Effects of an Arkansas strain of infectious bronchitis vaccine on the head-associated lymphoid tissue (HALT).

Chicks were vaccinated with an Arkansas strain of infectious bronchitis virus (IBV) vaccine when they were 1 day (Trial 1) or 4 weeks old (Trial 2). Starting at 4 weeks 3 days of age, chicks in both trials were subjected to an assay that measures the immunofunctional response of the gland of Harder (GH), one of the components of the head-associated lymphoid tissue (HALT). The assay involved multiple ocular exposures to killed Brucella abortus antigen, after which tears were collected and titered for antibodies to B. abortus. Following this, select tissues from vaccinated and unvaccinated chicks were collected and examined microscopically for specific lesions. Both functional and structural alterations were detected in the HALT of IBV-vaccinated chicks. Antibody titers to B. abortus in vaccinated chicks were significantly lower (P less than 0.05) than in unvaccinated controls. Structurally, there were elevations (P less than 0.01) in the number of lymphoid cells and follicles found in the mucosal lining of the nasal cavity. This occurred in the vaccinated chicks of both trials. Otherwise, histologic changes were confined to the chicks vaccinated at 4 weeks of age (Trial 2). In that trial, there were elevations in lymphoid-cell and follicle numbers in the eyelid (P less than 0.01) and lacrimal gland (P less than 0.05).     

Particle uptake by conjunctiva-associated lymphoid tissue (CALT) in turkeys

Uptake of tracer particles was assessed in lower eyelid conjunctiva-associated lymphoid tissue (CALT) of 3-week-old turkeys. Tracer particle suspensions, including carbon, iron oxide, or three sizes of latex beads (0.81 micron, 1.7 microns, and 2.9 microns), were placed into the experimentally sealed conjunctival space. After 5, 15, or 30 minutes, eyelids were removed and CALT was examined by light microscopy. Uptake was confirmed for all tracers and occurred within the lymphoepithelium of CALT. The uptake of latex beads was not as frequent as for carbon and iron. Tracers were increasingly evident in lymphoepithelium and subepithelial macrophage clusters as contact time increased. These findings provide additional evidence that CALT is capable of antigen uptake and may play a role in paraocular and upper respiratory immunity in turkeys.     

Conjunctiva-associated lymphoid tissue (CALT) in normal and Bordetella avium-infected turkeys

Conjunctiva-associated lymphoid tissue (CALT) was characterized in normal and Bordetella avium-infected turkey poults during the first 5 weeks of life. At 1, 5, 12, 19, 25, and 33 days post-hatching (DPH), upper and lower eyelids were examined by gross, histologic, and electron microscopic techniques. CALT was confined to the proximal part of the lower eyelid near the conjunctival fornix; it appeared by 5 DPH as individual lymphoid nodules and as dense masses by 19 DPH. In the upper eyelid, CALT was present only as isolated nodules. Histologically, CALT was composed of dense lymphocyte infiltrates within subepithelial connective tissue, intraepithelial lymphocytes, and flattened lymphoid-associated epithelium that lacked goblet cells. Germinal centers were in CALT by 19 DPH. By scanning electron microscopy, epithelial cells over lymphoid areas were flat and had short, irregular microvilli; non-lymphoid areas were covered by cells with tall, regular microvilli. Transmission electron microscopy revealed that with increasing age of birds, the epithelium over conjunctival lymphoid infiltrates became progressively flattened and infiltrated by lymphocytes. Some blood vessels in CALT had high endothelial cells; lymphocytes were in the lumen and between or beneath endothelial cells. In B. avium-infected poults, CALT was increased, developed earlier, and contained more germinal centers than in normal poults. We conclude that CALT of turkeys closely resembles other mucosal lymphoid tissues and may serve as a site for local antigen uptake.(ABSTRACT TRUNCATED AT 250 WORDS)     

Morphologic characterization of conjunctiva-associated lymphoid tissue in chickens.

