Lymphocyte proliferation in lymphoid organs of the dromedary camel using the monoclonal antibody MIB-5 against the proliferation-associated nuclear epitope Ki-67

Detection of proliferating lymphocytes is useful for studying immune reactions and for the prognosis of tumours of lymphocyte origin. Markers detecting proliferating cells are lacking in the dromedary camel. This study deals with the immunohistochemical detection of the Ki-67 proliferation-associated nuclear epitope using MIB-5 in frozen sections from spleens, different lymph nodes and haemal nodes of eight camels (0.5-12 years old). Frozen sections from rat spleens were labelled in parallel with camel tissue as a positive control. Large numbers of cells expressing the Ki-67 epitope were localized in germinal centres of all lymphoid organs tested. A few cells were found in the periarterial lymphoid sheath and the red pulp of the spleen, also in the lymphatic cords of the lymph nodes and the haemal nodes. There were no obvious differences in respect to the age of the animals. The Ki-67 epitope is well expressed by proliferating cells in camel lymphoid organs. MIB-5 can be applied to identify this epitope and will be a useful marker for cell production in immune reactions.     

Immunohistology of the splenic compartments of the one humped camel (Camelus dromedarius)

The cellular composition of the different splenic compartments is well characterized in several species, but the spleen of the camel has not been studied due to the lack of specific antibodies detecting its leukocyte subsets. Therefore, 5microm frozen sections from 15 camel spleens (0.5-15 years) were studied for acid and alkaline phosphatases and for cross-reaction with antibodies specific for bovine (n=181), swine (n=14) and human (n=6) leukocyte determinants. Fifteen antibodies cross-reacted with camel spleen cells. These included 13 anti-bovine, two anti-human, but no anti-swine antibodies. The lymph follicles mainly consisted of B cells. The germinal centers showed a strong alkaline phosphatase activity. The periarterial lymphatic sheath harbored T lymphocytes. The marginal zone contained gammadelta T cells, CD45R0+, MHC class II DR+, CD44+, IL-A 24+ cells and few macrophages. The red pulp contained B, T, MHC class II DR+, IL-A24+ and gammadelta T cells and few macrophages. The periarterial macrophage sheaths contained many more macrophages than the marginal zone, so they may play a central role in the phagocytosis of the blood born particles. The alkaline phosphatase probably labeled activated B cells, but in contrast to other species no positive cells were found in the marginal zone. In general, lymphocyte compartmentalization in the camel spleen is similar to that in other species except for lower numbers of macrophages and the absence of alkaline phosphatase positive cells in the marginal zone. No age related differences were observed in the splenic compartments.     

A Study on the Productivity and Diseases of Camels in Eastern Ethiopia

A study concerning performance traits of the Ethiopian camel indicated that, in the camel herds examined, there was one active bull camel for 25 females. The bull camel was 5 years old at puberty; it reached rutting vigour at the age of 9 years, the number of mountings per day was 8 during the breeding season, and the reproduction span was 10 years. The female camel reached puberty at 4 years of age; the age at first calving was 5 years, and the lactation period was one year; the calving interval was 2 years, the calving rate was 50%, and the reproduction span was 10–15 years. The survival rate of the newborn calves was 50%. The average milk yield was 2.5 L per day; the price of camel's milk was higher than that of cow's milk at US$0.5. Adult camels weighed around 500 kg; the dressing-out percentage was 52%. Mutton was preferred to camel meat, which came second in popularity, costing US$2/kg. Owing to their poor reproductive performance, camels are not efficient for producing meat. The camels worked for 16 h per day, covering 60 km. Animal health problems encountered were trypanosomosis, camel pox, camel pustular dermatitis, camel cephalopsis, dermatomycosis, mange mite, tick infestation and balantidiosis, most of which mainly affected the young animals.     

