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Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents

BACKGROUND: Tick-borne encephalitis virus (TBEV) can cause severe neurological disease in humans. Its geographical distribution is expanding in Western Europe with unresolved causes and spatial patterns, necessitating enhanced surveillance. Monitoring the virus in the environment is complicated, as...

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Autores principales: Pascoe, Emily L., de Vries, Ankje, Esser, Helen J., Koenraadt, Constantianus J. M., Sprong, Hein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018976/
https://www.ncbi.nlm.nih.gov/pubmed/36927723
http://dx.doi.org/10.1186/s13071-023-05717-0
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author Pascoe, Emily L.
de Vries, Ankje
Esser, Helen J.
Koenraadt, Constantianus J. M.
Sprong, Hein
author_facet Pascoe, Emily L.
de Vries, Ankje
Esser, Helen J.
Koenraadt, Constantianus J. M.
Sprong, Hein
author_sort Pascoe, Emily L.
collection PubMed
description BACKGROUND: Tick-borne encephalitis virus (TBEV) can cause severe neurological disease in humans. Its geographical distribution is expanding in Western Europe with unresolved causes and spatial patterns, necessitating enhanced surveillance. Monitoring the virus in the environment is complicated, as it usually relies on destructive sampling of small rodents to test organs for TBEV, which in addition to ethical considerations also raises issues for long-term monitoring or longitudinal studies. Moreover, even when the virus is not detected in the blood or organs of the rodent, TBEV can still be transmitted from an infected tick to uninfected ticks feeding nearby. This is due to the ability of TBEV to replicate and migrate locally within the epidermis of small mammals, including those that do not appear to have systemic infection. This suggests that the virus may be detectable in skin biopsies, which has been confirmed in experimentally infected laboratory rodents, but it remains unknown if this sample type may be a viable alternative to destructively obtained samples in the monitoring of natural TBEV infection. Here we test ear tissue and dried blood spot (DBS) samples from rodents to determine whether TBEV-RNA can be detected in biological samples obtained non-destructively. METHODS: Rodents were live-trapped and sampled at three woodland areas in The Netherlands where presence of TBEV has previously been recorded. Ear tissue (n = 79) and DBSs (n = 112) were collected from a total of 117 individuals and were tested for TBEV-RNA by real-time RT-PCR. RESULTS: TBEV-RNA was detected in five rodents (4.3% of tested individuals), all of which had a TBEV-positive ear sample, while only two out of four of these individuals (for which a DBS was available) had a positive DBS. This equated to 6.3% of ear samples and 1.8% of DBSs testing positive for TBEV-RNA. CONCLUSIONS: We provide the first evidence to our knowledge that TBEV-RNA can be detected in samples obtained non-destructively from naturally infected wild rodents, providing a viable sampling alternative suitable for longitudinal surveillance of the virus. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-100189762023-03-17 Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents Pascoe, Emily L. de Vries, Ankje Esser, Helen J. Koenraadt, Constantianus J. M. Sprong, Hein Parasit Vectors Brief Report BACKGROUND: Tick-borne encephalitis virus (TBEV) can cause severe neurological disease in humans. Its geographical distribution is expanding in Western Europe with unresolved causes and spatial patterns, necessitating enhanced surveillance. Monitoring the virus in the environment is complicated, as it usually relies on destructive sampling of small rodents to test organs for TBEV, which in addition to ethical considerations also raises issues for long-term monitoring or longitudinal studies. Moreover, even when the virus is not detected in the blood or organs of the rodent, TBEV can still be transmitted from an infected tick to uninfected ticks feeding nearby. This is due to the ability of TBEV to replicate and migrate locally within the epidermis of small mammals, including those that do not appear to have systemic infection. This suggests that the virus may be detectable in skin biopsies, which has been confirmed in experimentally infected laboratory rodents, but it remains unknown if this sample type may be a viable alternative to destructively obtained samples in the monitoring of natural TBEV infection. Here we test ear tissue and dried blood spot (DBS) samples from rodents to determine whether TBEV-RNA can be detected in biological samples obtained non-destructively. METHODS: Rodents were live-trapped and sampled at three woodland areas in The Netherlands where presence of TBEV has previously been recorded. Ear tissue (n = 79) and DBSs (n = 112) were collected from a total of 117 individuals and were tested for TBEV-RNA by real-time RT-PCR. RESULTS: TBEV-RNA was detected in five rodents (4.3% of tested individuals), all of which had a TBEV-positive ear sample, while only two out of four of these individuals (for which a DBS was available) had a positive DBS. This equated to 6.3% of ear samples and 1.8% of DBSs testing positive for TBEV-RNA. CONCLUSIONS: We provide the first evidence to our knowledge that TBEV-RNA can be detected in samples obtained non-destructively from naturally infected wild rodents, providing a viable sampling alternative suitable for longitudinal surveillance of the virus. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2023-03-16 /pmc/articles/PMC10018976/ /pubmed/36927723 http://dx.doi.org/10.1186/s13071-023-05717-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Brief Report
Pascoe, Emily L.
de Vries, Ankje
Esser, Helen J.
Koenraadt, Constantianus J. M.
Sprong, Hein
Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
title Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
title_full Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
title_fullStr Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
title_full_unstemmed Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
title_short Detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
title_sort detection of tick-borne encephalitis virus in ear tissue and dried blood spots from naturally infected wild rodents
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018976/
https://www.ncbi.nlm.nih.gov/pubmed/36927723
http://dx.doi.org/10.1186/s13071-023-05717-0
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