Mavenyengwa_321-332.qxd INTRODUCTION Ruminant amphistomosis is an infection of cattle, sheep, goats and other wild ruminants caused by severe infections of immature amphistomes in the small intestines of immunologically incompetent hosts (Horak 1967; Dutt 1980; Gupta 1993). The disease is characterised by sporadic epidemics of acute parasitic gastroenteritis and loss of produc- tion associated with high mortality and morbidity particularly in young stock (Butler & Yeoman 1962; Boray 1969; Horak 1971; Singh & Lakra 1971; Dutt 1980). 321 Onderstepoort Journal of Veterinary Research, 72:321–332 (2005) A macro- and light microscopical study of the pathology of Calicophoron microbothrium infection in experimentally infected cattle M. MAVENYENGWA1, S. MUKARATIRWA1, M. OBWOLO1 and J. MONRAD2 ABSTRACT MAVENYENGWA, M., MUKARATIRWA, S., OBWOLO, M.J. & MONRAD, J. 2005. A macro- and light microscopical study of the pathology of Calicophoron microbothrium infection in experimentally infected cattle. Onderstepoort Journal of Veterinary Research, 72:321–332 Twelve Tuli weaner steers aged 1 year were randomly subdivided into three groups of four animals and infected with different doses of Calicophoron microbothrium metacercariae. Each animal in Group I received a low dose (LD) of 5 000 metacercariae, Group II a medium dose (MD) of 15 000 metacer- cariae, Group III a high dose (HD) of 25 000 metacercariae and one additional animal was kept as an uninfected control (C). After infection, one animal from each group was slaughtered on Day 28, 42, 56 and 84 post infection (pi) and samples from the ileum, jejunum, duodenum, abomasum and the rumen were collected for histopathological and cytological examination. On Day 28 pi, the gross pathological lesions observed in the duodenum of the LD and the MD ani- mals were similar and comprised duodenal thickening, corrugation, hyperaemia, petechiation and ulceration. In the HD animal the duodenal lesions were similar but more severe. The abomasal folds were severely oedematous in the MD group and nearly occluded the abomasal lumen. Moderate oedema of the abomasal folds was also present in the LD and HD animals. The gross pathological lesions regressed in all the infected groups with increasing age of infection and had disappeared completely by Day 56 pi. On Day 28 pi the histopathological lesions in the duodenum and jejunum of the LD and MD groups were similar, comprising subtotal villous atrophy, hyperplasia of Brunner’s glands and Peyer’s patch- es and moderate infiltration of eosinophils, mast cells and a few globule leukocytes, basophils and lymphocytes in the lamina propria. The HD group had total villous atrophy, severe hyperplasia and cystic dilatation of Brunner’s glands, which had expanded to cover the entire submucosa. On Day 42 pi the histopathological lesions were still present in the MD and the HD groups comprising subto- tal villous atrophy and hyperplasia of Brunner’s glands. Heavy infiltrations of eosinophils, moderate amounts of mast cells and a few basophils, globule leukocytes and lymphocytes were still present in the lamina propria of all three groups. On Day 56 pi, a few glands were still cystic in the MD and the HD groups. Moderate cell infiltrations were still present in the lamina propria of all the three groups and by Day 84 pi complete regeneration had occurred in all animals. Keywords: Calicophoron microbothrium, cattle, pathology, intestinal tract, metacercariae, rumen, Tuli 1 Faculty of Veterinary Science, Paraclinical Veterinary Studies, University of Zimbabwe, Harare, Zimbabwe 2 Danish Centre for Experimental Parasitology, Frederiksberg, Copenhagen, Denmark Accepted for publication 5 July 2005—Editor Infection follows ingestion of herbage heavily con- taminated with amphistome metacercariae (Dutt 1980; Boray 1985). The adult ruminal amphistomes are not associated with clinical disease and have been described as commensals living on ruminal contents of the host (Boray 1985; Cheruiyot & Wa- mae 1988). The amphistome species responsible for the major- ity of outbreaks of immature amphistomosis in rumi- nants and their related snail intermediate hosts have been recorded in many countries (Dinnik & Dinnik 1962; Dinnik 1964; Horak 1971; Dutt 1980; Over 1982; Boray 1985; Eduardo 1982a, 1983, 1988; Sey 1991; Mukaratirwa, Siegismund, Kristensen & Chan- diwana 1996; Mukaratirwa, Kristensen, Siegismund & Chandiwana 1998; Chingwena, Mukaratirwa, Kris- tensen & Chimbari 2002; Madzingira, Mukaratirwa, Pandey & Dorny 2002). In Zimbabwe, amphistome species recovered from domestic and wild ruminants include Calicophoron calicophorum, Calicophoron microbothrium, Calico- phoron clavula, Calicophoron phillerouxi, Calico- phoron sukumum, Calicophoron raja, Paramphisto- mum cervi, Cotylophoron cotylophorum and Cotylo- phoron jacksoni (Eduardo 1982a, 1983, 1988; Jooste 1989; Sey 1991; Madzingira et al. 2002). In southern Africa, including Zimbabwe, C. micro- bothrium, with the snail species Bulinus tropicus as the main intermediate host, has a wide distribution and has been incriminated in the majority of out- breaks of immature amphistomosis in ruminants (Dinnik & Dinnik 1962; Swart & Reinecke 1962a; Dinnik 1964, 1965; Horak 1971; Over 