author_facet Koetsveld, Joris
Manger, Annemijn
Hoornstra, Dieuwertje
Draga, Ronald O.
Oei, Anneke
Kolyasnikova, Nadezhda M.
Toporkova, Marina G.
Sarksyan, Denis S.
Wagemakers, Alex
Platonov, Alexander E.
Hovius, Joppe W.
Koetsveld, Joris
Manger, Annemijn
Hoornstra, Dieuwertje
Draga, Ronald O.
Oei, Anneke
Kolyasnikova, Nadezhda M.
Toporkova, Marina G.
Sarksyan, Denis S.
Wagemakers, Alex
Platonov, Alexander E.
Hovius, Joppe W.
author Koetsveld, Joris
Manger, Annemijn
Hoornstra, Dieuwertje
Draga, Ronald O.
Oei, Anneke
Kolyasnikova, Nadezhda M.
Toporkova, Marina G.
Sarksyan, Denis S.
Wagemakers, Alex
Platonov, Alexander E.
Hovius, Joppe W.
spellingShingle Koetsveld, Joris
Manger, Annemijn
Hoornstra, Dieuwertje
Draga, Ronald O.
Oei, Anneke
Kolyasnikova, Nadezhda M.
Toporkova, Marina G.
Sarksyan, Denis S.
Wagemakers, Alex
Platonov, Alexander E.
Hovius, Joppe W.
Antimicrobial Agents and Chemotherapy
In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
Infectious Diseases
Pharmacology (medical)
Pharmacology
author_sort koetsveld, joris
spelling Koetsveld, Joris Manger, Annemijn Hoornstra, Dieuwertje Draga, Ronald O. Oei, Anneke Kolyasnikova, Nadezhda M. Toporkova, Marina G. Sarksyan, Denis S. Wagemakers, Alex Platonov, Alexander E. Hovius, Joppe W. 0066-4804 1098-6596 American Society for Microbiology Infectious Diseases Pharmacology (medical) Pharmacology http://dx.doi.org/10.1128/aac.00419-18 <jats:title>ABSTRACT</jats:title> <jats:p> <jats:named-content content-type="genus-species">Borrelia miyamotoi</jats:named-content> is an emerging relapsing fever (RF) <jats:named-content content-type="genus-species">Borrelia</jats:named-content> species that is reported to cause human disease in regions in which Lyme borreliosis is endemic. We recently showed that <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates are resistant to amoxicillin <jats:italic>in vitro</jats:italic> ; however, clinical isolates have not been studied. Therefore, our aim was to show the antimicrobial susceptibility of recently obtained clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> . A dilution series of various antibiotics was made in modified Kelly-Pettenkofer medium with 10% fetal calf serum. The susceptibilities of different <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical, <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick, RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> , and <jats:named-content content-type="genus-species">Borrelia burgdorferi</jats:named-content> <jats:named-content content-type="genus-species">sensu lato</jats:named-content> isolates were tested by measuring MICs through colorimetric changes and by counting motile spirochetes by dark-field microscopy after 72 h of incubation. The ceftriaxone and azithromycin MIC ranges of the six <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates tested were 0.03 to 0.06 mg/liter and 0.0016 to 0.0032 mg/liter, respectively. These values are similar to MICs for RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains and <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates. All tested RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains were susceptible to doxycycline (microscopic MIC range, 0.0625 to 0.25 mg/liter). In contrast to the MICs of the tested <jats:named-content content-type="genus-species">B. burgdorferi sensu lato</jats:named-content> strains and in line with our previous findings, the amoxicillin MICs (range, 8 to 32 mg/liter) of all RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains, including <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates, were above the clinical breakpoint for resistance (≤4 mg/liter). Clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> are highly susceptible to doxycycline, azithromycin, and ceftriaxone <jats:italic>in vitro</jats:italic> . Interestingly, as described previously for tick isolates, amoxicillin shows poor <jats:italic>in vitro</jats:italic> activity against <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates. </jats:p> <i>In Vitro</i> Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi Antimicrobial Agents and Chemotherapy
