Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs. / Herrero Fresno, Ana; Zachariasen, Camilla; Hansen, Monica Hegstad; Nielsen, Alexander Schlenzig; Hendriksen, Rene S.; Nielsen, Søren Saxmose; Olsen, John Elmerdahl.

I: Veterinary Research, Bind 47, 12, 2016.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Herrero Fresno, A, Zachariasen, C, Hansen, MH, Nielsen, AS, Hendriksen, RS, Nielsen, SS & Olsen, JE 2016, 'Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs', Veterinary Research, bind 47, 12. https://doi.org/10.1186/s13567-015-0291-z

APA

Herrero Fresno, A., Zachariasen, C., Hansen, M. H., Nielsen, A. S., Hendriksen, R. S., Nielsen, S. S., & Olsen, J. E. (2016). Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs. Veterinary Research, 47, [12]. https://doi.org/10.1186/s13567-015-0291-z

Vancouver

Herrero Fresno A, Zachariasen C, Hansen MH, Nielsen AS, Hendriksen RS, Nielsen SS o.a. Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs. Veterinary Research. 2016;47. 12. https://doi.org/10.1186/s13567-015-0291-z

Author

Herrero Fresno, Ana ; Zachariasen, Camilla ; Hansen, Monica Hegstad ; Nielsen, Alexander Schlenzig ; Hendriksen, Rene S. ; Nielsen, Søren Saxmose ; Olsen, John Elmerdahl. / Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs. I: Veterinary Research. 2016 ; Bind 47.

Bibtex

@article{1fdc78ce8ece4f7fb2f86c6f14e70e94,
title = "Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs",
abstract = "The effect of apramycin treatment on transfer and selection of an Escherichia coli strain (E. coli 912) in the intestine of pigs was analyzed through an in vivo experiment. The strain was sequenced and assigned to the sequence type ST101 and serotype O11. It carried resistance genes to apramycin/gentamicin, sulphonamide, tetracycline, hygromycin B, β-lactams and streptomycin [aac(3)-IV, sul2, tet(X), aph(4), bla TEM-1 and strA/B], with all but tet(X) located on the same conjugative plasmid. Nineteen pigs were randomly allocated into two inoculation groups, one treated with apramycin (pen 2) and one non-treated (pen 3), along with a non-inoculated control group (pen 1). Two pigs of pen 2 and 3 were inoculated intragastrically with a rifampicin resistant variant of the strain. Apramycin treatment in pen 2 was initiated immediately after inoculation. Strain colonization was assessed in the feces from all pigs. E. coli 912 was shown to spread to non-inoculated pigs in both groups. The selective effect did not persist beyond 3 days post-treatment, and the strain was not detected from this time point in pen 2. We demonstrated that E. coli 912 was able to spread between pigs in the same pen irrespective of treatment, and apramycin treatment resulted in significantly higher counts compared to the non-treated group. This represents the first demonstration of how antimicrobial treatment affects spread of resistant bacteria in pig production. The use of apramycin may lead to enhanced spread of gentamicin-resistant E. coli. Since gentamicin is a first-choice drug for human bacteremia, this is of concern.",
author = "{Herrero Fresno}, Ana and Camilla Zachariasen and Hansen, {Monica Hegstad} and Nielsen, {Alexander Schlenzig} and Hendriksen, {Rene S.} and Nielsen, {S{\o}ren Saxmose} and Olsen, {John Elmerdahl}",
year = "2016",
doi = "10.1186/s13567-015-0291-z",
language = "English",
volume = "47",
journal = "Veterinary Research",
issn = "0928-4249",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Apramycin treatment affects selection and spread of a multidrug-resistant Escherichia coli strain able to colonize the human gut in the intestinal microbiota of pigs

AU - Herrero Fresno, Ana

AU - Zachariasen, Camilla

AU - Hansen, Monica Hegstad

AU - Nielsen, Alexander Schlenzig

AU - Hendriksen, Rene S.

AU - Nielsen, Søren Saxmose

AU - Olsen, John Elmerdahl

PY - 2016

Y1 - 2016

N2 - The effect of apramycin treatment on transfer and selection of an Escherichia coli strain (E. coli 912) in the intestine of pigs was analyzed through an in vivo experiment. The strain was sequenced and assigned to the sequence type ST101 and serotype O11. It carried resistance genes to apramycin/gentamicin, sulphonamide, tetracycline, hygromycin B, β-lactams and streptomycin [aac(3)-IV, sul2, tet(X), aph(4), bla TEM-1 and strA/B], with all but tet(X) located on the same conjugative plasmid. Nineteen pigs were randomly allocated into two inoculation groups, one treated with apramycin (pen 2) and one non-treated (pen 3), along with a non-inoculated control group (pen 1). Two pigs of pen 2 and 3 were inoculated intragastrically with a rifampicin resistant variant of the strain. Apramycin treatment in pen 2 was initiated immediately after inoculation. Strain colonization was assessed in the feces from all pigs. E. coli 912 was shown to spread to non-inoculated pigs in both groups. The selective effect did not persist beyond 3 days post-treatment, and the strain was not detected from this time point in pen 2. We demonstrated that E. coli 912 was able to spread between pigs in the same pen irrespective of treatment, and apramycin treatment resulted in significantly higher counts compared to the non-treated group. This represents the first demonstration of how antimicrobial treatment affects spread of resistant bacteria in pig production. The use of apramycin may lead to enhanced spread of gentamicin-resistant E. coli. Since gentamicin is a first-choice drug for human bacteremia, this is of concern.

AB - The effect of apramycin treatment on transfer and selection of an Escherichia coli strain (E. coli 912) in the intestine of pigs was analyzed through an in vivo experiment. The strain was sequenced and assigned to the sequence type ST101 and serotype O11. It carried resistance genes to apramycin/gentamicin, sulphonamide, tetracycline, hygromycin B, β-lactams and streptomycin [aac(3)-IV, sul2, tet(X), aph(4), bla TEM-1 and strA/B], with all but tet(X) located on the same conjugative plasmid. Nineteen pigs were randomly allocated into two inoculation groups, one treated with apramycin (pen 2) and one non-treated (pen 3), along with a non-inoculated control group (pen 1). Two pigs of pen 2 and 3 were inoculated intragastrically with a rifampicin resistant variant of the strain. Apramycin treatment in pen 2 was initiated immediately after inoculation. Strain colonization was assessed in the feces from all pigs. E. coli 912 was shown to spread to non-inoculated pigs in both groups. The selective effect did not persist beyond 3 days post-treatment, and the strain was not detected from this time point in pen 2. We demonstrated that E. coli 912 was able to spread between pigs in the same pen irrespective of treatment, and apramycin treatment resulted in significantly higher counts compared to the non-treated group. This represents the first demonstration of how antimicrobial treatment affects spread of resistant bacteria in pig production. The use of apramycin may lead to enhanced spread of gentamicin-resistant E. coli. Since gentamicin is a first-choice drug for human bacteremia, this is of concern.

U2 - 10.1186/s13567-015-0291-z

DO - 10.1186/s13567-015-0291-z

M3 - Journal article

C2 - 26739225

VL - 47

JO - Veterinary Research

JF - Veterinary Research

SN - 0928-4249

M1 - 12

ER -

ID: 160078550