Jay R. Georgi

Characteristics of parasite populations in endemic trichostrongylidosis.

Worm counts, faecal egg counts and erythrocyte losses are recorded for lambs which were exposed on a naturally infected pasture for different periods in different years. After each exposure period the lambs were kept under conditions in which no further infection could occur; at varying times, usually after the infections had had time to maturo, the lambs were killed and examined. A detailed analysis of the results is given. It is concluded that the negative binomial distribution of worms among sheep within a flock is not a reflexion of the pasture distribution of infective stages but is the result of a combination of Poisson distributions, these distributions being generated by genetic subsets within the flock. There is a remarkable correlation between the numbers of Haemonchus present and the numbers of worms of the other genera. It is suggested that there are host-mediated common elements in the biomass regulating parameters of mixed trichostrongyle infections and that there is a resource-allocating device. Three main hypotheses are proposed. The hypotheses are: (1) The dimensional constraints on the host-parasite system are the results of various kinds of pace-setters or biological clocks. In each annual cycle the parent worms programme the rate of development through each generation. (2) The rate of development of the worms is tied stochastically or deterministically to the rate of senescence and death. (3) The rate of development and death for each trichostrongyle is set at the start of each season by a host factor which acts on a comparable area of the genome in each trichostrongyle. Methods of testing these hypotheses are discussed and the work related to other systems.

Attrition and temporal distribution of Schistosoma mansoni and S. haematobium schistosomula in laboratory mice

The total number and distribution of schistosomula of Schistosoma mansoni and S. haematobium in all tissues and organs of mice from infection to 14-27 days was determined by compressed tissue autoradiography. Attrition of schistosomula, manifested as a decrease in the number of autoradiographic foci, was observed in organs other than the liver. Attrition commenced about 2 days after cercariae entered the skin, and conformed to a single exponential function with a rate constant (+/- standard error) of 7.0 +/- 0.5%/day for S. mansoni and 3.2 +/- 0.7%/day for S. haematobium. The temporal distribution of schistosomula of S. mansoni and S. haematobium differed quantitatively. In the case of S. mansoni, concomitant with a decrease in skin counts, the lung curve rose rapidly to a peak centred on day 6 and thereafter decreased more or less parallel to the total body curve. Significant accumulation in the liver was not observed until day 7, whereupon liver counts rose steadily to a plateau that extended from about day 14 to the end of the experiment and approximated the number of adult worms recovered from the hepatic portal vessels on day 42. A maximum of 26% and mean of 12% of all foci in the body were counted on autoradiograms of tissues other than the skin, lung and liver. The pelt averaged 14% of the body weight yet schistosomula were detected only in the area initially exposed to cercariae. The eviscerated carcass averaged 54% of the body weight yet contained only 0.8%-3.4% of the schistosomula during the period of accumulation in the liver. Between day 6 and day 14, the ratio of schistosomula in the pulmonary circulation to schistosomula in the systemic circulation did not remain constant, as would be the case if schistosomula circulated passively and randomly, but instead displayed a statistically significant decrease from 0.92 and 0.85. For these reasons, it was considered unlikely that schistosomula had circulated randomly and repeatedly through the pulmonary and systemic circulations and entered the hepatic portal system by chance as hypothesized by Miller & Wilson (1980). Instead it was considered more probable that schistosomula migrating from lungs to liver had followed a directed path through intervening vessels (Kruger, Heitman, van Wyk & McCully, 1969) or tissues (Wilks, 1967).(ABSTRACT TRUNCATED AT 400 WORDS)

Patency and transmission of Filaroides hirthi infection

Filaroides hirthi lungworm infection was diagnosed by the recovery of 1st-stage larvae from the faeces of dogs with heavy, artificially induced infections using zinc sulphate flotation. Diagnosis of low-grade natural infections was infrequently achieved. Zinc sulphate flotation was demonstrated to be about 100 times as efficient as the Baermann technique in concentrating F. hirthi larvae from dog faeces. Larvae recovered from faeces proved to be infective when fed to a pup and it was concluded that F. hirthi infection can be transmitted directly and immediately by fresh faecal contamination. Mongrel dogs of diverse ancestry were readily infected by feeding 1st-stage larvae from lung tissue. Thus, F. hirthi infection was shown not to be limited to the Beagle breed by biological restrictions. The observations that 1st-stage larvae pass through the alimentary tract on their way out of the body and that larvae are found in the mesenteric lymph nodes long after a single exposure to infection support the hypothesis that there is an autogenous re-infection of the host by a proportion of these larvae.

