TY - JOUR
T1 - Pseudomonas aeruginosa antibiotic susceptibility profiles, genomic epidemiology and resistance mechanisms
T2 - a nation-wide five-year time lapse analysis
AU - Sastre-Femenía, Miquel Àngel
AU - Fernández-Muñoz, Almudena
AU - Gomis-Font, María Antonia
AU - Taltavull, Biel
AU - López-Causapé, Carla
AU - Arca-Suárez, Jorge
AU - Martínez-Martínez, Luis
AU - Cantón, Rafael
AU - Larrosa, Nieves
AU - Oteo-Iglesias, Jesús
AU - Zamorano, Laura
AU - Oliver, Antonio
AU - Galán-Sánchez, Fátima
AU - Gracia-Ahufinger, Irene
AU - Liébana-Martos, Carmen
AU - Roldán, Carolina
AU - Sánchez-Calvo, Juan Manuel
AU - Clavijo, Encarnación
AU - Mora-Navas, Laura
AU - Aznar, Javier
AU - Lepe, José Antonio
AU - Rodríguez-Villodres, Ángel
AU - Recacha, Esther
AU - Casas-Círia, Francisco Javier
AU - Martínez-Rubio, Carmen
AU - Sempere-Alcocer, Marco Antonio
AU - Martín-Hita, Lina
AU - Seral, Cristina
AU - López-Calleja, Ana Isabel
AU - Aspiroz, Carmen
AU - Monforte, Marisa
AU - Iglesia-Martínez, Pedro de la
AU - Jimenez-Guerra, Gemma
AU - Riera-Pérez, Elena
AU - Collado, Carmen
AU - Gallegos, Carmen
AU - Mulet, Xavier
AU - Sastre-Femenía, Miquel Àngel
AU - Siller-Ruiz, María
AU - Calvo, Jorge
AU - Quesada, Dolores
AU - Wang, Jun Hao
AU - Pitart, Cristina
AU - Marco, Francesc
AU - Prim, Nuria
AU - Horcajada, Juan Pablo
AU - Padilla, Eduardo
AU - Del Barrio-Tofiño, Ester
AU - Capilla, Silvia
AU - Navarro, Ferrán
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/11
Y1 - 2023/11
N2 - BACKGROUND:
Pseudomonas aeruginosa healthcare-associated infections are one of the top antimicrobial resistance threats world-wide. In order to analyze the current trends, we performed a Spanish nation-wide high-resolution analysis of the susceptibility profiles, the genomic epidemiology and the resistome of
P. aeruginosa over a five-year time lapse.
METHODS: A total of 3.180 nonduplicated
P. aeruginosa clinical isolates from two Spanish nation-wide surveys performed in October 2017 and 2022 were analyzed. MICs of 13 antipseudomonals were determined by ISO-EUCAST. Multidrug resistance (MDR)/extensively drug resistance (XDR)/difficult to treat resistance (DTR)/pandrug resistance (PDR) profiles were defined following established criteria. All XDR/DTR isolates were subjected to whole genome sequencing (WGS).
FINDINGS: A decrease in resistance to all tested antibiotics, including older and newer antimicrobials, was observed in 2022 vs 2017. Likewise, a major reduction of XDR (15.2% vs 5.9%) and DTR (4.2 vs 2.1%) profiles was evidenced, and even more patent among ICU isolates [XDR (26.0% vs 6.0%) and DTR (8.9% vs 2.6%)] (p < 0.001). The prevalence of Extended-spectrum β-lactamase/carbapenemase production was slightly lower in 2022 (2.1%. vs 3.1%, p = 0.064). However, there was a significant increase in the proportion of carbapenemase production among carbapenem-resistant strains (29.4% vs 18.1%, p = 0.0246). While ST175 was still the most frequent clone among XDR, a slight reduction in its prevalence was noted (35.9% vs 45.5%, p = 0.106) as opposed to ST235 which increased significantly (24.3% vs 12.3%, p = 0.0062).INTERPRETATION: While the generalized decrease in
P. aeruginosa resistance, linked to a major reduction in the prevalence of XDR strains, is encouraging, the negative counterpart is the increase in the proportion of XDR strains producing carbapenemases, associated to the significant advance of the concerning world-wide disseminated hypervirulent high-risk clone ST235. Continued high-resolution surveillance, integrating phenotypic and genomic data, is necessary for understanding resistance trends and analyzing the impact of national plans on antimicrobial resistance.
FUNDING: MSD and the Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea-NextGenerationEU.
AB - BACKGROUND:
Pseudomonas aeruginosa healthcare-associated infections are one of the top antimicrobial resistance threats world-wide. In order to analyze the current trends, we performed a Spanish nation-wide high-resolution analysis of the susceptibility profiles, the genomic epidemiology and the resistome of
P. aeruginosa over a five-year time lapse.
METHODS: A total of 3.180 nonduplicated
P. aeruginosa clinical isolates from two Spanish nation-wide surveys performed in October 2017 and 2022 were analyzed. MICs of 13 antipseudomonals were determined by ISO-EUCAST. Multidrug resistance (MDR)/extensively drug resistance (XDR)/difficult to treat resistance (DTR)/pandrug resistance (PDR) profiles were defined following established criteria. All XDR/DTR isolates were subjected to whole genome sequencing (WGS).
FINDINGS: A decrease in resistance to all tested antibiotics, including older and newer antimicrobials, was observed in 2022 vs 2017. Likewise, a major reduction of XDR (15.2% vs 5.9%) and DTR (4.2 vs 2.1%) profiles was evidenced, and even more patent among ICU isolates [XDR (26.0% vs 6.0%) and DTR (8.9% vs 2.6%)] (p < 0.001). The prevalence of Extended-spectrum β-lactamase/carbapenemase production was slightly lower in 2022 (2.1%. vs 3.1%, p = 0.064). However, there was a significant increase in the proportion of carbapenemase production among carbapenem-resistant strains (29.4% vs 18.1%, p = 0.0246). While ST175 was still the most frequent clone among XDR, a slight reduction in its prevalence was noted (35.9% vs 45.5%, p = 0.106) as opposed to ST235 which increased significantly (24.3% vs 12.3%, p = 0.0062).INTERPRETATION: While the generalized decrease in
P. aeruginosa resistance, linked to a major reduction in the prevalence of XDR strains, is encouraging, the negative counterpart is the increase in the proportion of XDR strains producing carbapenemases, associated to the significant advance of the concerning world-wide disseminated hypervirulent high-risk clone ST235. Continued high-resolution surveillance, integrating phenotypic and genomic data, is necessary for understanding resistance trends and analyzing the impact of national plans on antimicrobial resistance.
FUNDING: MSD and the Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea-NextGenerationEU.
KW - COVID-19
KW - Electronic health records
KW - PASC
KW - Post-acute sequelae of SARS-CoV-2
KW - SARS-CoV-2
UR - http://www.scopus.com/inward/record.url?scp=85171433118&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/73577513-61be-3351-8e61-53f1222bf5f1/
U2 - 10.1016/j.lanepe.2023.100736
DO - 10.1016/j.lanepe.2023.100736
M3 - Article
C2 - 37753216
AN - SCOPUS:85171433118
VL - 34
SP - 100736
JO - The Lancet Regional Health - Europe
JF - The Lancet Regional Health - Europe
M1 - 100736
ER -