Conjunctiva-associated lymphoid tissue (CALT) in the eyelids of chickens was studied by gross, histologic, and electron microscopic techniques. Structural features were characterized at 1 day of age and at posthatching week (PHW) 1, 2, 3, 4, 6, 8, 12, and 16. Beginning at PHW 1, prominent lymphoid nodules containing a heterogenous population of lymphocytes, lymphoblasts, and macrophages were first observed within conjunctival folds and fissures of the lower eyelid. Nodules contained germinal centers by PHW 2 and plasma cells by PHW 4. The epithelium associated with these nodules was flat, had short, irregular microvilli, contained intraepithelial lymphocytes, and lacked goblet cells. High endothelial venules were located at the base of lymphoid nodules and contained lymphocytes within and below the cuboidal endothelium. In the upper eyelid, CALT was morphologically similar to lymphoid tissue in the lower eyelid, but nodules were smaller and more random, lacked association with epithelial folds and fissures, and were clustered around the opening of the nasolacrimal duct. By PHW 12, CALT was characterized by basal germinal centers outlined by collagenous stroma, suprafollicular plasma cells, columnar epithelium with goblet cells, and fewer intraepithelial lymphocytes. On the basis of these features, CALT in chickens has morphologic characteristics similar to other components of the mucosal immune system and, therefore, may have a role in mucosal immunity.     

Quantification of particle uptake by conjunctiva-associated lymphoid tissue (CALT) in chickens

Tracer particle uptake by conjunctiva-associated lymphoid tissue (CALT) was quantified in the lower eyelids of 1-, 3-, 5-, and 7-week-old broiler chickens. CALT was measured histologically by computerized image analysis in all birds and in additional 1-day-old and 16-week-old chickens not subjected to uptake assessment. Suspensions of carbon or iron oxide were placed in contact with CALT for 5, 15, or 30 minutes (contact time). After eyelid removal, tracer uptake was scored by light microscopy, CALT was measured, and a mathematically derived uptake index was evaluated statistically. At each age examined, computer-generated measurements showed a significant increase in the proportion of CALT lymphoepithelium within proximal eyelids. Within the conjunctival sites evaluated, tracer uptake was significantly greater in lymphoepithelium than in non-lymphoepithelium at all ages and at all contact times. Uptake increased significantly between 3 and 5 weeks of age and between 5 and 15 minutes of tracer contact. Based on these uptake data for CALT in chickens, a minimal age-specific maturity is suggested that may influence function in mucosal immunity.     

切除结膜结合淋巴组织鸡对新城疫疫苗点眼免疫反应 Ⅱ.组织学与免疫组织化学研究

60只 1日龄健康雏鸡随机分为 A、B、C三组。A组于 1日龄手术切除下眼睑结膜。A、B两组于 12日龄时结扎鼻泪管 ,用新城疫克隆 30苗点眼。C组为对照组。 2 3日龄分别采取其 CAL T和哈德氏腺 ,比较观察其组织细胞。结果 ,1日龄手术切除下眼睑结膜后造成鸡 CAL T缺失 ,点眼免疫后 ,哈氏腺的免疫细胞也较正常免疫鸡少 ,而正常接种 ND克隆 30 (B组 )后 ,CAL T发生早 ,生长快 ,淋巴细胞数量多 ,故本实验证实 CAL T对哈氏腺免疫细胞的数量与成分有一定的调控作用。 CAL T缺失鸡是研究黏膜免疫系统比较理想的模型     

切除结膜结合淋巴组织鸡对新城疫疫苗点眼免疫反应Ⅱ.组织学与免疫组织化学研究

60只1日龄健康雏鸡随机分为A、B、C三组。A组于1日龄手术切除下眼睑结膜。A、B两组于12日龄时结扎鼻泪管，用新城疫克隆30苗点眼。C组为对照组。23日龄分别采取其CALT和哈德氏腺，比较观察其组织细胞。结果，1日龄手术切除下眼睑结膜后造成鸡CALT缺失，点眼免疫后，哈氏腺的免疫细胞也较正常免疫鸡少，而正常接种ND克隆30（B组）后，CALT发生早，生长快，淋巴细胞数量多，故本实验证实CALT对哈氏腺免疫细胞的数量与成分有一定的调控作用。CALT缺失鸡是研究黏膜免疫系统比较理想的模型。     

结膜相关淋巴组织和哈氏腺免疫协同关系的研究Ⅰ．结膜相关淋巴组织缺失对哈氏腺点眼免疫应答的影响

采用ＥＬＩＳＡ、免疫组织化学方法、手术切除结膜相关淋巴组织（Ｃｏｎｊｕｎｃｔｉｖａ－ａｓｓｏｃｉａｔｅｄ Ｌｙｍｐｈｏｉｄ Ｔｉｓｓｕｅ，ＣＡＬＴ）法对结膜相关淋巴组织和哈氏腺（Ｈａｒｄｅｒｉａｎ Ｇｌａｎｄ，ＨＧ）在点眼免疫应答过程中的相互协同关系进行了研究。研究发现，采用外科手术于１日龄切除结 膜相关淋巴组织后切除组点眼免疫后泪液中ＮＤＶ－特异性ＩｇＡ、ＩｇＭ型抗体滴度及哈氏腺中ＩｇＡ、ＩｇＭ     

Colonization of Escherichia coli in young turkeys and chickens.

