TY - JOUR
T1 - Within-host genomic evolution of methicillin-resistant Staphylococcus aureus in long-term carriers
AU - Larsen, Tine Graakjær
AU - Worning, Peder
AU - Samaniego Castruita, Jose Alfredo
AU - Westh, Henrik
AU - Bartels, Mette Damkjær
N1 - © 2024. The Author(s).
PY - 2024/1/11
Y1 - 2024/1/11
N2 - Assessing the genomic evolution of Staphylococcus aureus can help us understand how the bacteria adapt to its environment. In this study, we aimed to assess the mutation rate within 144 methicillin-resistant Staphylococcus aureus (MRSA) carriers with a carriage time from 4 to 11 years, including some carriers who belonged to the same households. We found that 23 of the 144 individuals had completely different MRSA types over time and were therefore not long-term carriers of the same MRSA. From the remaining 121 individuals, we performed whole-genome sequencing (WGS) on 424 isolates and then compared these pairwise using core genome multilocus sequence typing (cgMLST) and single-nucleotide polymorphism (SNP) analyses. We found a median within-host mutation rate in long-term MRSA carriers of 4.9 (3.4-6.9) SNPs/genome/year and 2.7 (1.8-4.2) allelic differences/genome/year, when excluding presumed recombination. Furthermore, we stratified the cohort into subgroups and found no significant difference between the median mutation rate of members of households, individuals with presumed continued exposure, e.g., from travel and persons without known continued exposure. Finally, we found that SNPs occurred at random within the genes in our cohort. KEY POINTS: • Median mutation rate within long-term MRSA carriers of 4.9 (3.4-6.9) SNPs/genome/year • Similar median mutation rates in subgroups (households, travelers) • No hotspots for SNPs within the genome.
AB - Assessing the genomic evolution of Staphylococcus aureus can help us understand how the bacteria adapt to its environment. In this study, we aimed to assess the mutation rate within 144 methicillin-resistant Staphylococcus aureus (MRSA) carriers with a carriage time from 4 to 11 years, including some carriers who belonged to the same households. We found that 23 of the 144 individuals had completely different MRSA types over time and were therefore not long-term carriers of the same MRSA. From the remaining 121 individuals, we performed whole-genome sequencing (WGS) on 424 isolates and then compared these pairwise using core genome multilocus sequence typing (cgMLST) and single-nucleotide polymorphism (SNP) analyses. We found a median within-host mutation rate in long-term MRSA carriers of 4.9 (3.4-6.9) SNPs/genome/year and 2.7 (1.8-4.2) allelic differences/genome/year, when excluding presumed recombination. Furthermore, we stratified the cohort into subgroups and found no significant difference between the median mutation rate of members of households, individuals with presumed continued exposure, e.g., from travel and persons without known continued exposure. Finally, we found that SNPs occurred at random within the genes in our cohort. KEY POINTS: • Median mutation rate within long-term MRSA carriers of 4.9 (3.4-6.9) SNPs/genome/year • Similar median mutation rates in subgroups (households, travelers) • No hotspots for SNPs within the genome.
KW - Humans
KW - Methicillin-Resistant Staphylococcus aureus/genetics
KW - Staphylococcus aureus/genetics
KW - Staphylococcal Infections/microbiology
KW - Genomics
KW - Multilocus Sequence Typing
KW - Mutation Rate
KW - Recombination
KW - Within-host
KW - Genomic evolution
KW - SNP
KW - MRSA
KW - cgMLST
UR - http://www.scopus.com/inward/record.url?scp=85182098035&partnerID=8YFLogxK
U2 - 10.1007/s00253-023-12932-3
DO - 10.1007/s00253-023-12932-3
M3 - Journal article
C2 - 38212970
SN - 0175-7598
VL - 108
SP - 95
JO - Applied microbiology and biotechnology
JF - Applied microbiology and biotechnology
IS - 1
ER -