Histopathological and histoenzymatic studies on experimental Taenia saginata cysticercosis

In young Taenia saginata cysticerci the reactions for alkaline phosphatase (AlPh), acid phosphatase (AcPh), ATP-ases, succinic dehydrogenase (SDH) and lacto dehydrogenase (LDH) were mild. The reactions were concentrated in the walls of spiral canals (AlPh, SDH) and in the outer layer of the bladder (AlPh). The reactions were more intensive in older cysticerci. In these, the reaction of AlPh marked a network of blood vessels winding around the larva. In dying cysticerci the reactions for oxidative enzymes (SDH, LDH) were weaker but the activity of the hydrolytic enzymes (AlPh, AcPh) was increased. These findings suggest that histoenzymatic reactions may be helpful in determining the viability and the age of cysticerci. T. saginata cysticerci in sheep and goats provoked an early and intensive cellular reaction. The histopathological appearance of the cysticerci as they were destroyed in the abnormal hosts was similar to that of cysticerci localized in abnormal tissue of the natural host (e.g., lung of calves). Treatment with mebendazole caused an intensive infiltrative reaction against dying cysticerci and a degenerative process in the surrounding muscle tissue. The treatment with praziquantel provoked a weak infiltration around dead cysticerci and did not affect the muscle tissue. In both cases the remnants of T. saginata cysticerci disappeared very slowly.     

An outbreak of cysticercosis in feedlot cattle

An outbreak of cysticercosis (infestation with the larvae of Taenia saginata) occurred in feedlot cattle in Ontario in 1986. Two hundred and thirty-three of 271 steers were confirmed histologically to be positive for cysticerci. Nineteen (8.2%) animals had viable cysticerci, 87 (37.3%) had degenerated cysticerci, 77 (33.0%) had mineralized cysticerci, and 50 (21.5%) steers had lymphoid granulomas consistent with cysticercosis. Three viable cysticerci were partly evaginated and one degenerate cysticercus was fully evaginated.     

Taenia solium porcine cysticercosis: viability of cysticerci and persistency of antibodies and cysticercal antigens after treatment with oxfendazole

The aim of this study was to assess the effect of treating Taenia solium infected pigs with oxfendazole (OFZ) on viability and clearance of cysticerci and the corresponding persistence of specific antibody isotypes (IgG(total), IgG1, IgG2 and IgA) and circulating cysticercal antigen (CCA). Antibody isotypes and CCA responses were measured by antibody-ELISA (Ab-ELISA) and antigen ELISA (Ag-ELISA), respectively. Correlations were made between antibodies, CCA and the total number of cysticerci enumerated at necropsy. Forty pigs with cysticercosis were randomly allocated into two groups: Treatment group (n=20) was treated with OFZ at 30 mg/kg orally while the treatment control group (n=20) was not treated. Five uninfected pigs served as negative controls. Pigs were killed at 1, 4, 8 and 26 weeks post-treatment (wkpt). Overall, the mean total cyst count in treated pigs was 2904+/-5397 (mean+/-S.D.) while in the controls it was 6235+/-6705. Mean cyst viability was 5+/-11% (mean+/-S.D.) and 97+/-4% in treated and control pigs, respectively. Results showed that OFZ killed muscular cysticerci over a period of 4 weeks but failed to kill cerebral cysticerci. Antibodies, CCA responses and clearance of dead cysts from the meat, depended on the cyst intensity of individual pigs at time of treatment since both antibody and CCA correlated with intensity of cysticerci at necropsy (r=0.441, P=0.005; r=0.654, P<0.001), respectively. IgG1 responses were the best indicator of treatment efficacy because they were predominant in both infected treated and control pigs and disappeared early after treatment. Both Ab/Ag-ELISA failed to detect cysts in the brain. Though dead cysticerci took some time (26 wkpt) to clear from the meat, treatment of porcine cysticercosis with OFZ should, in combination with other intervention measures be considered as an important, cost-effective measure in the control of taeniosis/cysticercosis.     

Freezing times and temperatures required to kill cysticerci of Taenia saginata in beef

Calves were given viable Taenia saginata eggs by stomach tube and slaughtered 12, 16 or 24 weeks later. The cysticerci-infected carcasses were frozen at six different temperatures for variable lenghts of time. Meat samples were then allowed to thaw at room temperature and the cysticerci were manually isolated. Criteria of viablity of the metacestodes were scolex evagination and peristaltic movements of the bladder wall. Sixteen and especially 12-week-old cysticerci were much more susceptible to the lethal effects of freezing than were 24-week-old cysticerci. The time and temperature combinations required to ensure death of all cysticerci were 360 h at ?5°C, 216 h at ?10°C, and 144 h at ?15°C or lower.     

