Rainbow Lorikeet Research Articles

Cerebral baylisascariosis in a rainbow lorikeet (Trichoglossus moluccanus) in a German Zoo

BackgroundThe raccoon roundworm, Baylisascaris procyonis, can cause a meningoencephalitis as neural larva migrans which is known in avian species, including rainbow lorikeets in North America, but has not been described in Old World parrots in Germany yet.Case presentationA 2-month-old, male rainbow lorikeet from a zoo in Germany was submitted for necropsy. Prior to death the animal had progressive neurological signs like apathy and torticollis. In the cerebrum a focally extensive severe granulomatous to necrotizing encephalitis with an intralesional larval nematode was diagnosed. Based on the clinical and pathological findings, the larval morphology and the epidemiological background, the larva was identified as Baylisascaris procyonis.ConclusionsCerebral baylisascariosis should be considered as a differential diagnosis in zoo and pet birds with neurological signs having contact to racoons or rather racoon faeces in Germany due to the high prevalence of Baylisascaris procyonis in the German raccoon population.

Detection of a Novel Alphaherpesvirus and Avihepadnavirus in a Plantar Papilloma from a Rainbow Lorikeet (Trichoglosis moluccanus).

Cutaneous plantar papillomas are a relatively common lesion of wild psittacine birds in Australia. Next-generation sequencing technology was used to investigate the potential aetiologic agent(s) for a plantar cutaneous papilloma in a wild rainbow lorikeet (Trichoglosis moluccanus). In the DNA from this lesion, two novel viral sequences were detected. The first was the partial sequence of a herpesvirus with the proposed name, psittacid alphaherpesvirus 6, from the Mardivirus genus of the family alphaherpesviruses. This represents the first mardivirus to be detected in a psittacine bird, the first mardivirus to be detected in a wild bird in Australia, and the second mardivirus to be found in a biopsy of an avian cutaneous papilloma. The second virus sequence was a complete sequence of a hepadnavirus, proposed as parrot hepatitis B genotype H (PHBV-H). PHBV-H is the first hepadnavirus to be detected in a wild psittacine bird in Australia. Whether other similar viruses are circulating in wild birds in Australia and whether either of these viruses play a role in the development of the plantar papilloma will require testing of biopsies from similar lesions and normal skin from other wild psittacine birds.

Detection of beak and feather disease virus in India and its implications.

Beak and feather disease virus (BFDV) has been found in Oceania, Africa, Asia and Europe, but the virus has not yet been detected in India. Here we are reporting the detection of BFDV in exotic rainbow lorikeets (Trichoglossus haematodus) in India. In the phylogenetic analysis, India's witnessed BFDV complete genome, replication (Rep) and capsid (Cap) sequences were displayed close to previously reported T. haematodus infecting BFDV from Australia. Further, we observed that the Indian and exotic Psittaciformes except T. haematodus housed together with the BFDV infected rainbow lorikeets did not display clinical signs and were negative for 4-month genome detection. This observation raised the suspicion that BFDV could cause host-specific infections. In addition, our phylogenetic analysis using 361 BFDV complete genome sequences from various bird species revealed that they were mainly grouped according to the specific species. Likewise, similarity plot analysis shows that the BFDV complete genome sequences found in T. haematodus are significantly different in areas such as the origin of Rep, the intergenic region between the 3' ends of the Rep and capsid (Cap) genes, and the Cap gene, compared to the BFDVs found in other birds. Furthermore, the BFDV-host coevolution analysis clarifies that the TimeTree of the evolution of various Psittaciformes bird species is the coevolution of the BFDV complete genome/Rep gene/Rep protein/Cap gene/Cap protein sequences found in the respective bird species. To our best knowledge, it is essential to note that no research has yet provided conclusive scientific evidence or experimental evidence that BFDVs detected from Trichoglossus sp. can infect other bird species. Therefore, it can be expected that the BFDVs found in the exotic bird in India will not infect Indian Psittaciformes. However, we hope that large-scale surveillance of BFDV in Indian birds will help determine the BFDV genome present in Indian birds and take further action.

Comparative analysis of complete mitochondrial genomes of three Trichoglossus species (Psittaciformes: Psittacidae).

