Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA

Background: A TaqMan real-time PCR assay targeting the Anaplasma citrate synthase gene, gltA, was developed and used for detection of Anaplasma phagocytophilum in 765 Ixodes ricinus ticks collected from dogs and cats in northern Norway (n = 669) and Telemark county in southern Norway (n = 96). Resul...

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Published in:BMC Microbiology
Main Authors: Henningsson, Anna J., Hvidsten, Dag, Kristiansen, Bjørn Erik, Matussek, Andreas, Stuen, Snorre, Jenkins, Andrew
Format: Article in Journal/Newspaper
Language:English
Published: BioMed Central 2015
Subjects:
Online Access:https://hdl.handle.net/10037/8076
https://doi.org/10.1186/s12866-015-0486-5
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spelling ftunivtroemsoe:oai:munin.uit.no:10037/8076 2023-05-15T15:04:34+02:00 Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA Henningsson, Anna J. Hvidsten, Dag Kristiansen, Bjørn Erik Matussek, Andreas Stuen, Snorre Jenkins, Andrew 2015-08-01 https://hdl.handle.net/10037/8076 https://doi.org/10.1186/s12866-015-0486-5 eng eng BioMed Central BMC Microbiology (2015) 15:153 FRIDAID 1257977 doi:10.1186/s12866-015-0486-5 1471-2180 https://hdl.handle.net/10037/8076 URN:NBN:no-uit_munin_7664 openAccess Anaplasma phagocytophilum Ixodes ricinus TaqMan realtime PCR Norway gltA Prevalence VDP::Mathematics and natural science: 400::Basic biosciences: 470 VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470 Journal article Tidsskriftartikkel Peer reviewed 2015 ftunivtroemsoe https://doi.org/10.1186/s12866-015-0486-5 2021-06-25T17:54:25Z Background: A TaqMan real-time PCR assay targeting the Anaplasma citrate synthase gene, gltA, was developed and used for detection of Anaplasma phagocytophilum in 765 Ixodes ricinus ticks collected from dogs and cats in northern Norway (n = 669) and Telemark county in southern Norway (n = 96). Results: Among the ticks from northern Norway the prevalence of A. phagocytophilum was 3.0 %, while the prevalence in southern Norway was 2.1 % (p = 0.63). The gltA PCR assay showed a high analytical sensitivity (30 genomic units) and efficiency (98.5 %), and its utility in clinical diagnostics should be evaluated in future studies. Conclusion: This is the first report of A. phagocytophilum occurrence in ticks collected north of the Arctic Circle in Norway. The prevalence is comparable to that found in Telemark county in southern Norway. Article in Journal/Newspaper Arctic Northern Norway University of Tromsø: Munin Open Research Archive Arctic Norway BMC Microbiology 15 1
institution Open Polar
collection University of Tromsø: Munin Open Research Archive
op_collection_id ftunivtroemsoe
language English
topic Anaplasma phagocytophilum
Ixodes ricinus
TaqMan realtime PCR
Norway
gltA
Prevalence
VDP::Mathematics and natural science: 400::Basic biosciences: 470
VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470
spellingShingle Anaplasma phagocytophilum
Ixodes ricinus
TaqMan realtime PCR
Norway
gltA
Prevalence
VDP::Mathematics and natural science: 400::Basic biosciences: 470
VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470
Henningsson, Anna J.
Hvidsten, Dag
Kristiansen, Bjørn Erik
Matussek, Andreas
Stuen, Snorre
Jenkins, Andrew
Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA
topic_facet Anaplasma phagocytophilum
Ixodes ricinus
TaqMan realtime PCR
Norway
gltA
Prevalence
VDP::Mathematics and natural science: 400::Basic biosciences: 470
VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470
description Background: A TaqMan real-time PCR assay targeting the Anaplasma citrate synthase gene, gltA, was developed and used for detection of Anaplasma phagocytophilum in 765 Ixodes ricinus ticks collected from dogs and cats in northern Norway (n = 669) and Telemark county in southern Norway (n = 96). Results: Among the ticks from northern Norway the prevalence of A. phagocytophilum was 3.0 %, while the prevalence in southern Norway was 2.1 % (p = 0.63). The gltA PCR assay showed a high analytical sensitivity (30 genomic units) and efficiency (98.5 %), and its utility in clinical diagnostics should be evaluated in future studies. Conclusion: This is the first report of A. phagocytophilum occurrence in ticks collected north of the Arctic Circle in Norway. The prevalence is comparable to that found in Telemark county in southern Norway.
format Article in Journal/Newspaper
author Henningsson, Anna J.
Hvidsten, Dag
Kristiansen, Bjørn Erik
Matussek, Andreas
Stuen, Snorre
Jenkins, Andrew
author_facet Henningsson, Anna J.
Hvidsten, Dag
Kristiansen, Bjørn Erik
Matussek, Andreas
Stuen, Snorre
Jenkins, Andrew
author_sort Henningsson, Anna J.
title Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA
title_short Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA
title_full Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA
title_fullStr Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA
title_full_unstemmed Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA
title_sort detection of anaplasma phagocytophilum in ixodes ricinus ticks from norway using a realtime pcr assay targeting the anaplasma citrate synthase gene glta
publisher BioMed Central
publishDate 2015
url https://hdl.handle.net/10037/8076
https://doi.org/10.1186/s12866-015-0486-5
geographic Arctic
Norway
geographic_facet Arctic
Norway
genre Arctic
Northern Norway
genre_facet Arctic
Northern Norway
op_relation BMC Microbiology (2015) 15:153
FRIDAID 1257977
doi:10.1186/s12866-015-0486-5
1471-2180
https://hdl.handle.net/10037/8076
URN:NBN:no-uit_munin_7664
op_rights openAccess
op_doi https://doi.org/10.1186/s12866-015-0486-5
container_title BMC Microbiology
container_volume 15
container_issue 1
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