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The guanine–hypoxanthine permease GhxP of Erwinia amylovora facilitates the influx of the toxic guanine derivative 6‐thioguanine
Author(s) -
Gatchell I.T.,
Huntley R.B.,
Schultes N.P.,
Mourad G.S.
Publication year - 2021
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.14925
Subject(s) - guanine , hypoxanthine , erwinia , permease , derivative (finance) , chemistry , biochemistry , microbiology and biotechnology , biology , escherichia coli , nucleotide , gene , enzyme , financial economics , economics
Aim Erwinia amylovora is the causal agent of fire blight, a devastating disease of apples and pears. This study determines whether the E. amylovora guanine–hypoxanthine transporter (EaGhxP) is required for virulence and if it can import the E. amylovora produced toxic analogue 6‐thioguanine (6TG) into cells. Methods and Results Characterization of EaGhxP in guanine transport deficient Escherichia coli reveals that it can transport guanine, hypoxanthine and the toxic analogues 8‐azaguanine (8AG) and 6TG. Similarly, EaGhxP transports 8AG and 6TG into E. amylovora cells. EaGhxP has a high affinity for 6TG with a K i of 3·7 µmol l −1 . An E. amylovora ⊿ghxP::Cam r strain shows resistance to growth on 8AG and 6TG. Although EaGhxP is expressed during active disease propagation, it is not necessary for virulence as determined on immature apple and pear assays. Conclusions EaGhxP is not required for virulence, but it does import 6TG into E. amylovora cells. Significance and impact of the Study As part of the disease establishment process, E. amylovora synthesizes and exports a toxic guanine derivative 6TG. Our results are counter intuitive and show that EaGhxP, an influx transporter, can move 6TG into cells raising questions regarding the role of 6TG in disease establishment.