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. 2018 Apr;24(4):741–745. doi: 10.3201/eid2404.170095

Table 2. Mutations differentiating Clostridium difficile RT017 imipenem-resistant isolates found at hospital A from imipenem-susceptible isolates found at hospital B, Portugal.

Gene in M68 genome* Genome position* Nucleotide in M68 Nucleotide change† Amino acid change† Gene product
RS02665 512416 C C578T Ala193Val‡ Multidrug ATP-binding cassette transporter permease, associated with antimicrobial drug resistance
RS04280/pbp1 905394 G G1663A Ala555Thr‡ Penicillin-binding transpeptidase
RS04935 1048151 C T1010C Ile337Thr‡ 3-Isopropylmalate dehydratase large subunit
RS05670/pbp3 1221182 G A2162C Tyr721Ser‡ Penicillin-binding protein
RS07765 1666351 G G214T Gly72§ Hypothetical protein
RS07795/hisB 1671129 T T209C Ile70Thr‡ Imidazoleglycerol-phosphate dehydratase
RS07810 1673280 T C474T Ala158Ala Imidazoleglycerol-phosphate synthase cyclase subunit
RS08415 1792079 G A241G Lys81Glu‡ Hypothetical protein (domain of MerR-like transcriptional regulators)
RS08810 1882950 C C420T Asp140Asp Flavodoxin
RS14235 3083548 G G421T Gly141§ Haloacid dehalogenase
RS18530 4054525 C C220T Gln74§ S-adenosyl methionine–dependent methyltransferase
RS19130/gyrA 4174650 C C245T Thr82Ile‡ DNA gyrase subunit A
RS19545 4255124 C C400T His134Tyr‡ Phage portal, SPP1 Gp6-like family protein

*Relative to the annotation of the C. difficile M68 genome (GenBank accession no. NC_017175).
†Changes observed between imipenem-resistant and imipenem-susceptible isolates. 
‡Nonsynonymous mutations.
§Mutations leading to putative protein truncation.