Literature DB >> 6996801

Mechanisms of host defense and quantitative comparisons of bacterial populations in experimental peritonitis.

M M Jennings, S A Jennings, M C Robson, J P Heggers.   

Abstract

A model for the quantitative study of bacterial levels in blood, ascitic fluid, and liver, induced by Escherichia coli in the rat, has been devised. Three experimental situations were then studied: non-fatal peritonitis, fatal peritonitis induced by bacteria rendered more virulent by serial passage through test animals, and fatal peritonitis using haemoglobin adjuvant with the more virulent strain. Results indicate that a variety of defense mechanisms are operant in the host animal. In the non-fatal peritonitis, clearance of free bacteria from the peritoneum is observed with a late rebound in local and systemic populations. These phenomena correlate well with in vitro studies of bacterial uptake by peritoneal macrophages. In fatal peritonitis without adjuvant, much larger numbers of bacteria seem to escape initial clearance in the peritoneum and proximal reticuloendothelial system with resultant overwhelming septicaemia. In fatal peritonitis with adjuvant, much less clearance of organisms from the peritoneum is observed, with resultant overgrowth of bacteria and host death. It thus seems that the initial host defenses center around peritoneal clearance of introduced organisms, and that processes which interfere with this clearance prove fatal.

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Year:  1980        PMID: 6996801     DOI: 10.1139/m80-026

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  2 in total

1.  Transient behavior of a chemotaxis system modelling certain types of tissue inflammation.

Authors:  W Alt; D A Lauffenburger
Journal:  J Math Biol       Date:  1987       Impact factor: 2.259

2.  Role of resident macrophages, peripheral neutrophils, and translymphatic absorption in bacterial clearance from the peritoneal cavity.

Authors:  D L Dunn; R A Barke; N B Knight; E W Humphrey; R L Simmons
Journal:  Infect Immun       Date:  1985-08       Impact factor: 3.441

  2 in total

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