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Biomedical subjects

M L Eberhard

Publications and source records attributed to M L Eberhard.

At least 145 records · Page 8Linked to original sources

Development and larval morphology of Loa loa in experimental primate hosts.

Experimental infections with Loa loa were established in laboratory primates by inoculation of third-stage larvae recovered from either Chrysops silacea infected after engorging on a human volunteer with loiasis, or Chrysops atlanticus infected after blood feeding on experimentally infected primates. The third molt occurred at 16 to 20 days postinoculation of infective larvae, and the fourth at about 50 days. Early larval development was characterized by rapid growth and marked differentiation of the reproductive systems. Differences in the body's growth rate between the sexes were seen as early as 30 days and was especially marked by 60 days. Females grew more rapidly, and for a longer time than males. Males reach maximum size by 120 days, females not until about 300 days. Female worms were inseminated prior to day 90 developing eggs filled the uteri by 120 days, and microfilariae appeared in the peripheral blood at approximately 150 days. Morphological features of the larval and adult stages of human Loa loa are described.

Animals↗

Intestinal parasitism in an outdoor breeding colony of Macaca mulatta.

A portion of a large outdoor breeding colony of rhesus monkeys (Macaca mulatta) was surveyed for intestinal parasites. The results of this examination were compared to data obtained at the time of arrival for this same group of animals. In addition, a small number of infants born in the colony were examined. Although most species of parasites detected during quarantine were retained in the breeding colony, the parasite population changed. The number of helminthic infections doubled while protozoan infections decreased by 20%. Trichuris (47%), Strongyloides (34%), Entamoeba (59%), Endolimax (20%), and Iodamoeba (20%) were the most common parasites detected in the outdoor breeding colony.

Animal Husbandry↗

Dipetalonema (Cercopithifilaria) kenyensis subgen. et sp. n. (Nematoda: Filarioidea) from African baboons, Papio anubis.

Dipetalonema (Cercopithifilaria) kenyensis subgen. et sp. n. is described from the subcutaneous connective tissues of Papio anubis, from Kenya, Africa. Of the six recognized subgenera of the genus Dipetalonema, Cercopithifilaria most closely resembles Loxodontofilaria and Chenofilaria in having an undividied esophagus. The appearance of the female tail and the number and arrangement of the caudal papillae in the male distinguish it from these two subgenera. The species kenyensis is distinct from all other species by its body size, its microfilaria, and the size and shape of the spicules. This is the first species of Dipetalonema to be described from an African primate.

Animals↗

Studies on the Onchocerca (nematoda: Filarioidea) found in cattle in the United States. I. Systematics of O. gutturosa and O. lienalis with a description of O. stilesi sp. n.

Onchocerca gutturosa and O. lienalis are redescribed and comparative morphological descriptions provided. In addition, a third species of Onchocerca is described from cattle in the United States. This third species, Onchocerca stilesi sp. n., localizes in the connective tissues around the stifle joint, and can be distinguished morphologically from O. gutterosa and O. lienalis. Onchocerca gutturosa and O. lienalis apparently have widespread distribution in the eastern United States; however O. stilesi has been reported only from Minnesota.

Animals↗

Development of Dipetalonema gracile and D. caudispina to the infective stage in Culicoides hollensis.

The microfilariae of 2 species of Dipetalonema (i.e., D. gracile and D. caudispina), common parasites of South American monkeys, develop to the third (infective) stage in the biting midge, Culicoides hollensis. Development of both species occurs in the abdominal fat body; D. gracile requires 13 days and D. caudispina 9 days. Despite similarities in the patterns of development of both species, the third-stage larvae of each is morphologically distinct.

Animals↗

Tetrapeltalonema (t.) mystaxi sp. n. (Nematoda: Filarioidea) from Brazilian moustached marmosets, Saguinus m. mystax.

Tetrapetalonema (T.) mystaxi sp. n. is described from the subscapular connective tissues of Saguinus mystax. The parasite is placed in the subgenus Tetrapetalonema and most closely resembles Tetrapetalonema atelensis, from which it can be differentiated by its long esophagus, size and shape of the spicules, and the size and arrangement of nuclei in the tail of the microfilaria.

