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At least 361 records · Page 20Linked to original sources
USGS2021

Health surveillance of a potential bridge host: Pathogen exposure risks posed to avian populations augmented with captive-bred pheasants

Augmentation of wild populations with captive-bred individuals presents an inherent risk of co-introducing novel pathogens to naïve species, but it can be an important tool for supplementing small or declining populations. Game species used for human enterprise and recreation such as the ring-necked pheasant ( Phasianus colchicus ) are commonly raised in captivity and released onto public and private wildlands as a method of augmenting naturalized pheasant populations. This study presents findings on pathogen exposure from three sources of serological data collected in California during 2014–2017 including (a) 71 pen-reared pheasants sampled across seven game bird breeding farms, (b) six previously released pen-reared pheasants captured at two study sites where wild pheasants occurred and (c) 79 wild pheasants captured across six study sites. In both pen-reared and wild pheasants, antibodies were detected against haemorrhagic enteritis virus (HEV), infectious laryngotracheitis (ILT), infectious bursal disease virus (IBDV), paramyxovirus type 1 (PMV-1) and Pasteurella multocida (PM). Previously released pen-reared pheasants were seropositive for HEV, ILT, and PM. Generalized linear mixed models accounting for intraclass correlation within groups indicated that pen-reared pheasants were more than twice as likely to test positive for HEV antibodies. Necropsy and ancillary diagnostics were performed in addition to serological testing on 40 pen-reared pheasants sampled from five of the seven farms. Pheasants from three of these farms tested positive by PCR for Siadenovirus, the causative agent of both haemorrhagic enteritis in turkeys and marble spleen disease of pheasants, which are serologically indistinguishable. Following necropsy, owners from the five farms were surveyed regarding husbandry and biosecurity practices. Farms ranged in size from 10,000 to more than 100,000 birds, two farms raised other game bird species on premises, and two farms used some form of vaccination. Biosecurity practices varied by farm, but the largest farm implemented the strictest practices.

California↗
USGS2021

Field trials to test new trap technologies for monitoring Culex populations and the efficacy of the biopesticide formulation VectoMax® FG for control of larval Culex quinquefasciatus in the Alaka'i Plateau, Kaua'i, Hawaii

Mosquito-borne avian malaria Plasmodium relictum is a key limiting factor for endemic Hawaiian forest birds. In the past decade, populations of Kaua‘i’s endemic forest birds have been in a steep decline due to an increase in malaria transmission. To evaluate the use of available biopesticides for short-term mosquito control we tested the efficacy of the biopesticide VectoMax® FG against Culex quinquefasciatus larvae in naturally occurring perched stream pools, seeps, and ground pools in forest bird habitat in Kaua‘i’s remote Alaka‘i Plateau. We also tested the efficacy of conventional and newer traps and attractants for the capture of adult Culex quinquefasciatus in Hawaiian rain forests and monitored adult mosquito populations at the Kaua‘i field site. During field trials conducted on Hawai‘i Island we captured more Culex quinquefasciatus in gravid traps than in host-seeking traps. Among the host-seeking traps, Biogents BG-Sentinel 2 traps baited with CO2 and BG-Lure caught more Culex quinquefasciatus and Aedes japonicus japonicus than CDC (Centers for Disease Control and Prevention) traps baited with compressed CO2, CDC traps baited with dry ice, or Biogents BG-Sentinel 2 traps baited with BG-Lure and octenol but not CO2. Both Biogents BG-Sentinel 2 and CDC miniature traps baited with compressed CO2 or dry ice captured significantly more Culex quinquefasciatus than Biogents BG-Sentinel 2 traps baited with octenol and BG-Lure but without CO2. We also found that gravid traps baited with timothy hay infusions caught significantly more Culex quinquefasciatus than traps baited with either a commercial gravid mosquito attractant or an infusion made with pelleted rabbit feed. Traps baited with an infusion of timothy hay and donkey dung were the most effective for Culex quinquefasciatus. On Kaua‘i, we operated Biogents BG-Sentinel 2 traps baited with CO2 and gravid traps and captured 29 mosquitoes in 182 trap-nights from October–November 2016 and 126 mosquitoes in 254 trap-nights from September–October 2017. Contrary to our findings on Hawai‘i Island, most mosquitoes (96%) were captured in Biogents BG-Sentinel 2 traps indicating considerable site-to-site variability in trap efficacy. Weekly adult trapping on Kaua‘i indicates Culex quinquefasciatus populations peaked in October but provided no reliable evidence that larval control had any significant effect on adult populations. Overall, VectoMax® FG was very effective at larval control reducing larval abundance by 95% at 48 hours and out to 1-week post-treatment. Treatment was most effective (100% at 1-week post-treatment) in perched pools when early instar larvae were present and least effective in seeps when pupae and fourth instar larvae were most common. Although post-treatment counts fluctuated dramatically, we observed no evidence of population level impacts to the two most common non-target invertebrates: the water strider Microvelia vagans and endemic damselfly naiads (Megalagrion sp.). VectoMax® FG appears to be an effective and safe biopesticide for the local control of Culex quinquefasciatus larvae in forest bird habitat in the Alaka‘i Plateau. Further studies will be necessary to determine if local larval control significantly reduces adult mosquito abundance and, ultimately, avian malaria transmission, and if there are long term, non-target effects associated with repeated use of VectoMax® FG in natural Hawaiian waterways.

