Examination of Type IV Pilus Expression and Pilus-Associated Phenotypes in Kingella kingae Clinical Isolates

Author:

Kehl-Fie Thomas E.123,Porsch Eric A.23,Yagupsky Pablo4,Grass Elizabeth A.2,Obert Caroline5,Benjamin Daniel K.26,St. Geme Joseph W.23

Affiliation:

1. Department of Molecular Microbiology, Washington University School of Medicine, 660 S. Euclid Ave., St. Louis, Missouri 63110

2. Department of Pediatrics

3. Department of Molecular Genetics and Microbiology

4. Clinical Microbiology Laboratory, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel

5. Hartwell Center, St. Jude Children's Research Hospital, Memphis, Tennessee 38105

6. Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina 27710

Abstract

ABSTRACT Kingella kingae is a gram-negative bacterium that is being recognized increasingly as a cause of septic arthritis and osteomyelitis in young children. Previous work established that K. kingae expresses type IV pili that mediate adherence to respiratory epithelial and synovial cells. PilA1 is the major pilus subunit in K. kingae type IV pili and is essential for pilus assembly. To develop a better understanding of the role of K. kingae type IV pili during colonization and invasive disease, we examined a collection of clinical isolates for pilus expression and in vitro adherence. In addition, in a subset of isolates we performed nucleotide sequencing to assess the level of conservation of PilA1. The majority of respiratory and nonendocarditis blood isolates were piliated, while the majority of joint fluid, bone, and endocarditis blood isolates were nonpiliated. The piliated isolates formed either spreading/corroding or nonspreading/noncorroding colonies and were uniformly adherent, while the nonpiliated isolates formed domed colonies and were nonadherent. PilA1 sequence varied significantly from strain to strain, resulting in substantial variability in antibody reactivity. These results suggest that type IV pili may confer a selective advantage on K. kingae early in infection and a selective disadvantage on K. kingae at later stages in the pathogenic process. We speculate that PilA1 is immunogenic during natural infection and undergoes antigenic variation to escape the immune response.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference33 articles.

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2. Burrows, L. L. 2005. Weapons of mass retraction. Mol. Microbiol.57:878-888.

3. Chometon, S., Y. Benito, M. Chaker, S. Boisset, C. Ploton, J. Berard, F. Vandenesch, and A. M. Freydiere. 2007. Specific real-time polymerase chain reaction places Kingella kingae as the most common cause of osteoarticular infections in young children. Pediatr. Infect. Dis. J.26:377-381.

4. Craig, L., M. E. Pique, and J. A. Tainer. 2004. Type IV pilus structure and bacterial pathogenicity. Nat. Rev. Microbiol.2:363-378.

5. Froholm, L. O., and K. Bovre. 1972. Fimbriation associated with the spreading-corroding colony type in Moraxella kingii. Acta Pathol. Microbiol. Scand. B Microbiol. Immunol.80:641-648.

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