Relationships of Trichomonas gallinae to the palatal-esophageal junction of ring doves (Streptopelia risoria) as revealed by scanning electron microscopy.

Ring doves (Streptopelia risoria) were experimentally infected with pathogenic (virulent) Trichomonas gallinae so that trichomonad activities in the upper alimentary tract, prior to canker formation, could be examined with scanning electron microscopy. Between 6 and 15 hr postinoculation low numbers of ameboid T. gallinae were attached to apical microfolds and cell borders of the palatal-esophageal junction squamous epithelium. Initial parasite activities at tightly attached cell borders and apical microfolds suggest that some parasite-secreted factor or factors initiated squamous cell damage, separation, and removal. As squamous cell borders separated, trichomonads invaded areas beneath them and ultimately aided in their complete removal. Accelerated parasite-mediated desquamation, the invasion of increased mucosal surface area by trichomonads, and the eruption and expansion of cankers were the primary changes to the palatal-esophageal junction and other upper alimentary tract tissues that occurred between 19 and 240 hr postinoculation.

Ectoparasites of black-tailed prairie dogs (Cynomys ludovicianus) from South Dakota.

During the summers of 1982 and 1983, black-tailed prairie dogs (Cynomys ludovicianus) were examined for parasites. Those collected and their respective prevalence included Linognathoides cynomyis (46.3%), Opisocrostis hirsutus (53.7%), Opisocrostis tuberculatus cynomuris (2.4%), Androlaelaps fahrenholzi (12.2%), Ixodes sculptus (2.4%) and Dermacentor andersoni (4.9%). The collection data indicated that L. cynomyis, O. hirsutus and A. fahrenholzi were at low population densities during this period.

[Difficulties of fungus detection in corneal culture medium]. / Schwierigkeiten beim Pilznachweis in Hornhautkulturmedium.

UNLABELLED: It is not always possible to prevent the growth of microorganisms in organ culture for cornea preservation, despite many prophylactic measures. It is especially difficult to prove the presence of fungi in the cultural medium. MATERIALS AND METHODS: A culture medium was examined for sterility after 8 days' storage of cornea in organ culture. To prove the presence of fungi a culture of Sabouraud 2% glucose-agar was prepared and its growth examined by light microscopy. RESULTS: After 8 days of preservation we noticed a color change in the cultural medium and suspected contamination with fungi. Coagulase-negative Staphylococci could be cultivated from the conjunctival smear obtained before preparation of the cornea only. Routine screening of microbiological contamination did not show any results. We were able to identify an Aspergillus species only after preparing a special culture. The conjunctival smear as well as the cultural medium of the other eye of the same donor showed no contamination. CONCLUSIONS: In spite of the fact that microbiological contamination can be seen macroscopically, it is difficult to prove the presence of a specific microorganism and even more so when dealing with fungus. Especially in these cases the incubation of the cornea in media might have an advantage because contamination can be suspected by just looking at the medium. By excluding these preparations from transplantation we can possibly prevent infections, even when routine examinations show negative results.

[Studies on the reduction of microorganisms in icecream in production and storage (author's transl)]. / Untersuchungen über das Absterben von Mikroorganismen bei der Speiseeisbereitung und -lagerung

Experimental analyses referred to in this publication were to clarify two important hygienic-bacteriological issues: 1. Which is the capacity of survival owned by microorganisms in icecream in correspondence to temperature and storing time, and what significance have the results in regard to the length of intervals between the taking of samples of icecream and their examination. 2. Which nutritient media are suitable for a routine diagnostic of coliforms? Analyses were being made with an artificially contaminated, industrially produced icecream (Vanilla icecream with 10 per cent milk fat and strawberry icecream with 6,6 per cent milk fat and 21 per cent strawberries). Inoculations were only done with strains of bacteria isolated from icecream. We employed one strain of Escherichia coli, Staphyloccus aureus, Pseudomonas aeruginosa and three strains of Coliforms for each inoculation. Contaminated samples were stored in deep-freeze units at three different temperatures(-28, -18, -8 degrees C). In the beginning inspections in regard to microbial content were performed in daily intervals, but intervals grew longer in the course of time. At the utmost samples were under observation for 140 days. For quantitative measurement of Coli and Coliform microorganisms five different culture media were used (Endoagar, Hexachlorophene Endoagar, Desoxycholatcitrat Agar, Violet Red Bile Agar and Brilliant Green Broth). Generally results showed, that icecream, if being stored, looses approximately one to two quarters of the bacteria within hours after production, the third dies within days and the rest after weeks and months. Within the given period of observation sterility can only be reached with rather sour kinds of icecream. E. coli proved to be moderately resistant, Coliforms were somewhat more sensitive. Staphylococci showed in the beginning a lower drop, but in the course of time similar rates as Coli and Coliforms. Only with Pseudomonas inactivation was distinctly more rapid. Differences concerning kinds of icecream and temperatures were not to be secured statistically. Examination of cultur media for the demonstration of E. coli and Coliforms resulted that Hexachlorophene Endoagar is the best one. It is recommended, to take icecream samples at the earliest at the time the icecream is to be sold. Bacteriological cultures should be prepared within 14 days. Controls are to be made at the earliest possible date, but not later that two weeks after the official analysis. Findings with a lower count reached at a later date do not contradict an earlier result of two to five times higher rates. Reliable constants for the retrospect establishment of balances of microbial content were not to be found.

[Correlation between prognostically predicted and actually attained refraction]. / Zur Korrelation von prognostizierter und tatsächlich erreichter Refraktion.

BACKGROUND: In cataract surgery high quality is demanded. That is why high precision in calculation of IOL power is necessary for predicting postoperative refraction. MATERIALS AND METHODS: In a series of 103 patients the predicted refraction--calculated by the SRK II formula for only one type of IOL (A-constant 118.9)--was compared to the received early and late (3 month) postoperative refraction. RESULTS: The accuracy of IOL calculations in 95% was acceptable--within a range of 2 diopters. The prediction errors of extended values were only shown in cases of axial length of more than 26 millimeters. CONCLUSIONS: The results confirm the fact that by means of SRK II formula the accuracy of IOL calculation is satisfactory in respect of predicted refraction. In eyes of elongated axial length the accuracy is limited.