1982; Ching- wena et al. 2002). The clinical and pathological manifestations of am- phistomosis have been studied in both field and experimental infections particularly in sheep and goats (Horak & Clark 1963; Deorani & Katiyar 1967; Horak 1967; Boray 1969; Panda & Misra 1980; Singh, Sahai & Jha 1984; Rolfe, Boray & Collins 1994). Studies in cattle are limited and information on the clinical and pathological manifestations of the disease has been derived mainly from field out- breaks (Butler & Yeoman 1962; Singh & Lakra 1971; Kelly & Henderson 1973) and no experimen- tal infections have been conducted to follow the course of the disease and establish its pathogen- esis. The objective of this study was to describe the path- ology of C. microbothrium in experimentally infected cattle. MATERIALS AND METHODS Study area and selection of experimental animals The study was conducted at Grassland Research Station, a State owned farm in Marondera about 80 km south east of Harare, Zimbabwe. The farm is amphistome-free and mainly raises Tuli cattle for commercial beef production. It is subdivided into paddocks where cattle can graze and have access to clean borehole water provided in troughs. Prior to the commencement of the study, faecal samples were collected from 30 1-year-old Tuli weaner steers for coprological examination using the sedimentation technique and the modified McMaster technique (MAFF 1986) to screen for trematode and nematode infection respectively. Thirteen animals were ran- domly selected for the study from the parasite-free weaner steers, on the basis of age and mass. The animals selected were allowed to graze in pad- docks and had access to clean borehole water pro- vided in concrete troughs and were dewormed every month using 10 % fenbendazole. Identification of C. microbothrium and harvesting of metacercariae Adult B. tropicus naturally infected with C. micro- bothrium were collected from a single natural habi- tat and maintained under laboratory conditions for periodic shedding of metacercariae. The identity of the C. microbothrium metacercariae was confirmed through the infection of a single sheep and recovery of mature amphistomes from the rumen for identifi- cation. The amphistomes were identified as C. microbothrium using the methods described by Eduardo (1982b, 1983) and Gupta (1993). For mass production of metacercariae and to avoid the ingestion of the shed metacercariae by the snails, small nylon gauze bags with an aperture size of 2 mm, each capable of holding 20 snails, were used to confine snails during shedding. The open end of each snail bag was stapled close. Each bag was immersed in individual plastic containers holding 500 ml of dechlorinated pond water and exposed to direct sunlight for 3 h. The cercariae encysted at the water meniscus. Shedding was induced every 2 days whereafter the snails were placed back in the dark aquaria. The metacercariae were stored in individual plastic containers with de- chlorinated pond water added to just below the level of the band of metacercariae. They were kept at a temperature of between 24–25 °C for a minimum of 322 Pathology of Calicophoron microbothrium infection in experimentally infected cattle 6 days before they were harvested with a fine tooth- brush and dosed to the experimental animals. Infection of experimental animals The numbers of metacercariae dosed to cattle in this study were an extrapolation from Rolfe, Boray, Nichols & Collins (1991) and metacercaria viability studies conducted by Swart & Reinecke (1962b), which showed that less than 50 % of metacercariae administered to ruminants survive. Three dosing regimens were therefore designed: each animal in Group I received 5 000 metacercariae and acted as the low dose group (LD), in Group II each animal re- ceived 15 000 metacercariae representing the med- ium dose group (MD) and in Group III each animal received 25 000 metacercariae representing the high dose group (HD). The dose for individual ani- mals was estimated by counting the metacercaria in several aliquots, as described by Rolfe et al. (1994) and was administered by direct inoculation into the rumen using a trocar and canula. One animal remained as an uninfected control (C). The animals were monitored daily for the develop- ment of clinical signs. One animal from Groups I–III was randomly selected, stunned and slaughtered on Day 28, 42, 56 and 84 post infection (pi). The control animal was slaughtered on Day 28 and used as a reference for comparing pathological lesions. Sample collection from slaughtered animals A midline incision from the xyphoid cartilage to the inguinal region was made and the rumen and intes- tines were exposed by cutting through and reflect- ing the abdominal and paracostal muscles on either side of the midline incision. The small intestines of each animal slaughtered were separated from the rest of the organs with minimal manipulation. Start- ing from the distal end of the jejunum, one metre long small intestinal loops were tied at both ends, cut and placed in labelled plastic containers for fluke recovery. This was followed by the collection of samples of the intestines for histopathological examination. The samples were rinsed in physio- logical saline to