Genomics of the new species Kingella negevensis: diagnostic issues and identification of a locus encoding a RTX toxin

Autor: Trestan Pillonel, Gilbert Greub, Guy Prod'hom, Sacha Laurent, Marie Léger, Onya Opota, Katia Jaton, Sabrina Trachsel
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Neisseriaceae Infections
Bacterial Toxins
030106 microbiology
Immunology
Genomics
Locus (genetics)
Biology
Real-Time Polymerase Chain Reaction
Microbiology
DNA sequencing
Young Adult
03 medical and health sciences
RNA
Ribosomal
16S

Humans
Gene
Phylogeny
Comparative genomics
Bacterial Toxins/genetics
Female
Kingella/genetics
Kingella/isolation & purification
Neisseriaceae Infections/diagnosis
Neisseriaceae Infections/genetics
Neisseriaceae Infections/microbiology
RNA
Ribosomal
16S/genetics

Vaginosis
Bacterial/microbiology

Hemolysin proteins
Infection
Kingella kingae
Matrix-assisted laser desorption-ionization mass spectrometry
Real-time polymerase chain reaction
RTX toxin
Hemolysin
Vaginosis
Bacterial

biology.organism_classification
Virology
030104 developmental biology
Infectious Diseases
Kingella
Zdroj: Microbes and infection, vol. 19, no. 11, pp. 546-552
Popis: Kingella kingae, producing the cytotoxic RTX protein, is a causative agent of serious infections in humans such as bacteremia, endocarditis and osteoarticular infection, especially in young children. Recently, Kingella negevensis, a related species, has been isolated from the oral cavity of healthy children. In this study, we report the isolation of K. negevensis strain eburonensis, initially misidentified as K. kingae with MALDI-TOF MS, from a vaginal specimen of a patient suffering of vaginosis. The genome sequencing and analysis of this strain together with comparative genomics of the Kingella genus revealed that K. negevensis possesses a full homolog of the rtx operon of K. kingae involved in the synthesis of the RTX toxin. We report that a K. kingae specific diagnostic PCR, based on the rtxA gene, was positive when tested on K. negevensis strain eburonensis DNA. This cross-amplification, and risk of misidentification, was confirmed by in silico analysis of the target gene sequence. To overcome this major diagnostic issue we developed a duplex real-time PCR to detect and distinguish K. kingae and K. negevensis. In addition to this, the identification of K. negevensis raises a clinical issue in term of pathogenic potential given the production of a RTX hemolysin.
Databáze: OpenAIRE