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series Antimicrobial Agents and Chemotherapy
source_id 49
title In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_unstemmed In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_full In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_fullStr In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_full_unstemmed In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_short In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_sort <i>in vitro</i> antimicrobial susceptibility of clinical isolates of borrelia miyamotoi
topic Infectious Diseases
Pharmacology (medical)
Pharmacology
url http://dx.doi.org/10.1128/aac.00419-18
publishDate 2018
physical
description <jats:title>ABSTRACT</jats:title> <jats:p> <jats:named-content content-type="genus-species">Borrelia miyamotoi</jats:named-content> is an emerging relapsing fever (RF) <jats:named-content content-type="genus-species">Borrelia</jats:named-content> species that is reported to cause human disease in regions in which Lyme borreliosis is endemic. We recently showed that <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates are resistant to amoxicillin <jats:italic>in vitro</jats:italic> ; however, clinical isolates have not been studied. Therefore, our aim was to show the antimicrobial susceptibility of recently obtained clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> . A dilution series of various antibiotics was made in modified Kelly-Pettenkofer medium with 10% fetal calf serum. The susceptibilities of different <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical, <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick, RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> , and <jats:named-content content-type="genus-species">Borrelia burgdorferi</jats:named-content> <jats:named-content content-type="genus-species">sensu lato</jats:named-content> isolates were tested by measuring MICs through colorimetric changes and by counting motile spirochetes by dark-field microscopy after 72 h of incubation. The ceftriaxone and azithromycin MIC ranges of the six <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates tested were 0.03 to 0.06 mg/liter and 0.0016 to 0.0032 mg/liter, respectively. These values are similar to MICs for RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains and <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates. All tested RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains were susceptible to doxycycline (microscopic MIC range, 0.0625 to 0.25 mg/liter). In contrast to the MICs of the tested <jats:named-content content-type="genus-species">B. burgdorferi sensu lato</jats:named-content> strains and in line with our previous findings, the amoxicillin MICs (range, 8 to 32 mg/liter) of all RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains, including <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates, were above the clinical breakpoint for resistance (≤4 mg/liter). Clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> are highly susceptible to doxycycline, azithromycin, and ceftriaxone <jats:italic>in vitro</jats:italic> . Interestingly, as described previously for tick isolates, amoxicillin shows poor <jats:italic>in vitro</jats:italic> activity against <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates. </jats:p>
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author Koetsveld, Joris, Manger, Annemijn, Hoornstra, Dieuwertje, Draga, Ronald O., Oei, Anneke, Kolyasnikova, Nadezhda M., Toporkova, Marina G., Sarksyan, Denis S., Wagemakers, Alex, Platonov, Alexander E., Hovius, Joppe W.
author_facet Koetsveld, Joris, Manger, Annemijn, Hoornstra, Dieuwertje, Draga, Ronald O., Oei, Anneke, Kolyasnikova, Nadezhda M., Toporkova, Marina G., Sarksyan, Denis S., Wagemakers, Alex, Platonov, Alexander E., Hovius, Joppe W., Koetsveld, Joris, Manger, Annemijn, Hoornstra, Dieuwertje, Draga, Ronald O., Oei, Anneke, Kolyasnikova, Nadezhda M., Toporkova, Marina G., Sarksyan, Denis S., Wagemakers, Alex, Platonov, Alexander E., Hovius, Joppe W.