remove excess faecal material before each segment was preserved in Bouin’s fix- ative. Samples were also removed from the cranial ruminal pillar and the fundus of the abomasum and preserved in Bouin’s fixative fluid. Fluke recovery To determine the distribution of flukes established along the small intestines, the intestinal segments were scraped to the level of the muscular tunic using glass slides to recover the embedded flukes. The contents of the abomasum, omasum and the reticulum were washed into separate containers and serially sieved under pressure through 2400 µm and 850 µm sieves, respectively. The intestinal mucosal scrapings were similarly sieved and the flukes were collected after sedimentation at the bottom of a jar of 10 l capacity. Excess water was decanted and the recovered flukes were preserved in 70 % alco- hol for identification and enumeration. Gross pathology At each necropsy the intestinal portions were opened separately, examined for gross pathological lesions before their mucosal surfaces were scraped to remove embedded flukes (Boray 1969). In assess- ing the gross pathology of the small intestine, the duodenum, proximal jejunum, distal jejunum and the ileum were demarcated on the basis of their dis- tances from the pylorus. The duodenum constituted the first meter from the pylorus, the proximal jejunum extended for 3 m from the distal end of the duode- num while the distal jejunum extended for 4 m from the distal end of the proximal jejunum. The ileum extended up to the ileo-cecal junction. A checklist of gross pathological lesions was drawn up based on the severity of abomasal oedema, intestinal wall thickening, mucosal corrugation, hyperaemia, petechiation and ulceration. The severity of the gross pathological lesions present were compared between the different experimental groups. Histopathology The samples preserved in Bouin’s fluid were embed- ded in paraffin wax. Triplicate 4 µm thick sections were cut from each segment of the small intestines, abomasum and rumen and each section stained with haematoxylin and eosin (H&E), toluidine blue- ferric sulphate-ferrioxamine B or Giemsa-chromo- trope stain. The toluidine blue stain was used to dif- ferentiate mast cells while the Giemsa-chromotrope stain was used to differentiate eosinophils and basophils. The H&E stain was used to stain globule leukocytes and the evaluation of general histopath- ology of the gastrointestinal regions. Similar to the assessment of the gross pathology, a checklist of histopathological lesions was drawn up based on the severity of villous atrophy, cryptal hyperplasia, goblet cell hyperplasia, dilatation of Brunner’s glands and hyperplasia of Peyer’s patches. The histopath- ological lesions observed were compared between the different experimental groups. 323 M. MAVENYENGWA et al. Data analysis The villous crypt unit method for counting eosino- phils, mast cells, basophils and globule leukocytes as described by Miller & Jarret (1971) was used. For each intestinal segment, three intact villous crypt units were identified and the different cell types esti- mated. The populations of tissue eosinophils, mast cells, globule leukocytes and basophils in the differ- ent intestinal sections were estimated using a four point scale (0, +, ++, +++). RESULTS Clinical signs Animals in the LD and C groups remained clinically normal during the study period. An effortless and voluminous foul smelling projectile diarrhoea devel- oped in three of the four animals in the MD group on Day 21 pi and persisted for 3 days in two of the animals. In the third animal, the diarrhoea persisted for a week and the animal became inappetant, de- hydrated, emaciated, lagged behind the group and never fully recovered until it was slaughtered on Day 56 pi. No clinical signs were evident in the fourth animal in the group. In the HD group, a non-projectile diarrhoea devel- oped in all animals. The diarrhoea developed on Day 21 pi and persisted for 3 days before all the animals recovered. Thereafter no clinical signs or changes in body condition were observed in any of the animals until Day 84 pi when the last animal in the group was slaughtered. Fluke recovery and distribution The distribution patterns of flukes recovered from the various gastrointestinal sites among the different experimental groups on Day 28 pi are presented in Fig. 1. In the LD group, 781 (15.6 %) of juvenile flukes were recovered from the different regions of the gut of the animal slaughtered on Day 28 pi. Of the recovered flukes, 22.4 % were from the proximal third of the duodenum, 7.9 % from the abomasum and the remaining 69.7 % from the rumen along the oesophageal groove and the cranial pillar of the rumen. In the MD group, 4 044 (27 %) of juvenile flukes were recovered from the various intestinal sites of the animal slaughtered on Day 28 pi. Of the flukes present, 8.3 % occurred in the proximal third of the duodenum, 4.9 % in the abomasum and the remaining 86.8 % were recovered along the oeso- phageal groove and the cranial pillar of the rumen. In the HD group, 965 (4 %) of juvenile flukes were recovered from the various gut sites the animal slaughtered on Day 28 pi. Of the flukes present, 44.4 % were recovered from the proximal half of the duodenum, 35.3 % from the abomasum, 10.4 % from the omasum and the remaining 10 % from the oesophageal groove and the cranial pillar of the rumen. All the flukes were recovered from the cranial pillars of the rumen of all the animals slaughtered on Days 42, 56 and 84 pi, and the percentage that had become established in the slaughtered animals is presented in Fig. 2. The percentage of flukes recovered at each slaugh- ter occasion varied between animals, with recovery rates ranging from 4 % to 56 %. 