RESUMO
Kingella negevensis is a newly described gram-negative bacterium in the Neisseriaceae family and is closely related to Kingella kingae, an important cause of pediatric osteoarticular infections and other invasive diseases. Like K. kingae, K. negevensis can be isolated from the oropharynx of young children, although at a much lower rate. Due to the potential for misidentification as K. kingae, the burden of disease due to K. negevensis is currently unknown. Similarly, there is little known about virulence factors present in K. negevensis and how they compare to virulence factors in K. kingae. Using a variety of approaches, we show that K. negevensis produces many of the same putative virulence factors that are present in K. kingae, including a polysaccharide capsule, a secreted exopolysaccharide, a Knh-like trimeric autotransporter, and type IV pili, suggesting that K. negevensis may have significant pathogenic potential.
Assuntos
Kingella kingae/patogenicidade , Kingella/patogenicidade , Infecções por Neisseriaceae/microbiologia , Fatores de Virulência/análise , Proteínas de Bactérias/análise , Fímbrias Bacterianas/química , Fímbrias Bacterianas/microbiologia , Humanos , Kingella/química , Kingella kingae/química , Polissacarídeos Bacterianos/análise , VirulênciaRESUMO
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.
Assuntos
Kingella/isolamento & purificação , Infecções por Neisseriaceae/diagnóstico , Infecções por Neisseriaceae/microbiologia , Orofaringe/microbiologia , Criança , Meios de Cultura , Genótipo , Humanos , Kingella/classificação , Kingella/genética , Kingella/patogenicidade , Kingella kingae/classificação , Kingella kingae/genética , Kingella kingae/isolamento & purificação , Kingella kingae/patogenicidade , Fenótipo , VirulênciaAssuntos
Falência Renal Crônica/terapia , Kingella/patogenicidade , Infecções por Neisseriaceae/tratamento farmacológico , Diálise Peritoneal/efeitos adversos , Peritonite/microbiologia , Antibacterianos/uso terapêutico , Feminino , Seguimentos , Humanos , Falência Renal Crônica/diagnóstico , Kingella/classificação , Pessoa de Meia-Idade , Infecções por Neisseriaceae/etiologia , Diálise Peritoneal/métodos , Peritonite/tratamento farmacológico , Peritonite/etiologia , Doenças Raras , Resultado do TratamentoRESUMO
Kingella denitrificans possess type-4 pili, and the type strain, ATCC 33394, contains at least four complete copies of type-4 pilin-encoding genes. Previously reported hybridization patterns of K. denitrificans chromosomal DNA seen using a Neisseria gonorrhoeae pilin gene region probe, had been interpreted as representing possible partial, silent gene loci. This now appears to be due to cross-reaction to multiple copies of 18-bp inverted repeat structures. Data are presented on a variety of colony variants which have changed from a spreading-corroding (SC) phenotype to a nonspreading-noncorroding (N) phenotype. Interestingly, while the SC to N transition is most often associated with loss of piliation in other bacteria containing type-4 pili, many of the K. denitrificans N variants still produce pilin, and some still produce pili.
Assuntos
Proteínas da Membrana Bacteriana Externa/genética , Fímbrias Bacterianas/química , Genes Bacterianos , Kingella/química , Southern Blotting , Western Blotting , Sondas de DNA , Proteínas de Fímbrias , Fímbrias Bacterianas/genética , Dosagem de Genes , Regulação Bacteriana da Expressão Gênica , Kingella/genética , Kingella/patogenicidade , Microscopia Eletrônica , FenótipoRESUMO
The oral distribution of Kingella oralis was investigated in 10 periodontally healthy subjects. 11 untreated adult periodontitis patients and 6 untreated localized juvenile periodontitis patients. From each subject, 6-8 each of supra- and subgingival tooth samples, 4 mucosa samples and a saliva sample were examined by culture for the presence of K. oralis. K. oralis was found in at least one oral site in 26 of the 27 study subjects, and in at least one tooth site in each of these 26 positive subjects. Its prevalence in dental plaque ranged from 23% to 59% in different subject groups. The mean percentage of K. oralis in total microbiota in the dental plaque ranged from 0.40% in the periodontally healthy group to 4.60% in localized juvenile periodontitis subjects. The organism was a significant species in a few periodontitis sites, constituting > 5% of the total microbiota.