In order to investigate the possibility of pathogenic Escherichia coli penetrating the bloodstream via the intestinal mucosa in normal and stressed turkeys and chickens, birds were inoculated orally with the bacteria or exposed environmentally to it. Immediately after hatch, intestines contained a substantial number of coliform bacteria that increased with time. In orally infected turkeys, the pathogenic bacteria (nalidixic-acid-resistant O78) replaced 10%-50% of the native coliform flora but could not be isolated from the trachea or blood. Environmentally exposed groups exhibited pathogenic bacteria in intestines but not in blood. Stressing of exposed turkeys resulted in isolation of the pathogenic bacteria from blood and even spleen. In orally infected broiler chickens, stress resulted in bacteremia and mortality. Chickens that were exposed to pathogenic bacteria at a young age and showed no mortality or morbidity demonstrated no detrimental effects due to challenge with the same pathogenic bacteria later in life. Stress seems to cause penetration of the pathogenic bacteria into the bloodstream, which in turn can cause severe disease and mortality.     

Plasma cell quantitation in the gland of Harder during infectious bursal disease virus infection of 3-week-old broiler chickens

Histopathologic changes in the gland of Harder (GH) and bursa of Fabricius (BF) were studied during and after infection of 3-week-old broiler chickens with a pathogenic strain of infectious bursal disease virus (IBDV). Plasma cell (PC) necrosis in the GH was seen from 5 to 14 days postinoculation (PI), BF follicular necrosis was observed from 1 to 7 days PI. PC numbers within the GH, counted for 28 days after inoculation, declined and were reduced (P less than 0.01) by 51% at 7 days after inoculation, which coincided with PC necrosis and heterophil infiltration. After 14 days PI, however, PC numbers were equal to those in uninfected controls. Since the GH is a major antibody-producing site in the paraocular area, the reduction in PC number at 7 days PI might indicate compromise of local immunity in the paraocular region and upper respiratory tract associated with IBD.     

Comparison of the oral bioavailability and tissue disposition of monensin and salinomycin in chickens and turkeys

Henri, J., Maurice, R., Postollec, G., Dubreil‐Cheneau, E., Roudaut, B., Laurentie, M., Sanders, P. Comparison of the oral bioavailability and tissue disposition of monensin and salinomycin in chickens and turkeys. J. Vet. Pharmacol. Therap.  35 , 73–81. The current study describes the pharmacokinetic parameters of two carboxylic polyether ionophores: monensin in turkeys and salinomycin in chickens. These data can be used to understand and predict the occurrence of undesirable residues of coccidiostats in edible tissues of these animal species. Special attention is paid to the distribution of residues between the different edible tissues during and at the end of the treatment period. For the bioavailability studies, monensin was administered to turkeys intravenously, in the left wing vein, at a dose of 0.4 mg /kg and orally at a dose of 20 mg /kg. Salinomycin was administered to chickens intravenously, in the left wing vein, at a dose of 0.25 mg /kg and orally at a dose of 2.5 mg /kg. Residue studies were carried out with supplemented feed at the rate of 100 mg /kg of feed for monensin in turkeys and 70 mg /kg for salinomycin in chickens, respectively. Coccidiostats had a low bioavailability in poultry (around 30% for monensin in chickens, around 1% for monensin in turkeys and around 15% for salinomycin in chickens). Monensin in chickens had a longer terminal half‐life (between 3.07 and 5.55 h) than both monensin in turkeys (between 1.36 and 1.55 h) and salinomycin in chickens (between 1.33 and 1.79 h). The tissue /plasma partition coefficients showed a higher affinity of both monensin and salinomycin for fat, followed by liver and muscle tissue. The depletion data showed a fairly rapid elimination of coccidiostats in all the tissues after cessation of treatment. According to the results of depletion studies, a withdrawal period of 1 day seems sufficient to avoid undesirable exposure of consumers.     

Inflammation of the nasal gland in domestic turkeys.

A prominent swelling above the eye of range-reared tom turkeys was found to be due to severe inflammation and hyperplasia of the nasal or salt gland. The incidence of affected turkeys was sporadic, and no mortality or other lesions were associated with the condition.     

