Data collected monthly over a period of two years were live weight, packed cell volume (PCV), nematode faecal egg counts (FECs) and coccidial oocyst counts from faecal analyses for 100 mixed age (3-7 years) indigenous Tswana does. The aims of this experiment were to determine seasonal FECs and coccidial oocysts in these goats and quantify the relationships of these burdens to liveweight and PCV. FECs significantly (P < 0.05) varied with season, with the warmer seasons viz spring, summer and autumn having higher log (x + 1) parasite burdens than the cooler winter, while seasonal trends for coccidial oocysts were not obvious. PCV was also significantly (P< 0.05) lower in the warmer seasons than winter. FECs and coccidial oocysts in all seasons were less than the mean log (x + 1) of 3.3 inferred to reduce production in small stock. Correlation coefficients were strongly negative: -0.95 for FECs and liveweight and -0.84 for FECS and PCV, indicating that these worms had a negative impact on productivity. A further study should be conducted to quantify the effects of controlling these parasites during the warm seasons on productivity.

Grazing cattle are vulnerable to the harmful effects of gastrointestinal parasites. Organically farmed cattle are even more so because conventional antiparasitic treatments are restricted, yet parasite infection patterns in Polish organic herds remain poorly documented.

The prevalence and intensity of Cryptosporidium infection were examined in 445 Holstein calves at 10 dairy farms in western Washington, near Seattle. Fifty-one percent (176) of calves in the 7- to 21-day-old age group (n = 342) were positive for oocysts in the feces by carbolfuchsin staining. Prevalence and intensity of infection were highest in calves 8 to 14 days old; prevalence was 60% in this group, and 48% of the Cryptosporidium-positive calves had oocyst shedding at a 4+ level. A seasonal pattern in prevalence was not evident.

A survey of 95 wild rats which were captured from various locations was conducted to determine the diversity and distribution of ectoparasites and endoparasites infesting wild rat population around the city of Ipoh and Kuala Lumpur. The rodents captured were Rat tus norvegicus and post mortem was carried out immediately after capture, with skin and organs examined for parasite infection. Ectoparasites recovered were blood sucking louse (Polyplax spinulosa) and mites (Myocoptes musculinus). Endoparasites recovered were nematodes (Aspiculuris tetraptera, Trichuris sp., and two strongyles, one of which is Strongyloides sp.) And three intestinal protozoan parasites (Blastocystis sp., Trichomonas sp., and a coccidia). Low diversity of ecto- and endoparasites were observed infecting wild rat population caught in Ipoh as compared to Kuala Lumpur.

A Survey of gastrointestinal helminthes/ parasites in camel migrated from Tehsil Jalapur Pir Wala to Multan Tehsil, was carried out during May, 2012.A total number of 50 samples (20 males and 30 females) were collected from various places at Multan. The revealed parasites were mixed helminthic infection and identified as strongylidae spp, trichostrongyle spp, coccidian/eimeria spp and isospora spp.

Trypanosomiasis positive cases were reported in Sahom Farm Retreatin Gopeng, Perak; with multispecies livestock animals. Nzi and Vavoua traps were applied to survey the population of biting flies; stable flies (Muscidae: Stomoxyinae) and horse flies (Tabanidae)as the vector for surra. Results indicated the presence of Trypanosomiasis infection diagnosed by buffy coat examination, thinblood stained smears and serological test (Surra Sero K-Set test) and identification of its insect vectors. The presence of bothbiting flies provides the missing link between the occurrence of the disease and host or environmental factors precipitatingthe disease. Besides trypanosomiasis in cattle, other parasitic infections were also recorded with heavy infections for liver fluke (Fasciola gigantica ova) and coccidia oocysts. Therefore, some control measures are recommended to eradicate the vectors and to treat infected animals in order to prevent the dissemination ofthe trypanosmiasis.

The worm ova estimation method is important to assess the degree of worm infestation in domestic animals. Currently, the method used in many veterinary laboratories is the McMaster method which can enumerate the number of eggs per gram of faeces. Due to emergingand re-emerging diseases currently being diagnosed in Veterinary Research Institute, Ipoh, it is important to seek new, less risky methods for diagnosis of faecal samples. In view of increasing risk to the laboratory personnel conducting tests on faecal samples, the Parasep® method was assessed to indicate its suitability as aroutine test method. The results indicate that there was no significant differences between the worm egg counts enumeratedby conventional McMaster method and Parasep® method (Z = -1.111, P = 0.267). It is however, critical that assessment based on costs, time and ease of conducting the tests for lab staff be done before adopting this method in diagnostic laboratories.

In 1985, 22 pony foals reared in a helminth-free environment were tested daily for oocysts of Cryptosporidium sp by use of fecal flotation. Oocysts were found in all foals. Oocysts were first observed in feces collected from foals 9 to 28 days after birth. The mean period of oocyst shedding was 10 days and ranged from 2 to 18 days in individual foals. Diarrhea was observed in 14 of 22 (64%) foals and began before the period of oocyst shedding. Fecal samples also wre examined for other infective agents. Salmonella poona was isolated from 1 foal that did not have diarrhea, and coronavirus particles were observed in the feces of 2 foals with diarrhea. Cryptosporidium sp oocytes also were observed in feces of 2 of 17 Thoroughbred foals, 3 of 14 Quarter Horse foals, and 3 of 26 pony foals reared on pastures with their dams. Samples from pasture-reared foals were collected at irregular intervals. Of the 11 Crytosporidium-positive fecal samples collected from pastured foals, 2 were from foals with diarrhea. A similar survey was conducted during the 1986 foaling season, using the same procedures. Examination of 300 samples from 58 Quarter Horse, Arabian, and pony foals did not detect oocysts. Daily examination of feces from 10 pony foals reared under helminth-free conditions for 30 days also failed to detect Cryptosporidium oocysts.

An avidin-biotin-peroxidase complex immunoperoxidase staining method was developed to detect Neospora caninum in formalin-fixed, paraffin-embedded tissue sections. Specific antiserum to N caninum was made in rabbits and used to probe tissues from dogs naturally and experimentally infected with N caninum. The test detected tachyzoites and bradyzoites of N caninum. A reaction was not observed to Toxoplasma gondii, Hammondia hammondi, Sarcocystis cruzi, S capricanis, S tenella, Besnoitia jellisoni, Caryospora bigenetica, Hepatazoon canis, Atoxoplasma sp, or the organism causing canine dermal coccidiosis. When antiserum made in rabbits to T gondii was used in the test, reaction to N caninum was not observed.