The isolation of salmonellae, Newcastle disease virus and other infectious agents from quarantined imported birds in Canada.

Necropsy and culture results are presented for 269 consignments of imported birds (mainly psittacine and passerine species) examined between January 1977 and August 1980. Consignments were submitted for diagnosis of clinical illness or deaths occurring among these birds while they were in quarantine before entry into Canada. Enteritis and injury were the most frequent diagnoses. Pathogens or potential pathogens were isolated from 77% of consignments. Newcastle disease virus was isolated nine times, and Chlamydia psittaci was isolated once. Escherichia coli (from 113 consignments) and salmonellae (from 49) were the most common bacteria isolated, and reoviruses (from 22) and paramyxoviruses other than Newcastle disease virus (from 22) were the most common viruses. Salmonella typhimurium was the most common Salmonella serovar. Salmonella hadar was isolated from turkey poults imported from Great Britain. The possible public health significance of the role of imported birds in the introduction of exotic Salmonella serovars, or of serovars resistant to several antimicrobials is discussed.     

Isolation of Newcastle disease virus and Salmonella typhimurium from the brain of double-crested cormorants (Phalacrocorax auritus)

Avian paramyxovirus type 1 (Newcastle disease virus) and Salmonella typhimurium were isolated from the brain and lung tissues of double-crested cormorants (Phalacrocorax auritus) from Lac Canard, Alberta, Canada. More than 100 birds died during this outbreak in 1999. Affected birds presented signs of central nervous system disease characterized by unilateral wing and leg paralysis. Other geographic locations in the provinces of Alberta and Saskatchewan have reported cases of cormorants suffering from diseases with signs compatible with Newcastle disease. The virus isolated in the 1999 outbreak was characterized as mesogenic. These findings suggest that other pathogens, like S. typhimurium, may influence the clinical presentation of disease caused by mesogenic strains of Newcastle disease virus in cormorants.     

鹅源新城疫病毒云南流行株动物回归试验

用分离的鹅源新城疫病毒KM2007株尿囊液分别接种25日龄非免疫雏鹅和25日龄非免疫雏鸡各20只,对照组每只鸡肌肉注射生理盐水。结果试验组鹅和鸡分别出现典型的鹅新城疫病和鸡新城疫的临床症状和病理变化,对照组全部健活。从发病及死亡鹅和鸡的脑/脾中分离到病毒。试验结果表明,分离病毒KM2007株与鹅自然感染发病的病原一致。     

鹅源新城疫病毒云南流行株免疫交叉保护试验

用分离的鹅新城疫病毒KM2007株尿囊液制成油乳剂灭活苗,和NDV油乳剂灭活苗分别接种10日龄未免疫雏鸡和未免疫雏鹅,并设非免疫对照组。免疫后21 d,试验组和对照组每只鸡和鹅分别注射0.1 mL鹅新城疫病毒KM2007株尿囊液10-1稀释液,结果对照组鹅和鸡分别出现典型的鹅新城疫和鸡新城疫的症状和病理变化,而试验组鹅和鸡全部健活。结果表明,鹅新城疫病毒KM2007株油乳剂灭活苗及NDV油乳剂灭活苗均可保护鹅和鸡免受鹅新城疫病毒野毒的攻击。     

Investigation of an outbreak of velogenic viscerotropic Newcastle disease in pet birds in Michigan, Indiana, Illinois, and Texas.

An outbreak of velogenic viscerotropic Newcastle disease in exotic pet birds in the United States from April through July 1991 was investigated. More than 2,000 pet birds in 5 states (Michigan, Indiana, Illinois, Texas, and Maryland) were tested. Infected birds were found in Michigan, Illinois, Indiana, and Texas. This disease was eradicated without spread to domestic poultry. Epidemiologic investigations revealed the source of infection to be double yellow-headed Amazon parrots suspected to be illegally imported into Texas.     

Hepatic intranuclear inclusion bodies in a cockatoo bird (Cacatua sulphurea)

One hundred and nineteen cockatoos (Cacatua sulphurea) were kept at the Animal Quarantine Station in Denpasar, Indonesia. These birds were intended to be exported overseas. Nine birds were found dead in a period of 17 days. Necropsies were performed on three, and tissues were taken for microbiological and histopathological examination. Examinations revealed that two birds had both Newcastle disease and aspergillosis, and one bird was found to contain hepatic intranuclear inclusion bodies suggestive of Pacheco's parrot disease. Newcastle disease and aspergillosis in cockatoos have frequently been diagnosed in our laboratory. However, the finding of hepatic intranuclear inclusion bodies in a cockatoo is considered to be the first in Indonesia.     