324 Pathology of Calicophoron microbothrium infection in experimentally infected cattle � �� �� �� �� �� �� � � �� ����� �� ����� ������ ����� �������� ���� ����� � � � � � �� � �� �� � �� � �� �� � � ��� �� �������� �� ������ �� � �� �� �� �� �� �� � � ����� ���� ����� � � � � � �� � �� �� � �� � �� �� � � ��� �� �������� �� ������ �� �� �� � FIG. 1 Distribution patterns of recovered Calicophoron micro- bothrium (%) in cattle infected with different doses of metacercariae and slaughtered on Day 28 post infection FIG. 2 Percentage establishment of Calicophoron microbothri- um recovered from the rumen of cattle infected with dif- ferent doses of metacercariae and slaughtered on Day 42, 56 and 84 post infection Pathology Gross pathology The gross pathological lesions of the gut observed in all the infected groups at different stages of infec- tion were confined to the abomasum, the duodenum and the jejunum and are summarized in Table 1. Histopathology The histopathological lesions of the gut observed in all the infected groups at different stages of infection were confined to the duodenum and the jejunum and were characterized by villous atrophy, goblet cell hyperplasia, cystic dilatation of Brunner’s glands and hyperplasia of Peyer’s patches. There was subtotal villous atrophy in the duodenum of the LD animal slaughtered on Day 28 pi. The vil- lous atrophy was characterized by fusion of villi, transformation of absorptive enterocytes into low cuboidal, and moderate hyperplasia of the crypts which were elongate and emptying into the intestin- al lumen. The goblet cells were hyperplastic and occurred in large numbers in the crypts and along epithelia of the villi. Necrotic debris and free-lying flukes were observed in the lumen. The lamina propria was moderately infiltrated by eosinophils, mast cells and a few globule leukocytes, basophils and lympho- cytes. In the submucosa Brunner’s glands were hyperplastic, and occupied nearly half of the sub- mucosal area. Some cystic glands were surrounded by eosinophils and a few lymphocytes. The Peyer’s patches were hyperplastic and expanded into the mucosal area in some sections. In the jejunum, subtotal villous atrophy characterized by shortening and blunting of the villi with elongate crypts empty- ing into the intestinal lumen was present. The lami- na propria was mildly infiltrated by eosinophils, mast cells and low levels of globule leukocytes and basophils. The duodenal and jejunal lesions in the MD animal were similar to those in the LD animal slaughtered on Day 28 pi. However, infiltration of eosinophils and mast cells into the lamina propria tended to be heavier. In the HD animal, Brunner’s glands were hyper- plastic and cystic and had expanded to cover the entire submucosal area on Day 28 pi. The cystic glands were surrounded by an intense eosinophilic cell reaction and a few lymphocytes. Total villous atrophy characterized by severe shortening of the villi and elongate crypts opening into the duodenal lumen was evident. Goblet cell and Peyer’s patch hyperplasia were present and comparable to those in the LD and MD animals. The lamina propria in both the duodenum and the proximal jejunum was heavily infiltrated by eosinophils, moderate amounts of mast cells and a few basophils, globule leukocytes and lymphocytes. The histopathological lesions in the distal jejunum were similar to those in the LD and MD animals slaughtered at the same time. On Day 42 pi the duodenal glands of the LD animal were hyperplastic, non-cystic and contained little mucin. Moderate villous atrophy and goblet cell hyperplasia were still present. The lamina propria was moderately infiltrated by eosinophils, mast cells, lymphocytes and a few globule leukocytes while basophils were not present. Similar cell infiltrations were present in the jejunum. In the MD animal, the submucosal area of the duo- denum was expanded to three times the size of the control animal and half the space was occupied by the hyperplastic Brunner’s glands. Some of the glands were cystic and contained mucin. An intense eosinophilic cell reaction was present in the sub- mucosa and around the cystic glands. Subtotal vil- lous atrophy and mild goblet cell hyperplasia was still present along the crypts and epithelia of the villi. The lamina propria was heavily infiltrated by eosinophils, mast cells and low numbers of globule leukocytes and basophils. In the jejunum, subtotal villous atrophy was still present. The lamina propria was heavily infiltrated by eosinophils, moderate amounts of mast cells and lymphocytes and low numbers of globule leukocytes. In the HD animal, the duodenal and jejunal lesions were similar to the MD animal. However, infiltration of eosinophils and mast