Hawaii↗
USGS2015

USGS role and response to highly pathogenic avian influenza

Avian influenza viruses are naturally occurring in wild birds such as ducks, geese, swans, and gulls. These viruses generally do not cause illness in wild birds, however, when spread to poultry they can be highly pathogenic and cause illness and death in backyard and commercial farms. Outbreaks may cause devastating agricultural economic losses and some viral strains have the potential to infect people directly. Furthermore, the combination of avian influenza viruses with mammalian viruses can result in strains with the ability to transmit from person to person, possibly leading to viruses with pandemic potential. All known pandemic influenza viruses have had some genetic material of avian origin. Since 1996, a strain of highly pathogenic avian influenza (HPAI) virus, H5N1, has caused infection in wild birds, losses to poultry farms in Eurasia and North Africa, and led to the deaths of several hundred people. Spread of the H5N1 virus and other influenza strains from China was likely facilitated by migratory birds. In December 2014, HPAI was detected in poultry in Canada and migratory birds in the United States. Since then, HPAI viruses have spread to large parts of the United States and will likely continue to spread through migratory bird flyways and other mechanisms throughout North America. In the United States, HPAI viruses have severely affected the poultry industry with millions of domestic birds dead or culled. These strains of HPAI are not known to cause disease in humans; however, the Centers for Disease Control and Prevention (CDC) advise caution when in close contact with infected birds. Experts agree that HPAI strains currently circulating in wild birds of North America will likely persist for the next few years. This unprecedented situation presents risks to the poultry industry, natural resource management, and potentially human health. Scientific knowledge and decision support tools are urgently needed to understand factors affecting the persistence of HPAI in wild birds, to forecast future spread of HPAI by wild birds, and to detect novel strains of HPAI that may emerge.

Fact Sheet↗
USGS2015

USGS highly pathogenic avian influenza research strategy

Avian influenza viruses are naturally occurring in wild birds such as ducks, geese, swans, and gulls. These viruses generally do not cause illness in wild birds, however, when spread to poultry they can be highly pathogenic and cause illness and death in backyard and commercial farms. Outbreaks may cause devastating agricultural economic losses and some viral strains have the potential to infect people directly. Furthermore, the combination of avian influenza viruses with mammalian viruses can result in strains with the ability to transmit from person to person, possibly leading to viruses with pandemic potential. All known pandemic influenza viruses have had some genetic material of avian origin. Since 1996, a strain of highly pathogenic avian influenza (HPAI) virus, H5N1, has caused infection in wild birds, losses to poultry farms in Eurasia and North Africa, and led to the deaths of several hundred people. Spread of the H5N1 virus and other influenza strains from China was likely facilitated by migratory birds. In December 2014, HPAI was detected in poultry in Canada and migratory birds in the United States. Since then, HPAI viruses have spread to large parts of the United States and will likely continue to spread through migratory bird flyways and other mechanisms throughout North America. In the United States, HPAI viruses have severely affected the poultry industry with millions of domestic birds dead or culled. These strains of HPAI are not known to cause disease in humans; however, the Centers for Disease Control and Prevention (CDC) advise caution when in close contact with infected birds. Experts agree that HPAI strains currently circulating in wild birds of North America will likely persist for the next few years. This unprecedented situation presents risks to the poultry industry, natural resource management, and potentially human health. Scientific knowledge and decision support tools are urgently needed to understand factors affecting the persistence of HPAI in wild birds, to forecast future spread of HPAI by wild birds, and to detect novel strains of HPAI that may emerge.