Velogenic Newcastle Disease Virus in Captive Wild Birds

Newcastle disease virus (NDV) was isolated from the faeces of seven different species of clinically healthy captive wild birds. All seven NDV isolates were characterized as velogenic, based on the mean death time in embryonated hens' eggs and the intracerebral pathogenicity index in day-old chicks. Three of the isolates were placed in group C₁ based on the reactions with monoclonal antibodies. The role of captive wild birds in the epidemiology of Newcastle disease is briefly discussed.     

Protective antibody response following oral vaccination of feral pigeons (<Emphasis Type="Italic">Columba livia</Emphasis>) with Newcastle disease vaccine (strain I-2) coated on oiled rice

The novel vaccination technique for feral pigeons was developed in the present study. Multi-age feral pigeons were vaccinated orally with Newcastle disease (ND) strain I-2 vaccine coated on oiled rice. The results showed that 14 days after vaccination 40% of pigeons seroconverted with HI GMT of ≥3 log₂ whereas 28 days after vaccination the seroconversion rate of these birds reached 100%. Moreover, all vaccinated pigeons survived the challenge of virulent Newcastle disease virus (NDV). The findings from the present study indicated that the use of ND (strain I-2) vaccine in feral pigeons is feasible and resulted into the production of protective antibody response. Thus ND I-2 vaccine may prevent the spread of NDV to other birds particularly chickens. Furthermore the use of oral vaccine in feral multi-age pigeons overcomes the difficulty of catching these birds for individual vaccination.     

Field trials of a food-based vaccine to protect village chickens against Newcastle disease

The food pellet vaccine has been shown to be effective in trials conducted under laboratory and simulated field conditions. The village chickens vaccinated with the food pellet vaccine during the field trial were protected against virulent Newcastle disease virus. The efficacy of the food pellet vaccine in the field was evaluated by challenge trial in which 60 per cent protection was obtained, or by monitoring the incidence of Newcastle disease in vaccinated and unvaccinated birds. There was no report of Newcastle disease outbreaks in the vaccinated birds during the two-year period of the field trial. The ease in administering the food pellet vaccine makes it readily accepted by the farmers.     

A controlled vaccination trial for Newcastle disease under village conditions

All the poultry in each of four distinct Moroccan villages were vaccinated against Newcastle disease using Hitchner B1 and inactivated vaccines. Poultry in a fifth village were monitored as controls. Mortality in the poultry was followed for 20 weeks after the first vaccination and blood samples were taken every 4 weeks from chickens for estimation of antibodies against Newcastle disease virus. Sixty-three percent of the chicken population and 60% of the turkey population in the control village died during the 20 weeks of observation. Necropsied birds showed lesions consistent with Newcastle disease. Mortality did not exceed 22% in the vaccinated villages.     

The role of indigenous wild, semidomestic, and exotic birds in the epizootiology of velogenic viscerotropic Newcastle disease in southern California, 1972-1973.

During an epornitic of velogenic viscerotropic Newcastle disease (VVND) in southern California, free-flying wild birds, captive and free-ranging semidomestic birds, and exotic birds were collected from the quarantine area to determine their role in the epizootiology of the disease. The VVND virus was isolated from 0.04% of 9,446 free-flying wild birds, 0.76% of 4,367 semidomestic birds, and 1.01% of 3,780 exotic birds examined. Three house sparrows and 1 crow directly associated with infected poultry flocks were the only free-flying wild birds from which VVND virus was isolated. Among semidomestic species, ducks, quail, chukars, pheasants, peafowl, pigeons, and doves were found to be infected. Psttacines, pittas, and toucans accounted for 92% of the VVND virus isolations from exotic birds. In addition, domestic Newcastle disease virus (NDV) was isolated from 0.29% of the free-flying wild birds, from 1.65% of the semidomestic birds, and from 0.19% of the exotic birds collected. Hemagglutination-inhibition against domestic NDV was demonstrated in 0.24% of 3,796 wild bird serums, 8.28% of 2,004 semidomestic bird serums, and 3.90% of 231 exotic bird serums tested. Although few free-flying wild birds were infected with VVND virus in this epornitic, the isolation of domestic NDV strains from free-flying wild ducks and mourning doves suggests the potential for transportation of NDV over long distances by migratory birds.     