猪囊虫病基因工程疫苗用于免疫治疗的研究

应用猪囊虫病基因工程疫苗分别对实验性猪囊虫病和自然感染的猪囊虫病进行了分组治疗,以探讨该疫苗的免疫治疗作用。１０头人工复制的囊虫病猪,随机分成３组。第１组４头猪,于感染于１个月注射该疫苗,连续３次,间隔１５天;第２组４头猪,于感染后２个月注射疫苗,同上连续３次;第３组２头猪,不注苗。第１组注射疫苗后１个月循环抗原滴度开始降低,２．０、２．５及３．５个月各有１头猪ＣＡ转阴,５个月ＯＤ值分别为０．１４、０．０９、０．１７、０．３８。第２组和第３组各猪血清ＯＤ值一直维持在１．０以上。感染后５个月剖检,第１组４头猪均未检出囊虫;第２组４头猪在咬肌、膈肌、腰肌、股内侧肌、肩胛外侧肌等部位均检测到囊虫,检测部位４０ｃｍ＾２面积发现囊虫３～７个,有部分虫体已钙化,胆汁卵化率为１５．４％;第３组各猪也在各检测部位检测到囊虫,４     

The effect of corticosteroids on the cysticerci of Taenia ovis in sheep.

The effect of two synthetic corticosteroids on the cysticerci of Taenia ovis in sheep has been investigated. Dexamethasone given from four days before infection had no effect on the number of cysticerci recovered but did enhance their survival. When betamethasone was used there was an increase in the number of cysts compared with controls. Corticosteroids given for 12 days after infection did not increase the number of viable cysticerci recovered at autopsy three months later but when treatment was continued until the time of autopsy, a very high proportion of cysticerci were viable.     

Effects of nitroscanate on adult Taenia pisiformis in dogs with experimentally induced infections.

Twenty-four specific-pathogen-free Beagles were each given 50 cysticerci of Taenia pisiformis that had been harvested from experimentally infected rabbits. Quantitative fecal egg counts and fecal screening for recovery of passed segments were performed on postinoculation days 56 through 70. Twenty-three of 24 dogs fed cysticerci developed patent infections. The 23 dogs with patent infections were assigned to 1 of 2 groups and treated with nitroscanate or a placebo 60 days after inoculation. Egg counts in the treated dogs had markedly decreased by the second day after treatment, and by the sixth day after treatment, segments were not found in the feces of any of the treated animals. The control dogs continued to pass eggs and segments in their feces throughout the 9 days after treatment. The dogs were euthanatized and necropsied 70 days after being inoculated. At necropsy, the mean number of scolices recovered from control dogs was 24.6, the mean number of scolices recovered from treated dogs was 0.25. Worms recovered from the control dogs were intact, gravid cestodes. Efficacy of treatment with nitroscanate at a mean dosage of 56 mg/kg of body weight was 98.9%.     

Limits of the therapeutic properties of synthetic S3Pvac anti-cysticercosis vaccine

The S3Pvac synthetic vaccine, composed of three peptides (GK1, KETc1 and KETc12) effectively protects against cysticercosis under experimental and field conditions. Additionally, S3Pvac vaccine can effectively damage early-established cysticerci in experimentally lightly infected young pigs. This study was designed to explore if also fully-developed cysticerci that eluded immunity induced by the infection can be damaged by S3Pvac-induced immunity in naturally, heavily infected adult pigs. Fourteen pigs identified as cysticercotic by tongue inspection from rural communities were purchased and moved to controlled conditions in the Faculty of Veterinary Medicine. Half of these pigs were treated once a month three times with S3Pvac plus saponin, and the other half received only saponin (controls). Twelve months later pigs were euthanized, and the number of cysticerci, their macro and microscopic status and their capacity to transform into tapeworms were determined. S3Pvac failed to damage fully-developed muscle cysticerci of naturally, heavily infected adult pigs. To explore possible factors involved in the failure of the therapeutic capacity pooled sera from control and treated cysticercotic pigs were added to mice mononuclear peripheral cells. Pooled sera from non-infected pigs were also tested. Sera from control and treated infected pigs almost completely suppressed the T cell proliferative responses, pointing to the presence of suppressor factors. In conclusion, S3Pvac vaccine failed to damage fully-developed cysticerci in pigs in which a host parasite relationship had evolved after months of infection with immunological implications.     