Fact Sheet↗
USGS2019

Use of blood clotting assays to assess potential anticoagulant rodenticide exposure and effects in free-ranging birds of prey

Non-target wildlife, particularly birds of prey, are widely exposed to and acutely poisoned by anticoagulant rodenticides (ARs). An unresolved issue surrounding such exposure, however, is the potential for sublethal effects. In particular, the consequences of AR exposure and resulting coagulopathy on health and survival of unintentionally exposed animals, which often encounter a multitude of anthropogenic stressors, are understudied. In a wildlife rehabilitation setting, AR intoxication may be masked by more obvious injuries related to collision with vehicles or electrocution, thereby obfuscating proximate from ultimate cause of mortality. An assessment of coagulation function of admitted wildlife may provide a means of identifying animals exhibiting sublethal coagulopathy, and ultimately ensuring provision of appropriate and swift treatment. In conjunction with routine diagnostics for injury and disease, we performed two blood clotting assays (prothrombin time, Russell's viper venom time) affected by vitamin K-dependent coagulopathy of samples from six species of live raptors admitted to a rehabilitation facility. We also measured clotting time in pre-fledgling barn owl chicks ( Tyto furcata ) from 10 nest sites in Lower Mainland Canada. Prolonged clotting time or failure to form a clot altogether was observed in 23.0% of 61 sampled raptors admitted to the rehabilitation facility. This is a biologically significant proportion of individuals given the fortuitous and likely biased nature by which raptors are found and admitted to rehabilitation facilities. In contrast, there was little evidence of coagulopathy in 19 pre-fledgling barn owl chicks. The utility of avian coagulation tests for diagnosing AR exposure is promising, yet there remains a need to establish species specific reference values and standardize assay methodologies among testing facilities.

Science of the Total Environment↗
USGS2022

Host plant associations of Lepidoptera and implications for forest bird management at Hakalau Forest National Wildlife Refuge

Forests dominated or co-dominated by ‘ōhi‘a ( Metrosideros polymorpha ) are critical to most Hawaiian forest birds, but fungal diseases causing Rapid ‘Ōhi‘a Death (ROD) threaten ‘ōhi‘a-based food webs that support native bird communities on Hawai‘i Island. Caterpillars are the most frequently consumed arthropod prey of native birds and their young and are especially frequent in the diets of one threatened (T) and three endangered (E) species (“listed” species) at Hakalau Forest National Wildlife Refuge (Hakalau): ‘akiapōlā‘au ( Hemignathus wilsoni , E), ‘alawī (Hawai‘i creeper; Loxops mana , E), Hawai‘i ‘ākepa ( L. coccineus , E), and ‘i‘iwi ( Drepanis coccinea , T). Hakalau harbors the largest and most stable populations of listed forest birds in Hawai‘i, presumably due to the availability of food resources and the extent of suitable, managed habitat above the range of mosquito-borne avian malaria. Because a previous study indicated that only a few caterpillar species were important in the diets of listed birds at Hakalau, we investigated the distribution of caterpillars on common host plants available to foraging birds. Eleven native plant species hosted two or more taxa identified to genus or species, with at least seven from ‘ōhi‘a, six from koa ( Acacia koa ), and five from ‘ākala ( Rubus hawaiensis ). We identified 16 taxa to genus or species from 9 families, assigning 11 to species. Leaves, which were the focus of our sampling effort, were the substrate used by 20 caterpillar taxa, and dead wood or bark was used by 7 taxa. In a previous study, we classified 19 morphotypes of caterpillar mandibles in the diets of native and alien birds at Hakalau, and in the present study we dissected mandibles from caterpillars that likely matched 10 of those morphotypes. These 10 morphotypes potentially represented >95% of caterpillar prey found in the earlier diet study and were collected from 11 host plant species, with ‘ōhi‘a hosting 8 morphotypes, 4 of which were exclusive to ‘ōhi‘a. The most widely hosted morphotype was found on all 11 plant species that we sampled, including ‘ōhi‘a, but the other 9 morphotypes were found on 1–7 hosts. As shown by the previous diet study, each of the listed bird species consumed caterpillar prey consisting mostly of combinations of two morphotypes drawn from a pool of only five, indicating a high degree of specialization. In the present study, we collected three of the five key morphotypes only on ‘ōhi‘a, highlighting the importance of this tree to listed bird species. Because ‘ōhi‘a forests in Hakalau remain vulnerable to ROD, measures to mitigate the impacts of reduced ‘ōhi‘a cover are important to consider from the perspective of forest bird food webs and diet. Ongoing reforestation of former pasturelands with koa and common understory species should provide alternative caterpillar prey for forest birds. Our results and information from the literature indicate that koa supports, to varying degrees, nearly all forest birds at Hakalau, while ‘ākala, ‘ōhelo ( Vaccinium calycinum ), kōlea ( Myrsine lessertiana ), ‘ōlapa ( Cheirodendron trigynum ), pūkiawe ( Leptecophylla tameiameiae ), and māmaki ( Pipturus albidus ) could benefit bird populations by increasing prey availability and structural complexity in koa-dominated stands. Foraging studies and additional research to identify species and host plant associations of important forest bird prey, including caterpillars and other arthropods, can help managers evaluate the complex interactions between native forest birds and their food webs and habitats.