Serological response of chickens to oral vaccination with Newcastle disease virus

Conventional Newcastle disease vaccines are not suitable for application to village chickens in tropical countries of Asia. Trials with food-based vaccines are being initiated and the following experiments were performed to evaluate oral vaccination with Newcastle disease virus. Experimental chickens were vaccinated orally with the avirulent V4 strain of Newcastle disease virus and haemagglutination-inhibition antibody responses were measured. V4 virus was introduced into the crop by tube and total faecal output was collected daily and assayed for Newcastle disease virus. Virus was recovered on Days 5 and 6 after vaccination from most chickens that had received 10(7.4) and 10(6.4) 50% egg-infectious doses (EID50) of virus. There was no recovery of virus from birds receiving a lower dose of vaccine. Groups of chickens kept in cages with wire floors were given various doses of vaccine into the crop. Higher antibody titres were achieved with higher doses of virus. This dose responsiveness was not observed when various doses of vaccine were presented on food pellets and the groups of chickens were kept on concrete floors. Similar antibody responses were then seen with nominal doses of 10(5.2) and 10(8.2) EID50 per bird, possibly as a result of excretion and re-ingestion of the vaccine virus. Spread of the vaccine virus was demonstrated when control chickens and chickens receiving 10(7.7) EID50 of V4 virus on food pellets were housed together on a concrete floor. Similar antibody titres were achieved in both vaccinated and in-contact chickens.     

A comparison of the Nigerian indigenous fowl with White Rock under conditions of disease and nutritional stress

Equal numbers of day old White Rock and Nigerian indigenous male chicks were reared to 10 weeks of age under 4 variables consisting of 2 dietary regimes and 2 regimes of immunity (natural versus vaccinal) to Newcastle disease challenge. Although White Rock grew significantly faster, ate more food and tended to be more efficient in feed utilisation than the indigenous chicks, the mortality of the latter was significantly lower. Growth rate and feed intake were significantly greater, feed efficiency better and prechallenge mortality lower in birds fed on the higher crude protein diet. Prechallenge mortality was significantly lower in birds that had been vaccinated against Newcastle disease.     

新城疫病毒基因组与基因演化

新城疫在世界范围内出现了4次大流行,造成了极大的经济损失和贸易影响。虽然新城疫病毒仅有1个血清型,但不同毒株生物学特性和毒力相差很大。近来,病毒宿主谱扩大,开始感染水禽,造成鹅的大规模发病。经典的新城疫病毒基因组长度为15 186个核苷酸(nt),如La Sota和V4毒株等,而我室报道的鹅源毒株ZJ1全长为15 192 nt。我们对基因组进行比对分析,发现新城疫病毒是在基因组水平上整体演化的。     

LaSota vaccination may not protect against the lesions of velogenic newcastle disease in chickens

Two groups of six weeks old cockerels comprising 40 immunized and 40 non-immunized birds were inoculated intramuscularly with VGF-1, which is a local Nigerian strain of velogenic Newcastle disease virus (VNDV). Immunized birds did not show any clinical signs except significant loss (p < 0.05) in body weight on days 5 and 20 post inoculation (PI). But the non-immunized birds showed clinical signs of disease characterized by anorexia and drowsiness from day 2 PI. These were followed on day 3 PI by depression, diarrhoea, opisthotonus, weight loss (p < 0.05) and high mortalities (96.9%). Both the immunized and non-immunized groups showed severe atrophy of the bursa, spleen and thymus. Histopathological section of these lymphoid organs showed necrosis and depletion of lymphocytes. Both the gross and microscopic lesions were more severe in the non-immunized birds. Marked ballooning degeneration was observed in the bursal follicles of the non-immunized birds. This lesion has not been described earlier for any other disease and could be diagnostic for VND. Our results also showed that VND can cause marked atrophy of the lymphoid organs, which may lead to immunosupression without the characteristic signs of Newcastle disease (ND) in vaccinated chickens. This no doubt emphasizes the limitation of vaccination as a biosecurity measure in poultry industry. Ezema, W.S., J.O.A. Okoye and Nwanta, J.A., 2008. LaSota vaccination may not protect against the lesions of velogenic Newcastle disease in chickens. Tropical Animal Health and Production     

