Vincent Groupé
New Jersey Agricultural Experiment Station
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Featured researches published by Vincent Groupé.
Experimental Biology and Medicine | 1951
Vincent Groupé; Leonora H. Pugh; David Weiss; Mutsuyuki Kochi
Summary Viscosin was found to exert a marked protective effect in embryonated eggs subsequently infected with infectious bronchitis virus. A slight but detectable suppressive effect on the progress of infection in mice infected with influenza A virus was demonstrated.
Experimental Biology and Medicine | 1947
Vincent Groupé
Summary A regular pattern of groovelike striations was observed on the pellicle of Euglena gracilis.
Experimental Biology and Medicine | 1952
Vincent Groupé; Leonora H. Pugh; Alvin S. Levine
Summary A material (APM) produced by a culture of Achromobacter sp., was found to possess a unique combination of biological characteristics, (a) APM was not inhibitory to representative species of bacteria or fungi in vitro, (b) Preparations capable of suppressing the development of pulmonary lesions in mice previously infected with influenza A virus were found to be devoid of virucidal activity in vitro and failed to affect the production of infectious virus in lung tissue or allantoic fluid. (c) The mouse was a far better host than the embryonated egg for the demonstration or detection of inhibitory effects of APM on influenza A virus. (d) Hemagglutination in vitro by influenza A or B virus was not affected by the presence of APM. (e) The most interesting characteristic of APM was its capacity to suppress the development of non-transmissible pneumonia in mice induced by intranasal inoculation of Newcastle disease virus.
Experimental Biology and Medicine | 1946
Vincent Groupé; John J. Oskay; Geoffrey Rake
Summary The elementary bodies of fowl pox closely resemble those of canary pox and have many morphological characteristics in common with the elementary bodies of vaccinia.
Experimental Biology and Medicine | 1946
Geoffrey Rake; Helen Rake; Dorothy Hamre; Vincent Groupé
Summary Electron microscope studies of the agent of feline pneumonitis suggest that the elementary bodies in nature have properties similar to those of jelly-filled sacs which in course of preparation for examination in the microscope settle to a form similar to a wrinkled pea with one flattened side. Such distorted bodies are approximate- 465 μ in diameter. They have several characteristics which resemble rickettsiae and bacteria.
Experimental Biology and Medicine | 1948
Vincent Groupé; John D. Winn; Erwin Jungherr
Summary An agent capable of producing clinical sinusitis in turkeys was isolated and propagated in the yolk sac of the developing chicken embryo. 2. Impression smears of infected yolk sacs stained by Machiavellos technic revealed morphologic forms closely resembling those found in the lymphogranuloma-psittaeosis group of agents (Chlamydozoaceae).
Experimental Biology and Medicine | 1945
Vincent Groupé
Summary Multiplication of Tetrahymena geleii was inhibited by 50 y of atabrine per ml. Resistance of the cells to atabrine was progressively decreased by the environmental changes occurring during growth of the culture and was strikingly decreased when the pH of the culture was increased.
Experimental Biology and Medicine | 1945
Vincent Groupé; Richard Donovick
Summary Under the conditions described, the toxicity of untreated yolk suspensions and the antigenicity of typhus vaccines prepared from embryos harvested on consecutive days rose together with the complement-fixing activity of the same antigens.
Experimental Biology and Medicine | 1950
Vincent Groupé; Leonora H. Pugh
Summary Experiments are described illustrating (a) the use of death of the embryo as a criterion for the measurement of infectivity and interference, (b) an increase in the amount of interfering material present in allantoic fluid following death of the embryo and (c) the absence of demonstrable auto-interference following inoculation into the yolk sac.
Science | 1946
Vincent Groupé; Richard Donovick
The specificity of epidemic and murine typhus has been shown by active immunization of mice with killed rickettsial suspensions and subsequent challenge with heterologous and homologoustoxic substance. During the preparation of this manuscript, Fitzpatrick published findings showing that 3 of 8 mice immunized with murine typhus vaccine were protected against 3 MLD of epidemic toxic substance administered intravenously and that 8 of 16 mice immunized with epidemic vaccine were protected against < 1 MLD of murine typhus rickettsiae administered intraperitoneally (2). These results suggested to Fitzpatrick that the toxic factor in the two strains is identical. Although there are antigens common to both strains, our findings do not support the suggestion that the two toxic substances are identical.