Hawaii↗
USGS2011

A novel member of the family Hepeviridae from cutthroat trout ( Oncorhynchus clarkii )

Beginning in 1988, the Chinook salmon embryo (CHSE-214) cell line was used to isolate a novel virus from spawning adult trout in the state of California, USA. Termed the cutthroat trout ( Oncorhynchus clarkii ) virus (CTV), the small, round virus was not associated with disease, but was subsequently found to be present in an increasing number of trout populations in the western USA, likely by a combination of improved surveillance activities and the shipment of infected eggs to new locations. Here, we report that the full length genome of the 1988 Heenan Lake isolate of CTV consisted of 7269 nucleotides of positive-sense, single-stranded RNA beginning with a 5' untranslated region (UTR), followed by three open reading frames (ORFs), a 3' UTR and ending in a polyA tail. The genome of CTV was similar in size and organization to that of Hepatitis E virus (HEV) with which it shared the highest nucleotide and amino acid sequence identities. Similar to the genomes of human, rodent or avian hepeviruses, ORF 1 encoded a large, non-structural polyprotein that included conserved methyltransferase, protease, helicase and polymerase domains, while ORF 2 encoded the structural capsid protein and ORF 3 the phosphoprotein. Together, our data indicated that CTV was clearly a member of the family Hepeviridae , although the level of amino acid sequence identity with the ORFs of mammalian or avian hepeviruses (13-27%) may be sufficiently low to warrant the creation of a novel genus. We also performed a phylogenetic analysis using a 262. nt region within ORF 1 for 63 isolates of CTV obtained from seven species of trout reared in various geographic locations in the western USA. While the sequences fell into two genetic clades, the overall nucleotide diversity was low (less than 8.4%) and many isolates differed by only 1-2 nucleotides, suggesting an epidemiological link. Finally, we showed that CTV was able to form persistently infected cultures of the CHSE-214 cell line that may have use in research on the biology or treatment of hepevirus infections of humans or other animals.

Virus Research↗
USGS2017

Reassortment of influenza A viruses in wild birds in Alaska before H5 Clade 2.3.4.4 Outbreaks

Sampling of mallards in Alaska during September 2014–April 2015 identified low pathogenic avian influenza A virus (subtypes H5N2 and H1N1) that shared ancestry with highly pathogenic reassortant H5N2 and H5N1 viruses. Molecular dating indicated reassortment soon after interhemispheric movement of H5N8 clade 2.3.4.4, suggesting genetic exchange in Alaska or surrounds before outbreaks.

Emerging Infectious Diseases↗
USGS2008

Avian wildlife mortality events due to salmonellosis in the United States, 1985-2004

Infection with Salmonella spp. has long been recognized in avian wildlife, although its significance in causing avian mortality, and its zoonotic risk, is not well understood. This study evaluates the role of Salmonella spp. in wild bird mortality events in the United States from 1985 through 2004. Analyses were performed to calculate the frequency of these events and the proportional mortality by species, year, month, state, and region. Salmonellosis was a significant contributor to mortality in many species of birds; particularly in passerines, for which 21.5% of all mortality events involved salmonellosis. The proportional mortality averaged a 12% annual increase over the 20-yr period, with seasonal peaks in January and April. Increased salmonellosis-related mortality in New England, Southeastern, and Mountain-Prairie states was identified. Based on the results of this study, salmonellosis can be considered an important zoonotic disease of wild birds.

