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G S Merz

Publications and source records attributed to G S Merz.

24 records · Page 2Linked to original sources

Decreased percentage of polymorphonuclear neutrophils in mouse peripheral blood after inoculation with material from multiple sclerosis patients.

Mice inoculated with brain homogenates from multiple sclerosis (MS) cases showed marked changes in their leukocyte differential counts, with a decrease in per cent polymorphonuclear neutrophils (PMN) and an increase in the per cent lymphocytes. These changes were based upon an absolute decrease in the number of circulating PMN. The decrease in PMN percentages was apparent at 16 hr after infection and persisted for at least 11 months. The factor responsible for the decrease in PMN was (a) recoverable from 12 hr to 8(1/2) months after inoculation, (b) present in human brain homogenate at a concentration of 3 x 10(12), and (c) between 25 and 50 nm in diameter. Inoculation of 100 units of factor into mice and subsequent titration showed that the factor had undergone a net increase in the mouse of at least 10(9)-fold. The factor causing the PMN decrease was found in all MS material thus far tested: three brains, one spleen, three sera, and two cerebrospinal fluid (CSF) from nine cases of MS. The factor was not found in normal human material that included two brains, one spleen, two sera, and two CSF.

Animals↗

Scrapie-induced changes in the percentage of polymorphonuclear neutrophils in mouse peripheral blood.

A decrease in the percentage of polymorphonuclear neutrophils (PMN) in the peripheral blood of mice appeared 3 days after intracerebral (IC) inoculation with scrapie mouse brain homogenate. Mice inoculated IC with normal mouse brain had PMN percentages similar to those found for uninoculated mice. This difference between normal and scrapie-inoculated mice continued throughout the preclinical phase of the disease. In the clinical phase of the disease, the percentage of PMN was either higher or lower than that found in normals. The factor causing the decrease in PMN percentages was found in the filtrates from 220-, 100-, and 50-nm filters, but not in the filtrates from a 25-nm filter. Sodium periodate treatment of the scrapie brain samples eliminated their ability to cause the decrease in PMN percentages, whereas sodium iodate had no effect. In addition to two genetically different scrapie mouse brain isolates, homogenates of mouse spleen, sheep brain, and sheep spleen from scrapie-affected animals caused a decrease in percent PMN, whereas the corresponding normal tissue homogenates did not.

Animals↗

Phage typing reactions on Brucella species.

The nature of the phage typing reactions on Brucella species was determined by rates of adsorption and infection, one-step growth experiments, and susceptibility to lysis from without. The highest rates of adsorption and infection were obtained on smooth B. abortus cultures, and large clear plaques were produced. One or a few phage particles per B. neotomae cell killed about one-half of the cells, but some went through an infective cycle and released mature phage that resulted in production of small clear plaques. With B. suis, more phage particles per cell were required to kill, replication did not occur, and plaques were not observed. Still greater numbers of phage particles were required to cause some inhibition of growth of B. melitensis lawns. Rough Brucella cultures and species, such as B. ovis and B. canis, were not affected by the highest concentrations of phage. B. abortus cultures of intermediate colonial morphology adsorbed phage, but only a few infected cells (after a delayed latent period) released mature phage. An infected culture or colony appeared normal until spontaneous phage mutants appeared which could penetrate the cell wall more effectively than the parent phage. The mutant phage multiplied more rapidly, and the colony changed to a sticky white form.

Adsorption↗

Spontaneous mutation and recombination among brucellaphages.

Merz, George S. (University of Wisconsin, Madison), and Joe B. Wilson. Spontaneous mutation and recombination among brucellaphages. J. Bacteriol. 91:2356-2361. 1966.-Two plaque morphology variants, as seen on Brucella abortus 544A, termed c (for clear plaque) and lc (for late-clearing plaque) were isolated from stocks of wild-type brucellaphage and from colonies of B. abortus 544A which had undergone an alteration in colonial morphology associated with the establishment of the phage carrier state. Single-burst experiments showed that the phage variants arise by spontaneous mutation of the wild-type phage during its replication on B. abortus strain R19. Two-factor crosses of independently occurring c mutant phages showed the presence of wild-type recombinants among the progeny. Control experiments showed that there are no strong selective forces against either wild-type or c mutant phage inherent in the cross-procedure. Other control experiments ruled out the possibility that wild-type phage in the cross-progeny resulted from either back mutation of the c mutants or the presence of wild-type phage among the input c mutants.

Bacteriophages↗