Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites

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Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites. / Lykkeberg, Anne Kruse; Halling-Sørensen, Bent; Jensen, Lars Bogø.

In: Veterinary Microbiology, Vol. 121, No. 1-2, 2007, p. 116-124.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lykkeberg, AK, Halling-Sørensen, B & Jensen, LB 2007, 'Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites', Veterinary Microbiology, vol. 121, no. 1-2, pp. 116-124. https://doi.org/10.1016/j.vetmic.2006.11.020

APA

Lykkeberg, A. K., Halling-Sørensen, B., & Jensen, L. B. (2007). Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites. Veterinary Microbiology, 121(1-2), 116-124. https://doi.org/10.1016/j.vetmic.2006.11.020

Vancouver

Lykkeberg AK, Halling-Sørensen B, Jensen LB. Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites. Veterinary Microbiology. 2007;121(1-2):116-124. https://doi.org/10.1016/j.vetmic.2006.11.020

Author

Lykkeberg, Anne Kruse ; Halling-Sørensen, Bent ; Jensen, Lars Bogø. / Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites. In: Veterinary Microbiology. 2007 ; Vol. 121, No. 1-2. pp. 116-124.

Bibtex

@article{62ff1200c36c11dcbee902004c4f4f50,
title = "Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites",
abstract = "Susceptibilities to metabolites of tiamulin (TIA) and enrofloxacin (ENR) were tested using selected bacteria with previously defined minimal inhibitory concentrations (MIC). The TIA metabolites tested were: N-deethyl-tiamulin (DTIA), 2{\ss}-hydroxy-tiamulin (2{\ss}-HTIA) and 8a-hydroxy-tiamulin (8a-HTIA), and the ENR metabolites were: ciprofloxacin (CIP) and enrofloxacin N-oxide (ENR-N). Bacteria, all of porcine origin, were selected as representatives of bacterial infections (Staphylococcus hyicus and Actinobacillus pleuropneumoniae), zoonotic bacteria (Campylobacter coli) and indicator bacteria (Escherichia coli and enterococci). Furthermore the effects of these compounds were tested on the microbial community of active sludge to test any negative effect on colony forming units (CFU). DTIA had a potency of 12.5-50% of the potency of TIA. 2{\ss}-HTIA and 8a-HTIA had potencies less than 1% of the potency of TIA. ENR-N had a potency of 0.75-1.5% of the potency of ENR, while CIP and ENR had similar potencies. Results obtained here indicate that CIP and DTIA could contribute to the selective pressure for upholding antimicrobial resistant bacteria in animals under ENR or TIA treatment. The most potent metabolites CIP and DTIA showed considerable potencies against activated sludge bacteria compared to the parent compounds. EC50 (µg/ml) for ENR, CIP, TIA and DTIA were 0.018 [95% CI: 0.028-0.149], 0.064 [95% CI: 0.007-0.046], 6.0 [95% CI: 3.6-9.8], and 9.7 [95% CI: 5.8-16.3], respectively. This indicates that the compounds can change the bacterial population in the sludge, and hereby alter the properties of the sludge. ",
keywords = "Former Faculty of Pharmaceutical Sciences",
author = "Lykkeberg, {Anne Kruse} and Bent Halling-S{\o}rensen and Jensen, {Lars Bog{\o}}",
year = "2007",
doi = "10.1016/j.vetmic.2006.11.020",
language = "English",
volume = "121",
pages = "116--124",
journal = "Veterinary Microbiology",
issn = "0378-1135",
publisher = "Elsevier",
number = "1-2",

}

RIS

TY - JOUR

T1 - Susceptibility of bacteria isolated from pigs to tiamulin and enrofloxacin metabolites

