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Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)

The Ixodes scapularis tick transmits a number of pathogens, including tick-borne flaviviruses (TBFVs). In the United States, confirmed human infections with the Powassan virus (POWV) TBFV have a fatality rate of ∼10% and are increasing in incidence. Tick salivary glands (SGs) serve as an organ barri...

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Autores principales: Grabowski, Jeffrey M., Nilsson, Olof R., Fischer, Elizabeth R., Long, Dan, Offerdahl, Danielle K., Park, Yoonseong, Scott, Dana P., Bloom, Marshall E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355982/
https://www.ncbi.nlm.nih.gov/pubmed/30696737
http://dx.doi.org/10.1128/mBio.02628-18
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author Grabowski, Jeffrey M.
Nilsson, Olof R.
Fischer, Elizabeth R.
Long, Dan
Offerdahl, Danielle K.
Park, Yoonseong
Scott, Dana P.
Bloom, Marshall E.
author_facet Grabowski, Jeffrey M.
Nilsson, Olof R.
Fischer, Elizabeth R.
Long, Dan
Offerdahl, Danielle K.
Park, Yoonseong
Scott, Dana P.
Bloom, Marshall E.
author_sort Grabowski, Jeffrey M.
collection PubMed
description The Ixodes scapularis tick transmits a number of pathogens, including tick-borne flaviviruses (TBFVs). In the United States, confirmed human infections with the Powassan virus (POWV) TBFV have a fatality rate of ∼10% and are increasing in incidence. Tick salivary glands (SGs) serve as an organ barrier to TBFV transmission, and little is known regarding the location of TBFV infection in SGs from fed ticks. Previous studies showed I. scapularis vanin (VNN) involved with TBFV infection of I. scapularis ISE6 embryonic cells, suggesting a potential role for this gene. The overall goal of this study was to use SG cultures to compare data on TBFV biology in SGs from fully engorged, replete (fed) ticks and from unfed ticks. TBFV multiplication was higher in SGs from fed ticks than in those from unfed ticks. Virus-like particles were observed only in granular acini of SGs from unfed ticks. The location of TBFV infection of SGs from fed ticks was observed in cells lining lobular ducts and trachea but not observed in acini. Transcript knockdown of VNN decreased POWV multiplication in infected SG cultures from both fed and unfed ticks. This work was the first to identify localization of TBFV multiplication in SG cultures from a fed tick and a tick transcript important for POWV multiplication in the tick SG, an organ critical for TBFV transmission. This research exemplifies the use of SG cultures in deciphering TBFV biology in the tick and as a translational tool for screening and identifying potential tick genes as potential countermeasure targets.
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spelling pubmed-63559822019-02-01 Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick) Grabowski, Jeffrey M. Nilsson, Olof R. Fischer, Elizabeth R. Long, Dan Offerdahl, Danielle K. Park, Yoonseong Scott, Dana P. Bloom, Marshall E. mBio Research Article The Ixodes scapularis tick transmits a number of pathogens, including tick-borne flaviviruses (TBFVs). In the United States, confirmed human infections with the Powassan virus (POWV) TBFV have a fatality rate of ∼10% and are increasing in incidence. Tick salivary glands (SGs) serve as an organ barrier to TBFV transmission, and little is known regarding the location of TBFV infection in SGs from fed ticks. Previous studies showed I. scapularis vanin (VNN) involved with TBFV infection of I. scapularis ISE6 embryonic cells, suggesting a potential role for this gene. The overall goal of this study was to use SG cultures to compare data on TBFV biology in SGs from fully engorged, replete (fed) ticks and from unfed ticks. TBFV multiplication was higher in SGs from fed ticks than in those from unfed ticks. Virus-like particles were observed only in granular acini of SGs from unfed ticks. The location of TBFV infection of SGs from fed ticks was observed in cells lining lobular ducts and trachea but not observed in acini. Transcript knockdown of VNN decreased POWV multiplication in infected SG cultures from both fed and unfed ticks. This work was the first to identify localization of TBFV multiplication in SG cultures from a fed tick and a tick transcript important for POWV multiplication in the tick SG, an organ critical for TBFV transmission. This research exemplifies the use of SG cultures in deciphering TBFV biology in the tick and as a translational tool for screening and identifying potential tick genes as potential countermeasure targets. American Society for Microbiology 2019-01-29 /pmc/articles/PMC6355982/ /pubmed/30696737 http://dx.doi.org/10.1128/mBio.02628-18 Text en https://doi.org/10.1128/AuthorWarrantyLicense.v1 This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply.
spellingShingle Research Article
Grabowski, Jeffrey M.
Nilsson, Olof R.
Fischer, Elizabeth R.
Long, Dan
Offerdahl, Danielle K.
Park, Yoonseong
Scott, Dana P.
Bloom, Marshall E.
Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)
title Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)
title_full Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)
title_fullStr Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)
title_full_unstemmed Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)
title_short Dissecting Flavivirus Biology in Salivary Gland Cultures from Fed and Unfed Ixodes scapularis (Black-Legged Tick)
title_sort dissecting flavivirus biology in salivary gland cultures from fed and unfed ixodes scapularis (black-legged tick)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355982/
https://www.ncbi.nlm.nih.gov/pubmed/30696737
http://dx.doi.org/10.1128/mBio.02628-18
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