Phenotypic and genotypic analysis of antimicrobial resistance in Nocardia species

Author:

Hershko Yizhak12,Levytskyi Katia1,Rannon Ella3,Assous Marc V4,Ken-Dror Shifra5,Amit Sharon6,Ben-Zvi Haim7,Sagi Orli8,Schwartz Orna9,Sorek Nadav10,Szwarcwort Moran11,Barkan Daniel1ORCID,Burstein David3,Adler Amos212ORCID

Affiliation:

1. Koret School of Veterinary Medicine, Robert H. Smith Faculty for Agriculture, The Hebrew University of Jerusalem , Rehovot , Israel

2. Tel Aviv Sourasky Medical Center , Tel Aviv , Israel

3. The Shmunis School of Biomedicine and Cancer Research, Faculty of Life Science, Tel Aviv University , Tel Aviv 6997801 , Israel

4. Clinical Microbiology Laboratory, Shaare Zedek Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem , Jerusalem , Israel

5. Clalit Health Services, Haifa and Western Galilee District , Israel

6. Sheba Medical Center , Tel Hashomer, Ramat Gan , Israel

7. Microbiology Laboratory, Rabin Medical Center, Beilinson Hospital , Petah Tikva , Israel

8. Clinical Microbiology Laboratory, Soroka University Medical Center , Beer-Sheva 84105 , Israel

9. Wolfson Medical Center , Holon , Israel

10. Assuta Ashdod University Hospital , Ashdod , Israel

11. Clinical Microbiology Laboratories, Laboratories Division, Rambam Health Care Campus , Haifa , Israel

12. Department of Epidemiology and Preventive Medicine, Faculty of Medicine, Tel Aviv University , Tel Aviv , Israel

Abstract

Abstract Background Antimicrobial resistance is common in Nocardia species but data regarding the molecular mechanisms beyond their resistance traits are limited. Our study aimed to determine the species distribution, the antimicrobial susceptibility profiles, and investigate the associations between the resistance traits and their genotypic determinants. Methods The study included 138 clinical strains of Nocardia from nine Israeli microbiology laboratories. MIC values of 12 antimicrobial agents were determined using broth microdilution. WGS was performed on 129 isolates of the eight predominant species. Bioinformatic analysis included phylogeny and determination of antimicrobial resistance genes and mutations. Results Among the isolates, Nocardia cyriacigeorgica was the most common species (36%), followed by Nocardia farcinica (16%), Nocardia wallacei (13%), Nocardia abscessus (9%) and Nocardia brasiliensis (8%). Linezolid was active against all isolates, followed by trimethoprim/sulfamethoxazole (93%) and amikacin (91%). Resistance to other antibiotics was species-specific, often associated with the presence of resistance genes or mutations: (1) aph(2″) in N. farcinica and N. wallacei (resistance to tobramycin); (ii) blaAST-1 in N. cyriacigeorgica and Nocardia neocaledoniensis (resistance to amoxicillin/clavulanate); (iii) blaFAR-1 in N. farcinica (resistance to ceftriaxone); (iv) Ser83Ala substitution in the gyrA gene in four species (resistance to ciprofloxacin); and (v) the 16S rRNA m1A1408 methyltransferase in N. wallacei isolates (correlating with amikacin resistance). Conclusions Our study provides a comprehensive understanding of Nocardia species diversity, antibiotic resistance patterns, and the molecular basis of antimicrobial resistance. Resistance appears to follow species-related patterns, suggesting a lesser role for de novo evolution or transmission of antimicrobial resistance.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

Reference53 articles.

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