Age-related changes in the anatomical characteristics of Peyer's patches in small intestine of Bactrian camels (Camelus bactrianus)

The distribution, size, and appearance of Peyer's patches vary according to species. In order to determine the anatomical characteristics of Peyer's patches in small intestine of Bactrian camel, and age-related changes in the number of Peyer's patches, 40 Bactrian camels of the following four age groups were studied: young (0.5–2 years), pubertal (3–5 years), middle-aged (6–16 years), and old (17–20 years). The exact number of Peyer's patches was recorded, and the appearance of Peyer's patches was described in detail. The results indicated that Peyer's patches of Bactrian camels not only have a particular anatomical location and distinct appearance but also change with age. They were distributed in the whole small intestine and there were four distinct types of Peyer's patches: nodular, faviform, cup-shaped, and cystic form Peyer's patches. However, the nodular and cystic form Peyer’s patches are specific to Bactrian camel, which have not been found in other animals including Dromedary camel. In addition, the distribution density of Peyer's patches in ileum was the maximum, then was jejunum and duodenum. Further statistical analysis showed that the number of Peyer's patches was altered with age. The number peaked in 5-year-old camels and declined subsequently with age. However, there was little change in the size of Peyer's patches in different age groups; no age-related macroscopic variations in the shape or size of the Peyer's patches were found. Results obtained from this study provide the basic information to further study on the gastrointestinal mucosal immunity of Bactrian camel.     

The prevalence of Middle East respiratory syndrome coronavirus (MERS‐CoV) antibodies in dromedary camels in Israel

Middle East respiratory syndrome coronavirus, MERS‐CoV, was identified in Saudi Arabia in 2012, and as of January 29, 2018, there were 2,123 laboratory‐confirmed MERS‐CoV cases reported to WHO (WHO, 2018, https://www.who.int/emergencies/mers-cov/en/ ). Multiple studies suggest that dromedary camels are a source for human MERS‐CoV infection. MERS‐CoV‐specific antibodies have been detected in the serum of dromedary camels across Northern Africa and across the Arabian Peninsula. Israel's geographic location places Israel at risk for MERS‐CoV infection. To date, MERS‐CoV‐related illness has not been reported and the burden of MERS‐CoV infection in the Israeli population is unknown. The seroprevalence of MERS‐CoV‐specific antibodies in Israeli dromedary camels is unknown. The objective of this study was to determine the prevalence of MERS‐CoV seropositivity in dromedary camels in Israel. The prevalence of MERS‐CoV antibodies in Israeli camels was examined in 71 camel sera collected from four farms across Israel by MERS‐CoV‐specific microneutralization (Mnt) assay and confirmed by MERS‐CoV‐specific immunofluorescence assay (IFA). Although this study cannot rule out potential antibody cross‐reactivity by IFA, the presence of bovine coronavirus‐specific antibodies do not appear to impact detection of MERS‐CoV antibodies by Mnt. MERS‐CoV neutralizing antibodies were detectable in 51 (71.8%) camel sera, and no association was observed between the presence of neutralizing antibodies and camel age or gender. These findings extend the known range of MERS‐CoV circulation in Middle Eastern camels. The high rate of MERS‐CoV‐specific antibody seropositivity in dromedary camels in the absence of any reported human MERS cases suggests that there is still much to be learned about the dynamics of camel‐to‐human transmission of MERS‐CoV.     

Copper status in breeding and racing camels (<Emphasis Type="Italic">Camelus dromedarius</Emphasis>) and response to cupric oxide needle capsules

Copper was determined in the blood of breeding camels, camel calves and racing camels to evaluate copper status in these animals in UAE. Low blood copper concentrations were reported in newly born camel calves (100%) and calves 2–4 months old (68%), breeding camels at early (55.6%) and at mid lactation (48%) and at late pregnancy (69%). This is attributed to the low copper and high sulfate in the Rhodes grass which is the only diet offered to the breeding camels. On the other hand only 9.7% of racing camels showed low copper levels. This is because copper is routinely offered to racing camels when their blood copper is low. Cupric oxide needle capsules orally administered at the rate of 8 g per adult camel was effective in elevating blood copper from 7.083 μmol/L at day zero to 10.074 μmol/L at day 28 after dosing.     

Spatial association between primary Middle East respiratory syndrome coronavirus infection and exposure to dromedary camels in Saudi Arabia

