Genomic changes in Mycoplasma pneumoniae caused by adaptation to environmental or ecologic pressures are poorly understood. We collected M. pneumoniae from children who had confirmed pneumonia in Taiwan during 2017-2020. We used whole-genome sequencing to compare these isolates with a worldwide collection of current and historical clinical strains for characterizing population structures. A phylogenetic tree for 284 strains showed that all sequenced strains consisted of 5 clades: T1-1 (sequence type [ST]1), T1-2 (mainly ST3), T1-3 (ST17), T2-1 (mainly ST2), and T2-2 (mainly ST14). We identified a putative recombination block containing 6 genes (MPN366-371). Macrolide resistance involving 23S rRNA mutations was detected for each clade. Clonal expansion of macrolide resistance occurred mostly within subtype 1 strains, of which clade T1-2 showed the highest recombination rate and genome diversity. Functional characterization of recombined regions provided clarification of the biologic role of these recombination events in the evolution of M. pneumoniae.
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MIT, Dept Biol, Cambridge, MA 02139 USA
Univ Penn, Perelman Sch Med, Dept Microbiol, Philadelphia, PA 19104 USAMIT, Dept Biol, Cambridge, MA 02139 USA
Minot, Samuel
Melo, Mariane B.
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MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Dept Biol, Cambridge, MA 02139 USA
Melo, Mariane B.
Li, Fugen
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MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Dept Biol, Cambridge, MA 02139 USA
Li, Fugen
Lu, Diana
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MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Dept Biol, Cambridge, MA 02139 USA
Lu, Diana
Niedelman, Wendy
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MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Dept Biol, Cambridge, MA 02139 USA
Niedelman, Wendy
Levine, Stuart S.
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MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Dept Biol, Cambridge, MA 02139 USA
Levine, Stuart S.
Saeij, Jeroen P. J.
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MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Dept Biol, Cambridge, MA 02139 USA