Beyond CC398: Characterisation of Other Tetracycline and Methicillin-Resistant <em>Staphylococcus aureus</em> Genetic Lineages Circulating in Spanish Hospitals
Sara Ceballos,
Carmen Lozano,
Carmen Aspiroz,
Laura Ruiz-Ripa,
Paula Eguizábal,
Allelen Campaña-Burguet,
Emilia Cercenado,
Ana Isabel López-Calleja,
Javier Castillo,
Jose Manuel Azcona-Gutiérrez,
Luis Torres,
Jorge Calvo,
Carmen Martin,
María Navarro,
Myriam Zarazaga,
Carmen Torres,
the Study Group of Clinical LA-MRSA
Affiliations
Sara Ceballos
Area Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain
Carmen Lozano
Area Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain
Carmen Aspiroz
Servicio de Microbiología, Hospital Royo Villanova, 50015 Zaragoza, Spain
Laura Ruiz-Ripa
Area Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain
Paula Eguizábal
Area Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain
Allelen Campaña-Burguet
Area Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain
Emilia Cercenado
Servicio de Microbiología y Enfermedades Infecciosas, Hospital General Universitario Gregorio Marañón, CIBERES (CIBER de Enfermedades Respiratorias), 28007 Madrid, Spain
Ana Isabel López-Calleja
Hospital Universitario Miguel Servet/IIS Aragón, 50009 Zaragoza, Spain
Tetracycline resistance (TetR) has been evidenced as a good phenotypic marker for detection of livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA) isolates of the clonal complex CC398. The aim of this study was to characterise a collection of 95 TetR-MRSA isolates, not belonging to the lineage CC398, that were obtained in a previous multicentre study, to detect other MRSA clonal complexes that could be associated with this phenotypic TetR marker. The TetR-MRSA isolates were recovered from 20 Spanish hospitals during 2016 and they were characterised to determine their antimicrobial resistance and virulence phenotypes/genotypes as well as the presence of the immune evasion cluster (IEC). A high proportion of isolates belonging to the CC1 lineage (46%) were observed, as well as to the CC5, CC8 and CC45 lineages (11% each one). Thirty-two different spa-types were identified, being predominantly CC1-t127 (40%) and CC45-t1081 (11%). The IEC system (with the gene scn as marker) was present in 73% of isolates and 16% produced the Panton Valentine leucocidin (PVL). A high proportion of MRSA-CC1 isolates were scn-negative (38.6%) and 52.9% of them were blaZ-negative. A multidrug resistance (MDR) phenotype was identified in 86% of MRSA isolates. The knowledge of other TetR-MRSA genetic lineages, in addition to CC398, is highly relevant, since most of them were MDR and some of them presented important virulence factors. Strains potentially associated with livestock (as the subpopulation CC1-t127-scn-negative) or with humans (as the CC45 lineage or the subpopulation CC1-scn-positive) have been found in this study. The use of tetracycline-resistance for detection, not only of CC398 but also of other LA-MRSA lineages should be tracked in the future.