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Haemophilus somnus-induced interference with bovine neutrophil functions
Veterinary Microbiology
|June 1, 1986
Summary
Haemophilus somnus inhibits bovine polymorphonuclear leukocyte (PMN) functions, including protein iodination and Staphylococcus aureus ingestion. Specific bacterial surface components were identified as responsible for these inhibitory effects on immune cells.
Area of Science:
- Bovine immunology
- Bacterial pathogenesis
- Cellular immunology
Background:
- Haemophilus somnus is a significant pathogen in cattle.
- Bovine polymorphonuclear leukocytes (PMNs) are crucial immune cells for combating bacterial infections.
- Understanding bacterial interference with host immune function is vital for disease control.
Purpose of the Study:
- To investigate the in vitro effects of Haemophilus somnus on bovine PMN function.
- To identify bacterial components responsible for inhibiting PMN activity.
Main Methods:
- Incubation of bovine PMNs with live and heat-killed Haemophilus somnus cells, cell-free supernatant, and extracted bacterial fractions.
- Assays to measure PMN protein iodination and Staphylococcus aureus ingestion.
- Analysis of nitroblue tetrazolium (NBT) reduction by PMNs.
Main Results:
- Live, heat-killed whole cells, and supernatant fluid of Haemophilus somnus significantly inhibited PMN protein iodination and S. aureus ingestion.
- Washed, heat-killed cells did not inhibit these functions, suggesting soluble or surface-associated factors.
- No inhibition of NBT reduction was observed.
- The factor inhibiting S. aureus ingestion was heat-stable with a molecular weight >300,000 MW.
- The factor inhibiting protein iodination was <10,000 MW.
Conclusions:
- Haemophilus somnus produces factors that impair critical bovine PMN functions.
- These bacterial factors, particularly a high molecular weight surface component and a low molecular weight soluble factor, contribute to immune evasion.
- Further research into these factors could inform strategies to enhance bovine immune responses against H. somnus infections.