1日龄火鸡新城疫免疫后局部体液免疫球蛋白含量的动态变化

本实验应用Lasota苗及其灭活苗联合免疫接种1日龄火鸡,60日龄攻毒。分别在免疫后第7、14、21、35和60日检泪液、气管液、胆汁和肠道冲洗液中IgG、IgM、IgA含量及泪液HI抗体滴度的动态变化。结果表明免疫火鸡上述各项指标明显高于对照,联合免疫组高于Lasota单独免疫组,说明火鸡早期免疫可明显提高呼吸道和消化道相关局部体液的抗体水平和抗感染能力,其中联合免疫优于单独弱毒苗免疫。     

新城疫与传染性法氏囊疫苗疫苗对雏鸡联合免疫的研究

将１１４只１１日龄海赛克斯褐公鸡随机分成５组：Ⅰ组为空白对照，Ⅱ组用新城疫弱毒苗和ＮＤ油佐剂灭活苗同时免疫，Ⅱ组用传染性法氏囊病地方毒株油佐剂灭活苗免疫，Ⅳ组用ＮＤ弱毒苗，ＮＤ油佐剂灭活苗，ＩＢＤ地方毒株油佐剂灭活苗同时免疫，Ｖ组在Ⅳ组的基础上增加ＩＢＤ弱毒苗免疫。５组鸡分别隔离饲养，定期测定血清ＮＤＨＩ效价与ＩＢＤ琼扩效价。选择时机用强毒攻击，观察各组鸡的保护情况。结果：（１）Ⅱ、Ⅳ、Ⅴ组鸡均能     

感染鸡贫血病毒雏鸡ND免疫后血清Igs和HI抗体的动态变化

本试验对１日龄感染鸡传染性贫血病毒（ＣＩＡＶ）雏鸡接种新城疫（ＮＤ）疫苗及其强毒攻击后外周血液免疫球蛋白ＩｇＧ、ＩｇＭ、ＩｇＡ含量和ＨＩ抗体滴度的动态变化进行研究。结果发现，ＣＩＡＶ感染雏鸡ＮＤ疫苗免疫后，其外周血液ＩｇＧ、ＩｇＭ、ＩｇＡ含量和ＨＩ抗体滴度，于接种ＮＤ疫苗后７￣２８ｄ较未感染ＣＩＡＶ的免疫对照雏鸡明显减少，表明ＣＩＡＶ感染雏鸡对ＮＤ疫苗免疫的体液免疫应答功能明显降低。ＮＤ强毒攻击后     

雏鸡早期新城疫弱毒疫苗与灭活疫苗联合免疫方法的研究

在鸡新城疫（ＮＤ）流行的地区，雏鸡早期应用弱毒疫苗和灭活疫苗联合免疫的方法，可以较好地控制ＮＤ的发生。作者对弱毒疫苗与灭活疫苗的单独免疫和联合免疫分八个试验组进行了试验，并对试验结果进行了分析比较。结果表明：Ｂ３（弱毒疫苗→＾１０日龄 灭活疫苗）组于３、６、１０、２０、３０、４０、６０日龄分别随机取样检测ＮＤＨＩ抗体效价，值为５．８３Ｌｏｇ２，与其他各试验组相比，效价高且平稳；于２０、４０、６０、     