cells into the lamina propria was moderate and comparable to the LD animal. On Day 56 pi, the villi were elongate and leaf-like with normal epithelia in both the duodenum and jejunum of the LD, MD and the HD animals. Some Brunner’s glands were still cystic in the MD and HD animals. Goblet cell numbers had reduced to mini- mal levels in the majority of sections, while regen- erative fibrous tissue deposition became evident in the lamina propria and in the submucosal area of all animals. The lamina propria of the MD animal was, however, still infiltrated by large numbers of eosin- ophils, lymphocytes and moderate numbers of mast cells in comparison to the LD and the HD animals. On Day 84 pi, the villi in both the duodenum and the jejunum of all infected animals were elongate and 325 M. MAVENYENGWA et al. 326 Pathology of Calicophoron microbothrium infection in experimentally infected cattle Days pi Group Gut site Main gross lesions 28 LD Abomasum Mild oedema of abomasal folds present but only appreciated on cut surfaces MD Severe oedema of abomasal folds present, abomasal folds swol- len and nearly occluded the lumen HD Moderate oedema of abomasal folds present, abomasal folds moderately swollen and could be easily flipped over C No gross lesions observed LD, MD Duodenum and Duodenal wall thickened and corrugated. Height from muscularis jejunum mucosa to tip of mucosal rugae varied from 8 mm in the proximal duodenum to 4 mm in the distal end. The duodenal and jejunal contents were watery and mucoid HD Duodenal wall severely thickened and corrugated. Height from muscularis mucosa to tip of mucosal rugae varied from 10 mm in the proximal duodenum to 4 mm in the distal end. The duodenal and jejunal contents similar to the LD and MD groups C No lesions detected. Duodenal wall thickening and corrugation absent. Height from muscularis mucosa to tip of mucosal rugae varied from 3 mm in the proximal duodenum to 2 mm in the distal distal end. Duodenal and jejunal contents normal 42 LD, C Abomasum No lesions detected MD, HD Mild oedema of abomasal folds present but only appreciated on cut surfaces LD, MD, HD Duodenum and Mild thickening and corrugation of duodenal wall. Height from jejunum muscularis mucosa to tip of mucosal rugae varied from 5 mm in the proximal duodenum to 3 mm in the distal end. Duodenal and jejunal contents viscous with mucus floccules present C No lesions detected 56 LD, HD, C Abomasum No lesions detected MD Mild oedema of abomasal folds present but only appreciated on cut surfaces LD, MD, HD Duodenum and Mild thickening and corrugation of duodenal wall. Height from jejunum muscularis mucosa to tip of mucosal rugae varied from 5 mm in the proximal duodenum to 3 mm in the distal end. Duodenal and jejunal contents viscous with mucus floccules present C No lesions detected 84 LD, MD, Abomasum, No lesions detected HD, C duodenum and jejunum MD Rumen anterior Fragmentation of papillary tips, Flukes firmly attached to the base pillar of the ruminal papillae. Foci of papillae inhabited by the flukes were pale and some of the papillae had fallen off the ruminal wall leaving non-ulcerated surface patches LD, HD Some papillae had fragmented tips but maintained their normal colour C No lesions detected LD = Low dose MD = Medium dose HD = High dose C = Control TABLE 1 Summary of gross pathological lesions of the abomasum, duodenum and the jejunum of groups of cattle experimentally infected with different doses of Calicophoron microbothrium and slaughtered on different days post infection covered with normal epithelium. The lamina propria was infiltrated with mainly lymphocytes, fibrocytes and a few eosinophils. Brunner’s glands were nor- mal in the LD and MD animals while in the HD ani- mal a few were still cystic and surrounded by lym- phocytes. Histopathological lesions of the rumen were evident on Days 56 and 84 pi in the MD animals and were characterized by thickening and vacuolation of the stratum corneum. In areas where the papillae had fallen off due to parasite feeding and anchorage, microabcesses were present confined to the stra- tum corneum. A mild cell reaction comprising scat- tered eosinophils and a few lymphocytes was pres- ent around the affected areas at the dermal-epider- mal junction. No significant histopathological lesions were seen in the rumen of the LD, HD and the control animals at any stage of infection. DISCUSSION The pathology of amphistome infection has been systematically studied in goats and sheep (Horak & Clark 1963; Singh et al. 1984; Rolfe et al. 1994) in which experimental infections were conducted and the disease followed until after patency. Besides a few reports which describe the pathology of amphi stomes in cattle following acute field outbreaks (But- ler & Yeoman 1962; Singh & Lakra 1971; Kelly & Henderson 1973) this study is the first in cattle, where periodic tissue alterations following infection with different doses of C. microbothrium metacer- cariae are described. The clinical signs exhibited by the infected cattle in the present study are similar to experimental and field observations made in other reports (Butler & Yeoman 1962; Horak & Clark 1963; Horak 1967; Deorani & Katiyar 1967; Boray 1969; Singh & Lakra 1971; Panda & Misra 1980; Rolfe et al. 1994; Pillai & Alikutty 1995). However, polydypsia as described in sheep by Horak & Clark (1963) and by Boray (1969) was not observed and could have been missed since the study animals were not constant- ly under observation. The occurrence of clinical amphistomosis and sub- sequent pathology in ruminants is dependent on the dose, the virulence and the establishment levels of the infecting metacercaria in the small intestine of the host (Horak 1966, 1967; Rolfe et al. 1994). The doses of metacercariae used in this study managed to reproduce the clinical disease. The parasite estab- lishment rates obtained for the LD and MD groups are comparable to those obtained by Horak (1967) in sheep and induced the expected clinical trends of the disease. However, parasite establishment in the HD group was low and could be due to either com- plete failure of parasites to establish or overcrowd- ing of the immature amphistomes in the small intes- tine and subsequent expulsion of unattached para- sites by the host during the diarrhoeic phase of the infection (Boray 1969). The highest concentration of immature amphistomes was recovered from the small intestines of the HD group making the later theory more likely. It is also evident that fluke migra- tion to the rumen was slow in the HD group and only a small proportion of the flukes had migrated to the rumen by Day 28 pi. Similar trends have been observed in sheep and cattle heavily infected with immature amphistomes (Horak 1967; Boray 1971; Rolfe et al. 1994). In this study, the gross pathological lesions were confined to the jejunum, duodenum and the abo- masum of all infected groups and this is related to the migratory habits of the immature flukes which upon establishment in the duodenum migrate to the rumen through the abomasum and omasum caus- ing tissue destruction (Boray 1969; Singh & Lakra 1971; Rolfe et al. 1994). Similar lesion distribution has also been observed in cattle (Butler & Yeoman 1962; Singh & Lakra 1971; Kelly & Henderson 1973) and in sheep (Horak & Clark 1963; Deorani & Katiyar 1967; Horak 1967; Boray 1969). The inten- sity of lesions appeared correlated with the estab- lishment rate and subsequent migration of immature flukes to the rumen. Large numbers of immature flukes in the duodenum have been reported to cause overcrowding and competition among the parasites which results in delayed migration and exacerbates the disease (Horak 1967; Boray 1971; Rolfe et al. 1994). At the same time, poorly attached flukes, particularly those which excyst beyond the duode- nal area, are ejected (Horak 1971). This scenario probably explains the massive duodenal pathology observed in the HD group compared to the other infected groups. Although overall fluke establish- ment was low in the HD group, the highest number of immature flukes was recorded in the duodenum of this group. The duodenal and abomasal changes observed in the infected groups in this study are similar to obser- vations made by Butler & Yeoman (1962), Singh & Lakra (1971) and Kelly & Henderson (1973) in cat- tle. The immature flukes cause tissue destruction by 327 M. MAVENYENGWA et al. anchoring and burrowing into the intestinal mucosa during migration to the submucosa for sojournment in Brunner’s glands (Deorani & Katiyar 1967; Boray 1969; Singh & Lakra 1971). The lesions were pres- ent until Day 42 pi after which they regressed and by Day 84 pi no appreciable differences in gross pathology could be detected between the infected and the control groups. The disappearance of the lesions coincided with the completion of migration of the immature amphistomes from the duodenum to the rumen, confirming earlier reports that the path- ogenic mechanisms of amphistomes are related to duodenal damage caused the by immature flukes (Horak 1971). Mature amphistomes are considered non-patho- genic in the rumen (Cheruiyot & Wamae 1988), but the finding of ruminal lesions in this study seem to suggest that when present in large numbers they may cause disease directly or indirectly through sys- temic absorption of ruminal microflora via necrotic papillary ends. However, the dose of metacercariae used in this study appeared insufficient to cause clinical ruminal dysfunction. The ruminal lesions observed in this study have also been described in sheep and goats (Mukherjee & Deorani 1962; Singh et al. 1984; Rolfe et al. 1994). The ruminal lesions were pronounced on Day 84 pi particularly in the MD group from which a large number of flukes were recovered. This is probably attributable to the attainment of maturity and the crowding effect at a single predilection site by the flukes (Horak 1971). Histopathological examination of the duodenal mucosa did not reveal any flukes embedded in Brunner’s glands in any of the infected groups as has been observed in sheep and goats (Varma 1961; Rolfe et al. 1994). Brunner’s glands provide an ideal environment for fluke growth until they become mature enough to withstand the acid envi- ronment in the abomasum during migration to the rumen (Deorani & Katiyar 1967; Boray 1969; Deo- rani & Jain 1969). Brunner’s glands were, however, cystic with an atrophied basal epithelium suggest- ing prior occupation. Some