Middle East respiratory syndrome coronavirus (MERS‐CoV) is an emerging zoonotic disease. Exposure to dromedary camels (Camelus dromedaries) has been consistently considered the main source of primary human infection. Although Saudi Arabia reports the highest rate of human MERS‐CoV infection and has one of the largest populations of dromedary camels worldwide, their spatial association has not yet been investigated. Thus, this study aimed to examine the correlation between the spatial distribution of primary MERS‐CoV cases with or without a history of camel exposure reported between 2012 and 2019 and dromedary camels at the provincial level in Saudi Arabia. In most provinces, a high proportion of older men develop infections after exposure to camels. Primary human infections during spring and winter were highest in provinces characterized by seasonal breeding and calving, increased camel mobilization and camel–human interactions. A strong and significant association was found between the total number of dromedary camels and the numbers of primary camel‐exposed and non‐exposed MERS‐CoV cases. Furthermore, spatial correlations between MERS‐CoV cases and camel sex, age and dairy status were significant. Via a cluster analysis, we identified Riyadh, Makkah and Eastern provinces as having the most primary MERS‐CoV cases and the highest number of camels. Transmission of MERS‐CoV from camels to humans occurs in most primary cases, but there is still a high proportion of primary infections with an ambiguous link to camels. The results from this study include significant correlations between primary MERS‐CoV cases and camel populations in all provinces, regardless of camel exposure history. This supports the hypothesis of the role of an asymptomatic human carrier or, less likely, an unknown animal host that has direct contact with both infected camels and humans. In this study, we performed a preliminary risk assessment of prioritization measures to control the transmission of infection from camels to humans.     

Ultrasonographic and macroscopic anatomy of the enucleated eyes of the buffalo (Bos bubalis) and the one-humped camel (Camelus dromedarius) of different ages

The ultrasonographic appearance and measurements of the normal buffalo and camel eye globes were described in 60 buffaloes (Bos bubalis) aged 1?year (28 eyes) and 10?years (32 eyes), and in 51 humped camels (Camelus dromedarius) aged 1?year (26 eyes) and 10?years (24 eyes). Ocular measurements were recorded by A- and B-scan ultrasonographic examination of 40 buffalo eyes (18 young and 22 adult eyes) and 34 camel eyes (14 young and 20 adult eyes) using a KANGH ultrasound scanner equipped with 10?MHz probe. For gross measurements, 20 buffalo and 16 camel eye globes were frozen and dissected and the same measurements were made using fine callipers macroscopically. The aqueous and vitreous humour of the buffalo and camel eyes appeared anechoic. The cornea, anterior and posterior lens capsule and iris appeared hyperechoic. The ocular measurements for the axial length, vitreous chamber depth (VCD), corneal thickness, lens thickness and scleroretinal rim thickness increase with the advance of age in both buffaloes and camels. Except for the anterior chamber depth, VCD and lens thickness, which were larger in adult camels than in adult buffaloes, no other differences between ocular dimensions were observed in both species. The results of this study are valuable for comparative ocular anatomy and will be useful for ultrasonographic evaluation of ocular diseases in buffaloes and camels.     

Onchocerca fasciata Railliet and Henry, 1910 and its nodule development in camels in Saudi Arabia

A total of 192 male camels of three age groups (young, adult and old) from Saudi Arabia were examined for Onchocerca fasciata infection by detection of microfilariae in skin snips and nodules in the nuchal ligaments and subcutaneous tissues of the neck and shoulder. The overall prevalence rates were 10.9 and 33.3%, respectively. The prevalence rate by the skin snip technique and the number of microfilariae per gram of skin were higher in young and adult camels than in old camels. However, the prevalence rate by the detection of nodules and the number of nodules per infected camel, increased with increase in age of the camels. An increase in size and weight of nodules was reported with an increase in age of the camels. Nodules varied in diameter from 2 to 36 mm and in weight from 0.5 to 5.0 g. The overall percentage of soft viable and calcified nodules was 42.5 and 57.5%, respectively. The viability of worms decreased, but calcification increased with increased age of the camels. Four levels of degeneration and calcification of worms were described following scanning electron microscopy.     

Species of Ticks on Camels and Their Seasonal Population Dynamics in Eastern Ethiopia

A study was conducted to identify the species of ticks found on camels (Camelus dromedarius) and their seasonal population dynamics in Eastern Ethiopia. Collection and identification of the ticks were undertaken at 2-month intervals from December 1997 to August 1999. On each occasion, all the visible adult ticks were collected from one side of the body of each of the same 17 camels. The most abundant species of ticks on the camels were Rhipiephalus pulchellus (85.2%), Hyalomma dromedarii (5.9%), Amblyomma gemma (4.0%) and Amblyomma variegatum (1.8%). The average tick load per camel was higher during rainy months than during dry months. The smallest number of ticks per camel was observed during the driest month (December), whereas the highest was recorded in the wettest month (August). Any strategy intended to mitigate problems of tick infestation of camels in this area should take into account the identified tick species and their season of abundance.     