新城疫与传染性法氏囊病疫苗对雏鸡联合免疫的研究

将１１４只１１日龄海赛克斯褐公鸡随机分成５组：Ⅰ组为空白对照，Ⅱ组用新城疫（ＮＤ）弱毒苗和ＮＤ油佐剂灭活苗同时免疫，Ⅲ组用传染性法氏囊病（ＩＢＤ）地方毒株油佐剂灭活苗免疫，Ⅳ组用ＮＤ弱毒苗、ＮＤ油佐剂灭活苗、ＩＢＤ地方毒株油佐剂灭活苗同时免疫，Ⅴ组在Ⅳ组的基础上增加ＩＢＤ弱毒苗免疫。５组鸡分别隔离饲养，定期测定血清ＮＤＨＩ效价与ＩＢＤ琼扩效价。选择时机用强毒攻击，观察各组鸡的保护情况。结果：（１）Ⅱ、Ⅳ、Ⅴ组鸡均能很好地抵抗ＮＤＶ强毒的攻击，Ⅲ、Ⅳ、Ⅴ组鸡无论对ＩＢＤＶ人工感染，还是自然感染，均有坚强的保护力；（２）ＩＢＤ地方毒株油佐剂灭活疫苗不干扰ＮＤ疫苗的免疫应答；（３）ＩＢＤ弱毒苗对ＮＤ疫苗的免疫应答有一定影响，在免疫初期能促进机体尽快对ＮＤ疫苗产生应答，但后期ＮＤ疫苗的ＨＩ抗体降低较快；（４）ＮＤ疫苗对ＩＢＤ疫苗的免疫效果无显著影响。作者提出，对雏鸡首免（无论有、无母源抗体）可采用ＮＤ弱毒苗＋ＮＤ油佐剂灭活苗＋ＩＢＤ（地方毒株）油佐剂灭活苗同时进行免疫，至少可以保护到上笼后或开产前免受ＮＤＶ和ＩＢＤＶ的感染，既简化了免疫程序，又可减少对鸡群的应激，值得推广应用。     

1日龄火鸡新城疫LaSota苗与灭活苗联合接种后的免疫应答

火鸡１日龄时用新城疫ＬａＳｏｔａ苗与油乳剂灭活苗联合免疫后，在７、１４、２１、３５日龄及攻毒后，检测了火鸡免疫器官组织法氏囊、胸腺、脾脏、盲肠扁桃体、哈德尔腺中浆细胞、ＴＡＮＡＥ＋＿数量变化。结果表明：免疫火鸡法氏囊、脾脏、盲肠扁桃体、哈德尔腺的浆细胞明显增多，机体体液免疫应答显著增强；胸腺、脾脏、盲肠扁桃体、哈德尔腺中ＴＡＮＡＥ＋也程度不同地增多，细胞免疫应答也明显增强，免疫后６０ｄ，用新城疫苗强毒攻击，免疫火鸡获得了良好的保护。     

1日龄火鸡新城疫La Sota苗与灭活苗联合接种后的免疫应签

火鸡１日龄时用新城疫Ｌａ Ｓｏｔａ苗与油乳剂灭活苗联合免疫后，在７、１４、２１、３５日龄及攻毒后，检测了火鸡免疫器官组织法氏囊、胸腺、脾脏、盲肠扁桃体、哈德尔腺中浆细胞、ＴＡＮＡＥ＾＋数量变化。结果表明：免疫火鸡法氏囊、脾脏、盲肠扁桃体、哈德尔腺的浆细胞明显增多，机体体液免疫应签显著增强；胸腺、脾脏、盲肠扁桃体、哈德尔腺中ＴＡＮＡＥ＾＋也程度不同地增多，细胞免疫应答也明显增强，免疫后６０ｄ，用新城     

鸡用天然缓释免疫增强剂的研究：天然缓释免疫增强剂对IBD等4？…

对７日龄艾维茵雏鸡投服天然缓释免疫增强剂１丸,１０日龄时分别用ＩＢＤ、ＮＤ、ＩＢ弱毒疫苗及ＮＤ油乳剂灭活苗免疫;免疫后７、１５、２５、３５一５５ｄ定期检测抗体效价;弱毒苗免疫后３５ｄ、灭活苗免疫后５５ｄ分别用强毒攻击。结果各试验组抗体效价显著高于对照组,试验组攻毒保护率提高１６．７￣３３．３个百分点。表明该缓释免疫增强剂能显著增强雏鸡的免疫应答,提高疫苗的免疫效力。     