The genus Trichoglossus belongs to the family Psittacidae and includes fourteen species distributed worldwide. According to the International Union for Conservation of Nature and Natural Resources (IUCN) Red List of Threatened Species, most Trichoglossus species have shown a decreasing population trend recently. In particular, Trichoglossus forsteni is listed as "Endangered" in the IUCN Red List of Threatened Species. Moreover, Trichoglossus haematodus and Trichoglossus moluccanus are one of the most traded and illegally traded parrots. However, only a few genetic studies have been conducted regarding the conservation of this genus. In the present study, complete mitochondrial genomes of three species (T. forsteni, T. haematodus, and T. moluccanus) were sequenced and compared with Trichoglossus rubritorquis, species whose mitochondrial genome is already reported. Results indicate that the complete mitochondrial genomes of the three species were similar in length (17,906bp for T. haematodus to 17,909bp for T. forsteni). Furthermore, the organization and order of these three mitochondrial genomes were identical, including thirteen protein-coding genes (PCGs), two ribosomal RNA genes, 22 transfer RNA genes, and two control regions (CRs) categorized into three domains containing nine conserved motifs. In addition, the genus Trichoglossus formed a well-supported monophyletic lineage. The results of this study may be useful for future genetic studies toward the conservation of the genus Trichoglossus.

Home is where the hollow is: Revealing vertebrate tree hollow user biodiversity with eDNA metabarcoding

AbstractTree hollows are essential for many vertebrate species, providing both nesting sites and shelter. Globally, old hollow‐bearing trees are in decline resulting in many dependent species being under threat. It is, therefore, imperative that vital hollow‐bearing trees are preserved, but it is logistically difficult to rapidly determine which hollows are being used and by which taxa. Here, we investigate the efficacy of eDNA metabarcoding as a survey tool for vertebrate hollow users. We compared the identity and richness of hollow‐inhabiting vertebrate taxa using eDNA metabarcoding of both sediment from the tree hollows, and material collected using roller swabs. Samples (n = 138) were collected from hollow‐bearing tuart trees (Eucalyptus gomphocephala; N = 28), within both an urban remnant and a relatively undisturbed forested area of South‐West Western Australia. We detected a wide range of vertebrate taxa, including cryptic species such as the brush‐tailed phascogale (Phascogale tapoatafa), while also providing ecologically informative data, such as hollow use by invasive Rainbow Lorikeet (Trichoglossus moluccanus) within the study areas. Our results showed variation in the species detected between methods, with the roller swab method detecting a greater number of species and a higher mean species richness per sample than hollow sediment did. The species detected from both methods did not perfectly overlap, highlighting the value of using multiple methods or substrates to detect a greater number of taxa. Our results suggest eDNA metabarcoding from tree hollow samples offers a sensitive and resource‐efficient method of monitoring vertebrate hollow users, if enough hollows are sampled. This provides not only a broad biodiversity assessment tool, but also an effective method for detecting taxa that may be elusive using other methods.

Polycystic Kidney Disease in 3 Juvenile Rainbow Lorikeets (Trichoglossus moluccanus).

This case series describes polycystic kidney disease in 3 (2 male, 1 female) 2-month-old, juvenile rainbow lorikeets (Trichoglossus moluccanus). The lorikeets diagnosed with polycystic kidney disease were the progeny of full sibling parents that were being intentionally line bred for the purpose of establishing a rainbow lorikeet with the blue color mutation. Clinically the juvenile lorikeets were presented with clinical signs of lethargy, dehydration, regurgitation, anorexia, polyuria, and pelvic limb paresis. Multiple abnormalities were identified on the complete blood count and plasma biochemistry panel, including a normocytic normochromic nonregenerative anemia, hyperuricemia, hyperphosphatemia, hypercalcemia, and azotemia. Severe renal dysfunction was diagnosed in all birds on the basis of clinical presentation, physical examination, and complete blood count and plasma biochemistry results. Radiographically marked renomegaly was noted in one of the cases. Although intensive critical care and supportive therapy was provided, 1 lorikeet died, and the remaining 2 were euthanatized because of client financial constraints and a rapid deterioration of their clinical condition associated with severe renal dysfunction. Postmortem pathology results found that all birds had marked renomegaly, visceral gout, and polycystic kidney disease. Because of the age of the birds and the line breeding within this group of lorikeets, the disease was believed to be inherited. Polycystic kidney disease should be considered as a possible differential diagnosis in juvenile psittacine birds with a history of line breeding when presented with severe renal dysfunction. From the current case series, polycystic kidney disease appears to carry a grave prognosis in juvenile rainbow lorikeets.