flukes, however, could be seen in the mucosal tissue probably migrating to the duodenal surface. The absence of flukes em- bedded in Brunner’s glands is probably related to the design of the study in which the animals were slaughtered late in the course of the infection after parasitic migration to the rumen had commenced. There was glandular enlargement with severe villous atrophy characterized by destruction of absorptive enterocytes, fusion of villi and subsequent cryptal hyperplasia as reported in sheep (Rolfe et al. 1994). Villous atrophy characterized by villous and cryptal epithelial differentiation, hyperplasia and loss of func- tion is a known feature of helminth infections and its mechanisms are obscure but could be related to immunological mechanisms against gastrointestinal parasites (Miller 1984). Similarly, with amphistome infections, the mechanisms of villous atrophy are unknown but have been ascribed to either traumatic destruction of tissues or enzymatic dissolution of the mucosa by the migrating flukes (Singh & Lakra 1971). Villous atrophy together with cystic dilatation of Brunner’s glands, hyperplasia of lymphoid follicles and marked mixed cellular infiltration into the lamina propria were probably responsible for the duodenal thickening and corrugation of the mucosa observed grossly in this study. The severity of the lesion appeared correlated with the magnitude of the dose of metacercariae as lesion intensity tended to increase with increasing dose and this could be related to the different levels of sensitization that occur following metacercaria excystment and sub- sequent migration to the rumen. In this study, the migration of immature flukes into the duodenal submucosa induced an acute inflam- matory reaction characterized by an infiltration of eosinophils, mast cells, basophils, globule leuko- cytes, lymphocytes and macrophages into the mu- cosal parenchyma. The goblet cell population also increased and the cells appeared active. Similar responses have been observed as a feature of gas- trointestinal nematode infection in sheep (Huntley, Patterson, Mackellar, Jackson, Stevenson & Coop 1995; Pfeffer, Douch, Shaw, Gatehouse, Rabel, Green, Shirer, Jonas & Bisset 1996; Winter, Wright & Lee 1997). The increase in the number of the var- ious cell types infiltrating the intestinal mucosa dur- ing helminth infections has been associated with the development of resistance to parasitic infections, but the mechanisms of the resistance remain unclear (Huntley et al. 1995). The response of eosinophils, mast cells and goblet cells to C. microbothrium infection occurred at the same time since their kinetic pattern appeared sim- ilar. The cells were seen in significant numbers in the mucosa from Day 28 pi, peaked on Day 42 pi and were maintained at more or less this level till Day 56 when they subsided in all the infected groups. This cellular response coincided with the migration of parasites from the duodenum to the rumen. A severe infiltration of tissue eosinophils was observed in the mucosa and the submucosa around the dilated Brunner’s glands. A similar eosinophil infiltration pattern has been observed in sheep and 328 Pathology of Calicophoron microbothrium infection in experimentally infected cattle goats (Deorani & Katiyar 1967). Tissue eosinophil- ia has been reported to be a feature of helminth infections (Rainbird, Macmillan & Meeusen 1998). The eosinophils, following activation by Th2 cell- derived interleukin-3 and interleukin-5 and through the mediation of parasite-induced IgE, IgG and com- plement C3b (Butterworth 1984; Rainbird et al. 1998 ) can bind to the parasite surface and degran- ulate to release potent biological molecules includ- ing major basic protein, eosinophilic cationic protein, eosinophil-derived neurotoxin, eosinophil peroxidase and toxic oxygen-derived metabolites such as superoxide anions, hydroxyl radicals, hydrogen per- oxide and singlet oxygen (McLaren, McKean, Ols- son, Venge & Kay 1981; Butterworth 1984; Jones 1993; Behm & Ovington 2000; Falcone, Pritchard & Gibbs 2001). The biological products released form a potent helminthicidal system believed to be re- sponsible for parasite damage (Spry 1988; Behm & Ovington 2000). Considering the eosinophil antipar- asite mechanisms as hypothesized by several work- ers (McLaren et al. 1981; Butterworth 1984; Jones 1993; Behm & Ovington 2000; Falcone et al. 2001) to be valid, the presence of high numbers of eosin- ophils in early infection in the duodenum in this study, would be regarded as part of the host defence mechanism against C. microbothrium infection. Despite the presence of severe lesions in the duo- denum of the HD group the mucosal eosinophilic cell infiltration was not as heavy in this group on Day 42 pi as compared to the MD group. It might be possible that the majority of the eosinophils could have been lost through desquamation and exfolia- tion during the antiparasite reaction that followed. Once in tissues the eosinophils can survive for sev- eral weeks (Spry 1988; Behm & Ovington 2000) and this might probably explain their continued pres- ence in the duodenum despite the completed migra- tion of the parasite to the rumen. Intestinal mastocytosis has been associated with