鸡痘疫苗与新城疫疫苗免疫接种对新城疫血凝抑制抗体干 …

试验结果证明，鸡痘（ＦＰ）弱毒疫苗对新城疫（ＮＤ）弱毒疫苗血凝抑制（ＨＩ）抗体产生有严重的干扰作用，在ＦＰ疫苗接种后１５天内再接种ＮＤ疫苗，ＦＰ疫苗以 苗的ＨＩ抗体的产竽均膛同程度的干扰作用，其ＮＤ抗体平均效价低于单独用ＮＤ疫苗组０．１５￣１．３５个滴度。对雏鸡用ＦＰ弱毒疫苗和ＮＤ弱毒疫苗同时接种，或间隔１５天后再接种ＮＤ疫苗，其ＮＤ抗体平均值与单独用ＮＤ疫苗免疫组无明显差异。本实验观察结果表明，     

污染场鸡新城疫灭能苗与弱毒苗联合免疫的试验效果

在鸡场暴发鸡新城疫（ＮＤ）、污染严重的情况下，对１１日龄肉鸡采用鸡ＮＤ灭能苗与弱毒苗联合免疫的方法，有效地控制了疫情。采用本方法的试验组保护率为９２．３５％，对照组存活率仅有１５％。     

鸡马立克病CVI988疫苗不同接种部位对免疫效果的影响

探讨鸡马立克病CVI988疫苗不同的接种部位对免疫效果的影响,将96只1日龄海兰褐公雏鸡随机分成对照组(C)、腹腔注射接种组(PI)和颈部皮下接种组(HI),C组腹腔注射0.2mL疫苗稀释液,PI组和HI组注射0.2mL CVI988疫苗。在第3、6、10、15、20、26、35、45天对3组各4只鸡进行心脏采血,制作血涂片,分别进行ANAE和甲基绿-派洛宁染色,观察血液中阳性B淋巴细胞和T淋巴细胞百分率的变化。结果显示,在免疫早期(3日龄～6日龄),免疫组的阳性T淋巴细胞显著低于对照组,而阳性B淋巴细胞在第3天就显著高于对照组;在免疫中后期,免疫组的阳性T淋巴细胞和B淋巴细胞基本都显著高于对照组;并且PI组的阳性T淋巴细胞高于或显著高于HI组,阳性B淋巴细胞在第15天显著高于HI组。由此可见,CVI988疫苗接种第3天产生体液免疫效应,10d后细胞免疫效应高于对照组,即早期免疫效果主要靠体液免疫,腹部免疫接种效果优于颈部免疫,为马立克病更有效的免疫接种提供了理论依据。     

In vitro DNA synthesis in lymphocytes from turkeys vaccinated with LaSota, TC, and inactivated Newcastle disease vaccines.

In vitro cultures of peripheral blood lymphocytes from turkeys vaccinated and revaccinated with Newcastle disease (ND) vaccines were stimulated to transformation when exposed to the homologous and heterologous strains of ND virus. The mitogenesis was measured by the uptake of 3H-thymidine into newly synthesized DNA. There was considerable difference in DNA synthesis by lymphocytes drawn 0, 2, 5, and 10 days after vaccination and revaccination with the three vaccines. Stimulation of DNA synthesis, evident as early as the 2nd day, was highest in lymphocytes from turkeys vaccinated or revaccinated with TCND intramuscularly. Stimulation was least in lymphocytes from turkeys vaccinated and revaccinated with LaSota vaccine by aersol. Stimulation was intermediate from an inactivated vaccine given subcutaneously. DNA synthesis was greater with the homologous than with the heterologous strains of NDV. Synthesis was even greater when the same strain was used as a viral suspension in allantoic or cell-culture fluid than the commercial vaccine. The bovine paramyxovirus (PI3) resulted in a minimum DNA synthesis or completely inhibited it. A many-fold (order of magnitude) stimulatory effect was observed when PHA was used as an antigen. The stimulation of DNA synthesis did not parallel the HI antibody response.     