Journal of Wildlife Diseases↗
USGS2005

Attempts to identify the source of avian vacuolar myelinopathy for waterbirds

Attempts were made to reproduce avian vacuolar myelinopathy (AVM) in a number of test animals in order to determine the source of the causative agent for birds and to find a suitable animal model for future studies. Submerged vegetation, plankton, invertebrates, forage fish, and sediments were collected from three lakes with ongoing outbreaks of AVM and fed to American coots ( Fulica americana ), mallard ducks and ducklings ( Anas platyrhynchos ), quail ( Coturnix japonica ), and laboratory mice either via gavage or ad libitum. Tissues from AVM-affected coots with brain lesions were fed to ducklings, kestrels ( Falco sparverius ), and American crows ( Corvus brachyrhynchos ). Two mallards that ingested one sample of Hydrilla verticillata along with any biotic or abiotic material associated with its external surface developed brain lesions consistent with AVM, although neither of the ducks had clinical signs of disease. Ingestion of numerous other samples of Hydrilla from the AVM affected lakes and a lake with no prior history of AVM, other materials (sediments, algae, fish, invertebrates, and water from affected lakes), or tissues from AVM-affected birds did not produce either clinical signs or brain lesions in any of the other test animals in our studies. These results suggest that waterbirds are most likely exposed to the causative agent of AVM while feeding on aquatic vegetation, but we do not believe the vegetation itself is the agent. We hypothesize that the causative agent of AVM might either be accumulated by aquatic vegetation, such as Hydrilla , or associated with biotic or abiotic material on its external surfaces. In support of that hypothesis, two coots that ingested Hydrilla sampled from a lake with an ongoing AVM outbreak in wild birds developed neurologic signs within 9 days (ataxia, limb weakness, and incoordination), and one of two coots that ingested Hydrilla collected from the same site 13 days later became sick and died within 38 days. None of these three sick coots had definitive brain lesions consistent with AVM by light microscopy, but they had no gross or histologic lesions in other tissues. It is unclear if these birds died of AVM. Perhaps they did not ingest a dose sufficient to produce brain lesions or the lesions were ultrastructural. Alternatively, it is possible that a separate neurotoxic agent is responsible for the morbidity and mortality observed in these coots.

Journal of Wildlife Diseases↗
USGS2014

Spatial and temporal patterns of avian paramyxovirus-1 outbreaks in Double-Crested Cormorants ( Phalacrocorax auritus ) in the USA

Morbidity and mortality events caused by avian paramyxovirus-1 (APMV-1) in Double-crested Cormorant (DCCO; Phalacrocorax auritus ) nesting colonies in the US and Canada have been sporadically documented in the literature. We describe APMV-1 associated outbreaks in DCCO in the US from the first reported occurrence in 1992 through 2012. The frequency of APMV-1 outbreaks has increased in the US over the last decade, but the majority of events have continued to occur in DCCO colonies in the Midwestern states. Although morbidity and mortality in conesting species has been frequently reported during DCCO APMV-1 outbreaks, our results suggest that isolation of APMV-1 is uncommon in species other than DCCO during APMV-1 outbreaks and that the cause of mortality in other species is associated with other pathogens. Populations of DCCO do not appear to have been significantly affected by this disease; however, because at least 65% of the APMV-1 outbreaks in DCCO in the US have involved APMV-1 strains classified as virulent to poultry (virulent Newcastle disease virus), its persistence and increased occurrence in DCCO warrants continued research and surveillance.

Journal of Wildlife Diseases↗
USGS2025

Variation in gene expression across infection status and elevation in a Hawaiian honeycreeper

Introduced pathogens exert novel selection on hosts, and although many host species have experienced drastic population declines in the absence of adaptation, some hosts have adapted to highly virulent pathogens. For instance, mosquitoes and Plasmodium relictum introduced to the Hawaiian Islands have resulted in extinctions and catastrophic population declines due to avian malaria, particularly in the diverse clade of Hawaiian honeycreepers. However, some species, such as the Hawai'i 'amakihi ( Chlorodrepanis virens ), can survive infection. Immunity exists in low-elevation populations where mosquitoes are abundant, whereas high-elevation, unexposed populations of 'amakihi display greatly reduced immunity. To explore the basis of adaptation to P. relictum in low-elevation 'amakihi, we sequenced transcriptomes from 24 low-elevation and 15 high-elevation 'amakihi. We tested for differential gene expression between (i) infected and uninfected birds and (ii) low- and high-elevation birds. Infected birds showed significant differences in expression across many transcripts with diverse cellular functions involved in different pathways of immune response; eight of the top 13 transcripts blasted to genes previously implicated in immunity to malaria in 'amakihi, and 11 have been identified in other infectious disease systems. Thirteen transcripts showed a trend of higher expression in high-elevation birds. These transcripts blasted to genes involved in metabolism, blood coagulation, and immune response. Our results provide increasing support for a subset of genes involved in immunity to malaria in 'amakihi and hint at possible antagonistic interactions between response to pathogens and environmental characteristics associated with elevation. Further work clarifying the nature of these interactions could benefit conservation efforts of Hawaiian honeycreepers in upper elevation refugia that are increasingly subject to malaria exposure.

