Summary The experimental data herein presented have demonstrated that the rates of oxygen consumption of embryonated eggs vary directly with the temperature of incubation. Thus, ten-day-old embryos incubated at 32.2 C have a Qeo2 amounting to about 50 per cent of that obtained with eggs incubated at 37.8 C. The experiment performed at an elevated temperature of 39.4 C yielded slight, but not statistically significant evidence of an increased rate of oxygen consumption. It is interesting to note that eggs injected with the NJ-KD strain of Newcastle disease virus (NDV) and incubated under standard conditions (37.8 C at 52 per cent relative humidity) do not exhibit any appreciable deviation in their Qeo2 from normal eggs or from embryonated eggs, injected with an equivalent amount of normal allantoic fluid, until near the terminal stage of the infection. At that time, there appears to be a rapid reduction in the rate of oxygen consumption, to the low level established for infertile eggs. Eggs inoculated with NDV and incubated (32.2 C) approximately 10 degrees below the standard environmental temperature responded to the infection as above, except that the survival time was increased from approximately 40 hours to 70 hours; furthermore, the slope of the drop in the Qeo2 at the terminal stage of infection appeared to be far more gradual. Repeated experiments with control and NDV-infected eggs incubated at 39.4 C failed to show any significant difference in the mean Qeo2 or in the survival time, from that observed with eggs incubated under standard conditions. The results presented tend to support the hypothesis that the rates of virus multiplication within a host cell may be regulated by the over-all respiratory quotient of that system. That is to say, a reduced Qeo2 of the embryonated egg is presumably accompanied by a reduction in the rate of virus proliferation. In the case of the hens' egg, the variation of environmental temperatures constitutes an easy mechanism for altering the Qeo2 to any desired level. We have been unable to demonstrate any significant stimulation in the oxygen uptake of infected eggs. This has been observed to be true also in the case of eggs infected with Western equine encephalitis virus3. It is appreciated that these results are not in accordance with those reported by Parodi, et al. (1) and Pinkerton et al. (2). A possible discrepancy between our findings and those of the above authors may be due to the entirely different types of technique employed.
Read full abstract