J 2024

Resistome in the indoor dust samples from workplaces and households: a pilot study

KLVAŇOVÁ, Eva; Petra VÍDEŇSKÁ; Vojtěch BARTOŇ; Jan BÖHM; Petra ŠPLÍCHALOVÁ et. al.

Základní údaje

Originální název

Resistome in the indoor dust samples from workplaces and households: a pilot study

Autoři

KLVAŇOVÁ, Eva; Petra VÍDEŇSKÁ; Vojtěch BARTOŇ; Jan BÖHM; Petra ŠPLÍCHALOVÁ; Viktorie KOKSOVÁ; Milan URÍK; Barbara LÁNÍČKOVÁ; Roman PROKEŠ; Eva BUDINSKÁ; Jana KLÁNOVÁ a Petra BOŘILOVÁ LINHARTOVÁ

Vydání

Frontiers in Cellular and Infection Microbiology, Lausanne, Frontiers, 2024, 2235-2988

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Organizace

Přírodovědecká fakulta – Masarykova univerzita – Repozitář

UT WoS

001378646400001

EID Scopus

2-s2.0-85212207012

Klíčová slova anglicky

antibiotic resistance gene; indoor environment; microbiome; antimicrobial resistance; hospital

Návaznosti

EF15_003/0000469, projekt VaV. GA22-32743S, projekt VaV. LM2023069, projekt VaV. 857560, interní kód Repo.
Změněno: 15. 1. 2025 00:50, RNDr. Daniel Jakubík

Anotace

V originále

The antibiotic resistance genes (ARGs) limit the susceptibility of bacteria to antimicrobials, representing a problem of high importance. Current research on the presence of ARGs in microorganisms focuses mainly on humans, livestock, hospitals, or wastewater. However, the spectrum of ARGs in the dust resistome in workplaces and households has gone relatively unexplored. This pilot study aimed to analyze resistome in indoor dust samples from participants' workplaces (a pediatric hospital, a maternity hospital, and a research center) and households and compare two different approaches to the ARGs analysis; high-throughput quantitative PCR (HT-qPCR) and whole metagenome shotgun sequencing (WMGS). In total, 143 ARGs were detected using HT-qPCR, with ARGs associated with the macrolides, lincosamides, and streptogramin B (MLSB) phenotype being the most abundant, followed by MDR (multi-drug resistance) genes, and genes conferring resistance to aminoglycosides. A higher overall relative quantity of ARGs was observed in indoor dust samples from workplaces than from households, with the pediatric hospital being associated with the highest relative quantity of ARGs. WMGS analysis revealed 36 ARGs, of which five were detected by both HT-qPCR and WMGS techniques. Accordingly, the efficacy of the WMGS approach to detect ARGs was lower than that of HT-qPCR. In summary, our pilot data revealed that indoor dust in buildings where people spend most of their time (workplaces, households) can be a significant source of antimicrobial-resistant microorganisms, which may potentially pose a health risk to both humans and animals.

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