Biology of cestodes of domestic ducks and wild water birds

Life cycles of 16 cestode species of the families Hymenolepididae and Diploposthidae were studied in 52 ponds of the State Fishery in Bohemia and Moravia. The parasites were recovered from domestic ducks kept on the ponds and from wild birds, mostly of the genera Anas and Aythya, occurring in these water biotopes. Cestode larvae were found in 9 species of Copepoda (9669 out of 1 600 200 examined specimens, i. e. 0.6%) and 3 species of Ostracoda (500 out of 272 300 examined specimens, i. e. 0.18%). Five species of water snails serving as reservoir hosts harboured cysticercoids of 5 cestode species (680 out of 10 212 examined specimens, i. e. 6%). The studies of cestode life cycle under natural conditions were supplemented with 680 successful experiments with intermediate hosts and 179 successful experiments with definitive hosts. The development of larvae was related to the temperature and lasted approximately 13-20 days at 18-25 degrees C. The highest intensity of infection occurred incrustaceans under experimental conditions, a lower intensity was found in crustaceans from duck farms and the lowest in crustaceans from other parts of ponds (e. g., in the case of Fimbriaria fasciolaris in Copepoda, 37, 22 and 10 cysticercoids). The intermediate hosts infected with cestode larvae can live for 3-6 weeks (Copepoda) and 4-7 weeks (Ostracoda) and after invagination of cysticercoids for 20-25 days, on the average. The cysticercoids survive their hosts for 14-18 h at 4-6 degrees C, for 10-11 h at 12-14 degrees C, for 6-7 h at 18-20 degrees C and for 3-4 h at 24-26 degrees C. If they are swallowed by water snails at that time (dead crustaceans are a component of their food), they survive in their digestive tract even for two years (the longest period demonstrated experimentally) and after this time they are able to develop into an adult cestode in the definitive host. The infectivity of cysticercoids increases with their age. It is the lowest immediately after invagination (10-15%), during the stay of cysticercoids in crustaceans it gradually increases (30-60% on days 10-20 after invagination) and it is the highest in cysticercoids from snails (45-55% after 20-50 days in snails, 60-80% after 50-100 days in snails and 70-90% after more than 100 days in snails).     

A survey of gastro-intestinal parasitic infection in domestic and wild birds in Chittagong and Greater Sylhet,Bangladesh

A survey of gastrointestinal parasitic infection as determined by faecal examination was conducted among domestic and wild birds in Bangladesh. Birds were sampled from households, wet markets and wetlands in Chittagong and Greater Sylhet districts during April 2012 to February 2013. Mist nets were used to catch resident wild and migratory birds. The overall prevalence of parasitic infection ranged among locations from 25 to 55% in indigenous domestic ducks (live bird samples = 304), 20% in resident wild birds (environmental faecal samples = 40) and 40% in migratory birds (live bird samples = 35). The prevalence of parasitic infection was significantly higher in indigenous domestic ducks collected during summer (39%) than winter (22%) (p = 0.04). In domestic indigenous ducks and Muscovy ducks, both single and multiple types of parasitic infections were found. However, other domestic birds and wild birds often had a single type of parasitic infection. Ascaridia spp. with an average egg load of 50–900, was commonly detected in faecal samples of domestic and wild birds in this study. Other identified parasites were Capillaria spp. and Heterakis spp. both in domestic and wild birds. Improvement of biosecurity measures for household duck farms through educating and motivating household farmers could help mitigate the effects of parasitic infection on production.     

