Literature DB >> 30045866

Detection of Respiratory Colonization by Kingella kingae and the Novel Kingella negevensis Species in Children: Uses and Methodology.

Pablo Yagupsky1.   

Abstract

The recognition of the role of Kingella kingae as one of the main etiologic agents of skeletal system infections in young children and the recent discovery of the novel Kingella negevensis species have resulted in an increasing interest in these two emerging pediatric pathogens. Both bacteria colonize the oropharynx and are not detected in nasopharyngeal specimens, and the colonized mucosal surface is their portal of entry to the bloodstream. Although species-specific nucleic acid amplification assays have significantly improved the detection of kingellae and facilitated patients' management, the increasing use of this diagnostic approach has the potential drawback of neglecting culture recovery of these organisms. The isolation of Kingella species enables the thorough genotyping of strains for epidemiological purposes, the study of the dynamics of asymptomatic colonization and person-to-person transmission, the investigation of the pathogenesis of invasive infections, and the determination of antibiotic susceptibility patterns. The culture isolation of pharyngeal strains and their comparison with isolates derived from normally sterile body sites may also aid in identifying virulence factors involved in the transition from colonization to invasive disease which could represent potential targets for a future protective vaccine. The two species are notoriously fastidious, and their isolation from upper respiratory tract specimens requires a short transport time, plating on selective vancomycin-containing blood-agar medium, and incubation under capnophilic and aerobic conditions. The identification of K. kingae and K. negevensis can be performed by a combination of the typical Gram stain and biochemical tests and confirmed and differentiated by molecular assays that target the groEL and mdh genes.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  Kingella kingae; Kingella negevensis; carriage; culture; method; oropharynx

Mesh:

Substances:

Year:  2018        PMID: 30045866      PMCID: PMC6156323          DOI: 10.1128/JCM.00633-18

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  30 in total

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Journal:  Clin Microbiol Infect       Date:  2012-03-06       Impact factor: 8.067

4.  A New Highly Sensitive and Specific Real-Time PCR Assay Targeting the Malate Dehydrogenase Gene of Kingella kingae and Application to 201 Pediatric Clinical Specimens.

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5.  Molecular Tests That Target the RTX Locus Do Not Distinguish between Kingella kingae and the Recently Described Kingella negevensis Species.

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6.  Identification and characterization of an RTX toxin in the emerging pathogen Kingella kingae.

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9.  Outbreaks of Invasive Kingella kingae Infections in Closed Communities.

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Journal:  J Pediatr       Date:  2015-11-03       Impact factor: 4.406

10.  Possible association of Kingella kingae with infantile spondylodiscitis.

Authors:  Dimitri Ceroni; Wilson Belaieff; Akatarina Kanavaki; Rebecca Anderson Della Llana; Pierre Lascombes; Victor Dubois-Ferriere; Romain Dayer
Journal:  Pediatr Infect Dis J       Date:  2013-11       Impact factor: 2.129

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Review 2.  Kingella kingae RtxA Cytotoxin in the Context of Other RTX Toxins.

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3.  Cytotoxic activity of Kingella kingae RtxA toxin depends on post-translational acylation of lysine residues and cholesterol binding.

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