Literature DB >> 3335403

Adherence of Pasteurella multocida or Bordetella bronchiseptica to the swine nasal epithelial cell in vitro.

T Nakai1, K Kume, H Yoshikawa, T Oyamada, T Yoshikawa.   

Abstract

The interaction of Bordetella bronchiseptica or Pasteurella multocida with swine nasal epithelial cells was studied in vitro. The mean number of B. bronchiseptica organisms adhered per cell was about three times as high as that of P. multocida (P less than 0.01), and the adherence was specifically inhibited by the homologous antiserum prepared with the whole-cell antigen of each bacterium. The poor affinity of P. multocida to the swine nasal mucosa as compared with that of B. bronchiseptica was also demonstrated in the cultured fragments of the nasal mucosa. When observed with a scanning electron microscope, B. bronchiseptica organisms colonized the fragments, whereas few P. multocida organisms adhered. Morphologically, the P. multocida-infected fragments had an essentially normal structure, whereas marked degeneration and marked desquamation of the epithelial cells and severe inflammatory reactions were observed in many areas of the B. bronchiseptica-infected fragments. These morphological observations were consistent with those for the nasal mucosa of P. multocida- or B. bronchiseptica-infected neonatal pigs (T. Nakai, K. Kume, H. Yoshikawa, T. Oyamada, and T. Yoshikawa, Jpn. J. Vet. Sci. 48:693-701, 1986; T. Oyamada, T. Yoshikawa, H. Yoshikawa, M. Shimizu, T. Nakai, and K. Kume, Jpn. J. Vet. Sci. 48:377-387, 1986). Cultured swine nasal fragments, however, were equally injured when they were incubated in a medium containing purified dermonecrotic toxin (DNT) preparations of B. bronchiseptica or P. multocida. Therefore, these DNT preparations can induce morphological damage closely resembling that induced in vivo. Hence, colonization of B. bronchiseptica and production of its DNT on the swine nasal mucosa appear to result in the production of mucosal damage. On the other hand, P. multocida seems to lack the ability to colonize normal swine nasal mucosa, thus resulting in no production or the slight production of DNT to such an extent as to produce mucosal damage. The present data support our previous hypothesis (Nakai et al.; Oyamada et al.) that B. bronchiseptica induces swine atrophic rhinitis, whereas P. multocida does not.

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Year:  1988        PMID: 3335403      PMCID: PMC259262          DOI: 10.1128/iai.56.1.234-240.1988

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  25 in total

1.  Intranasal infection with Bordetella bronchiseptica in gnotobiotic piglets.

Authors:  M Brassinne; A Dewaele; M Gouffaux
Journal:  Res Vet Sci       Date:  1976-03       Impact factor: 2.534

2.  Serological studies on Pasteurella multocida. I. A simplified method for capsule typing of the organism.

Authors:  S NAMIOKA; M MURATA
Journal:  Cornell Vet       Date:  1961-10

3.  Scanning electron microscopic study of hamster tracheal organ cultures infected with Bordetella pertussis.

Authors:  K E Muse; A M Collier; J B Baseman
Journal:  J Infect Dis       Date:  1977-12       Impact factor: 5.226

4.  Production of lesions similar to naturally occurring swine atrophic rhinitis by cell-free sonicated extract of Bordetella bronchiseptica.

Authors:  M Hanada; K Shimoda; S Tomita; Y Nakase; Y Nishiyama
Journal:  Nihon Juigaku Zasshi       Date:  1979-02

5.  Pathology of experimental atrophic rhinitis in swine infected with Alcaligenes bronchisepticus or Pasteurella multocida.

Authors:  M Nakagawa; T Shimizu; Y Motoi
Journal:  Natl Inst Anim Health Q (Tokyo)       Date:  1974

6.  Atrophic rhinitis produced by intranasal inoculation of Bordetella bronchiseptica in hysterectomy produced colostrum-deprived pigs.

