Molecular analysis of the tlyA gene in Campylobacter lari
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25906999
DOI
10.1007/s12223-015-0389-8
PII: 10.1007/s12223-015-0389-8
Knihovny.cz E-resources
- MeSH
- Bacterial Proteins chemistry genetics MeSH
- Campylobacter lari chemistry classification genetics isolation & purification MeSH
- Phylogeny MeSH
- Hemolysin Proteins chemistry genetics MeSH
- Campylobacter Infections microbiology veterinary MeSH
- Chickens microbiology MeSH
- Environmental Microbiology MeSH
- Bivalvia microbiology MeSH
- Molecular Sequence Data MeSH
- Open Reading Frames MeSH
- Promoter Regions, Genetic MeSH
- Birds microbiology MeSH
- Amino Acid Sequence MeSH
- Base Sequence MeSH
- Sequence Alignment MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins MeSH
- Hemolysin Proteins MeSH
Full-length tlyA gene and its adjacent genetic loci from the urease-positive thermophilic Campylobacter (UPTC) CF89-12 [approximately 15,000 base pairs (bp) in length], as well as a reference strain Campylobacter lari RM2100 (approximately 9,000 bp), were analyzed. The possible open-reading frame of tlyA from UPTC CF89-12 was shown to have 720 bp with a calculated molecular mass of approximately 26.7 kDa. Using a primer pair designed in silico, a total of approximately 1.1 kbp consisting of putative promoter region, structural gene for tlyA, and its adjacent genetic loci were identified in all 17 C. lari isolates [n = 13 for UPTC; n = 4 for urease-negative (UN) C. lari]. Although sequence differences were demonstrated at approximately 20 loci within the 90 bp non-coding (NC) region, including the putative promoter structure candidates immediately upstream of the tlyA gene among the 18 isolates including C. lari RM2100, no sequence differences were identified within the NC region among the five UN C. lari isolates examined. A start codon ATG and a probable ribosome-binding site, AGGC(T)GG(A), for the tlyA gene were identified in all 18 isolates, including C. lari RM2100. The putative intrinsic ρ-independent transcriptional terminator structure candidate was also identified for the tlyA gene in both UPTC CF89-12 and C. lari RM2100. Additionally, the hemolysis assay was performed with some of the C. lari isolates. The tlyA gene nucleotide sequence data may possibly be useful for discrimination between UN C. lari and UPTC organisms, as well as for the differentiation among the four thermophilic Campylobacter species.
Centre for Infection and Immunity Queen's University Belfast BT9 7AB Northern Ireland UK
Faculty of Pharmaceutical Sciences Hokuriku University Kanazawa 920 1181 Japan
School of Biomedical Sciences University of Ulster Coleraine BT52 1SA UK
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