鸡新城疫和传染性法氏囊病灭活疫苗抗原量对鸡细胞免疫的影响

将不同抗原含量的鸡新城疫和传染性法氏囊病油乳剂灭活疫苗分别免疫１７日龄雏鸡，测定了疫苗抗原含量与细胞免疫应答之间的关系。经Ｔ淋巴细胞转化试验结果表明，两种疫苗的抗原含量－细胞免疫应答曲线是一致的，随着抗原量的增加，活化的Ｔ淋巴细胞数量也相应增多，但是细胞免疫应答的可测时间是暂时的，于免疫７天达高峰，１７天后下降接近正常水平。     

Dynamics of lymphocyte subpopulation changes in the cecal tonsils of chickens infected with Salmonella enteritidis

Salmonella enteritidis (SE)-induced changes in various T and B lymphocyte subpopulations in the cecal tonsils of chickens were analyzed using flow cytometry. At 1 day post-SE inoculation, the percentages of CD3(+) and CD8(+) T lymphocytes were significantly decreased in the group inoculated with 1x10(9) SE colony-forming units (CFU) (SE high) and in the group inoculated with 1x10(6) SE CFU (SE low) compared with the uninfected control group. The percentage of CD4(+) T lymphocytes was significantly increased in the SE high group compared to the uninfected and the SE low groups at 4 days after SE inoculation. The percentage of IgG(+) B lymphocytes was also significantly increased in both SE high and low groups compared to the uninfected control at 6 days post-SE inoculation. In contrast, the SE low group showed significantly fewer IgM(+) B lymphocytes compared to the uninfected and SE high groups. These results show that SE infection induces significant changes in the cecal tonsil lymphocytes subpopulations shortly following SE inoculation.     

Duration of cross-protection between subtypes A and B avian pneumovirus in turkeys

The degree and duration of clinical and virological cross-protection between avian pneumovirus subtypes A and B were examined in two-week-old pneumovirus antibody-free turkeys. The turkeys were inoculated with either a virulent subtype A (Belgian isolate A/T6/96), a virulent subtype B (Belgian isolate B/T9/96), an attenuated subtype A or an attenuated subtype B, and challenged homologously and heterologously with virulent avian pneumovirus two, five and 11 weeks after inoculation. Birds inoculated with virulent A or B virus showed typical respiratory signs from three to seven days after inoculation. After challenge, no clinical signs were observed in any of the groups, and no virus was isolated from the turkeys that had been initially inoculated with a virulent strain. Virulent virus was recovered from the birds that had been initially inoculated with attenuated subtypes and challenged five and/or 11 weeks later with a heterologous virulent strain. Birds challenged after five weeks showed a serological booster reaction only when they had been inoculated initially with a virulent or attenuated subtype B and challenged with subtype A. Seroconversion was observed in all the groups challenged after 11 weeks except when they had been inoculated initially with attenuated subtype B and challenged with subtype B.     

Histologic evaluation of lung and bronchus-associated lymphoid tissue in young turkeys infected with Bordetella avium

One-day-old turkeys were inoculated intranasally with Bordetella avium. Noninoculated hatchmates were housed separately. At postinoculation weeks 1, 2, 3, 4, and 5, B avium-infected (BA+) and B avium-free (BA-) turkeys were necropsied; specimens of tracheas, intrapulmonary primary bronchi, and lung adjacent to primary bronchi were bacteriologically cultured. Lung tissue was collected for histologic examination. Lungs perfused with acetic acid were collected for evaluation to determine the size, number, and distribution of lymphoid nodules associated with primary bronchi. Bordetella avium was isolated from trachea and primary bronchi of all BA+ turkeys, but was never isolated from lung parenchyma. Acute purulent bronchitis was associated with colonization of the primary bronchi by B avium from postinoculation weeks 1 to 3. Macrophages and lymphocytes persisted in the peribronchial connective tissue for 5 weeks after inoculation. Bronchus-associated lymphoid tissue consisted of discrete lymphoid nodules protruding into the lumens of primary bronchi. Lymphoid nodules, morphologically similar in BA+ and BA- turkeys, were composed of nonciliated, cuboidal epithelium covering a zone of loosely arranged lymphocytes and macrophages and a deeper, sharply demarcated lymphoid follicle. Compared with bronchus-associated lymphoid tissue of BA- turkeys, lymphoid nodules of bronchus-associated lymphoid tissue in BA+ turkeys were more numerous and widely distributed along primary bronchi. In both BA- and BA+ turkeys, the mean diameter of lymphoid nodules doubled between 1 and 5 weeks of age.     