Toxoplasma gondii, Neospora caninum e Sarcocystis spp. em espécies de aves naturalmente infectadas

ABSTRACT: Toxoplasma gondii, Neospora caninum and Sarcocystis spp. are parasites detected in tissues of domestic and wild animals. Birds are relevant in the life cycle and epidemiology of protozoa due to the wide variety of bird species, feeding and migratory habits. The aim of this study was the molecular detection of T. gondii, N. caninum and Sarcocystis spp. in several species of naturally infected birds. Therefore, samples of brain and heart tissue were collected from birds received and necropsied at the Central Laboratory for the Diagnosis of Avian Pathologies (LCDPA), undergoing DNA extraction and amplification by the polymerase chain reaction (PCR) of the 18S rRNA gene to Sarcocystis spp., NC5 gene for N. caninum and repetitive gene 529 base pairs for T. gondii. N. caninum was detected in two birds (02/65, 3.07%), in a brain sample of Rupornis magnisrostris (accession number: ON182081, 267pb) and in a brain and heart sample of Dendrocygna bicolor (accession number: ON211312, 267pb). DNA of the genus Sarcocystis was detected in three birds (03/65, 4.62%), and in the genetic sequencing Sarcocystis spp. (accession number: MW463929) in brain of Nymphicus hollandicus and Sarcocystis speeri (accession number: MW464125) in brain and heart of Amazona aestiva. Phylogenetic analysis revealed that Sarcocystis spp. formed a clade with Sarcocystis spp. that use skunk (Didelphis aurita) as definitive host and Sarcocystis falcatula that use Moluccan loris (Trichoglossus moluccanus) as intermediate host. S. speeri formed a clade with S. speeri that used Mus musculus as an experimental intermediate host and formed a clade with Sarcocystis columbae, Sarcocystis corvusi, Sarcocystis halieti and Sarcocystis sp. that affect bird species. T. gondii DNA was not detected in any tissue. This is the first report of DNA detection of N. caninum, Sarcocystis spp. and S. speeri in tissue samples for these bird species extending the list of intermediate hosts.

Molecular and Phylogenetic Characterisation of a Highly Divergent Novel Parvovirus (Psittaciform Chaphamaparvovirus 2) in Australian Neophema Parrots.

Parvoviruses under the genus Chaphamaparvovirus (subfamily Hamaparvovirinae) are highly divergent and have recently been identified in many animals. However, the detection and characterisation of parvoviruses in psittacine birds are limited. Therefore, this study reports a novel parvovirus, tentatively named psittaciform chaphamaparvovirus 2 (PsChPV-2) under the genus Chaphamaparvovirus, which was identified in Australian Neophema birds. The PsChPV-2 genome is 4371 bp in length and encompasses four predicted open-reading frames, including two major genes, a nonstructural replicase gene (NS1), and a structural capsid gene (VP1). The NS1 and VP1 genes showed the closest amino acid identities of 56.2% and 47.7%, respectively, with a recently sequenced psittaciform chaphamaparvovirus 1 from a rainbow lorikeet (Trichoglossus moluccanus). Subsequent phylogenetic analyses exhibited that the novel PsChPV-2 is most closely related to other chaphamaparvoviruses of avian origin and has the greatest sequence identity with PsChPV-1 (60.6%). Further systematic investigation is warranted to explore the diversity with many avian-associated parvoviruses likely to be discovered.

Investigation into clinicopathological and pathological findings, prognosis, and aetiology of lorikeet paralysis syndrome in rainbow lorikeets (Trichoglossus haematodus).

ObjectiveTo report the temporal and spatial distribution of rainbow lorikeets presenting with lorikeet paralysis syndrome (LPS) and their clinicopathologic and pathologic findings, exposure to toxins, and response to treatment.MethodsRecords of lorikeets admitted in 2017 and 2018 to facilities in south‐east Queensland (QLD) were reviewed and LPS and non‐LPS cases were mapped and their distribution compared. Plasma biochemistries and complete blood counts were done on 20 representative lorikeets from south‐east QLD and Grafton, New South Wales (NSW). Tissues from 28 lorikeets were examined histologically. Samples were tested for pesticides (n = 19), toxic elements (n = 23), botulism (n = 15) and alcohol (n = 5).ResultsLPS occurred in warmer months. Affected lorikeets were found across south‐east QLD. Hotspots were identified in Brisbane and the Sunshine Coast. Lorikeets had a heterophilic leucocytosis, elevated muscle enzymes, uric acid and sodium and chloride. Specific lesions were not found. Exposure to cadmium was common in LPS and non‐LPS lorikeets. Treated lorikeets had a 60–93% See Table 2 depending on severity of signs.Clinical significanceThe primary differential diagnosis for lorikeets presenting with lower motor neuron signs during spring, summer and autumn in northern NSW and south‐east Queensland should be LPS. With supportive care, prognosis is fair to good.

