A PRÉCIS AND CHECKLIST OF HELMINTH PARASITES FOR 14 SPECIES OF WATERFOWL FROM THE CHIHUAHUA DESERT IN THE UNITED STATES AND MEXICO.

A précis of helminth parasite infections and a host-parasite checklist are presented for the following 14 species of waterfowl from the Chihuahua Desert in the United States and Mexico: Chen rossii, Chen caerulescens, Anas platyrhynchos, Anas diazi, Anas acuta, Anas strepera, Anas americana, Anas clypeata, Anas cyanoptera, Anas crecca, Bucephala albeola, Oxyura jamaicensis, Fulica americana, and Podiceps nigricollis. There was a total of 127 species of helminths recovered from the 14 species of waterfowl. Total abundance, which included data available for 12 species of waterfowl, was 134,202 (mean = 11,184, median = 1,376, and 95% confidence limit [CL] = 14,485). Mean species richness ranged from 1.5 in Ross's goose, C. rossii, to 4.3 in the bufflehead, B. albeola. Host mean abundance ranged from 7.5 in the Mexican duck, A. diazi, and green-winged teal, A. crecca, to a high of 811 for the ruddy duck, O. jamaicensis. Ninety-one percent of the helminth species were generalists. Most specialists were associated with the American coot, F. americana (7), and the eared grebe, P. nigricollis (5). Percent helminth species contribution was cestodes 45%, nematodes 25%, trematodes 22%, and acanthocephalans 8%. The most commonly occurring helminth species among the 14 host species were the trematode Notocotylus attenuatus (12), the cestode Cloacotaenia megalops (10), the acanthocephalan Corynosoma constrictum (9), and the nematode Capillaria anatis (6). Low ingestion of invertebrates may have contributed to the lower number of helminth species and abundance in wintering and spring dabbling ducks (Anatini). Wild dabbling ducks ranging in age from 6 mo to 8 yr and 8 mo were infected with helminth parasites. Helminth parasite data from resident and nesting hosts and pre-fledged young birds indicated as many as 43 helminth life cycles may be occurring in the Chihuahua Desert. Host-parasite species checklists are included.

Iron and contact with host cells induce expression of adhesins on surface of Trichomonas vaginalis.

The proteins AP65, AP51, AP33 and AP23 synthesized by Trichomonas vaginalis organisms in high iron play a role in adherence. Multigene families encode enzymes of the hydrogenosome organelles, which have identity to adhesins. This fact raises questions regarding the compartmentalization of the proteins outside the organelle and about the interactions of adhesins with host cells. Data here demonstrate the presence of the proteins outside the organelle under high-iron conditions. Fluorescence and immuno-cytochemical experiments show that high-iron-grown organisms coexpressed adhesins on the surface and intracellularly in contrast with low-iron parasites. Furthermore, the AP65 epitopes seen by rabbit anti-AP65 serum that blocks adherence and detects surface proteins were identified, and a mAb reacting to those epitopes recognized the trichomonal surface. Two-dimensional electrophoresis and immunoblot of adhesins from surface-labelled parasites provided evidence that all members of the multigene family were co-ordinately expressed and placed on the trichomonal surface. Similar two-dimensional analysis of proteins from purified hydrogenosomes obtained from iodinated trichomonads confirmed the specific surface labelling of proteins. Contact of trichomonads with vaginal epithelial cells increased the amount of surface-expressed adhesins. Moreover, we found a direct relationship between the levels of adherence and amount of adhesins bound to immortalized vaginal and ureter epithelial cells, further reinforcing specific associations. Finally, trichomonads of MR100, a drug-resistant isolate absent in hydrogenosome proteins and adhesins, were non-adherent. Overall, the results confirm an important role for iron and contact in the surface expression of adhesins of T. vaginalis organisms.

Biology of trichomonosis.

Trichomonas vaginalis is emerging as a major pathogen of men and women and is associated with serious health consequences. Advances in diagnosis and treatment are presented. The complexity of trichomonad pathogenesis is illustrated in the interaction of this parasite with human cells, tissues and the immune system. It is now becoming evident that the interaction of trichomonads with the host is frequently modulated by environmental signals. The molecular biology of trichomonads is still in its infancy, but analysis of genes, genomic structure and transcriptional mechanisms suggest that trichomonads combine both prokaryotic and eukaryotic features. Evidence for the ancient divergence of trichomonads from other eukaryotic lineages is discussed.