Uptake of ferritin and Bordetella avium in bronchus-associated lymphoid tissue of turkeys

The uptake of macromolecular and particulate materials in bronchus-associated lymphoid tissue (BALT) in turkeys was examined using transmission electron microscopy. Tracer materials used were live and ultraviolet-killed (UV-killed) Bordetella avium and ferritin. Suspensions of bacteria and ferritin were instilled via intratracheal catheterization and allowed to remain in contact with the respiratory surfaces for 0, 10, 30, 60, 90, and 120 min. Ferritin and B. avium were taken up by both ciliated and non-ciliated cells of the epithelium overlying BALT (BALT epithelium). Ferritin was found in organelles associated with endocytosis (i.e. apical vesicles, endosomes, cytoplasmic vacuoles) and was apparently transported across epithelial cells, since it was also found in intercellular spaces. Bacteria were found in vacuoles within BALT epithelial cells, but not free in intercellular spaces. Some macrophages in BALT epithelium also contained bacteria. No differences were observed between uptake of live and UV-killed bacteria. We conclude that both ciliated and non-ciliated cells of BALT epithelium in turkeys are able to take up macromolecular and particulate materials. Bacteria are also accessible to intraepithelial macrophages, although whether they are taken up directly from the bronchial surface or whether they pass through epithelial cells first could not be determined. This evidence suggests that antigens, including respiratory pathogens, could gain access to cells of the avian immune system by transepithelial passage in BALT.     

Pathogenicity of Campylobacter jejuni for turkeys and chickens.

A Campylobacter jejuni isolate obtained from a turkey liver, designated C101, and a C. jejuni isolate obtained from the feces of a chicken, designated C111, were used to inoculate their respective hosts. Isolate C101 depressed weight gain by 20% when inoculated into newly hatched poults or 4-day-old poults. It also caused death, hepatic necrosis, and generalized hemorrhages in turkey embryos. The chicken-derived isolate, C111, did not reduce weight gain in newly hatched chicks, but it did induce mortality in chicken embryos. The supernatant of the cultures of both C. jejuni isolates also caused mortality in embryos.     

不同日龄鸡眼结膜相关淋巴组织的形态学观察

(目的)本试验旨在观察不同日龄鸡眼结膜相关淋巴组织(conjunctiva-associate lymphoid tissue,CALT)的形态结构,从而了解其不同时期的免疫状态。(方法)选择不同日龄的雏鸡,每个时期取3只雏鸡的下眼睑结膜制成冰冻切片,片厚5μm,然后进行H.E.染色。(结果)结果发现,鸡CALT的黏膜上皮为复层扁平上皮,常见杯状细胞。固有层内的淋巴细胞随着日龄增长逐渐增多,21日龄时可观察到生发中心,与淋巴滤泡相关的上皮常缺乏杯状细胞,27日龄CALT的各种组织结构基本成熟。(结论)结果表明,鸡CALT的组织结构随着日龄增长逐渐发育成熟,并在27日龄时其免疫功能基本达到成熟水平。     

NALT (nasal cavity-associated lymphoid tissue) in the rabbit

Due to its many advantages, interest in intranasal vaccination of domestic mammals and humans is currently increasing. Successful stimulation of the immune system by intranasal vaccines requires, however, the presence of lymphoid tissue in the nasal cavity. This nasal cavity-associated lymphoid tissue (NALT) has already been described in humans and many laboratory rodents, but data about rabbits are very scarce. For this purpose, histological sections of the nasal cavities of 10 female adult New Zealand White rabbits were examined for the presence of lymphoid tissue. Primary (I) and secondary (II) lymphoid follicles divided by interfollicular regions were mainly present at the bottom of the ventral nasal meatus and the nasopharyngeal meatus from 1 to 3.3 cm from the tip of the nose. In this region intraepithelial and lamina propria lymphocytes, and isolated lymphoid follicles (ILF's) were additionally seen at the dorsal and dorsolateral sides of the nasopharyngeal meatus and within the mucosae of the nasal conchae and the lateral nasal walls. Intraepithelial and lamina propria lymphocytes, and ILF's were, just like in humans, randomly distributed along the entire nasal mucosa. The rabbit NALT is more voluminous compared to rodents in which lymphoid tissue is only present at the bottom of the nasopharyngeal meatus. Since the relative volume of the rabbit nasal cavity is also similar to that of humans, the rabbit could be a valuable research model not only for animal but also for human intranasal vaccine development.