Wet kiss: water transfer as part of couple bonding in Rainbow Lorikeets?

Wet kiss: water transfer as part of couple bonding in Rainbow Lorikeets?

Rainbow Lorikeets apparently harvesting orange fungal spores from the underside of willow leaves

The diet of Rainbow Lorikeets Trichoglossus moluccanus consists largely of nectar and pollen, with some fruit, leaf buds, bark and insects and, more recently, meat provided at bird-feeders. Here, I describe an instance of Rainbow Lorikeets apparently harvesting fungal spores from the underside of leaves of Weeping Willow Salix babylonica, a food item not previously recorded.

An Australian Pelican Pelecanus conspicillatus attacking a Rainbow Lorikeet Trichoglossus moluccanus being fed by people

Pelicans are generally piscivores, but occasionally prey on smaller waterbirds and other animals. I observed an Australian Pelican Pelecanus conspicillatus capture a Rainbow Lorikeet Trichoglossus moluccanus after both species had been attracted to people scattering seed for birds. The Pelican briefly caught the Lorikeet by the tail, but the Lorikeet escaped and flew away. To my knowledge, this is the first report of any pelican species capturing a parrot. It is unclear whether the Pelican was attempting to eat the Lorikeet.

Controlling the rainbow lorikeet in Tasmania: is it too late?

ABSTRACT Throughout the world, many parrot species have established wild populations outside their natural range through accidental escapes and deliberate releases from captivity. The Rainbow Lorikeet (Trichoglossus moluccanus), native to coastal northern and eastern continental Australia, has established viable populations in Western Australia and New Zealand from escaped or released pets and more recently have established in Tasmania. The Western Australian experience with introduced Rainbow Lorikeets, clearly shows that significant costs and impacts to agriculture, the environment and human amenities can be expected if this species is not controlled in the early stages of population increase, while in New Zealand, early intervention has proven successful in removing the species from the wild. This study examines sighting records of Rainbow Lorikeets in Tasmania which have gradually established over 20 years and we present a model to assist in determining likely population trajectories under various scenarios of control. Modelling indicates that the removal of 200 birds per year from each of the three Tasmanian sub-populations would decrease numbers to near-zero within 4.6 years. This demonstrates the opportunity to effectively control the Rainbow Lorikeet in Tasmania still exists and substantial damage to agriculture and impacts to conservation values can be avoided, resulting in significant cost savings to the Tasmanian community.

Impact of removal on occupancy patterns of the invasive rainbow lorikeet (Trichoglossus moluccanus) in Tasmania

AbstractIntroduced species may threaten both biodiversity and agriculture, necessitating an understanding on the factors that influence their distribution, and the efficacy of control measures. In Tasmania, Australia, the introduced rainbow lorikeet (Trichoglossus moluccanus) may be widespread, but data on where they occur and the efficacy of control methods are limited. We used an occupancy modelling framework (presence–absence data) to undertake a survey of two populations of invasive rainbow lorikeets to: (i) understand their distribution across the north and south of the island, and (ii) evaluate the impact of removing birds from the southern population by quantifying occupancy before (2016) and after (2018) removal. The best model explaining occupancy in both populations included a negative relationship with distance from central urban areas. We found no change in site occupancy or detectability in the southern population after removal of 208 birds (potentially comprising >50% of their original population size). This result may be explained by one of three possibilities: (i) the population is larger than previously thought, (ii) the population recovered quickly after reduction, or (iii) removal of birds reduced population density but not area of occupancy. We highlight the importance of urban habitats for the invasive rainbow lorikeet and suggest that alternative methods (e.g. abundance/density‐based monitoring) may better detect impacts of removal.

