Literature DB >> 3946910

Pasteurella haemolytica leukotoxin: chemiluminescent responses of peripheral blood leukocytes from several different mammalian species to leukotoxin- and opsonin-treated living and killed Pasteurella haemolytica and Staphylococcus aureus.

Y F Chang, H W Renshaw, R J Martens, C W Livingston.   

Abstract

A luminol-dependent chemiluminescence (LDCL) assay was used to assess the response of polymorphonuclear leukocyte (PMN) preparations from 4 species of ruminants (ie, cattle, sheep, goats, and antelopes) and 6 species of nonruminants (ie, swine, dogs, cats, rabbits, horses, and persons) to both opsonized and nonopsonized preparations of living and heat-killed Pasteurella haemolytica and Staphylococcus aureus and to opsonized and nonopsonized heat-killed strains of each bacterium in the presence of sterile culture supernatant (leukotoxin) from P haemolytica. The LDCL responses of PMN preparations from each of the species studied were greater for living than for heat-killed S aureus. The most efficient LDCL emission was observed with reaction mixtures containing opsonized living S aureus. Regardless whether they contained killed or living bacteria, the opsonized S aureus preparations elicited LDCL emissions more efficiently than did the corresponding nonopsonized preparations. Living P haemolytica cells and their sterile culture supernatant inhibited the LDCL emissions of phagocytically stimulated PMN preparations from ruminants, but not those from nonruminants. The LDCL response of ruminant PMN to nonopsonized living P haemolytica was characterized by the development of a peak response at 10 minutes of incubation followed by a precipitous decrease and a subsequent complete cessation of chemiluminescence. The peak LDCL response was higher for opsonized living P haemolytica than for nonopsonized living bacteria, and the increased response lasted longer. However, opsonization of living P haemolytica with the serum samples tested only temporarily spared the ruminant PMN preparations from the detrimental effects of leukotoxin.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3946910

Source DB:  PubMed          Journal:  Am J Vet Res        ISSN: 0002-9645            Impact factor:   1.156


  9 in total

1.  Evidence for vertical inheritance and loss of the leukotoxin operon in genus Mannheimia.

Authors:  Jesper Larsen; Anders G Pedersen; Henrik Christensen; Magne Bisgaard; Øystein Angen; Peter Ahrens; John E Olsen
Journal:  J Mol Evol       Date:  2007-04-13       Impact factor: 2.395

2.  Alterations in bovine platelet function and acute phase proteins induced by Pasteurella haemolytica A1.

Authors:  L A Cheryk; K E Hooper-McGrevy; P A Gentry
Journal:  Can J Vet Res       Date:  1998-01       Impact factor: 1.310

3.  Intact signal peptide of CD18, the beta-subunit of beta2-integrins, renders ruminants susceptible to Mannheimia haemolytica leukotoxin.

Authors:  Sudarvili Shanthalingam; Subramaniam Srikumaran
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-24       Impact factor: 11.205

4.  Identification and characterization of the Pasteurella haemolytica leukotoxin.

Authors:  Y F Chang; R Young; D Post; D K Struck
Journal:  Infect Immun       Date:  1987-10       Impact factor: 3.441

5.  Granulocyte plasma membrane damage by leukotoxic supernatant from Pasteurella haemolytica A1 and protection by immune serum.

Authors:  B Styrt; R D Walker; J C White; L D Dahl; J C Baker
Journal:  Can J Vet Res       Date:  1990-01       Impact factor: 1.310

6.  Bovine CD18 is necessary and sufficient to mediate Mannheimia (Pasteurella) haemolytica leukotoxin-induced cytolysis.

Authors:  M S Deshpande; T C Ambagala; A P N Ambagala; M E Kehrli; S Srikumaran
Journal:  Infect Immun       Date:  2002-09       Impact factor: 3.441

7.  Induction of acute bronchopneumonia in mice by intrabronchial inoculation of Pasteurella haemolytica serotype 1.

Authors:  L W Pace; J R Turk; R E Corstvet; F M Enright; W Henk
Journal:  Can J Vet Res       Date:  1994-04       Impact factor: 1.310

8.  Leukotoxin of Bibersteinia trehalosi Contains a Unique Neutralizing Epitope, and a Non-Neutralizing Epitope Shared with Mannheimia haemolytica Leukotoxin.

Authors:  Arumugam Murugananthan; Sudarvili Shanthalingam; Sai Arun Batra; Sitara Alahan; Subramaniam Srikumaran
Journal:  Toxins (Basel)       Date:  2018-05-30       Impact factor: 4.546

9.  β-Hemolysis May Not Be a Reliable Indicator of Leukotoxicity of Mannheimia haemolytica Isolates.

Authors:  Jegarubee Bavananthasivam; Sudarvili Shanthalingam; Abirami Kugadas; Bindu Raghavan; Sai Batra; Subramaniam Srikumaran
Journal:  Toxins (Basel)       Date:  2018-04-25       Impact factor: 4.546

  9 in total

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