INVESTIGADORES
SERRADELL Maria De Los Angeles
artículos
Título:
Clostridioides difficile: Characterization of the circulating toxinotypes in an Argentinean public hospital Clostridioides difficile: caracterización de los toxinotipos circulantes en un hospital público de Argentina
Autor/es:
CRIVARO, ANDREA N.; CARASI, PAULA; SALTO, ILEANA; HUGO, AYELEN; SOLDAVINI PELICHOTTI, P. CECILIA; BENGOA, AGUSTINA; FRAGOMENO, MELISA; SERRADELL, MARÍA A.; MINNAARD, JESSICA; ROLNY, IVANNA; ALUL, EDUARDO; ARREGUI, LEANDRO; FABRA MARTINEZ, MACARENA E.; MORENO VALERO, OSCAR JAVIER; FACENTE, ANDREA; MAGARIÑOS, FRANCISCO; JEWTUCHOWICZ, VIRGINIA; PÉREZ, PABLO F.; TREJO, FERNANDO M.
Revista:
REVISTA ARGENTINA DE MICROBIOLOGíA
Editorial:
ASOCIACION ARGENTINA MICROBIOLOGIA
Referencias:
Año: 2022
ISSN:
0325-7541
Resumen:
Clostridioides difficile is a spore-forming anaerobe microorganism associated to nosocomial diarrhea. Its virulence is mainly associated with TcdA and TcdB toxins, encoded by their respective tcdA and tcdB genes. These genes are part of the pathogenicity locus (PaLoc). Our aim was to characterize relevant C. difficile toxinotypes circulating in the hospital setting. The tcdA and tcdB genes were amplified and digested with different restriction enzymes: EcoRI for tcdA; HincII and AccI for tcdB. In addition, the presence of the cdtB (binary toxin) gene, TcdA and TcdB toxins by dot blot and the cytotoxic effect of culture supernatants on Vero cells, were evaluated. Altogether, these studies revealed three different circulating toxinotypes according to Rupnik´s classification: 0, I and VIII, being the latter the most prevalent one. Even though more studies are certainly necessary (e.g. sequencing analysis), it is worth noting that the occurrence of toxinotype I could be related to the introduction of bacteria from different geographical origins. The multivariate analysis conducted on the laboratory values of individuals infected with the most prevalent toxinotype (VIII) showed that the isolates associated with fatal outcomes (GCD13, GCD14 and GCD22) are located in regions of the biplots related to altered laboratory values at admission. In other patients, although laboratory values at admission were not correlated, levels of urea, creatinine and white blood cells were positively correlated after the infection was diagnosed. Our study reveals the circulation of different toxinotypes of C. difficile strains in this public hospital. The variety of toxinotypes can arise from pre-existing microorganisms as well as through the introduction of bacteria from other geographical regions. The existence of microorganisms with different pathogenic potential is relevant for the control, follow-up, and treatment of the infections.