The histological characteristics of the aggregated lymphoid nodules area in abomasum of Bactrian camels (Camelus bactrianus) of different ages

The aggregated lymphoid nodules area (ALNA) in abomasum of Bactrian camels is a special immune structure discovered only in Bactrian camels in recent years (2003). The anatomy research found that there was a close relationship between degree of development, anatomical characteristics and age. To further establish the relationship between histological characteristics of this special structure and animal age, 24 Alashan Bactrian camels of the following four age groups were studied: young (1-2 years), pubertal (3-5 years), middle-aged (6-16 years) and old (17-20 years). Mucosal-associated lymphoid tissue (MALT) of ALNA in abomasum was particularly observed and analyzed by histology, histochemistry and statistical methods. The results showed that the average number of lymphoid nodules in reticular mucosal folds region of ALNA in abomasum from young group to old group was in order of 26.8, 32.7, 17.6 and 7.8, and in longitudinal mucosal folds region was 20.1, 26.0, 10.3 and 5.1. The number of lymphoid nodules in the four experimental groups first increased and then decreased with increasing age (P<0.01). In young and pubertal camels lymphoid nodules were distributed evenly on both sides of the axis of mucosal folds and mostly displayed round, oval or wedge shape. The number of lymphoid nodules, follicle-associated epithelium (FAE), reticular fibers and plasmocytes in mucosal folds gradually increased from 1 to 2 years and peaked at puberty. There were up to 37 visible lymphoid nodules in a mucosal fold. However, ALNA of middle-aged and old camels gradually degenerated as aging. Lymphoid nodules were unevenly distributed on both sides of the axis of mucosal folds, which mostly displayed oval or irregular shape. Lymphoid tissue in old camels mostly existed as diffuse form. Although germinal centers of the lymphoid nodules were still obvious, the number of reticular fiber and plasmocyte and lymphoid nodules gradually decreased. The results indicated that in accord with the anatomical results, there was a close relationship between histology characteristics of lymphoid tissue of ALNA in abomasum and animal age. In summary, the lymphoid tissue of ALNA in abomasums gradually increased from young to pubertal groups with increasing age, peaked in 3-5 year-old camels, and subsequently declined with age and when 17-20 years old this immunity structure had severely atrophied.     

Serum protein electrophoretic pattern in young and adult camels

OBJECTIVE: To compare the electrophoretic pattern of serum proteins in clinically healthy adult camels (between 3 and 8 years of age) and camel calves (less than 3 months of age). DESIGN: Laboratory analysis of serum from healthy camels. PROCEDURE: Blood was collected from 30 healthy adult camels and 30 camel calves and the serum separated. Total protein of each serum sample was estimated by automated chemistry analyser. The proteins were fractionated by automated electrophoresis on agarose gel. RESULTS: Serum proteins migrated on the agarose gel as one albumin, two alpha (alpha1 and alpha2-globulins), two beta (beta1 and beta2-globulins) and one gamma-globulin fractions. In adult camels the mean concentration of total protein, albumin alpha1, alpha2, beta1, beta2 and gamma-globulins was 56.8 +/- 1.5, 30.7 +/- 0.8, 2.4 +/- 0.1, 3.2 +/- 0.1, 9.7 +/- 0.3, 3.4 +/- 0.2 and 8.6 +/- 0.3 g/L, respectively. These values in calves were 49.7 +/- 1.8, 23.7 +/- 0.8, 3.2 +/- 0.2, 3.1 +/- 0.2, 14.2 +/- 0.2, 4.0 +/- 0.2 and 4.1 +/- 0.2 g/L, respectively. CONCLUSION: The concentration of total proteins, albumin and gamma-globulins was higher (P < 0.05) in the adult camels than in camel calves. The concentrations of beta1 globulins was higher (P < 0.05) in calves as compared to adult camels.     

