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Rapid evolution and host immunity drive the rise and fall of carbapenem resistance during an acute Pseudomonas aeruginosa infection.

Rachel M WheatleyJulio Diaz CaballeroNatalia KapelFien H R De WinterPramod JangirAngus M QuinnEster Del Barrio-TofiñoCarla López-CausapéJessica HedgeGabriel TorrensThomas Ewout van der SchalkXavier Basil BrittoFelipe Fernández-CuencaAngel ArenzanaClaudia RecanatiniLeen TimbermontFrangiscos SifakisAlexey RuzinOmar AliChristine LammensHerman GoossensJan KluytmansSamir Kumar-SinghAntonio OliverSurbhi Malhotra-KumarPauline Hall Barrientos
Published in: Nature communications (2021)
It is well established that antibiotic treatment selects for resistance, but the dynamics of this process during infections are poorly understood. Here we map the responses of Pseudomonas aeruginosa to treatment in high definition during a lung infection of a single ICU patient. Host immunity and antibiotic therapy with meropenem suppressed P. aeruginosa, but a second wave of infection emerged due to the growth of oprD and wbpM meropenem resistant mutants that evolved in situ. Selection then led to a loss of resistance by decreasing the prevalence of low fitness oprD mutants, increasing the frequency of high fitness mutants lacking the MexAB-OprM efflux pump, and decreasing the copy number of a multidrug resistance plasmid. Ultimately, host immunity suppressed wbpM mutants with high meropenem resistance and fitness. Our study highlights how natural selection and host immunity interact to drive both the rapid rise, and fall, of resistance during infection.
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