Published online July 15, 2005
PEDIATRICS Vol. 116 No. 2 August 2005, pp. e206-e213 (doi:10.1542/peds.2004-2051)
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kiang, K. M.
Right arrow Articles by Lynfield, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kiang, K. M.
Right arrow Articles by Lynfield, R.
Related Collections
Right arrow Infectious Disease & Immunity
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

ELECTRONIC ARTICLE

Outbreak of Osteomyelitis/Septic Arthritis Caused by Kingella kingae Among Child Care Center Attendees

Karen M. Kiang, MD*,§, Folashade Ogunmodede, MBBS, MPH*, Billie A. Juni, MS{ddagger}, David J. Boxrud, MS{ddagger}, Anita Glennen, BS{ddagger}, Joanne M. Bartkus, PhD{ddagger}, Elizabeth A. Cebelinski, BS{ddagger}, Kathleen Harriman, PhD, MPH, RN*, Steven Koop, MD||, Ralph Faville, MD||, Richard Danila, PhD, MPH* and Ruth Lynfield, MD*

* Acute Disease Investigation and Control Section
{ddagger} Public Health Laboratory, Minnesota Department of Health, Minneapolis, Minnesota
§ Epidemic Intelligence Service, Epidemiology Program Office, Centers for Disease Control and Prevention, Atlanta, Georgia
|| Gillette Children's Hospital, St Paul, Minnesota

Objective.Kingella kingae often colonizes the oropharyngeal and respiratory tracts of children but infrequently causes invasive disease. In mid-October 2003, 2 confirmed and 1 probable case of K kingae osteomyelitis/septic arthritis occurred among children in the same 16- to 24-month-old toddler classroom of a child care center. The objective of this study was to investigate the epidemiology of K kingae colonization and invasive disease among child care attendees.

Methods.Staff at the center were interviewed, and a site visit was performed. Oropharyngeal cultures were obtained from the staff and children aged 0 to 5 years to assess the prevalence of Kingella colonization. Bacterial isolates were subtyped by pulsed-field gel electrophoresis (PFGE), and DNA sequencing of the 16S rRNA gene was performed. A telephone survey inquiring about potential risk factors and the general health of each child was also conducted. All children and staff in the affected toddler classroom were given rifampin prophylaxis and recultured 10 to 14 days later. For epidemiologic and microbiologic comparison, oropharyngeal cultures were obtained from a cohort of children at a control child care center with similar demographics and were analyzed using the same laboratory methods. The main outcome measures were prevalence and risk factors for colonization and invasive disease and comparison of bacterial isolates by molecular subtyping and DNA sequencing.

Results.The 2 confirmed case patients required hospitalization, surgical debridement, and intravenous antibiotic therapy. The probable case patient was initially misdiagnosed; MRI 16 days later revealed evidence of ankle osteomyelitis. The site visit revealed no obvious outbreak source. Of 122 children in the center, 115 (94%) were cultured. Fifteen (13%) were colonized with K kingae, with the highest prevalence in the affected toddler classroom (9 [45%] of 20 children; all case patients tested negative but had received antibiotics). Six colonized children were distributed among the older classrooms; 2 were siblings of colonized toddlers. No staff (n = 28) or children aged <16 months were colonized. Isolates from the 2 confirmed case patients and from the colonized children had an indistinguishable PFGE pattern. No risk factors for invasive disease or colonization were identified from the telephone survey. Of the 9 colonized toddlers who took rifampin, 3 (33%) remained positive on reculture; an additional toddler, initially negative, was positive on reculture. The children of the control child care center demonstrated a similar degree and distribution of K kingae colonization; of 118 potential subjects, 45 (38%) underwent oropharyngeal culture, and 7 (16%) were colonized with K kingae. The highest prevalence again occurred in the toddler classrooms. All 7 isolates from the control facility had an indistinguishable PFGE pattern; this pattern differed from the PFGE pattern observed from the outbreak center isolates. 16S rRNA gene sequencing demonstrated that the outbreak K kingae strain exhibited >98% homology to the ATCC-type strain, although several sequence deviations were present. Sequencing of the control center strain demonstrated more homology to the outbreak center strain than to the ATCC-type strain.

Conclusions.This is the first reported outbreak of invasive K kingae disease. The high prevalence in the affected toddler class and the matching PFGE pattern are consistent with child-to-child transmission within the child care center. Rifampin was modestly effective in eliminating carriage. DNA sequence analysis suggests that there may be considerable variability within the species K kingae and that different K kingae strains may demonstrate varying degrees of pathogenicity.


Key Words: Kingella kingae • osteomyelitis • septic arthritis

Abbreviations: MDH, Minnesota Department of Health • PHL, Public Health Lab • PFGE, pulsed field gel electrophoresis • rRNA, ribosomal RNA • MIC, minimum inhibitory concentration • WBC, white blood cell • ESR, erythrocyte sedimentation rate • CRP, C-reactive protein


Accepted Jan 25, 2005.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Clin. Microbiol.Home page
B. Ilharreborde, P. Bidet, M. Lorrot, J. Even, P. Mariani-Kurkdjian, S. Liguori, C. Vitoux, Y. Lefevre, C. Doit, F. Fitoussi, et al.
New Real-Time PCR-Based Method for Kingella kingae DNA Detection: Application to Samples Collected from 89 Children with Acute Arthritis
J. Clin. Microbiol., June 1, 2009; 47(6): 1837 - 1841.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
A. Cherkaoui, D. Ceroni, S. Emonet, Y. Lefevre, and J. Schrenzel
Molecular diagnosis of Kingella kingae osteoarticular infections by specific real-time PCR assay
J. Med. Microbiol., January 1, 2009; 58(1): 65 - 68.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
M. Matta, D. Wermert, I. Podglajen, O. Sanchez, A. Buu-Hoi, L. Gutmann, G. Meyer, and J.-L. Mainardi
Molecular Diagnosis of Kingella kingae Pericarditis by Amplification and Sequencing of the 16S rRNA Gene
J. Clin. Microbiol., September 1, 2007; 45(9): 3133 - 3134.
[Abstract] [Full Text] [PDF]