The serological response of dogs to Taenia ovis

The effect of 4-weekly anthelmintic dosing and other treatment regimes on the serological response of dogs to Taenia ovis was examined. Most dogs which were frequently fed infected meat and dosed with a cestocidal anthelmintic at 4-week intervals eventually showed a positive ELISA absorbance. The absence of dosing, or intermittent dosing, of repeatedly infected dogs raised ELISA absorbances to very high levels in most dogs and these absorbances took an increasingly longer time to fall after each new infection. The feeding of large numbers of frozen, dead cysts to sensitised dogs raised absorbance levels. The serological test for T. ovis infections in dogs does not detect false postives. Positive tests result from the dog being exposed to T. ovis scolex secretory antigen.     

The serological response of dogs to Taenia ovis

The effect of 4-weekly anthelmintic dosing and other treatment regimes on the serological response of dogs to Taenia ovis was examined. Most dogs which were frequently fed infected meat and dosed with a cestocidal anthelmintic at 4-week intervals eventually showed a positive ELISA absorbance. The absence of dosing, or intermittent dosing, of repeatedly infected dogs raised ELISA absorbances to very high levels in most dogs and these absorbances took an increasingly longer time to fall after each new infection. The feeding of large numbers of frozen, dead cysts to sensitised dogs raised absorbance levels. The serological test for T. ovis infections in dogs does not detect false positives. Positive tests result from the dog being exposed to T. ovis scolex secretory antigen.     

与PCV2有关的血清学试验重要性

鉴于由PCV2引起感染的高流行性,以及它可出现在健康和患病的猪中,针对这种病原体的血清学试验作为疾病的诊断性试验已受到质疑.众所周知,圆环病毒的诊断必须以Sorden标准为依据.然而,这些试验的重要性建立在试验类型、试验有效性、我们希望使用这种方法的情况或条件以及它们的目标基础上. 由于间接免疫荧光法(Indirect Immunofluorescence,IFA)试验在我们的环境中没有得到使用,免疫过氧化物酶单层试验(Immunoperoxidase Monolayer,IPMA)出于其操作麻烦和可利用性有限,实际上局限于科学领域的应用.本文我们将不对它们进行讨论.我们只是说,对于一些专家来说,后者将是参考试验,免疫酶测定法或ELISA试验将进行评估.     

The serological response of foals to vaccination against strangles.

A group of 100 foals was given either a commercial bacterin or an autogenous vaccine consisting of whole cells and an acid extract of Streptococcus equi. During the study, some of the foals developed clinical strangles. Various sets of sera were collected from these foals prevaccination, during vaccination, postvaccination and postinfection. The serological response of these foals was measured by passive haemagglutination and long chain tests. In foals which remained healthy, the highest titres were reached within one to two months postvaccination with a passive haemagglutination 10 x log2 mean titre of 6.78 and the long chain indices of 4.41. These levels persisted for 120 days postvaccination. Those foals which had clinical strangles exhibited lower passive haemagglutination titres (3.78) at one to two months postimmunization, but rose significantly after recovery. Four ponies immunized with formalinized Str. equi bacterin showed a partial protection against the challenge infection. The passive haemagglutination titres, long chain indices and serum bactericidal activity in these ponies were highest at 35 days postvaccination but did not increase after infection.     

Comparison of serological techniques to measure antibody to Pasteurella haemolytica A1.

Analysis of 45 sera was performed employing five techniques which are currently in use in three laboratories to measure anti-Pasteurella haemolytica antibodies. The enzyme linked immunosorbent assay, passive hemagglutination, complement fixation and direct and indirect bacterial agglutination assays were employed and a relationship between tests in the measurement of anti-P. haemolytica antibodies was demonstrated. Regression analysis together with prediction and confidence intervals were tabulated also. The conclusion drawn from statistical analysis was that all five tests are similar in their ability to detect immune responses (antibody and antigen(s) interactions) to Pasteurella haemolytica.     

The epidemiological interpretation of serological responses to leptospiral serovars in sheep

Serum samples were examined for evidence of leptospiral agglutinins from 928 sheep from 45 lines and kidneys from 12 of these lines for evidence of leptospiral infection. All sheep had been submitted for slaughter at meat works in the Manawatu. Serological results were analysed using the results at a minimum serum dilution in the microscopic agglutination test (MAT) of 1:24 and at a minimum dilution of 1:48. It was shown that a minimum dilution of 1:24 resulted in many non-specific or cross-reactions. A minimum dilution of 1:48 was more accurate for detecting the serological prevalence of specific agglutinins to leptospires in ovine sera. Twenty percent of the sheep had titres of 1:48 or greater to hardjo, 3.8% to pomona, 2.6% to tarassovi, 2.3% to copenhageni and 2.7% to ballum. No titres of 1:48 or greater to australis were detected. Serovar hardjo was isolated from the kidneys of three animals in one line. Eighteen months later 291 serum samples and 95 urine samples were collected from live animals on the property from which the three hardjo infected animals originated. No titres to hardjo were detected in the sera of lambs, but a serological prevalence of 44% and 84% to this serovar was demonstrated in the hoggets and ewes respectively. No leptospires were demonstrated in any of the urine samples. These results show that sporadic infection of sheep with hardjo can occur but they also indicate that infection with this serovar is not endemic and that sheep are unlikely to act as maintenance hosts for hardjo in New Zealand.     