helminth infections in sheep (Miller 1984; Huntley, Newlands & Miller 1984; Huntley 1992) and similar to the eosinophils, the role of mastocytes remains unclear. In this study, the mucosal mast cell infiltra- tion peaked at the same time as the eosinophils, showing a similar kinetic pattern. Such a kinetic pat- tern would be expected as the two cells are interre- lated in their functional roles during helminth expul- sion. The mast cells, following activation by Th2 cell- derived interleukin-3 and interleukin-5 and cross- linkage of parasite antigens to mast cell surface bound IgE receptors (Lee, Swieter, & Befus 1986; Falcone et al. 2001; Kawakami & Galli 2002) de- granulate and release vasoactive amines including histamin, serotonin, proteases and leukotrines C, D and E, collectively known as slow reactive sub- stances of anaphylaxis (SRS-A) (Lee et al. 1986). Degranulation of mast cells provokes a Type-I hypersensitivity reaction characterized by smooth muscle contraction and increased vascular perme- ability and subsequent influx of fluids into the gut making the environment hostile to the parasite (Miller 1992; Falcone et al. 2001). In this study the goblet cell population also increased at the same time as the mast cells and eosinophils increased. Goblet cell hyperplasia has been report- ed in the intestines of parasitized animals, particu- larly in sheep (Miller 1984) and the mucin compo- nent of their secretory products intermingles with other epithelial secretory products like IgA and IgE antibodies resulting in an increase in the viscosity of intestinal contents. The increased viscosity fixes the parasite for antibody binding and subsequent lethal attack by the effector cells (Miller 1984). In this study, increased fluidity and viscocity of the gut contents were observed till Day 42 pi and could be related to the activities of the mast and goblet cell populations. Such mechanisms would be expected to be important in the rejection of immature amphis- tomes excysting in the distal jejunum and ileum where the environment is unsuitable for growth and subsequent migration to the rumen. The origin of the globule leukocyte is controversial (Gregory 1979), but it has been reported to occur in high numbers in sheep infected with gastrointesti- nal helminths (Miller 1984; Huntley 1992). In this study the globule leukocyte levels had a kinetic pat- tern similar to those of the mast cell and the eosin- ophils, but in lower intensities. The levels of the globule leukocyte cell infiltration seem to suggest that while the globule leukocyte might be important in sheep where it is associated with the develop- ment of resistance to parasitic infections (Douch, Harrison, Elliott, Buchanan, & Greer 1986; Douch & Morum 1993; Stankiewicz, Jonas, Douch, Rabel, Bisset, & Cabaj 1993; Rolfe et al. 1994; Pfeffer et al. 1996) the same cannot be said for cattle infect- ed with amphistomes. The globule leukocyte kinet- ic pattern resembled that of mast cells. This could be expected considering the theory of its derivation as described by Huntley et al. (1984) where the glob- ule leukocyte is derived from the mast cell. While the composition of the granular contents of the glob- ule leukocyte is more or less similar to that of the mast cell granules, the mechanisms of how the glob- ule leukocyte is involved in resistance are unknown. 329 M. MAVENYENGWA et al. Some authors, however, have linked the globule leukocyte mechanism of action to a Type-I hyper- sensitivity reaction (Stankiewicz et al. 1993). Like the globule leukocyte, basophil numbers were found in low numbers and they appeared to be of minor importance in cattle infected with C. micro- bothrium. Presently there is very little evidence that basophils are involved in ruminant defence mecha- nisms against gastrointestinal parasites. However, basophils have been seen in large numbers in guinea pigs infected with Trichostrongylus colubri- formis (Rothwell & Dineen 1972; Rothwell & Love 1975). Although the number of experimental animals used in the present study was limited, the study has demonstrated the chronology of pathological lesions which occur in cattle experimentally infected with different doses of C. microbothrium. The chronolo- gy of pathological lesions observed in the present study are similar to those described in goats exper- imentally infected with Paramphistomum cervi (Singh et al. 1984) and in sheep experimentally infected with P. ichikawai (Rolfe et al. 1994). How- ever, this study might not have mimicked field con- ditions where infection gradually builds up resulting in variations of the lesions induced by the parasite. ACKNOWLEDGEMENTS DANIDA through the ENRECA-Livestock Helminths Research Project is acknowledged for the provision of funds. Thanks also goes to all support staff in the Department of Paraclinical Veterinary Studies, Uni- versity of Zimbabwe, for their assistance with the collection of samples, and to the staff in the Histol- ogy section of the Central Veterinary Laboratory for the production of tissue slides and the staff at Blair Research Laboratory for the provision of facilities for maintenance of snails and cercarial shedding of the snails. 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