Author/Editor     Rupnik, Maja; Kato, Naoki; Grabnar, Miklavž; Kato, Haro
Title     New types of toxin A-negative, toxin B-positive strains among Clostridium difficile isolates from Asia
Type     članek
Source     J Clin Microbiol
Vol. and No.     Letnik 41, št. 3
Publication year     2003
Volume     str. 1118-25
Language     eng
Abstract     A total of 56 C. dificile strains were selected from 310 isolates obtained from different hospitals in Japan and Korea and from healthy infants from Indonesia. Strains that had been previously typed by pulsed-field gel electrophoresis and PCR ribotyping, were characterized by toxinotyping and binary toxin gene detection. When toxinotyped, 35 strains were determined to be toxinotype 0, whereas 21 strains showed variations in toxin genes and could be grouped into 11 variant toxinotypes. Six of the toxinotypes had been described before (I, III, IV, VllI, IX, and XII). In addition, five new toxinotypes were defined (XVI to XX). Three of the new toxinotypes (XVIII, XIX, and XX) vary only in repetitive regions of tcdA and produce both toxins. In two strains from toxinotypes XVI and XVII, the production of TcdA could not be detected with commercial immunological kits. Strain J9965 (toxinotype XVII) was in PaLoc similar but not identical to another known A-B+ strain, C. difficile 8864. Strain SUC 36 (toxinotype XVI), on the other hand, was similar to well-defined group consisting of toxinotypes V, VI, and VII, which thus far includes only A+B+ strains. Toxinotypes XVI and XVII represent two new groups of AB+ strains. Strains of the well-known A-B+ group from toxinotype VIII have a nonsense mutation at the beginning of tcdA gene, and the introduction of a stop codon at amino acid position 47 results in nonproduction of TcdA. The 5`-end sequence of tcdA in two newly described A-B+ strains does not contain an identical mutation. The prevalence of variant C. difficile strains varied greatly among nine hospitals. Only five strains from four different hospitals were positive in PCR for amplification of the binary toxin gene.
Descriptors     CLOSTRIDIUM DIFFICILE
BACTERIAL TYPING TECHNIQUES
BACTERIAL TOXINS
ELECTROPHORESIS, GEL, PULSED-FIELD
POLYMERASE CHAIN REACTION