Differential expression of sheep beta-defensin-1 and -2 and interleukin 8 during acute Mannheimia haemolytica pneumonia

Mark R. Ackermann, Jack M. Gallup, Joseph Zabner, Richard B. Evans, Charles W. Brockus, David K. Meyerholz, Branka Grubor, Kim A. Brogden

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Beta-defensins are antimicrobial peptides produced by several cell types, including respiratory epithelia and leukocytes. Expression of some beta-defensins is increased by bacterial-induced inflammatory responses whereas expression of other beta-defensins is constitutive. Two beta-defensins are expressed in lungs of sheep (sheep beta-defensin-1 and -2; SBD-1/-2) and expression of SBD-1 is increased during parainfluenza virus type 3 (PI-3) infection. The effect of Mannheimia haemolytica, a Gram-negative bacteria known to induce expression of bovine beta-defensins and NF-kappa B in lung, has not been determined for SBD-1/-2. In this study, different concentrations of M. haemolytica were inoculated into pulmonary bronchi of lambs. SBD-1 and SBD-2 mRNA levels detected by real time reverse transcriptase polymerase chain reaction in lung homogenates did not increase. In fact, SBD-1 mRNA levels were significantly decreased with the highest administered inoculum concentration (109). In contrast, mRNA levels of interleukin-8 (IL-8) were significantly increased over controls and progressively increased with M. haemolytica concentrations. Co-inoculation of M. haemolytica with xylitol, an osmotic agent, did not alter mRNA levels of SBD-1, SBD-2 or IL-8. SBD-1 mRNA expression was detected in lung epithelia, but not in leukocytes. This study suggests that SDB-1 expression occurs in epithelia and decreases during severe bacterial pneumonia, which is in contrast to the increase that occurs with PI-3 infection.

Original languageEnglish (US)
Pages (from-to)21-27
Number of pages7
JournalMicrobial Pathogenesis
Volume37
Issue number1
DOIs
StatePublished - Jul 2004
Externally publishedYes

Bibliographical note

Funding Information:
The authors acknowledge the assistance of Rachel Derscheid and Erin Costello for their assistance with RNA and cDNA-related laboratory procedures. This work is partially funded by the J.G. Salsbury Endowment, Iowa State University, USDA/CSREES/NRI-CGP (2003-35204-13492) (Ackermann); USDA/ARS-NADC Respiratory Disease Unit CRIS (Brogden); and NIDDK (DK54759) (Zabner).

Keywords

  • Antimicrobial peptides
  • Innate immunity
  • Interleukin-8
  • Mannheimia haemolytica
  • Pneumonia
  • Sheep beta-defensin

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