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Phagocytosis and killing of Actinobacillus pleuropneumoniae by alveolar macrophages and polymorphonuclear leukocytes isolated from pigs

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To study the cellular response of phagocytic cells to Actinobacillus pleuropneumoniae, we investigated whether porcine alveolar macrophages (AM) and polymorphonuclear leukocytes (PMN) are able to phagocytize and intracellularly kill A. pleuropneumoniae in vitro. Bacterial cultivation methods of A. pleuropneumoniae were used to assess in vitro phagocytosis and the ability to kill. A specific-pathogen-free pig was killed, blood was collected, and PMN were isolated and counted. The AM were isolated by lung lavage of the same animal and counted. In addition, convalescent-stage serum was collected from a specific-pathogen-free pig that was infected with A. pleuropneumoniae. Both porcine AM and porcine PMN effectively phagocytized A. pleuropneumoniae in the presence of convalescent-stage pig serum. PMN killed 90 to 99% of the bacteria intracellularly, whereas AM did not. Because A. pleuropneumoniae produces exotoxins that kill porcine AM and porcine PMN, we incubated equal amounts of bacteria and phagocytic cells and tested the viability of the cells 120 min later. In the presence of convalescent-stage pig serum, A. pleuropneumoniae was toxic to AM but not to PMN. Probably in porcine AM, intracellular released toxins of A. pleuropneumoniae lessen the ability of the cell to kill the bacterium. Consecutive lysis of AM and release of viable A. pleuropneumoniae may initiate the characteristic porcine pleuropneumonia.
Title: Phagocytosis and killing of Actinobacillus pleuropneumoniae by alveolar macrophages and polymorphonuclear leukocytes isolated from pigs
Description:
To study the cellular response of phagocytic cells to Actinobacillus pleuropneumoniae, we investigated whether porcine alveolar macrophages (AM) and polymorphonuclear leukocytes (PMN) are able to phagocytize and intracellularly kill A.
pleuropneumoniae in vitro.
Bacterial cultivation methods of A.
pleuropneumoniae were used to assess in vitro phagocytosis and the ability to kill.
A specific-pathogen-free pig was killed, blood was collected, and PMN were isolated and counted.
The AM were isolated by lung lavage of the same animal and counted.
In addition, convalescent-stage serum was collected from a specific-pathogen-free pig that was infected with A.
pleuropneumoniae.
Both porcine AM and porcine PMN effectively phagocytized A.
pleuropneumoniae in the presence of convalescent-stage pig serum.
PMN killed 90 to 99% of the bacteria intracellularly, whereas AM did not.
Because A.
pleuropneumoniae produces exotoxins that kill porcine AM and porcine PMN, we incubated equal amounts of bacteria and phagocytic cells and tested the viability of the cells 120 min later.
In the presence of convalescent-stage pig serum, A.
pleuropneumoniae was toxic to AM but not to PMN.
Probably in porcine AM, intracellular released toxins of A.
pleuropneumoniae lessen the ability of the cell to kill the bacterium.
Consecutive lysis of AM and release of viable A.
pleuropneumoniae may initiate the characteristic porcine pleuropneumonia.

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