author_sort koetsveld, joris
container_issue 7
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description <jats:title>ABSTRACT</jats:title> <jats:p> <jats:named-content content-type="genus-species">Borrelia miyamotoi</jats:named-content> is an emerging relapsing fever (RF) <jats:named-content content-type="genus-species">Borrelia</jats:named-content> species that is reported to cause human disease in regions in which Lyme borreliosis is endemic. We recently showed that <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates are resistant to amoxicillin <jats:italic>in vitro</jats:italic> ; however, clinical isolates have not been studied. Therefore, our aim was to show the antimicrobial susceptibility of recently obtained clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> . A dilution series of various antibiotics was made in modified Kelly-Pettenkofer medium with 10% fetal calf serum. The susceptibilities of different <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical, <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick, RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> , and <jats:named-content content-type="genus-species">Borrelia burgdorferi</jats:named-content> <jats:named-content content-type="genus-species">sensu lato</jats:named-content> isolates were tested by measuring MICs through colorimetric changes and by counting motile spirochetes by dark-field microscopy after 72 h of incubation. The ceftriaxone and azithromycin MIC ranges of the six <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates tested were 0.03 to 0.06 mg/liter and 0.0016 to 0.0032 mg/liter, respectively. These values are similar to MICs for RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains and <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates. All tested RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains were susceptible to doxycycline (microscopic MIC range, 0.0625 to 0.25 mg/liter). In contrast to the MICs of the tested <jats:named-content content-type="genus-species">B. burgdorferi sensu lato</jats:named-content> strains and in line with our previous findings, the amoxicillin MICs (range, 8 to 32 mg/liter) of all RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains, including <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates, were above the clinical breakpoint for resistance (≤4 mg/liter). Clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> are highly susceptible to doxycycline, azithromycin, and ceftriaxone <jats:italic>in vitro</jats:italic> . Interestingly, as described previously for tick isolates, amoxicillin shows poor <jats:italic>in vitro</jats:italic> activity against <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates. </jats:p>
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spelling Koetsveld, Joris Manger, Annemijn Hoornstra, Dieuwertje Draga, Ronald O. Oei, Anneke Kolyasnikova, Nadezhda M. Toporkova, Marina G. Sarksyan, Denis S. Wagemakers, Alex Platonov, Alexander E. Hovius, Joppe W. 0066-4804 1098-6596 American Society for Microbiology Infectious Diseases Pharmacology (medical) Pharmacology http://dx.doi.org/10.1128/aac.00419-18 <jats:title>ABSTRACT</jats:title> <jats:p> <jats:named-content content-type="genus-species">Borrelia miyamotoi</jats:named-content> is an emerging relapsing fever (RF) <jats:named-content content-type="genus-species">Borrelia</jats:named-content> species that is reported to cause human disease in regions in which Lyme borreliosis is endemic. We recently showed that <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates are resistant to amoxicillin <jats:italic>in vitro</jats:italic> ; however, clinical isolates have not been studied. Therefore, our aim was to show the antimicrobial susceptibility of recently obtained clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> . A dilution series of various antibiotics was made in modified Kelly-Pettenkofer medium with 10% fetal calf serum. The susceptibilities of different <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical, <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick, RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> , and <jats:named-content content-type="genus-species">Borrelia burgdorferi</jats:named-content> <jats:named-content content-type="genus-species">sensu lato</jats:named-content> isolates were tested by measuring MICs through colorimetric changes and by counting motile spirochetes by dark-field microscopy after 72 h of incubation. The ceftriaxone and azithromycin MIC ranges of the six <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates tested were 0.03 to 0.06 mg/liter and 0.0016 to 0.0032 mg/liter, respectively. These values are similar to MICs for RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains and <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> tick isolates. All tested RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains were susceptible to doxycycline (microscopic MIC range, 0.0625 to 0.25 mg/liter). In contrast to the MICs of the tested <jats:named-content content-type="genus-species">B. burgdorferi sensu lato</jats:named-content> strains and in line with our previous findings, the amoxicillin MICs (range, 8 to 32 mg/liter) of all RF <jats:named-content content-type="genus-species">Borrelia</jats:named-content> strains, including <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates, were above the clinical breakpoint for resistance (≤4 mg/liter). Clinical isolates of <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> are highly susceptible to doxycycline, azithromycin, and ceftriaxone <jats:italic>in vitro</jats:italic> . Interestingly, as described previously for tick isolates, amoxicillin shows poor <jats:italic>in vitro</jats:italic> activity against <jats:named-content content-type="genus-species">B. miyamotoi</jats:named-content> clinical isolates. </jats:p> <i>In Vitro</i> Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi Antimicrobial Agents and Chemotherapy
spellingShingle Koetsveld, Joris, Manger, Annemijn, Hoornstra, Dieuwertje, Draga, Ronald O., Oei, Anneke, Kolyasnikova, Nadezhda M., Toporkova, Marina G., Sarksyan, Denis S., Wagemakers, Alex, Platonov, Alexander E., Hovius, Joppe W., Antimicrobial Agents and Chemotherapy, In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi, Infectious Diseases, Pharmacology (medical), Pharmacology
title In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_full In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_fullStr In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_full_unstemmed In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_short In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
title_sort <i>in vitro</i> antimicrobial susceptibility of clinical isolates of borrelia miyamotoi
title_unstemmed In Vitro Antimicrobial Susceptibility of Clinical Isolates of Borrelia miyamotoi
topic Infectious Diseases, Pharmacology (medical), Pharmacology
url http://dx.doi.org/10.1128/aac.00419-18