Serodiagnosis of bovine cysticercosis by detecting live Taenia saginata cysts using a monoclonal antibody-based antigen-ELISA

An ante mortem antigen-ELISA-based diagnosis of Taenia saginata cysticercosis was studied in artificially (n = 24) and naturally (n = 25) infected cattle with the objective of further validating the assay as a field diagnostic test. Based on total dissection as the definitive method of validity, the assay minimally detected 14 live cysticerci in artificially infected calves and 2 in naturally infected steers. In natural infections, the minimum number of live cysticerci consistently detected by Ag-ELISA was 5 while in artificial infections it was above 14. However, other animals with 12 and 17 live cysticerci in artificially infected calves, and 1 and 2 live cysticerci in naturally infected steers, escaped detection for unknown reasons. Animals harbouring dead cysticerci gave negative reactions in the assay as was the case in non-infected experimental control calves. There was a statistically significant positive linear correlation between Ag-ELISA optical density values and burdens of live cysticerci as obtained by total dissection of both artificially infected calves (r = 0.798, n = 24; P < 0.05) and naturally infected steers (r = 0.631, n = 25; P < 0.05). These results clearly show the potential effectiveness of ante mortem monoclonal antibody-based antigen detection ELISA in the diagnosis of bovine cysticercosis in cattle. Its value lies in the diagnosis of infection in cattle as a screening test in a herd, rather than as a diagnostic test at the individual level, due to false positive and negative reactions. In a herd of heavily infected cattle, the assay may, however, provide for individual diagnosis. Nevertheless, more work is recommended to increase its sensitivity so as to be able to diagnose light infections consistently in the field.     

Generalized Taenia crassiceps cysticercosis in a chinchilla (Chinchilla lanigera)

Taenia crassiceps is a cestode parasite that uses carnivores as definitive hosts and rodents and rabbits as main intermediate hosts, but other animal species and humans may also get infected. One adult male chinchilla (Chinchilla lanigera) from an animal shelter in Switzerland presented widespread subcutaneous fluctuant swellings extended over the forehead, nose, face and thoracic regions with a progressive growth over 3 months. The thoracic swelling was surgically resected, and it consisted of numerous 3–4 mm small transparent vesicles, mainly confined to the subcutaneous tissue, which were morphologically identified as cysticerci of T. crassiceps. The diagnosis was confirmed by PCR and DNA sequence analysis of fragments of the mitochondrial small subunit rRNA and NADH dehydrogenase subunit 1 genes. After 1.5 months, due to enlargement of the swollen areas and deterioration of the general health condition, the chinchilla was euthanized and a necropsy was performed. Thousands of small cysticerci were observed widespread in the subcutis, involving underlying musculature of the whole body, in the thoracic cavity, larynx, pharynx and in the retropharyngeal region. Additionally, three larger metacestodes were detected in the liver and morphologically and molecularly identified as Taenia taeniaeformis strobilocerci. The present case represents an indicator of the environmental contamination with Taenia eggs, highlighting the risk of infection for susceptible animals and humans. Besides the clinical relevance for pets, T. crassiceps is a zoonotic parasite and can be also cause of severe cysticercosis in humans.     

Preferential infection sites of Cysticercus bovis in cattle experimentally infected with Taenia saginata eggs