复方中药提取物在新城疫B_1株免疫中的免疫增强作用

用自制的中药提取物与新城疫Ｂ１株混合后免疫５５日龄鸡，以血凝抑制试验测定新城疫抗体效价。结果表明，５５日龄鸡的中药提取物最佳用量为１．０ｍＬ，试验组鸡ＮＤ抗体效价明显高于对照组。免疫后６０ｄ用Ｆ４８Ｅ８新城疫强毒进行攻击，试验组的保护率达到１００％，而对照组相对较低。     

Effect of infection of turkeys with haemorrhagic enteritis adenovirus isolate on the selected parameters of cellular immunity and the course of colibacillosis

The aim of the study was to determine the effect of a Polish low-virulence isolate of haemorrhagic enteritis adenovirus (HEV) on the immune system in turkeys and on the course of colibacillosis in birds infected under laboratory conditions. Turkeys were infected per os with HEV at the dose of 10(4.3)EID50/mL and with E. coli (APEC) (serotypes 078:K80:H9) at the dose of 4x10(9)CFU/mL by injection to the thoracic air sac. The birds infected with the HEV were infected with the APEC either simultaneously or after 5 days. Five days after HEV infection, the percentages of subpopulations of the CD3+CD4+ and CD3+CD8alpha+ T cells and the IgM+ B cells were determined in blood and spleens of the HEV-infected turkeys and in the control (uninfected) birds. The course of colibacillosis was more severe in turkeys infected with the APEC 5 days after infection with the HEV than in those infected with the HEV and APEC simultaneously and than in those infected only with APEC. Five turkeys out of the 18 infected with the APEC 5 days after infection with HEV, died. Their body weights were statistically significantly lower with higher FCR values 41 days after the infection in comparison to turkeys in the other groups. A considerable decrease in the percentage of the T and B cells subpopulations in the blood were found in turkeys infected with the HEV and while the percentage of CD3+CD4+ T cells subpopulation in the spleen increased significantly, the contribution of the CD3+CD8alpha+ T cells and IgM+ B cells subpopulations were decreased. These changes in the immune system of turkeys, occurring 5 days after infection with the HEV, made them more susceptible to infection with the APEC.     

The clinical, pathological and microbiological outcome of an Escherichia coli O2:K1 infection in avian pneumovirus infected turkeys

The purpose of this study was to evaluate the effect of an Escherichia coli infection in avian pneumovirus (APV)-infected turkeys. One group of 2-week-old specific pathogen-free (SPF) and two groups of 3-week-old conventional (CON) turkeys were inoculated oculonasally with virulent APV subtype A alone, with E. coli O2:K1 alone or with both agents at varying intervals (1, 3, 5 or 7 days) between the two inoculations. The birds were followed clinically and examined for macroscopic lesions at necropsy. Titres of APV were determined in the turbinates, trachea, lungs and air sacs. The number of E. coli O2:K1were assessed in the turbinates, trachea, lungs, air sacs, liver and heart. In both SPF and CON turkeys, dual infection resulted in an increased morbidity and a higher incidence of gross lesions compared to the groups given single infections, especially with a time interval between APV and E. coli inoculations of 3 and 5 days. APV was isolated from the respiratory tract of all APV-infected groups between 3 and 7 days post inoculation. E. coli O2:K1 was isolated only from turkeys that received a dual infection. It was recovered from the turbinates, trachea, lungs, heart and liver. These results show that APV may act as a primary agent predisposing to E. coli colonization and invasion.