or inversely with latitude.

A species-specific multiplex polymerase chain reaction targeting the cytochrome b gene of cattle, horses, humans, and dogs was developed to determine the blood meal sources of stable flies, Stomoxys calcitrans (L.), collected from Florida equine facilities. Of 595 presumptive blood-fed stable flies analyzed, successful host amplification was obtained in 350, for a field host-detection efficiency of 58.8%. The majority of analyzed stable flies had fed on cattle (64.6%), followed by horses (24.3%), humans (9.5%), and dogs (1.6%). A survey of animal-enclosed pastures occurring within 3 km of stable fly collection sites revealed that the nearest cattle were between 0.8 and 1.5 km from the four horse farm sampling sites. Cattle-feeding frequencies were greater on farms where cattle were located at distances of 0.8 km, suggesting that between farm differences in host-feeding frequency is related to the number of and distance from a particular host type. Time course evaluations of previously laboratory-fed stable flies demonstrated that host-detection efficiency with this system was 100, 50, and 0% when flies were evaluated at 16, 24, and 48 h postblood feeding, respectively. The results of this study suggest short-term stable fly dispersal of up to 1.5 km in a 48-h time period. The implications of these findings are discussed.

ABSTRACT Bacteria carried by wild house flies (Musca domestica L.) collected near the rear entrances and dumpsters of 4 restaurants in north central Florida were identified. Live house flies were collected and individually transferred to blood agar plates for 1 h. After removing the flies, the plates were incubated overnight at 37C. Bacterial colonies that were morphologically distinct were isolated from other colonies by streaking onto new plates. The bacteria were identified by fatty acid analysis and sequence of their 16S rRNA gene. The bacterial isolates included 5 new bacterial records for house flies: Acinetobacter baumanni, Bacillus pumilus, Cronobacter sakazakii, Methylobacterium persicinum, and Staphylococcus sciuri. Other bacteria identified have been associated previously with house flies, including Bacillus cereus, B. thuringiensis, Escherichia coli 0157:H7, Shigella dysenteriae, Staphylococcus saprophyticus, and Staphylococcus xylosus. Most of the organisms recovered from the house fly are serious pathogens, known to produce diseases such as meningitis, food poisoning, diarrhea, abscesses, bloodstream infections, and hemorrhagic colitis. The possible exception is Bacillus thuringiensis, a known pathogen for insects that only occasionally produces allergic reactions in humans. If these organisms are not prevented from entering the food preparation and consumption areas, they could become a serious risk in the transmission of diseases.

The Musca domestica salivary gland hypertrophy virus (MdSGHV) is a large dsDNA virus that infects and sterilizes adult houseflies. The transcriptome of this newly described virus was analysed by rapid amplification of cDNA 3'-ends (3'-RACE) and RT-PCR. Direct sequencing of 3'-RACE products revealed 78 poly(A) transcripts containing 95 of the 108 putative ORFs. An additional six ORFs not amplified by 3'-RACE were detected by RT-PCR. Only seven of the 108 putative ORFs were not amplified by either 3'-RACE or RT-PCR. A series of 5'-RACE reactions were conducted on selected ORFs that were identified by 3'-RACE to be transcribed in tandem (tandem transcripts). In the majority of cases, the downstream ORFs were detected as single transcripts as well as components of the tandem transcripts, whereas the upstream ORFs were found only in tandem transcripts. The only exception was the upstream ORF MdSGHV084, which was differentially transcribed as a single transcript at 1 and 2 days post-infection (days p.i.) and as a tandem transcript (MdSGHV084/085) at 2 days p.i. Transcriptome analysis of MdSGHV detected splicing in the 3' untranslated region (3'-UTR) and extensive heterogeneity in the polyadenylation signals and cleavage sites. In addition, 23 overlapping antisense transcripts were found. In conclusion, sequencing the 3'-RACE products without cloning served as an alternative approach to detect both 3'-UTRs and transcript variants of this large DNA virus.

The Miami blue butterfly (Cyclargus thomasi bethunebakeri) is a state-endangered taxon in Florida and a candidate for federal listing. Here we report 12 polymorphic microsatellite loci appropriate for use in population and conservation studies. We genotyped 114 individuals sampled from a metapopulation in the lower Florida Keys over a 2-year period (2005-2006). These results show 4-14 alleles per locus, and ranges of observed and expected heterozygosities are 0.02679-0.79630 and 0.06154-0.69565, respectively. Large deviations from Hardy-Weinberg equilibrium (HWE) are observed across the whole sample set. When a single breeding population is analysed alone, seven of the loci are in HWE.

Salivary gland hypertrophy viruses (SGHVs) have been identified from different dipteran species, such as the tsetse fly Glossina pallidipes (GpSGHV), the housefly Musca domestica (MdSGHV) and the narcissus bulbfly Merodon equestris (MeSGHV). These viruses share the following characteristics: (i) they produce non-occluded, enveloped, rod-shaped virions that measure 500–1,000 nm in length and 50–100 nm in diameter; (ii) they possess a large circular double-stranded DNA (dsDNA) genome ranging in size from 120 to 190 kbp and having G + C ratios ranging from 28 to 44%; (iii) they cause overt salivary gland hypertrophy (SGH) symptoms in dipteran adults and partial to complete sterility. The available information on the complete genome sequence of GpSGHV and MdSGHV indicates significant co-linearity between the two viral genomes, whereas no co-linearity was observed with baculoviruses, ascoviruses, entomopoxviruses, iridoviruses and nudiviruses, other large invertebrate DNA viruses. The DNA polymerases encoded by the SGHVs are of the type B and closely related, but they are phylogenetically distant from DNA polymerases encoded by other large dsDNA viruses. The great majority of SGHV ORFs could not be assigned by sequence comparison. Phylogenetic analysis of conserved genes clustered both SGHVs, but distantly from the nudiviruses and baculoviruses. On the basis of the available morphological, (patho)biological, genomic and phylogenetic data, we propose that the two viruses are members of a new virus family named Hytrosaviridae. This proposed family currently comprises two unassigned species, G. pallidipes salivary gland hypertrophy virus and M. domestica salivary gland hypertrophy virus, and a tentative unassigned species, M. equestris salivary gland hypertrophy virus. Here, we present the characteristics and the justification for establishing this new virus family.

Mosquitoes from different species endemic to North Florida were collected over a 12-month period and blood meal analyses were conducted on engorged females to determine the range of vertebrate hosts each species fed on. Thirty-one mosquito blood meals from 6 mosquito species were identified and blood meal hosts identified included horse, cow, armadillo, deer, raccoon rabbit, and owl. Several mosquitoes captured in the study should be considered potential bridge vectors for encephalitis viruses considering their ubiquity, their preference for mammalian blood meals, and their competence as viral vectors.