The preferential sites of infection of Cysticercus bovis were evaluated in the skeletal muscle and entrails of 25 cattle that were experimentally infected with Taenia saginata (2 × 10⁴ eggs). Two other animals were not inoculated (control). Ninety days after inoculation, all the cattle were euthanized. The carcasses were deboned and dissected into 26 anatomical sections (masseter muscles, brain, tongue, esophagus, heart, diaphragm, lungs, liver, kidneys, spleen, top sirloin butt, bottom sirloin butt, outside round, top (inside) round, transversus abdominus, top sirloin cap, strip loin, full tenderloin, eye of round, knuckle, shoulder clod, foreshank, shank, chuck, back ribs, and tail muscles). The dissected tissues were sliced into 5 mm sections. From the 25 cattle, 9258 C. bovis (cysticerci) were recovered; 75.02% (6946) of these were recovered from skeletal muscles and 24.98% (2312) from the entrails. A high parasitism level was found in the shoulder clod (12.55%), heart (11.02%), liver (9.48%), masseter muscles (8.51%), chuck (8.25%), strip loin and full tenderloin (7.26%), knuckle (6.63%), and back ribs (5.53%), totaling 69.23% (5738) of all of the detected cysticerci. On the other hand, there was a low C. bovis parasitism level in the brain, spleen, tail muscles, kidneys, esophagus, and diaphragm, representing just 3.9% of the total number of cysticerci. Given these results, we conclude that specific skeletal musculature regions, such as the shoulder blade, chuck, strip loin and full tenderloin, knuckle, back ribs and top round, which are not officially examined in many countries, are effective sites to efficiently screen C. bovis infection. To date, these regions have not been considered as preferential sites of C. bovis infection. Based on our work, however, these regions deserve greater attention from health inspectors because they contained a greater number of Cysticercus than the other regions of carcasses that are parasitized by T. saginata larvae.     

In vivo cross-reactivity of Taenia saginata and Taenia crassiceps antigens in bovine cysticercosis

Steers sensitized or infected with Taenia saginata exhibited similar delayed-type dermal hypersensitivity (DTH) responses after intradermal inoculation with T. saginata or T. crassiceps skin test antigens. Steers sensitized to T. crassiceps cysticerci exhibited similar DTH responses to intradermal inoculation with T. crassiceps, T. saginata whole worm and T. saginata cysticerci antigens. No correlation existed between the DTH responses and the number of cysticerci in the carcasses. One sensitized/infected and one infected steer harbored cysticerci but exhibited no DTH responses. Infection with cysticerci did not elevate DTH responsiveness in sensitized animals.     

Cerebral cysticercosis in pigs studied by computed tomography and necropsy

An original technique for computed tomography (CT) of the pig's brain is described. Brains of 11 cysticercotic pigs were studied by CT and by macroscopic and microscopic examination after necropsy, in order to compare the tomographic images with the anatomic findings. By CT, cysticerci could be seen in all the brains except one which had only one parasite. Good correlation was found when the CT sections were compared with the anatomic slices, nevertheless not all cysticerci seen during necropsy examination could be identified in the CT images. Only two parasites were found in the ventricles. There were difficulties in differentiating submeningeal and parenchymal localization of the cysticerci. Most cysticerci had similar morphologic appearance; inflammatory reactions of different degrees and characteristics were observed around some of them.     

Immunizing potential of various stages of Taenia ovis eggs injected subcutaneously into neonatal or sixteen-week-old lambs

When viable eggs of Taenia ovis were given orally to 1-week-old lambs, infection occurred only in those lambs that had been deprived of colostrum. When viable eggs were injected subcutaneously into 1-week-old lambs, no larvae developed at the injection site, and no resistance was stimulated against an oral challenge of T. ovis eggs given 11 weeks later. However, when eggs, oncospheres or developing cysticerci were subcutaneously injected into 16-week-old lambs, all grew at the injection site and stimulated a high degree of immunity to oral infection. Colostrum-derived antibodies against T. ovis apparently suppressed the immunizing potential of T. ovis eggs injected subcutaneously into neonatal lambs.     

Host--parasite relationship in cysticercosis: immunologic study in different compartments of the host

Cysticerci parasitize several mammalian species, including man, in which the parasitic disease shows unique characteristics since cysticerci are established mainly in immunologically privileged sites and can survive for many years. The study of the human immune response to cysticerci is helpful in diagnosis and could perhaps also aid in preventing or curing the disease. Anti-cysticercus IgG can be detected in serum and cerebrospinal fluid (CSF) of almost all patients with neurocysticercosis, by the enzyme-linked immunosorbent assay (ELISA); antibodies of the other classes are found less frequently. Antibodies react with up to eight Taenia solium cysticercus antigens, mainly with antigen B. This antigen has an affinity for collagen and is not commonly found in the CSF. It could therefore be participating in vasculitic processes spotted in the brain of neurocysticercotic patients. Immunoglobulins are also identified on the surface of the parasites: IgG is detected on parasites obtained from various tissues; IgM, IgA and IgE mostly on extracerebral cysticerci. We discuss the possibility of extraneural cysticerci being destroyed by the immune response of the host whereas natural aging may cause brain cysticerci death.     