AU - Lykkeberg, Anne Kruse

AU - Halling-Sørensen, Bent

AU - Jensen, Lars Bogø

PY - 2007

Y1 - 2007

N2 - Susceptibilities to metabolites of tiamulin (TIA) and enrofloxacin (ENR) were tested using selected bacteria with previously defined minimal inhibitory concentrations (MIC). The TIA metabolites tested were: N-deethyl-tiamulin (DTIA), 2ß-hydroxy-tiamulin (2ß-HTIA) and 8a-hydroxy-tiamulin (8a-HTIA), and the ENR metabolites were: ciprofloxacin (CIP) and enrofloxacin N-oxide (ENR-N). Bacteria, all of porcine origin, were selected as representatives of bacterial infections (Staphylococcus hyicus and Actinobacillus pleuropneumoniae), zoonotic bacteria (Campylobacter coli) and indicator bacteria (Escherichia coli and enterococci). Furthermore the effects of these compounds were tested on the microbial community of active sludge to test any negative effect on colony forming units (CFU). DTIA had a potency of 12.5-50% of the potency of TIA. 2ß-HTIA and 8a-HTIA had potencies less than 1% of the potency of TIA. ENR-N had a potency of 0.75-1.5% of the potency of ENR, while CIP and ENR had similar potencies. Results obtained here indicate that CIP and DTIA could contribute to the selective pressure for upholding antimicrobial resistant bacteria in animals under ENR or TIA treatment. The most potent metabolites CIP and DTIA showed considerable potencies against activated sludge bacteria compared to the parent compounds. EC50 (µg/ml) for ENR, CIP, TIA and DTIA were 0.018 [95% CI: 0.028-0.149], 0.064 [95% CI: 0.007-0.046], 6.0 [95% CI: 3.6-9.8], and 9.7 [95% CI: 5.8-16.3], respectively. This indicates that the compounds can change the bacterial population in the sludge, and hereby alter the properties of the sludge.

AB - Susceptibilities to metabolites of tiamulin (TIA) and enrofloxacin (ENR) were tested using selected bacteria with previously defined minimal inhibitory concentrations (MIC). The TIA metabolites tested were: N-deethyl-tiamulin (DTIA), 2ß-hydroxy-tiamulin (2ß-HTIA) and 8a-hydroxy-tiamulin (8a-HTIA), and the ENR metabolites were: ciprofloxacin (CIP) and enrofloxacin N-oxide (ENR-N). Bacteria, all of porcine origin, were selected as representatives of bacterial infections (Staphylococcus hyicus and Actinobacillus pleuropneumoniae), zoonotic bacteria (Campylobacter coli) and indicator bacteria (Escherichia coli and enterococci). Furthermore the effects of these compounds were tested on the microbial community of active sludge to test any negative effect on colony forming units (CFU). DTIA had a potency of 12.5-50% of the potency of TIA. 2ß-HTIA and 8a-HTIA had potencies less than 1% of the potency of TIA. ENR-N had a potency of 0.75-1.5% of the potency of ENR, while CIP and ENR had similar potencies. Results obtained here indicate that CIP and DTIA could contribute to the selective pressure for upholding antimicrobial resistant bacteria in animals under ENR or TIA treatment. The most potent metabolites CIP and DTIA showed considerable potencies against activated sludge bacteria compared to the parent compounds. EC50 (µg/ml) for ENR, CIP, TIA and DTIA were 0.018 [95% CI: 0.028-0.149], 0.064 [95% CI: 0.007-0.046], 6.0 [95% CI: 3.6-9.8], and 9.7 [95% CI: 5.8-16.3], respectively. This indicates that the compounds can change the bacterial population in the sludge, and hereby alter the properties of the sludge.

KW - Former Faculty of Pharmaceutical Sciences

U2 - 10.1016/j.vetmic.2006.11.020

DO - 10.1016/j.vetmic.2006.11.020

M3 - Journal article

C2 - 17194550

VL - 121

SP - 116

EP - 124

JO - Veterinary Microbiology

JF - Veterinary Microbiology

SN - 0378-1135

IS - 1-2

ER -

ID: 2307113