Noisy neighbours and myna problems: Interaction webs and aggression around tree hollows in urban habitats

Abstract Interaction networks among native and invasive species in a community can inform both invasion impacts and applied management of invasive species. The intensity of aggressive interactions may be related to the overlap in species’ ecological niche and functional traits, especially in cavity‐breeding species, that often compete for limited nesting sites. Australia is home to over 100 native and introduced cavity‐nesting species, including several invasive species that are widespread globally, such as the common myna Acridotheres tristis. Here, we aimed to test the extent to which shared functional traits inform the intensity of aggression between cavity‐nesting birds. We quantified the outcomes of aggressive interactions between birds in large hollow‐bearing trees in SE Queensland, Australia. We examined whether more similarly sized birds interacted more frequently, whether larger species won aggressive interactions more often, and whether cavity‐breeding species with similar preferences for nesting sites (breeding‐niche space) interacted more frequently. We recorded a total of 410 aggressive interactions and 48 interacting bird species around tree hollows, including 20 cavity‐nesting bird species. These interactions were dominated by the invasive common myna, the native noisy miner (a non‐cavity‐breeder) and the native rainbow lorikeet Trichoglossus moluccanus, but the common myna won the largest total number of interspecific interactions. On average, larger birds won aggressive interactions more frequently, yet there were some important exceptions to this finding; the common myna (113 ± 30 g) won 26 of the 29 interactions against the larger native rainbow lorikeet (126 ± 44 g). Importantly, species with more similar nest‐site preferences were observed aggressively interacting more frequently. Synthesis and applications. The impact of the invasive common myna was higher‐site preferences. Control efforts for the myna should focus on birds that nest in natural tree hollows. An analysis of shared traits by managers could be used to help identify how many local species would benefit from common myna control in a given area and test if further behavioural studies of common myna are warranted.

Beak and feather disease virus (BFDV) prevalence, load and excretion in seven species of wild caught common Australian parrots.

Pathogens pose a major risk to wild host populations, especially in the face of ongoing biodiversity declines. Beak and feather disease virus (BFDV) can affect most if not all members of one of the largest and most threatened bird orders world-wide, the Psittaciformes. Signs of disease can be severe and mortality rates high. Its broad host range makes it a risk to threatened species in particular, because infection can occur via spill-over from abundant hosts. Despite these risks, surveillance of BFDV in locally abundant wild host species has been lacking. We used qPCR and haemagglutination assays to investigate BFDV prevalence, load and shedding in seven abundant host species in the wild in south-east Australia: Crimson Rosellas (Platycercus elegans), Eastern Rosellas (Platycercus eximius), Galahs (Eolophus roseicapillus), Sulphur-crested Cockatoos (Cacatua galerita), Blue-winged Parrots (Neophema chrysostoma), Rainbow Lorikeets (Trichoglossus moluccanus) and Red-rumped Parrots (Psephotus haematonotus). We found BFDV infection in clinically normal birds in six of the seven species sampled. We focused our analysis on the four most commonly caught species, namely Crimson Rosellas (BFDV prevalence in blood samples: 41.8%), Sulphur-crested Cockatoos (20.0%), Blue-winged Parrots (11.8%) and Galahs (8.8%). Species, but not sex, was a significant predictor for BFDV prevalence and load. 56.1% of BFDV positive individuals were excreting BFDV antigen into their feathers, indicative of active viral replication with shedding. Being BFDV positive in blood samples predicted shedding in Crimson Rosellas. Our study confirms that BFDV is endemic in our study region, and can inform targeted disease management by providing comparative data on interspecies variation in virus prevalence, load and shedding.

Avian coxiellosis in nine psittacine birds, one black-browed barbet, and one paradise tanager

ABSTRACTInfection with a novel species of the genus Coxiella was first described in three Swainson’s blue mountain rainbow lorikeets from a zoological collection, and days later in a group of seven other psittacine birds and a toucan. We provide an update on coxiellosis in nine additional psittacines, and two non-psittacines. Psittacines originated in New England, the mid Atlantic, the Midwest, the South, and the Northwest. Psittacines most commonly had lesions in the brain, spleen, liver, and lungs, consisting of meningoencephalitis, hepatosplenomegaly, and interstitial pneumonia. Lesions contained histiocytic infiltrate, with intracytoplasmic, Gimenez-positive coccobacilli. Transmission electron microscopy revealed bacteria with trilaminar cell walls, electron dense cores, and spore-like forms. PCR revealed homology to the organism in index cases. In addition, one black-browed barbet and one paradise tanager were found with systemic coxiellosis; sequencing identified the same pathogen. These are the second piciforme and the first passerine affected by this pathogen, indicating expanded infectivity and pathogenicity.RESEARCH HIGHLIGHTSReport of coxiellosis in nine psittacines; lesions often in brain, spleen, liver, lung.Second piciforme with coxiellosis, a black-browed barbet.First case of avian coxiellosis described in a passerine, a paradise tanager.