Schistosoma mansoni: temporal distribution of radioselenium-labelled schistosomula in lungs of mice during the first two weeks of infection

The number of schistosomula in lungs was determined by compressed organ autoradiography at intervals up to 14 days after exposure of mice to 75Se-labelled cercariae by tail immersion. Probit analysis of compressed lung autoradiogram focus counts, expressed as percentages of initial infection level, yielded estimates of the average time of arrival, peak accumulation in the lungs and average time of departure of schistosomula: 4.5 +/- 0.87, 6.3 +/- 0.45 and 11 +/- 0.58 days, respectively. At peak accumulation 92 +/- 3.5% of the initial number of schistosomula were found in the lungs. It thus appears that little or no significant attrition of schistosomula occurred in the skin and, instead, that most of the 50-70% of penetrant cercariae that fail to reach adulthood are lost somewhere between the pulmonary and hepatic phases of development. Loss of 75Se label from schistosomula during the first 14 days was exponential, with an average half-life of 4.5 +/- 0.81 days. However, the high sensitivity of autoradiography tended to compensate for this rather rapid rate of label loss. It was pointed out that autoradiographic detection of schistosomula as discrete loci of radioactivity can also be expected to overcome the problem posed by the accumulation in such tissues as liver and kidney of 75Se label that has become separated from larvae.

Radiolabeling and autoradiographic tracing of Toxocara canis larvae in male mice.

Artificially hatched infective larvae of Toxocara canis were labeled with 75Se in Medium 199 (Gibco) containing 75Se-methionine. Male CD-1 mice were infected with radiolabeled larvae by intragastric intubation or by intraperitoneal injection. At intervals of 3-56 days mice were killed and the organs prepared for compressed organ autoradiography. Radioactivity of parasitic larvae showed an exponential decrease with time, reflecting catabolism of label with a biological half life of 26 days (effective half life of 21 days) making possible experiments lasting several months. Total body larva counts, estimated by total body autoradiography, displayed an overall downward trend, but the rate of reduction was probably not constant because no significant positive or negative trends were noted from day 14 onward in the numbers of larvae. The carcass accumulated the greatest number of larvae followed by the central nervous system, liver, and lung in that order. When the numbers of larvae were considered in relationship to the mass of tissue, there were 4 groupings: central nervous system, liver, lung, carcass, and kidney, and genito-urinary organ, pelt, and intestine. No significant difference between intragastric and intraperitoneal administration was observed in the larval distribution after the larvae had left the initial site of deposition.

Parasites of the Respiratory Tract

The author discusses the parasites that infect the nasal passages, trachea, bronchi, and lung parenchyma of dogs and cats. The clinical signs, diagnosis, epidemiology, treatment, and control of infection are also considered.

203Hg and other gamma-emitting radio-isotopes as labels for Dirofilaria immitis microfilariae.

The in vitro uptake of gamma-emitting radionuclides by microfilariae of Dirofilaria immitis was investigated. Radionuclides tested were 133Ba, 207Bi, 82Br, 109Cd, 51Cr, 60Co, 59Fe, 203Hg, 125I, 54Mn, 32P, 125Sb, 46Sc, 75Se and 65Zn. Only 207Bi, 59Fe, 203Hg, 54Mn and 46Sc showed more than 2% of the available radioactivity to bind to the microfilariae. When tested for retention in vitro only 203Hg showed retention levels approaching 90%. Moreover, when dimethyl-sulphoxide was incorporated into the medium at levels of 1% (v/v) the uptake of 203Hg could be increased by 3-5 times; no other radio-isotope tested responded in this manner. The uptake of 203Hg was directly related to temperature and time of incubation. Mercury, as mercuric chloride, was toxic to the microfilariae and represents an impediment to the incorporation of high levels of 203Hg in microfilariae.

External monitoring of 203Hg-labelled Dirofilaria immitis microfilariae in mice and dogs.

Microfilariae of Dirofilaria immitis were labelled with 203Hg2+ in vitro and injected into irradiated mice and Beagle dogs. With irradiated mice it was possible to demonstrate microfilariae present in the blood and to detect 203Hg by external counting as long as 28 days after dosing. The 203Hg2+ label had a half-time of 4-5 days; the amount of stable mercury in the labelling medium strongly influenced the survival of microfilariae in vivo. In dogs, external counting showed the lungs to be a major location of the microfilariae soon after reinjection into the host. Evidence was obtained that labelled microfilariae can circulate; however, the detection of dispersed microfilariae is difficult because of the relative insensitivity of the detecting system. For radiomercury the accumulation of the inorganic form in the liver and kidneys limits the long-term usefulness of 203Hg2+ as a label if the organism being studied also accumulates in these organs.