Pathology and molecular diagnosis of paratuberculosis of camels

Camels are the prime source of meat and milk in many desert regions of the world including Saudi Arabia. Paratuberculosis of camels, locally called Silag, is a serious and invariably fatal disease in the Arabian camel. Six camels were used in this study. Five camels with clinical paratuberculosis were used to study the pathology of the disease and confirm its aetiology. The sixth camel was clinically healthy and used as a control. The camels were examined clinically and bled for haematological and blood chemistry analysis. They were then humanely killed with a high intravenous dose of thiopental sodium (10 mg/kg) for pathological studies as well as obtaining tissues for microbiological and molecular studies. The clinical signs of the disease were emaciation, diarrhoea, alopecia, wry neck and pale mucous membranes. Laboratory diagnosis showed reduced haemoglobin concentration, low haematocrit and high activity of the serum enzyme alanine aminotransferase. Serum creatinine concentration was normal. These results indicated the infected camels were anaemic and the function of their livers was affected. Postmortem examination showed thickened and corrugated intestinal mucosa, enlarged granulomatous mesenteric lymph nodes, miliary and diffuse granulomas in the liver (in four camels), generalized lymph node granulomas (in one camel), splenic granuloma (in one camel) and mediastinal lymph node granuloma (in two camels). Histopathological examination showed diffuse infiltration of macrophages in all organs showing lesions. Ziehl–Neelsen staining of tissue scraping and tissue sections showed masses of acid fast bacilli, except for the spleen. Infection with Mycobacterium avium subsp. paratuberculosis was confirmed by PCR by targeting the IS900 gene.     

基于瘤胃转录组探究双峰驼沙漠适应性分子机制

旨在比较胚胎期和成年期双峰驼瘤胃在组织形态、编码基因表达上的变化,挖掘影响双峰驼瘤胃发育的关键基因和通路,从消化系统探究双峰驼的沙漠适应性机制。本研究选取3峰10~12岁健康状况良好的成年期阿拉善双峰驼,以及3峰9~10月龄健康状况良好的胚胎期阿拉善双峰驼,采集瘤胃组织样品,制作石蜡组织切片,观察成年期与胚胎期双峰驼瘤胃,比较其组织结构之间的差异。分别提取成年期和胚胎期双峰驼的瘤胃组织总RNA,利用Illumination Hiseq 2000测序平台分别进行转录组测序,对转录组数据进行质控、比对、差异基因筛选、GO、KEGG富集分析。随机选择6个差异表达基因进行荧光定量试验,关联转录组数据与荧光定量试验的表达趋势。结果表明,胚胎期瘤胃组织中上皮细胞和肌纤维细胞清晰可见,分布密集,在成年期的瘤胃组织中,可见明显的肌纤维,肌纤维直径较宽,肌纤维间的空隙较大。转录组测序结果显示,每个样本获得至少10G的数据量,各样本的质控率都在90%以上,Q30数据都在88%以上。对测序数据进行分析,以胚胎期为对照组,成年期为试验组,筛选到1 207个差异表达基因,其中上调基因456个,下调基因751个;对差异表达基因进行层次聚类分析,结果显示,成年期的3个个体（M1、M2、M3）表达模式接近,胚胎期的3个个体（T1、T2、T3）表达模式接近。对差异表达基因进行GO和KEGG富集分析,结果显示,上调差异表达基因显著富集到62条显著的GO条目,下调差异表达基因显著富集到366条显著的GO条目,73条显著的KEGG通路。差异表达基因主要富集在代谢过程的负调控、RNA生物合成过程的负调控、基因表达的负调控等GO条目中,KEGG主要富集到MAPK信号通路、PI3K-Akt信号通路、糖尿病并发症中的AGE-RAGE信号、胰岛素信号通路、醛固酮的合成与分泌等通路中。同时筛选到MAPK12、MAPK13、FABP5、PPARγ、CaMK1等与双峰驼沙漠适应性相关的基因。荧光定量结果显示,差异基因在成年期和胚胎期瘤胃组织中的表达模式与RNA-Seq的结果一致。上述结果表明,双峰驼的瘤胃组织可能与脂肪细胞分化有关。在沙漠环境中,双峰驼可能降低瘤胃组织代谢效率、通过胰岛素抵抗作用提高血糖耐受性以及促进醛固酮的合成与分泌以调节血压平衡,以更好地在沙漠干燥缺水的环境中生存。     

Pathogenesis of mouse scrapie: distribution of agent in the pulp and stroma of infected spleens