Investigation of aberrant positive reactions to serological tests for bovine brucellosis

Fifty cattle thought not to be infected with Brucella abortus but giving persistent positive serological reactions, were investigated. It was concluded that only one of these was infected since exhaustive bacteriological examination produced only one isolate of B. abortus (strain 19) and none of the herds of origin was subsequently shown to be infected with brucellosis. Antibody was detected in stifle joint fluid of 15 cattle, which may have been stimulated by the presence of Strain 19 antigen that persisted in collagenous tissue long after the viable organisms had been eliminated.     

Characterisation, experimental infection and serological response to caprine retrovirus

A virus (151) isolated from synovial membrane explant cultures from a goat with arthritis-synovitis was characterised with respect to cytopathic effect in synovial membrane cell cultures, virus morphology, buoyant density and presence of RNA dependent DNA polymerase. Virus 151 was shown to be a retrovirus with similar properties to caprine arthritis-encephalitis virus in the United States of America. Inoculation of the virus into uninfected goats caused the development of arthritis-synovitis lesions and the virus was recovered from affected joints and lung 361 days post-inoculation. The development of antibody to virus 151 was detected using an enzyme linked immunosorbent assay (ELISA). Other goats with arthritis-synovitis, progressive pneumonia or viral leukoencephalomyelitis all had antibody that reacted in this ELISA. Viruses similar to virus 151 were recovered from a number of cases. Goats inoculated with one of the viruses produced serum antibody that cross-reacted in ELISA using maedi-visna virus and virus 151 as antigens.     

National survey to determine uniformity of serological test results for avian mycoplasmosis

A national survey was conducted to address the concern over the uniformity of serological test results for avian mycoplasmosis. The National Veterinary Services Laboratories produced chicken and turkey mycoplasma serum-check test kits. Each kit had a total of 25 sera that consisted of negative and positive sera. Participating laboratories were requested to examine their kits using the serum plate agglutination test with the plate antigens currently being used and the hemagglutination inhibition test with the hemagglutinating antigens provided. A conclusion whether serum plate agglutination-positive sera were positive, negative, or suspicious was based on the hemagglutination inhibition test results. Results in each category were scored on the basis of 100 points. The average scores on the serum plate agglutination test, hemagglutination inhibition test, and conclusion were 95, 71, and 91, respectively, for the chicken serum test kit and 91, 71, and 89, respectively, for the turkey serum test kit. The results indicated a high degree of uniformity among laboratories in reporting serological test results for mycoplasmosis in chickens and turkeys.     

Factors affecting the serological response of dogs and cats to rabies vaccination

After being vaccinated against rabies some cats and dogs fail to show an antibody titre adequate to meet the requirements of the UK Pet Travel Scheme. To investigate this problem, the data derived from 16,073 serum samples submitted to the Veterinary Laboratories Agency for serological testing between 1999 and 2002, 1002 samples submitted to BioBest during March and April 2001, and 1264 samples associated with one make of vaccine submitted to BioBest between June 2001 and January 2003, were analysed. The probability of antibody titre failing to reach at least 0.5 iu/ml was analysed by logistic regression as a function of the choice of vaccine, the interval between vaccination and sampling, the sex and age of the animal, and its country of origin. In dogs, all these factors, except sex, had highly significant (P < 0.001) effects on the test failure rate, and in cats all the factors had a significant effect (P < 0.05).     

The epidemiological interpretation of serological responses to leptospiral serovars in sheep.

Serum samples were examined for evidence of leptospiral agglutinins from 928 sheep from 45 lines and kidneys from 12 of these lines for evidence of leptospiral infection. All sheep had been submitted for slaughter at meat works in the Manawatu.

Serological results were analysed using the results at a minimum serum dilution in the microscopic agglutination test (MAT) of 1:24 and at a minimum dilution of 1:48. It was shown that a minimum dilution of 1:24 resulted in many non-specific or cross-reactions. A minimum dilution of 1:48 was more accurate for detecting the serological prevalence of specific agglutinins to leptospires in ovine sera. Twenty percent of the sheep had titres of 1:48 or greater to hardjo, 3.8% to pomona, 2.6% to tarassovi, 2.3% to copenhageni and 2.7% to ballum. No titres of 1:48 or greater to australis were detected. Serovar hardjo was isolated from the kidneys of three animals in one line.

Eighteen months later 291 serum samples and 95 urine samples were collected from live animals on the property from which the three hardjo infected animals originated. No titres to hardjo were detected in the sera of lambs, but a serological prevalence of 44% and 84% to this serovar was demonstrated in the hoggets and ewes respectively. No leptospires were demonstrated in any of the urine samples.

These results show that sporadic infection of sheep with hardjo can occur but they also indicate that infection with this serovar is not endemic and that sheep are unlikely to act as maintenance hosts for hardjo in New Zealand.