“…Massively parallel sequencing combined with traditional transposon mutagenesis [101] , as well as high-throughput screening of transposon insertion libraries, have been used to track genes whose inactivation modifies the susceptibility to antibiotics [102] , [103] . This method has been used to analyse the resistome of different pathogens, including Pseudomonas aeruginosa [104] , [105] , [106] , [107] , [108] , [109] , [110] , [111] , [112] , [113] , [114] , [115] , [116] , [117] , [118] , [119] , E. coli [110] , Staphylococcus aureus [111] , [112] or Klebsiella pneumoniae [113] , among other bacteria [114] , [115] .…”