Animals↗

Dirofilaria cancrivori sp. n. (Nematoda: Filarioidea from the crabdog, Procyon cancrivorus, in Guyana.

Dirofilaria cancrivori sp. n. is described from subcutaneous tissues of the crabdog, Procyon cancrivorus, in Guyana, South America. The filarid is morphologically distinct from Dirofilaria tenuis, parasite of a related host, the raccoon, in the southern United States, and all other species of Dirofilaria. The parasite can be distinguished from other dirofilarias based on a combination of morphological features including its size, number, and arrangement of caudal papillae on the male tail, size and shape of the spicules, the presence of longitudinal ridges and transverse striations on the cuticle, and the microfilaria.

Animals↗

Dirofilaria macrodemos and D. panamensis spp. n. (Nematoda: Filarioidea) from Central and South Americal sloths.

Two new species of Diorfilaria, Dirofilaria macrodemos and Dirofilaria panamensis, are described from the subserosa of Central and South American sloths. Dirofilaria macrodemos, described from the three-toed sloth, Bradypus tridactylus, in Guyana, is characterized and differentiated from other dirofilarias by its length (female 214mm, male 64mm), relatively long tail (female 140 micron, male 110 micron), and the number and distribution of the caudal papillae (7 pairs) in the male. Dirofilaria panamensis, parasite of the two-toed sloth, Cholopeus hoffmanni, in Panama, was previously described as Dirofilaria incrassata by Caballero (1947), but can be distinguished from both D. macrodemos and D. incrassata on the basis of body size (female 66 mm long by 360 micron wide, male 34 mm long by 250 micron wide), tail length (female 80 micron, male 80 micron), and number (6 pairs) of caudal papillae in the male.

Animals↗

Development of Tetrapetalonema marmosetae to the infective stage in Culicoides hollensis and C. furens.

Development of the microfilaria of Tetrapetalonema marmosetae to the infective stage is described in 2 species of biting midges, Culicoides furens and C. hollensis. Development takes place in the thoracic muscles where the microfilaria requires 8 days to reach the third, or infective, stage. These observations suggest that species of Culicoides are the probable natural vectors of T. marmosetae in enzootic areas and that possibly a wide range of midges will serve as suitable vectors for the parasite in the laboratory. The elucidation of the life cycle, the first for a filaria from a neotropical primate, opens the way for the maintenance of this parasite in the laboratory and provides another useful tool for experimental study.

Animals↗

Cruorifilaria tuberocauda gen. et sp. n. (Nematoda: Filarioidea) from the capybara, Hydrochoerus hydrochaeris in colombia.

Cruorifilaria tuberocauda gen. et sp. n. is described from blood vessels of the kidney, heart, and lungs of the capybara, Hyrochoerus hydrochaeris, in Colombia, S.A. The adult worms are robust, of moderate size (females approximately 42 mm long, males about 27 mm long), and tapered at both ends. The males have unequal, dissimilar spicules, lack a gubernaculum and possess both pre- and postanal papillae. The unsheathed microfilaria is found in the peripheral blood. Even though a severe tissue response is seen in the walls of the blood vessels occupied by the adult worms, it appears to be a common parasite in the population of capybaras surveyed.

Animals↗

Differential humoral and cellular immunoreactivity to saline- and detergent-extracted filarial antigens.

The immunoreactivity to saline- and detergent-extracted filarial antigens of 31 Haitian subjects exposed to or infected with Wuchereria bancrofti was analysed. Cellular reactivity, monitored by blastogenesis in vitro, was significantly greater to a soluble extract of Brugia pahangi than to a detergent-extracted antigenic preparation. In contrast, serum antibody levels against the detergent extract were significantly higher. These differences were consistently observed in symptomatic, microfilaraemic, and asymptomatic/amicrofilaraemic groups of patients. These patterns of immunoreactivity may reflect intrinsic differences between the 2 antigenic preparations in terms of composition or their mode of presentation to the host immune system.

Adolescent↗