Hawaii↗
USGS1978

Avian cholera in eider ducks in Maine

Outbreaks of avian cholera ( Pasteurella multocida ) occur frequently in common eiders ( Somateria mollissima dresseri ) in Maine during early summer. Studies over a seven year period show that over 90% of the loss occurred in incubating females and might be associated with their weakened condition because females and might be associated with their weakened condition because females do not feed during the incubation period. High nesting densities also may contribute to the losses. The exact source of P. Multocida is unknown although carrier birds were found.

Maine↗
USGS2025

Safety and immunogenicity of poultry vaccine for protecting critically endangered avian species against highly pathogenic avian influenza virus, United States

In 2023, an outbreak of highly pathogenic avian influenza occurred among critically endangered California condors ( Gymnogyps californianus ), and > 21 died. We evaluated safety, immunogenicity, vaccination strategies, and correlates of antibody response of an influenza vaccine for poultry in black vultures ( Coragyps atratus ) and then California condors. We noted differences in antibody titers between vaccinated and unvaccinated birds (vultures p < 0.004; condors p­ < 0.02) but no adverse effects of vaccination. All vaccinated vultures and 80% of vaccinated condors showed maximum measured antibody response within the published range associated with survival of vaccinated and virally challenged chickens. We noted weak evidence of higher antibody responses for birds given two 0.5-mL vaccines versus those given one 1-mL vaccine but no correlation between antibody titers and sex for either species or between antibody titers and bone lead concentrations in vultures. Our results prompted initiation of a vaccination program for condors that could reduce spread of this disease among highly threatened species.

Emerging Infectious Diseases↗
USGS1981

Evaluation of coproexamination as a diagnostic test for avian botulism

Fecal extracts and blood sera from 113 ducks showing clinical signs of botulism were examined for Clostridium botulinum type C toxin by means of the mouse toxicity test to evaluate coproexamination as a diagnostic procedure, as compared with demonstration of toxin in serum. When death of test mice unprotected with type specific antitoxin (while protected controls survived) was the criterion, 78.8% of the sera and 5.3% of the fecal extracts were positive. When characteristic signs of intoxication in the unprotected mice was included as evidence of toxin in the specimens, these percentages increased to 86.7 and 6.2, respectively. Fecal specimens were collected hourly for the first 6 h after peroral dosing of eight mallards ( Anas platyrhynchos ) with 1.0 LD 50 , of type C toxin and at 24, 48, and 72 h from birds surviving that long. From 2 to 4 toxin-positive specimens were passed by all eight ducks during the first 6 h, five specimens were positive at 24 h, and three were positive at 48 h. Only three specimens were collected at 72 h, all of which were negative. These findings suggest that attempts to detect toxin in the feces of wild ducks might have been more successful had the birds been captured earlier in the course of the disease.

Utah↗
USGS2000

Characterization of poxviruses from forest birds in Hawaii

Two strains of avian pox viruses were isolated from cutaneous lesions in Hawaiian crows ( Corvus hawaiiensis ) examined in 1994 and a third from a biopsy obtained in 1992 from an infected bird of the Apapane species ( Himatione sanguinea ) by inoculation of the chorioallantoic membranes (CAM) of developing chicken embryos. The resulting proliferative CAM lesions contained eosinophilic cytoplasmic inclusion bodies characteristic of pox virus infection. The pathogenicity of these three viruses in domestic chickens was mild as evidenced by the development of relatively minor lesions of short duration at the sites of inoculation. Their virulence in this host was similar to that of a fowlpox virus (FPV) vaccine strain and contrasted greatly with the ability of two field strains of FPV to produce extensive proliferative lesions. One of the Hawaiian crow pox virus isolates as well as the one originating from the Apapane species could be propagated in two secondary avian cell lines, QT-35 and LMH. A comparison of the restriction fragment length polymorphisms (RFLP) of the genomes of the two cell line-adapted viruses, generated by Eco RI digestion, revealed a limited degree of similarity. Moreover, neither profile was comparable to those of the two field isolates of FPV, which were almost indistinguishable from each other. Thus, based on the genetic distinctness of the two Hawaiian bird viruses, they appear to represent different strains of avipoxvirus.

Hawaii↗