RESUMEN
Staphylococcus aureus is known worldwide as an invasive pathogen, but information on S. aureus from bloodstream infections in Central Africa remains scarce. A collection of S. aureus blood culture isolates recovered from hospitals in four provinces in the Democratic Republic of the Congo (2009-2013) was assessed. A total of 27/108 isolates were methicillin-resistant S. aureus (MRSA), of which >70% were co-resistant to aminoglycosides, tetracyclines, macrolides and lincosamides. For MRSA and methicillin-susceptible S. aureus (MSSA) isolates, resistance to chloramphenicol and trimethoprim-sulphamethoxazole (TMP-SMX) was <10%. However, 66.7% (72/108) of all isolates harboured the trimethoprim resistance gene dfrG. More than three-quarters (84/108, 77.8%) of isolates belonged to CC5, CC8, CC121 or CC152. Genetic diversity was higher among MSSA (31 spa types) compared to MRSA (four spa types). Most MRSA (23/27, 85.2%) belonged to CC8-spa t1476-SCCmec V and 17/23 (73.9%) MRSA ST8 were oxacillin susceptible but cefoxitin resistant. Among MRSA and MSSA combined, 49.1% (53/108) and 19.4% (21/108) contained the genes encoding for Panton-Valentine leucocidin (lukS-lukF PV, PVL) and toxic shock syndrome toxin-1 (tst, TSST-1), respectively. PVL was mainly detected among MSSA (51/53 isolates harbouring PVL were MSSA, 96.2%) and associated with CC121, CC152, CC1 and CC5. TSST-1 was associated with CC8-spa t1476-SCCmec V. The immune evasion cluster (IEC) genes scn, sak and chp were detected in 81.5% of isolates (88/108, equally represented among MSSA and MRSA). The present study confirms the occurrence of MRSA with high levels of multidrug co-resistance and PVL-positive MSSA among invasive S. aureus isolates in Central Africa.
Asunto(s)
Antibacterianos/farmacología , Farmacorresistencia Bacteriana , Variación Genética , Sepsis/microbiología , Infecciones Estafilocócicas/microbiología , Staphylococcus aureus/clasificación , Staphylococcus aureus/efectos de los fármacos , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Preescolar , República Democrática del Congo , Femenino , Genotipo , Humanos , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Staphylococcus aureus/genética , Staphylococcus aureus/aislamiento & purificación , Factores de Virulencia/genética , Adulto JovenRESUMEN
Introduction: Le diagnostic de la primo-infection tuberculeuse de l'enfant est difficile en situation de ressources limitées et c'est généralement à la tuberculine qu'on a recours. Le but de cette étude est de déterminer les facteurs qui peuvent influencer la réponse positive de l'intradermoréaction à la tuberculine en situation d'endémie Matériel et Méthode: Etude transversale analytique réalisée à Kisangani du 05 mars 2012 au 27 décembre 2013 chez 593 enfants d'âge compris entre 6 mois et 15 ans suivis au «Village de Pédiatrie». Chacun a subi l'intradermoréaction à la tuberculine et la lecture était faite 72 heures après. Le Chi-carré de tendance et le Test exact de Ficher, où c'est approprié, ont été utilisés Résultat: A Kisangani, le taux de prévalence de l'intradermoréaction positive (IDR+) s'élève à 31,53%. Il est identique dans les deux sexes. Celui-ci décroit significativement avec l'âge (p<0,0002): 38,0% entre 6 et 11mois, 26,4% entre 12 et 24mois, 21,4% entre 6 et 10ans puis remonte à partir de 11ans (47,0%). La positivité de l'IDR augmente avec la notion de BCG dans 69,7% de cas (p<0,0017) et avec la notion de contage tuberculeux (p<0,006) Conclusion: A Kisangani, le taux de prévalence de l'intradermoréaction positive est similaire à celui décrit en situation d'endémie. Le taux de positivité décroit avec l'âge. La cicatrice BCG et la notion de contage augmentent la positivité de l'IDR+
Asunto(s)
Niño , República Democrática del Congo , Lactante , Pruebas Intradérmicas , Prueba de Tuberculina , Tuberculosis/diagnósticoRESUMEN
Methicillin-resistant Staphylococcus aureus (MRSA) is a global health concern, but there are few data from Central Africa. The objective of our study was to characterise S. aureus colonisation isolates from healthcare-exposed professionals in the Democratic Republic of the Congo (DRC). Healthcare workers and medical students (n = 380) in Kisangani, DRC were screened for S. aureus nasal carriage in a single-centre cross-sectional study in the University Hospital of Kisangani. The isolates were identified and characterised using phenotypic and genotypic methods. The nasal carriage rate of S. aureus was 16.6 % and 10 out of 63 isolates (15.9 %) were MRSA. We found 28 different spa types. Most MRSA isolates belonged to ST8-spa t1476-SCCmec V. The majority of MRSA were multidrug-resistant to non-beta-lactam antibiotics. Overall, 28.5 % of S. aureus carried Panton-Valentine leucocidin (PVL)-encoding genes (all methicillin-sensitive) and 17.5 % carried toxic shock syndrome toxin-1 (TSST-1)-encoding genes. The finding of MRSA carriage among healthcare workers in a setting with limited access to diagnostic microbiology and appropriate therapy calls for improved education on infection control practices and supports the introduction of surveillance programmes.