USE OF POLYMERASE CHAIN-REACTION FINGERPRINTING TO COMPARE CLINICAL ISOLATES OF BACTEROIDES-FRAGILIS AND BACTEROIDES-THETAIOTAOMICRON FROM GERMANY AND THE UNITED-STATES
Mc. Claros et al., USE OF POLYMERASE CHAIN-REACTION FINGERPRINTING TO COMPARE CLINICAL ISOLATES OF BACTEROIDES-FRAGILIS AND BACTEROIDES-THETAIOTAOMICRON FROM GERMANY AND THE UNITED-STATES, Clinical infectious diseases, 25, 1997, pp. 295-298
Accurate identification of Bacteroides species is often problematic. T
herefore, we used a polymerase chain reaction (PCR) fingerprinting tec
hnique with either a single nonspecific primer derived from tDNA inter
genic spacer or a single primer that anneals to mini-and microsatellit
e DNA sequences to compare 34 clinical isolates of B. fragilis and 21
clinical isolates of B. thetaiotaomicron from Southern California with
32 clinical isolates of B. fragilis and 10 isolates of B. thetaiotaom
icron from Germany. All German B. fragilis isolates (32 of 32) formed
one PCR fingerprint group that matched the PCR profile of the B. fragi
lis reference strain ATCC (American Type Culture Collection) 25285, re
presentative of DNA homology group I, In contrast, the isolates from S
outhern California formed two PCR fingerprint groups, Although most of
these strains (29 of 34) also matched B. fragilis ATCC 25285, some st
rains (4 of 34) matched the DNA homology group II reference strain VPI
(Virginia Polytechnic Institute) 2393, One of the 34 strains showed a
unique profile, German B. thetaiotaomicron strains (10 of 10) formed
one PCR fingerprint group, matching the reference strain B. thetaiotao
micron ATCC 29742, whereas the B. thetaiotaomicron isolates from South
ern California showed heterogenous profiles.