ArticleAntimicrobial agents and chemotherapy2006
Distribution of tetracycline resistance genes in Actinobacillus pleuropneumoniae isolates from Spain.
Article in Antimicrobial agents and chemotherapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Serotyping and antimicrobial resistance of Actinobacillus pleuropneumoniae isolates from fattening pigs in Poland from 2019 to 2024.BMC veterinary research · 2025Article
- Characterization of small plasmids carrying florfenicol resistance geneFrontiers in veterinary science · 2023Article
- Genetic Diversity ofVeterinary sciences · 2022Article
- Antimicrobial Resistance Genes in PorcineAntibiotics (Basel, Switzerland) · 2020Article
- Antimicrobial Resistance inMicrobiology spectrum · 2018Review
- Evidence of Illegitimate Recombination Between TwoFrontiers in microbiology · 2018Article
- PCR-Based Analysis of ColE1 Plasmids in Clinical Isolates and Metagenomic Samples Reveals Their Importance as Gene Capture Platforms.Frontiers in microbiology · 2018Article
- ICEApl1, an Integrative Conjugative Element Related to ICEHin1056, Identified in the Pig Pathogen Actinobacillus pleuropneumoniae.Frontiers in microbiology · 2016Article
- Review
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5 authors.
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Abstract
Actinobacillus pleuropneumoniae is the etiological agent of porcine pleuropneumonia. Tetracycline is used for therapy of this disease, and A. pleuropneumoniae carrying the tet(B) gene, coding for an efflux protein that reduces the intercellular tetracycline level, has been described previously. Of the 46 tetracycline-resistant (Tc(r)) Spanish A. pleuropneumoniae isolates used in this study, 32 (70%) carried the tet(B) gene, and 30 of these genes were associated with plasmids. Eight (17%) isolates carried the tet(O) gene, two (4%) isolates carried either the tet(H) or the tet(L) gene, and all these genes were associated with plasmids. This is the first description of these tet genes in A. pleuropneumoniae. The last two Tc(r) isolates carried none of the tet genes examined. Except for tet(O)-containing plasmids, the other 34 Tc(r) plasmids were transformable into an Escherichia coli recipient. Two plasmids were completely sequenced. Plasmid p11745, carrying the tet(B) gene, was 5,486 bp and included a rep gene, encoding a replication-related protein, and two open reading frames (ORFs) with homology to mobilization genes of Neisseria gonorrhoeae plasmid pSJ7.4. Plasmid p9555, carrying the tet(L) gene, was 5,672 bp and, based on its G+C content, consisted of two regions, one of putative gram-positive origin containing the tet(L) gene and the other comprising four ORFs organized in an operon-like structure with homology to mobilization genes in other plasmids of gram-negative bacteria.
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