Persistence of the V4 strain of Newcastle disease virus in an open-range flock of chickens

The V4 strain of Newcastle disease virus was introduced into a small open range flock of bantam chickens, by dosing half the birds directly into the crop. As indicated by rises in titres of haemagglutination inhibition antibody, the virus spread to the uninoculated birds and persisted in the flock for two years, infecting chickens that were introduced by natural brooding and rearing. All new clutches of chicks seroconverted by 80 days of age, and the titres of adult birds showed a concurrent rise, suggesting that the chicks were amplifying the virus. The modes of spread and of persistence of the virus were not determined; although cloacal swabs were taken regularly, only one yielded virus. Antibody titres of the inoculated birds remained above the presumptive protective level of 3 (log2) for over a year, whereas the titres of birds infected by contact were generally less than 3.     

野鸟传播的重要传染病研究进展

野鸟在迁徙和飞行过程中,因能携带和散播多种病原体,在公共卫生学方面具有重要的意义.通过野鸟能潜在性传播人和动物的重要传染病,包括禽类疫病(禽流感、新城疫、禽痘、禽肺病毒感染、禽分支杆菌感染和鸭瘟)和其他重要疫病(口蹄疫、衣原体病、日本脑炎、莱姆病、西尼罗病毒感染、博尔纳病、Q热、东方马脑炎及致病菌感染),由此应对野鸟传播的疫病予以必要的重视和警惕,并提出有效的防范措施.     

一起朱鹮雏鸟新城疫的诊治

2018年5月,陕西省珍稀野生动物救护基地突然有10只人工育雏的朱鹮雏鸟在短暂厌食后相继死亡,经病理剖检及实验室病原检测诊断为新城疫.剩余18只朱鹮雏鸟经检测12只新城疫阳性,后经抗NDV异源高免血清治疗和新城疫疫苗紧急免疫后,16只雏鸟成活.朱鹮感染新城疫偶有报道,但尚无成功治愈的案例.这次朱鹮雏鸟新城疫的诊治为今后...     

Failure to demonstrate viscerotropic velogenic Newcastle disease in psittacine birds in the Republic of the Philippines

Birds on the islands of Luzon, Mindanao, and Palawan in the Republic of the Philippines were surveyed for viscerotropic velogenic Newcastle disease (VVND). Virus isolation was attempted on 728 cloacal samples from native and exotic psittacine birds, non-psittacine birds, and domestic chickens and ducks. A VVND virus isolate was obtained from a single domestic chicken that had exhibited ocular discharge and diarrhea 3 days before sampling. All other birds were negative for VVND.     

Avian paramyxovirus type 1 infections of racing pigeons: 4 laboratory assessment of vaccination

The immune response and protection from challenge afforded to adult pigeons by four different vaccination schedules were assessed. Intravenous challenge with a field pigeon isolate was done four weeks after the second of two doses of vaccine given four weeks apart. Little difference in protection was seen between two 0.25 ml and two 0.5 ml doses of oil emulsion vaccine, although the latter produced a slightly higher immune response. In both cases one of 10 challenged pigeons became sick and died. One dose of Newcastle disease virus B1 live vaccine followed four weeks later by 0.5 ml oil emulsion vaccine gave a comparable immune response to two 0.25 ml doses of oil emulsion but only six birds survived challenge. Two doses of Newcastle disease virus B1 vaccine gave a poor immune response and little protection from challenge; all 10 birds became sick and eight died. Assessment of the onset of protection following one dose of either 0.5 ml oil emulsion vaccine or Newcastle disease virus B1 indicated some partial protection in the latter group as early as five days after vaccination. Both groups showed protection at 10 days but by 21 days, although protection was sustained in the oil emulsion group, birds receiving live vaccine were fully susceptible. Measurement of the duration of protection in pigeons given two 0.5 ml doses of oil emulsion vaccine indicated that protection had begun to wane by 40 weeks after the first dose.