The in vitro inhibition of growth of intracellular Listeria monocytogenes by lymphocyte products

1973 ◽  
Vol 9 (3) ◽  
pp. 353-362 ◽  
Author(s):  
Tobi Jones ◽  
Guy P. Youmans
1984 ◽  
Vol 11 (4) ◽  
pp. 296-300 ◽  
Author(s):  
JEAN-GUY BISAILLON ◽  
PIERRE TURGEON ◽  
DANIEL DUBREUIL ◽  
REJEAN BEAUDET ◽  
MICHEL SYLVESTRE ◽  
...  

1970 ◽  
Vol 48 (3) ◽  
pp. 631-637
Author(s):  
R. D. Lumsden ◽  
G. C. Papavizas ◽  
W. A. Ayers

β-Methylaspartic acid (MAA) effectively reduced root rot of pea, caused by Aphanomyces euteiches, at concentrations as low as 4 p.p.m., and prevented disease at 15–20 p.p.m. The degree of methylation of pectic materials in healthy pea plants was not increased by MAA, which thus could not account for induced resistance to root rot. Further studies revealed that MAA in the absence of glutamic acid affected zoospore germination and inhibited growth of A. euteiches in vitro. Inhibition of growth and of root rot development was almost completely reversed by glutamic and aspartic acids, and partly reversed by several other amino acids. Studies of the mechanism of inhibition of growth of A. euteiches by MAA indicated that MAA did not affect glutamine synthetase or aspartate oxoglutarate transaminase, two amino acid metabolizing enzymes produced by A. euteiches, nor did it affect the uptake of 14C-labeled glutamic acid by mycelium of the fungus and the incorporation of glutamate into alcohol-insoluble material. It was concluded that MAA directly affects growth of A. euteiches and in this way controls root rot of pea.


1959 ◽  
Vol 101 (1) ◽  
pp. 145-147 ◽  
Author(s):  
A. R. Hennes ◽  
H. G. Muchmore ◽  
H. G. McClure ◽  
J. F. Hammarsten

2007 ◽  
Vol 70 (1) ◽  
pp. 65-69 ◽  
Author(s):  
GIOVANNI FORMATO ◽  
IFIGENIA GEORNARAS ◽  
IOANNA M. BARMPALIA ◽  
PANAGIOTIS N. SKANDAMIS ◽  
KEITH E. BELK ◽  
...  

The fate of acid-adapted and nonadapted Listeria monocytogenes inoculated onto bologna slices (formulated with or without antimicrobials) was examined during storage and after exposure to in vitro gastric challenge. Bologna slices formulated with no antimicrobials (control), 3% sodium lactate (SL), or 1.8% SL plus 0.25% sodium diacetate (SD) were inoculated (2 log CFU/cm2) with a 10-strain composite of acid-adapted or nonadapted L. monocytogenes strains. Growth or survival of the two inocula on bologna was evaluated during vacuum-packaged storage (10°C) for up to 36 days. Survival of previously acid-adapted or nonadapted L. monocytogenes on stored bologna exposed to simulated gastric fluid (adjusted to pH 1.0 with HCl) for 20, 40, and 60 min also was determined. As expected, inclusion of antimicrobials in the product formulation inhibited growth of L. monocytogenes during storage of vacuum-packaged bologna compared with growth on control samples. Acid adaptation of L. monocytogenes prior to product inoculation did not affect subsequent survival or growth on bologna or resistance to simulated gastric fluid (P > 0.05). Survival of L. monocytogenes exposed to simulated gastric fluid during storage increased with product age, growth phase of the cells, and possibly age of the cells, particularly for control samples (no antimicrobials), in which the pathogen grew uninhibited to approximately 6 log CFU/cm2 by day 8 of storage. Inhibition of L. monocytogenes growth on product formulated with antimicrobials was associated with only sporadic and small numbers of survivors following exposure of these samples to simulated gastric fluid, especially in samples stored longer. However, cell numbers in these treatment groups before the gastric challenge did not exceed 3.8 log CFU/cm2. Inhibition of growth on product with antimicrobials precluded detection of survivors resistant to the effects of simulated gastric fluid.


1992 ◽  
Vol 55 (7) ◽  
pp. 542-544 ◽  
Author(s):  
GEORGE THARRINGTON ◽  
KENT M. SORRELLS

Milk culture filtrates from Lactobacillus delbrueckii subsp. lactis were found to be inhibitory to test strains of Listeria monocytogenes. Effective in vitro inhibition was found in broth cultures and well diffusion assays. The causative factor(s) of inhibition was lactic acid and hydrogen peroxide.


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