Fourteen spleens were collected from mice infected with the 139A strain of scrapie, at a time when the concentration of agent in spleen was at a plateau. Scrapie infectivity was present in both the pulp and stromal fractions, but the concentration in stroma was about 10 times greater than that in pulp. On average, 1000 pulp cells were required to give 1 LD50 unit of scrapie infectivity. Linear regression analysis of data from 64 mouse spleens showed that the total infectivity correlated with tissue weight (P less than 0.001). The titres of the 14 stromal fractions were significantly correlated with whole spleen weight (P less than 0.02) and with the weight of stroma (P less than 0.02), but not with pulp weight. Hence, the titres in the isolated stroma probably reflect those of the stroma in vivo. In contrast, there was no correlation between total pulp titre and spleen weight, pulp weight or pulp cell number. Moreover, gentle washing of pulp cells removed about 80% of the total infectivity. This suggests that much of the pulp titre is adventitiously associated with cells and is in fact agent released from damaged stroma.     

Prevalence of Linguatula serrata nymphs in one-humped camel (Camelus dromedarius) in Najaf-Abad, Iran

The prevalence of Linguatula serrata nymphs in livers and mesenteric lymph nodes (MLNs) of 400 camels of different sex and age groups was investigated. The lymph nodes and livers were examined macroscopically. A digestion method was also applied for investigation of liver samples. The MLNs in 84 camels out of 400 (21.0%) and the livers of 18 camels out of 400 (4.5%) were infected by L. serrata nymphs. The infection rate increased with age (p<0.01). No significant difference was observed between the prevalence in males and females (p>0.1). It is concluded that consumption of raw or under-cooked camel liver may result in nasopharyngeal linguatulosis in humans.     

Reactions of peripheral blood mononuclear cells (PBMC) of camels with monoclonal antibodies against ruminant leukocytes

The particular immune system of the camel has been but little investigated. In this work circulating camel peripheral blood mononuclear cells (PBMC) were studied by flow cytometry. Monoclonal antibodies (mAbs) raised against ruminant leukocytes were used for the detection of cell surface antigens. Monoclonals to T-cell markers, CD4 (CACT138A) and CD8 (CACT80C), exhibited no reactivity towards camel PBMC in contrast to their reactivity to PBMC of other ruminant species and those of cattle in particular. A relatively high percentage (29.1+/-8.9%) of camel PBMC reacted with a non-immunoglobulin cell surface marker, B-B2, comparable to the reactivity of bovine PBMC. The B-B7 cell marker revealed 22.4+/-10.0% of reactive camel PBMC while the CD45 leukocyte common antigen was identified only on 19.4+/-3.1% of camel PBMC as compared to 74.7+/-4.9% for bovine PBMC. IgM (PIg45A) was detected on 9.1+/-1.4% of camel PBMC and on 46.6+/-19.5% of the bovine PBMC. Double fluorescent labeling with two B-cell markers and an anti-ruminant lambda light-chain mAb revealed 7-9% of cells bearing both B and lambda L-chain markers. Light chain reactivity was also assessed using an anti-goat F(ab')(2) antiserum. The values obtained, 14.3+/-5.8% for the camel and 47.8+/-2.7% for the cattle, are close to the values observed for surface IgM. These data suggest that camels, like other ruminants, possess L-chain bearing cells of the B-cell lineage. However, in the camel, Igs are different in that in addition to regular four chain Igs, about 65% of them possess two heavy chain Igs devoid of light chains. Because different sets of V(H) gene segments are used by four and two chain Igs, it is possible that there might be two lineages of B-cells each secreting a different form of antibodies.     

Experimental camelpox infection in vaccinated and unvaccinated dromedaries

Four dromedaries were infected with a virulent camelpox virus strain which was isolated from the lung of a Saudi Arabian camel. The camels which were infected intradermally and subcutaneously developed severe generalized camelpox. One of these camels had to be euthanized on humane grounds and the second one died 13 days after being infected. This dromedary also developed internal pox. Neither dromedary showed camelpox antibodies before infection. The other two camels which had been vaccinated with Ducapox 6 years prior to the viral challenge did not develop any clinical symptoms when given 5 ml of the field virus intravenously and intramuscularly. They seroconverted after the challenge. Although only two camels were used for this trial, the results indicate that a single dose of Ducapox can protect 1-year-old camels from camelpox infection for several years.     

Involvement of spleen components of mature fowl in the primary and secondary humoral antibody response following experimental EDS'76 virus infection

Summary

Cellular changes in spleens of mature fowl in relation to both the primary and secondary humoral antibody response following experimentalEDS'76 virus infection were studied. The influence of splenectomy on humoral antibody response was also examined.