Opportunistic sampling of wild native and invasive birds reveals a rich diversity of adenoviruses in Australia.

Little is known about the diversity of adenoviruses in wild birds and how they have evolved and are maintained in complex ecosystems. In this study, 409 samples were collected from woodland birds caught for banding (droppings), birds submitted to a wildlife hospital (droppings and tissues), silver gulls (droppings or tissues), and feral pigeons (Columbia livia; oral, cloacal swabs, or tissues) from the Greater Sydney area in NSW, Australia. Additional samples were from native pigeons and doves (swabs) presented to the Healesville Sanctuary, VIC, Australia. Samples were screened for adenovirus DNA using degenerate primers and polymerase chain reaction. Adenovirus sequences were detected in eighty-three samples representing thirty-five novel amino acid sequences. Fourteen novel sequences were atadenoviruses, seven were aviadenoviruses, twelve were siadenoviruses, and one was a mastadenovirus. Sequences from passerine birds were predominately found to form a single lineage within the atadenoviruses, a second lineage in the siadenoviruses, and a third smaller aviadenovirus lineage. These viruses appeared to have co-evolved with a diverse group of woodland birds that share similar habitat. Evidence for host/virus co-evolution in some viruses and a wide host range in others was observed. A high prevalence of adenovirus infection was found in rainbow lorikeets (Trichoglossus haematodus), galahs (Eolophus roseicapilla), and sulphur-crested cockatoos (Cacatua galerita). Sequences were either identical to or mapped to already established lineages in the Aviadenovirus, Siadenovirus, and Atadenovirus genera, suggesting a possible origin of the psittacine adenoviruses in ancestral Australian psittacine birds. The sequences of passerine and psittacine origin provided insight into diversity and structure of the Atadenovirus genus and demonstrated for the first-time viruses of passerine origin in the Aviadenovirus genus. Four unrelated adenovirus sequences were found in silver gull samples (Chroicocephalus novaehollandiae), including one of pigeon origin, suggesting environmental virus exposure. Three pigeon adenovirus types were detected in feral pigeons and infection prevalence was high. Evidence for host switching between invasive species and native species and native species and invasive species was documented. A variant of a murine adenovirus was detected in kidney tissue from two bird species suggesting mouse to bird transmission.

Studi Pakan Burung Perkici Pelangi (Trichoglossus haematodus Linnaeus, 1771) dalam Laboratorium Penangkaran

During the 2002-2003 period, the research was done to study 11 Rainbow Lorikeetsreared in an animal house laboratory. The aim of this research was to find the foodrations formule of the Rainbow Lorikeets so that those birds can be able to grow andbreed well. The food rations were composed of 26.3% local bird foods (521), 35.09%lampung bananas, 8.77% slice corns, 10.5% boiled quails eggs, 1.75% white bread,bean sprouts and red sugar are 8.77%, respectively. All of food materials were mixedon the plastic cup and mixed with 450 ml of water, then pulverized like sweetporridge. That porridge was given to birds in cafeteria and the water was made ready“ad libitum” everyday. The results have shown that giving food rations formula canstimulate two pairs of the Rainbow Lorikeets breeding and during the 2002-2003period they produced three young birds.

A novel picornavirus in feces of a rainbow lorikeet (Trichoglossus moluccanus) shows a close relationship to members of the genus Avihepatovirus.

A novel picornavirus, named "lorikeet picornavirus 1" (LoPV-1), was detected in a fecal sample from rainbow lorikeets using viral metagenomic analysis, and its complete genome sequence was determined and analyzed. The genome of LoPV-1 is 7862 nt long, including a 617-nt 5' UTR, a type IV IRES 5'UTR with an '8-like' motif, a 7032-nt polyprotein ORF, and a 213-nt 3' UTR. Phylogenetic analysis and pairwise asequence comparisons based on the amino acid sequences of P1, P2, and P3 indicated that LoPV-1 showed the closest relationship to two picornaviruses that were isolated recently from red-crowned cranes and clustered together with members of the genus Avihepatovirus.