Prevalence of Campylobacter jejuni in selected domestic and wild birds in Louisiana

Prevalence of Campylobacter jejuni was determined in a selected population of domestic and free-living birds submitted for necropsy to the Louisiana State Veterinary Medical Diagnostic Laboratory. The 445 cases examined included 13 orders of birds and yielded C. jejuni in 45 cases, representing an isolation rate of 10.1%. Prevalence was highest in Galliformes (25.2%), followed by Anseriformes (12.9%) and Columbiformes (8.3%). Only one isolation was made out of 179 Psittaciformes examined. Penner serotypes 1, 2, 4, and 16 were most commonly identified among the C. jejuni isolates. This study emphasizes the importance of Galliformes as reservoirs of C. jejuni. The commonality of these serotypes with isolates derived from humans suggests the zoonotic potential of Galliformes in relation to human campylobacteriosis. The isolation rate of 12.9% in Anseriformes implicates free-living and migratory waterfowl as carriers of C. jejuni. Results confirm that Psittaciformes represent a low risk of C. jejuni infection in humans.     

Pigeon paramyxovirus: association with common avian pathogens in chickens and serologic survey in wild birds

Pigeon paramyxovirus-1 (PPMV-1) was isolated from pigeons from east-central Alabama and used in association with chicken anemia virus (CAV), infectious bursal disease virus (IBDV), or finch Mycoplasma gallisepticum (MG) in specific-pathogen-free chickens to assess dinical disease and pathology. PPMV-1 infection in all groups was conducted at day 10 of age via the ocular route. The low passage PPMV-1 isolate was inoculated into chickens in different groups at 10 days post-CAV infection, 6 days post-IBDV infection, and 6 days post-finch MG infection, respectively. Additionally, to obtain information on the status of paramyxovirus infection in the wild bird population of the region, we used a multispecies competitive enzyme-linked immunosorbent assay kit to assess serum samples from 180 wild birds representing 24 species obtained throughout 2001. Mild respiratory signs characterized by sneezing were observed in PPMV-1-infected chicks. In the brain, PPMV-1 caused disseminated vasculitis in the neuropile and meninges, sometimes with small foci of gliosis. Most brains had only mild lesions. In the upper respiratory tract, lesions were confined to the larynx and proximal trachea as hyperplasia of laryngeal mucosa-associated lymphoid tissue. In the lung, PPMV-1 caused minimal to moderate multifocal interstitial pneumonia. Lymphocytic expansion occurred in the interstitium of the Harderian gland. PPMV-1 in the spleen caused expansion of the white pulp as a result of hypertrophy of the macrophages in the periarteriolar sheaths accompanied by lymphocytic hyperplasia at the periphery. No severe aggravation of either signs or lesions could be attributed to any of the avian pathogens used in association with PPMV-1. The serologic survey in wild birds showed antibody levels that were considered negative or doubtful. Interestingly, significantly (P < 0.05) higher mean titers were observed during the months of October and November 2001, following closely multiple PPMV-1 episodes of mortality in wild collard doves in northwestern Florida.     

Isolation of avian paramyxovirus-2 from domestic and wild birds in Costa Rica

A survey for Newcastle disease virus (NDV) in wild birds of Costa Rica was conducted by swabbing wild-caught pet birds, backyard chickens, and wild birds captured in Japanese mist nets in tropical rain forests and agricultural areas. Cloacal swabs were collected from 876 birds of approximately 132 species representing 24 taxonomic families. Hemagglutinating agents were isolated from 18.7% of the birds. Paramyxovirus type 2(PMV-2) (Yucaipa-like), unreported in free-flying passerines in the Americas, was recovered from a finch, wren, and chicken, each from a different location. Pathogenicity trials with infected turkey poults and newly hatched chicks did not result in growth impairment or significant clinical signs of disease. Attempts to isolate NDV were negative.     

