Literature DB >> 9441859

Effect of Haemophilus somnus on nitric oxide production and chemiluminescence response of bovine blood monocytes and alveolar macrophages.

S M Gomis1, D L Godson, G A Wobeser, A A Potter.   

Abstract

Haemophilus somnus is able to survive and multiply in bovine blood monocytes (BBM) and alveolar macrophages (BAM), but the mechanisms used by H. somnus to evade killing mechanisms of bovine mononuclear phagocytes are not completely understood. To study the bactericidal ability of bovine mononuclear phagocytes following interaction with H. somnus, in vitro assay systems were developed to detect the luminol-dependent chemiluminescence response (LDCL) and nitric oxide (NO) production of BBM and BAM. Live logarithmically growing or stationary phase H. somnus inhibited the LDCL of BBM and BAM costimulated with opsonized Staphylococcus aureus. Inhibition of the LDCL response of BBM and BAM was not mediated by live H. somnus opsonized with hyperimmune serum, or by killed bacteria. H. somnus stimulated both BBM and BAM to produce NO at levels comparable with Escherichia coli lipopolysaccharide. While NO was being produced, viable H. somnus could still be isolated from the cell cultures. The ability of H. somnus to inhibit LDCL of both BBM and BAM, and resistance to NO killing may be an important mechanism that contributes to survival of the organism following ingestion by bovine mononuclear phagocytes. Copyright 1997 Academic Press Limited.

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Year:  1997        PMID: 9441859     DOI: 10.1006/mpat.1997.0162

Source DB:  PubMed          Journal:  Microb Pathog        ISSN: 0882-4010            Impact factor:   3.738


  2 in total

1.  Molecular characterization of phosphorylcholine expression on the lipooligosaccharide of Histophilus somni.

Authors:  Shaadi F Elswaifi; Frank St Michael; Avula Sreenivas; Andrew Cox; George M Carman; Thomas J Inzana
Journal:  Microb Pathog       Date:  2009-08-12       Impact factor: 3.738

2.  Histophilus somni Survives in Bovine Macrophages by Interfering with Phagosome-Lysosome Fusion but Requires IbpA for Optimal Serum Resistance.

Authors:  Yu Pan; Yuichi Tagawa; Anna Champion; Indra Sandal; Thomas J Inzana
Journal:  Infect Immun       Date:  2018-11-20       Impact factor: 3.441

  2 in total

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