Experimental fowl had been naturally infected with fowl adenovirus (FAV) but did not possess precipitins to these viruses at the time of EDS’ 76 virus infection. Since EDS'76 infection provokes a recall of the group antibody to FAV, this infection simultaneously induces a primary response against EDS’ 76 virus and a secondary response due to the recall of the group antibody to FAV.

HI and precipitating antibodies toEDS'76 virus (primary response) werefirst detected at 6 and 8 days p.i. respectively. Curves of HI, precipating and neutralising antibody titres were biphasic; the first peak (IgM peak) occurred at 10–11 days p.i., the second (IgG peak) at 16–28 days p.i.

Precipitating antibodies to FAV (secondary response) were demonstrated from 4 days p.i. The curve of these antibody titres was also biphasic, with peaks at the same times as in the primary response.

Based on HI and AGP testing of primary and secondary immune response in both splenectomised and non‐splenectomised fowl it is concluded that in the primary response the spleen of the adult fowl is involved significantly in only IgM secretion, while in the secondary response it is likely that bothIgM and IgG are secreted in considerable amounts.

Clusters of lymphoblasts and plasmablasts were observed at 3 days p.i. in the red pulp. It is very likely that antigen‐antibody complexes are formed from that time and circulate bound to the surface of lymphocytes. These antigen‐loaded lymphocytes are ‘picked up’ from the blood stream by

– red pulp macrophages, leading to enhanced formation of lymphoblasts in the red pulp. Great numbers of these cells (which are very probably IgM secreting cells) were present on days 6 and 7 p.i., but were no longer detectable after day 10 p.i.

– macrophages of the macrophagalellipsoidal corona (MEC), leading to significant enlargement of the periellipsoidal lymphoid tissue(PELT) by an increase of the number of lymphocytes observedfrom days 4–12 p.i. The MEC was significantly enlarged from 7–12 days p.i., very likely due to an increased number of macrophages.

Following deposition of antigen in the white pulp, formation of follicles begins. The number of small, intact follicles includingfollicle precursors increasedfrom 6 days p.i. From 15 days p.i. to the end of the experiment both the number and size of follicles increased significantly.

Uptake and processing of antigen by macrophages is probably accompanied by death of some of these cells. This might explain the degenerative changes observed in large mesenchymal cells, probably macrophages, at 3 and 5 days p.i. in the red pulp and at 5 and 6 days especially in the MEC. Splenitis which was present at 3 and 5 days p.i. and oedema observed in and around ellipsoidal cells at 5 days p.i. may be due to mediators released from these degenerative macrophages.

A significantly increased number of follicles with lymphoblasts was seen from 2–15 days p.i. while lymphoblasts and plasmablasts were present in the PELT from 5–15 days p.i., but predominantly at 6 and 7 days p.i. It is likely that disruption of follicles and blast transformation of white pulp lymphoid cells are secondary response events. White pulp lymphoblastsand plasmablastsare probably IgG secreting cells.

Splenomegaly was observed at 3, 5 and 6 days after infection and was mainly due to swelling of red pulp macrophages and infiltration of granulocytes in the red pulp. Ellipsoidal and periellipsoidal changes could contribute to the splenomegaly at 5 and 6 days p.i.     

Mastitis in lactating camels (Camelus dromedarius) in Afar Region, north-eastern Ethiopia.

Quarter milk samples (n = 543) from 152 traditionally managed lactating camels (Camelus dromedarius) in Afar Region, north-eastern Ethiopia were examined to determine the prevalence of camel mastitis and identify its bacterial causes. Out of 152 camels examined, 19 (12.5%) were diagnosed as clinical mastitis cases based on clinical signs and bacteriological examinations. Of the 257 California Mastitis Test (CMT) positive quarter milk samples 162 (63.0%) yielded pathogenic bacteria. A positive correlation was observed between CMT positive results and presence of major pathogens in camel milk samples. The main mastitis pathogens isolated were Staphylococcus aureus, coagulase-negative staphylococci, Streptococcus agalactiae, S. dysgalactiae, and other species of streptococci, Pasteurella haemolytica and E. coli. Results of the present study suggest that mastitis in Afar camels is prevalent, Gram-positive cocci are the major isolates from camel milk samples and the CMT can be used as a screening test for the detection of mastitis in camels.