Authors:  T Shimizu; M Nakagawa; S Shibata; K Suzuki
Journal:  Cornell Vet       Date:  1971-10

7.  Pathology of experimental Bordetella bronchiseptica infection in swine: atrophic rhinitis.

Authors:  J R Duncan; R F Ross; W P Switzer; F K Ramsey
Journal:  Am J Vet Res       Date:  1966-03       Impact factor: 1.156

8.  Nasal infection of Alcaligenes bronchisepticus (Bordetella bronchiseptica) and lesions in newborn rabbits.

Authors:  M Maeda; T Shimizu
Journal:  Natl Inst Anim Health Q (Tokyo)       Date:  1975

9.  Experimental atrophic rhinitis in gnotobiotic pigs.

Authors:  O P Miniats; J A Johnson
Journal:  Can J Comp Med       Date:  1980-10

10.  The aetiological significance of Bordetella bronchiseptica and Pasteurella multocida in atrophic rhinitis of swine.

Authors:  K B Pedersen; K Barfod
Journal:  Nord Vet Med       Date:  1981-12
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  11 in total

1.  A highly adherent phenotype associated with virulent Bvg+-phase swine isolates of Bordetella bronchiseptica grown under modulating conditions.

Authors:  K B Register; M R Ackermann
Journal:  Infect Immun       Date:  1997-12       Impact factor: 3.441

2.  Pasteurella multocida specific bacteriophage suppresses P. multocida-induced inflammation: identification of genes related to bacteriophage signaling by Pasteurella multocida-infected swine nasal turbinate cells.

Authors:  Ga Young Park; Hyun Jin Yu; Jee Soo Son; Sang Joon Park; Hee-Jae Cha; Kyoung Seob Song
Journal:  Genes Genomics       Date:  2019-12-18       Impact factor: 1.839

3.  Isolation and characterization of mutant strains of Bordetella bronchiseptica lacking dermonecrotic toxin-producing ability.

Authors:  H Nagano; T Nakai; Y Horiguchi; K Kume
Journal:  J Clin Microbiol       Date:  1988-10       Impact factor: 5.948

4.  Role of the dermonecrotic toxin of Bordetella bronchiseptica in the pathogenesis of respiratory disease in swine.

Authors:  Susan L Brockmeier; Karen B Register; Tibor Magyar; Alistair J Lax; Gillian D Pullinger; Robert A Kunkle
Journal:  Infect Immun       Date:  2002-02       Impact factor: 3.441

5.  Adherence of Bordetella bronchiseptica 276 to porcine trachea maintained in organ culture.

Authors:  F Dugal; C Girard; M Jacques
Journal:  Appl Environ Microbiol       Date:  1990-06       Impact factor: 4.792

6.  Virulence of capsulated and noncapsulated isolates of Pasteurella multocida and their adherence to porcine respiratory tract cells and mucus.

Authors:  M Jacques; M Kobisch; M Bélanger; F Dugal
Journal:  Infect Immun       Date:  1993-11       Impact factor: 3.441

Review 7.  Human infections associated with Bordetella bronchiseptica.

Authors:  B F Woolfrey; J A Moody
Journal:  Clin Microbiol Rev       Date:  1991-07       Impact factor: 26.132

8.  Enhanced adherence of Pasteurella multocida to porcine tracheal rings preinfected with Bordetella bronchiseptica.

Authors:  F Dugal; M Bélanger; M Jacques
Journal:  Can J Vet Res       Date:  1992-07       Impact factor: 1.310

9.  Experimental model of atrophic rhinitis in gnotobiotic pigs.

Authors:  M R Ackermann; R B Rimler; J R Thurston
Journal:  Infect Immun       Date:  1991-10       Impact factor: 3.441

10.  Interaction of Bordetella bronchiseptica and Its Lipopolysaccharide with In Vitro Culture of Respiratory Nasal Epithelium.

Authors:  Carolina Gallego; Andrew M Middleton; Nhora Martínez; Stefany Romero; Carlos Iregui
Journal:  Vet Med Int       Date:  2013-03-11
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