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Isogenic Variation of Helicobacter pylori Strain Resulting in Heteroresistant Antibacterial Phenotypes in a Single Host In Vivo
Author(s) -
Lee Yong Chan,
Lee SunYoung,
Pyo Jae Hee,
Kwon Dong H.,
Rhee Jong Chul,
Kim Jae J.
Publication year - 2005
Publication title -
helicobacter
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.206
H-Index - 79
eISSN - 1523-5378
pISSN - 1083-4389
DOI - 10.1111/j.1523-5378.2005.00316.x
Subject(s) - biology , genetics , phylogenetic tree , microbiology and biotechnology , gene
Background. Antibiotic‐susceptible and ‐resistant Helicobacter pylori can be present simultaneously in the same host. The aim of this study was to evaluate the genomic diversity of H. pylori strains resulting in heteroresistant antibacterial phenotypes. Materials and methods. Twenty‐one pairs of H. pylori strains isolated from the antrum and body displaying heteroresistant antibacterial phenotypes were included. We compared the genotypes of paired‐isolates by random arbitrarily primed polymerase chain reaction (PCR), flagella gene PCR‐based restriction fragment length polymorphism, and flaA gene sequencing. In metronidazole‐heteroresistant isolates, the sequence variation of rdxA and frxA genes was analyzed using phylogenetic analysis. Results. The DNA fingerprinting patterns of the paired isolates revealed that 12 pairs (57.1%) were identical, whereas one pair (3.8%) was different. The remaining eight pairs (38.1%) of isolates showed minor heterogenecity in fingerprinting patterns. In flaA gene sequencing, these identical and similar isolates showed close sequence similarity between the antrum and body, whereas different isolate showed 31 points of different nucleotide sequences. Phylogenetic analysis of the metronidazole‐heteroresistant pairs showed consistent genetic relatedness of each paired isolates despite the sequence variation of the rdxA or frxA genes in five pairs (71.4%). Conclusions. These results suggest that continuing genomic diversities in the same strain may play an important role in modulating the antibiotic‐heteroresistant H. pylori in vivo.