Parasites of Chamois in New Zealand

Abstract Sir, - Andrews'((2)) checklist of helminth parasites of wild ruminants in New Zealand recorded the presence of 10 species of gastrointestinal nematodes in chamois (Rupicapra rupicapra rupicapra L.) from "Central South Island". In October 1978 we examined 28 freshly-shot chamois cadavers from the Harper-Avoca watershed in the headwaters of the Rakaia River. Six of the nematode species reported by Andrews were found again; viz. Ostertagia ostertagi, O. circumcincta, O. trifurcata, Nematodirus filicollis, Oesophagostomum venulosum and Trichuris ovis. The 4 species found by Andrews that were not recovered by us from the animals we examined were: Trichostrongylus axei, T. vitrinus, Spiculotragia spiculoptera and S. asymmetrica. On the other hand we found 4 helminths not encountered by Andrews: 3 nematodes: Nematodirus spathiger (Railliet, 1896), N. abnormalis (May, 1920), and Chabertia ovina (Fabricius, 1794), and 7 specimens of the cestode Moniezia expansa (Rud., 1805). Nematodirus spathiger was the most commonly encountered Nematodirus species, but generally the numbers of all 3 species encountered were low as might be expected in a sample of adult and almost year-old animals. It is probable that most of the adults had acquired some measure of immunity((3)), and the most susceptible group, the kids, would not be born until late November. Because peptic digestion was not used to recover juveniles from the intestinal submucosa, only small numbers of adults were obtained.     

Determination of amphetamine by Schiff base formation and quantitative gas-liquid chromatography.

A procedure was developed to determine amphetamine salts in solid dosage forms. Amphetamine was extracted from the solid matrix with dilute hydrochloric acid and reacted with cyclohexanone in a strongly basic aqueous methanolic solution. The Schiff base reaction product was extracted with hexane for gas chromatographic determination. Reaction time and optimum conditions were studied. Phenethylamine, similarly treated, was used as an internal standard. Results compared favorably with those obtained by using USP methods.     

魁北克省多日龄猪接种FLEX系列茵格发(R)猪圆环病毒疫苗预防猪圆环病毒相关疾病(PCVAD)的初步结果

人们认为猪圆环病毒2型(PCV2)是发生断奶仔猪多系统衰竭综合征的一个必要因素.目前断奶仔猪多系统衰竭综合征在欧洲称作猪圆环病毒病(PCVD),在北美称作猪圆环病毒相关疾病(PCVAD).     

Diagnosis of ovine fascioliasis by a dot enzyme-linked immunosorbent assay: a rapid microdiagnostic technique

A microenzyme-linked immunosorbent assay (dot-ELISA) was modified for making an immunodiagnosis of Fasciola hepatica infections in sheep. Sheep were alloted as follows: group I-3 controls and 4 principals, each inoculated with 500 metacercariae; group II-3 controls and 7 principals, each inoculated with 250 metacercariae; and group III-3 controls and 7 principals, each inoculated with 500 metacercariae. Blood and fecal samples were collected from each animal every 2 weeks for 16 weeks. Presence (or absence) of flukes was confirmed by fecal examinations and examination of dissected livers at necropsy of the sheep. The dot-ELISA incubations were done at ambient room temperature. Nitrocellulose disks dotted with 1 microliter (50 ng of protein) of F hepatica excretory/secretory products were placed in 96-well tissue culture plates. After nonspecific binding sites on the disks were bound with bovine serum albumin-triethanolamine-buffered saline solution, dilutions (1:2) of positive- and negative-control serum samples or experimental serum samples were placed in appropriate wells for a 30-minute incubation. Wells were washed (3 times), and 50 microliters of horseradish peroxidase conjugated rabbit anti-sheep immunoglobulin G was added to each well for a 30-minute incubation and then aspirated. Substrate solution (4-chloro-1-naphthol, methanol, triethanolamine-buffered saline solution, and H2O2; 50 microliters) was added for a 30-minute incubation and then aspirated. Disks were air dried for visualization: solid purple dot = positive sample, or no dot = negative sample.(ABSTRACT TRUNCATED AT 250 WORDS)