Leptospira interrogans infection in domestic and wild animals in Fiji

Clinical and serological evidence has indicated that human leptospirosis in Fiji is an important disease, and the prevalence of antibody is exceptionally high. A serological survey of the rural population showed that only 12% of the people studied did not have complement fixing (CF) leptospiral antibody. As the origin of this infection could not be explained by the known distribution of leptospiral infection in domestic and wild animals, a serological survey using the complement fixation test (CFT) was undertaken as the first stage of an epidemiological investigation into human and animal leptospirosis. Sera from domestic and wild animals were tested for CF antibody to 12 leptospiral serovars, namely: pomona, copenhageni, grippotyphosa, hardjo, ballum, tarassovi, canicola, australis, bratislava, autumnalis, pyrogenes and bataviae. Antibody was detected in 27.5% of 480 cattle, 17.1% of 70 sheep, 10.3% of 252 goats, 10.0% of 480 pigs, 57.0% of 100 dogs, 55.8% of 34 rats (Rattus rattus, R. frugivorus, R. exulans and R. norvegicus), 53.1% of 32 mongooses (Herpestes auropunctatus) and 40.0% of 10 mice (species unknown.) Cross-reactivity precluded the identification of infecting serogroups with the exception of pomona in pigs and icterohaemorrhagiae, ballum and australis in dogs. Infection of dogs with a serovar of the australis serogroup may explain the predominance of serological reactions to bratislava in man. The survey revealed a significant level of leptospiral antibody in the animal populations of Fiji and indicated that cattle, dogs, rats, mongooses and mice are probably the most important maintenance hosts. Consequently, further investigation will concentrate on the attempted isolation of leptospires from these species.     

Serotyping of US isolates of Chlamydophila psittaci from domestic and wild birds.

The identities of chlamydial strains, which can infect a given host, are important to know for disease prognosis, disease control, and epidemiology. The microimmunofluorescence test (MIFT) was used with a panel of 14 serovar-specific monoclonal antibodies (MAbs) to serotype 150 chlamydial isolates from domestic and wild birds. The isolates were obtained from birds submitted to diagnostic laboratories or during investigation of outbreaks. The 150 US isolates included 96 from the order Psittaciformes, 14 isolates from the order Columbiformes, 2 from the order Passeriformes, 16 from the order Galliformes, 12 from the order Struthioniformes, and 3 from the order Falconiformes. A total of 93, or 97%, of the Psittaciformes isolates were of serovar A; 11, or 79%, of the Columbiformes isolates were of serovar B; 64% of the Galliformes isolates were of serovar D, and all the Struthioniformes isolates were of serovar E. The 3 Falconiformes isolates did not react with any of the MAbs to the avian and mammalian isolates and are presumed to represent a new strain. The results show that specific chlamydial strains are usually associated with certain types of birds and that some serovars may be unusually virulent for certain species of birds. The MIFT using serovar-specific MAbs provides a rapid method to serotype new isolates, making it a useful system for epidemiological studies.     

Survey for natural Neospora caninum infection in wild and captive birds

Neospora caninum is a protozoan parasite that presents worldwide distribution and is mainly implicated as responsible for bovine abortion. Although the presence of birds in cattle-raising properties is positively correlated to higher infection rates, very little has been described about the role of these animals in the parasite's life cycle. In that sense, this work aimed to investigate the serological and histological positivity of different avian species sampled in its natural habitat or in captivity. No serological positivity was observed in the 294 tested serum samples. On the other hand, Apicomplexa-like cysts found in muscular tissues of two Psittaciformes were immunostained with N. caninum antisera. These findings indicate that N. caninum may infect a wider range of hosts than described to date, and that further studies should be performed in order to determine the presence of the infection in different avian species.     

Strains of avian paramyxovirus type 1 of low pathogenicity for chickens isolated from poultry and wild birds in Denmark

Twenty-one strains of avian paramyxovirus type 1 of low virulence for chickens were isolated in Denmark between 1996 and the beginning of 2003. The low virulence of the strains was demonstrated by sequencing the fusion (F) gene at the cleavage site motif and in some cases by determining the intracerebral pathogenicity index in day-old chicks. By using a panel of monoclonal antibodies it was shown that the isolates belonged to four different antigenic groups (five C2 isolates, six E isolates, six H isolates and four G/Q isolates). They were placed in three distinguishable genetic groups by phylogenetic analysis of a partial sequence of the F gene. The origin of the six E isolates was probably contaminated vaccines; the other viruses were isolated from wild birds and from poultry which probably came into contact with wild birds.