“…The toxins are believed to slow down (dormancy) or suppress growth (cell death) in order to survive in rapidly changing environments or stress conditions (Gerdes et al, 1986;Yamaguchi and Inouye, 2009). TA systems have other diverse functions and roles, including ensuring persistence of plasmids during replication, virulence, antibiotic tolerance, phage defense and biofilm formation (Hayes, 2003;Sass et al, 2014;Shidore and Triplett, 2017). A number of genes related to different classes of TA systems were found in JZ38 ( Supplementary Table S16), including an adenylate cyclase toxin (cyaA) (Cannella et al, 2017), SOS-induced toxins (tisB, symE) and their regulator (lexA) (Gerdes and Wagner, 2007), membrane stress phage shock proteins (pspABCD) (Engl et al, 2010), toxins involved in cell division (cptAB, fstZ, merB) (Masuda et al, 2012) cell death (phd, doc, clpXP) (Smith and Magnuson, 2004), promoters of persister cells (hha-tomB, hipAB in plasmid p2).…”