The efficacy of mebendazole and praziquantel againstTaenia saginata cysticercosis in cattle

Approximately 50,000Taenia saginata eggs were given orally to bullocks. Ten weeks later, mebendazole or praziquantel was administered in the fodder in single or multiple doses. The animals were slaughtered at intervals after medication when the numbers and viability of cysticerci in various sites were recorded. Single doses of 5 mg/kg mebendazole or 10 mg/kg praziquantel had little effect on the viability of cysticerci. One single dose of 25 mg/kg or 10 daily doses of 5 mg/kg mebendazole had some effect. Praziquantel was completely effective against the viability of cysticerci in either one single dose of 100 mg/kg or 10 daily doses of 10 mg/kg.     

Morphological changes to early stage Taenia solium cysticerci following oxfendazole treatment

The progressive morphological changes to early stage Taenia solium cysticerci following the treatment of pigs with a single therapeutic dose of oxfendazole (30 mg/kg), are described. On Day 1 after treatment, no obvious changes occurred in the general appearance of the larvae but alternations were seen by electron microscope, with an apparent reduction in the number of microtriches, and a complete disappearance of the tegument. Numerous granules were seen to have accumulated in the tegument cells. As treatment progressed, damage to the cysticerci was more serious and, by five days, all cysticerci were seen to be in an advanced stage of degeneration. By 45 days post-treatment, all cysts were calcified. These results suggest that oxfendazole is a highly effective drug against T. solium cysticerci in the early stages of development.     

Oncospheres of Taenia solium develop into cysticerci in normal mice

In vitro-hatched oncospheres of Taenia solium, prepared by the sodium hypochlorite method and adjusted to approximately 5 x 10(2)/2ml phosphate buffer saline, were injected intramuscularly or intravenously into normal Balb/c mice. When these mice were sacrificed 2 months later, all cysticerci were exclusively recovered in the lungs from the mice with intravenous inoculation, but not with intramuscular injection. A high infection rate of 76% was obtained and a total of 45 cysticerci were collected from 50 mice. Thirty-five cysticerci were mature and with normal appearance but the rest were either with abnormal appearance (4) or degenerated (6). These findings give strong evidence that T. solium oncospheres may migrate to the normal mouse lung through venous circulation and develop in this organ.     

HYDATIDOSIS AND CYSTICERCOSIS

The distribution of 12,310 cysts of Taenia ovis in 212 experimentally infected lambs and of 46 cysts in 24 naturally infected 5-year-old sheep, has been analysed. It was determined that irrespective of the number of cysticerci in an infected group of animals, about two-thirds were present in the carcase meat, and the remainder were distributed between the heart, diaphragm and head including the tongue. In lightly infected animals, cysticerci were not necessarily present in any of these sites. In individual animals, the number of cysticerci present in any one or in all three of these sites, did not provide accurate information on the extent of the infection in the carcase meat.     

Clinico-pathological studies in cattle experimentally infected with Taenia saginata eggs

Calves 1-2 months old were experimentally infected with eggs of Taenia saginata and clinical and haematological deviations, development and distribution of cysticerci and pathological changes were recorded. The calves infected with 5,000, 10,000 or 50,000 eggs showed an increase in pulse and respiratory rates. The animals that received 50,000 eggs had significantly increased pulse (p < 0.05) and respiratory rates (p < 0.005). The symptoms were more severe in young, 30-day-old calves infected with 50,000 eggs. Haemoglobin concentration, haematocrit values and red blood cell count decreased, but white blood cell count increased slightly. Lymphocytes and eosinophils also increased up to 88% and 14% (p < 0.05), respectively. Most of the cysticerci were not fully formed 1 month post-infection, but at 2 months the cysts were fully mature and at 4 months, some cysts had degenerated. There was no uniform pattern of distribution of cysticerci in the body of infected calves, but the most commonly affected sites were masseter and heart muscles, followed by diaphragm, tongue and other skeletal muscles. The maximum concentration of 8-14 cysticerci per 10 g of tissue was recorded in masseter muscles and heart. The affected parts revealed tissue reactions that included pressure atrophy, necrosis and fibrosis. Microscopically, the lesions comprised infiltration with lymphocytes, plasma cells, eosinophils and macrophages, fibrosis, necrosis and calcification. The tissue reaction was severe in calves infected with 50,000 eggs. The severity of clinical signs, haematological and pathological changes depended mostly on the age of the animals and dose of infection.