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Extending the Enterovirus Lead: Could a Related Picornavirus be Responsible for Diabetes in Humans?
We found an association between the abundance of rodents in the wild and onset of type 1 diabetes (T1D) in humans. A picornavirus named Ljungan virus (LV) was subsequently isolated from wild bank voles. Both picornavirus-like particles detected by electron microscopy and LV antigen visualized by imm...
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Published in: | Microorganisms (Basel) 2020-09, Vol.8 (9), p.1382 |
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description | We found an association between the abundance of rodents in the wild and onset of type 1 diabetes (T1D) in humans. A picornavirus named Ljungan virus (LV) was subsequently isolated from wild bank voles. Both picornavirus-like particles detected by electron microscopy and LV antigen visualized by immunohistochemistry was seen in islets of Langerhans in diabetic wild bank voles. LV antigen has also been found in islets of Langerhans in a patient with recent onset of T1D and in the commonly used Bio Breeding (BB) T1D rat model. We discuss the possibility of T1D and type 2 diabetes (T2D) as parts of a single disease entity. Antiviral compounds directed against picornavirus have been found to be an effective treatment of diabetes in BB rats. We propose using the same currently available antiviral compounds in clinical trials in humans. Antiviral treatment would have the potential to be both proof of concept for involvement of a picornavirus in diabetes pathogenesis and also present a first-generation therapy. |
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A picornavirus named Ljungan virus (LV) was subsequently isolated from wild bank voles. Both picornavirus-like particles detected by electron microscopy and LV antigen visualized by immunohistochemistry was seen in islets of Langerhans in diabetic wild bank voles. LV antigen has also been found in islets of Langerhans in a patient with recent onset of T1D and in the commonly used Bio Breeding (BB) T1D rat model. We discuss the possibility of T1D and type 2 diabetes (T2D) as parts of a single disease entity. Antiviral compounds directed against picornavirus have been found to be an effective treatment of diabetes in BB rats. We propose using the same currently available antiviral compounds in clinical trials in humans. Antiviral treatment would have the potential to be both proof of concept for involvement of a picornavirus in diabetes pathogenesis and also present a first-generation therapy.</description><identifier>ISSN: 2076-2607</identifier><identifier>EISSN: 2076-2607</identifier><identifier>DOI: 10.3390/microorganisms8091382</identifier><identifier>PMID: 32927606</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>animal models ; Animals ; Antigens ; Clinical trials ; Cloning ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes mellitus (non-insulin dependent) ; Disease ; Electron microscopy ; Enteroviruses ; Genotype & phenotype ; Glucose ; Health services ; Hypotheses ; Immunohistochemistry ; Infections ; Insulin ; Islets of Langerhans ; Laboratories ; Ljungan virus ; Pathogenesis ; Pathogens ; picornavirus ; Population ; Pregnancy ; Review ; Rodents ; T1D ; T2D ; Viral infections ; Viruses</subject><ispartof>Microorganisms (Basel), 2020-09, Vol.8 (9), p.1382</ispartof><rights>2020. 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A picornavirus named Ljungan virus (LV) was subsequently isolated from wild bank voles. Both picornavirus-like particles detected by electron microscopy and LV antigen visualized by immunohistochemistry was seen in islets of Langerhans in diabetic wild bank voles. LV antigen has also been found in islets of Langerhans in a patient with recent onset of T1D and in the commonly used Bio Breeding (BB) T1D rat model. We discuss the possibility of T1D and type 2 diabetes (T2D) as parts of a single disease entity. Antiviral compounds directed against picornavirus have been found to be an effective treatment of diabetes in BB rats. We propose using the same currently available antiviral compounds in clinical trials in humans. Antiviral treatment would have the potential to be both proof of concept for involvement of a picornavirus in diabetes pathogenesis and also present a first-generation therapy.</description><subject>animal models</subject><subject>Animals</subject><subject>Antigens</subject><subject>Clinical trials</subject><subject>Cloning</subject><subject>Diabetes</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Disease</subject><subject>Electron microscopy</subject><subject>Enteroviruses</subject><subject>Genotype & phenotype</subject><subject>Glucose</subject><subject>Health services</subject><subject>Hypotheses</subject><subject>Immunohistochemistry</subject><subject>Infections</subject><subject>Insulin</subject><subject>Islets of Langerhans</subject><subject>Laboratories</subject><subject>Ljungan virus</subject><subject>Pathogenesis</subject><subject>Pathogens</subject><subject>picornavirus</subject><subject>Population</subject><subject>Pregnancy</subject><subject>Review</subject><subject>Rodents</subject><subject>T1D</subject><subject>T2D</subject><subject>Viral infections</subject><subject>Viruses</subject><issn>2076-2607</issn><issn>2076-2607</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1rFDEUhgdRbGn7E4SAN96szcdMMvFCke3WFhYU0euQj5NtlplkTWZK_fdNnSJWmpuENw8Ph3NO07wh-D1jEp-PweaU8k7HUMbSY0lYT180xxQLvqIci5f_vI-as1L2uJ4HrCOvmyNGJRUc8-PGbu4miC7EHZpuAG3iBDndhjwXtAXtPqB1mgeHNPoOg57AoW_Bphz1ghioeTmkWIIZAPmU0UXQBiYoKER0NY86lk-nzSuvhwJnj_dJ8_Ny82N9tdp-_XK9_rxd2ban00oQR6gU0mNjNBPcEMEZEZiJ1knLsZOsxdIZ64RrrZSOQyeZMyCE9pR27KS5Xrwu6b065DDq_FslHdSfoPZL6TwFO4AiVvjee8cwZ62BVvdSA6O-uok3vaiuj4vrMJsRnIU4ZT08kT79ieFG7dKtEh3vKCdV8O5RkNOvGcqkxlAsDIOOkOaiaNvSvu0EZRV9-x-6T3Pt8bBQXOJeykp1C1VHX0oG_7cYgtXDVqhnt4LdAxLArmo</recordid><startdate>20200910</startdate><enddate>20200910</enddate><creator>Klitz, William</creator><creator>Niklasson, Bo</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20200910</creationdate><title>Extending the Enterovirus Lead: Could a Related Picornavirus be Responsible for Diabetes in Humans?</title><author>Klitz, William ; Niklasson, Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-71d12979f0bba376b1763170374d9c60d93409dbcd7d4c99d6e593dbe77af2253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>animal models</topic><topic>Animals</topic><topic>Antigens</topic><topic>Clinical trials</topic><topic>Cloning</topic><topic>Diabetes</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Disease</topic><topic>Electron microscopy</topic><topic>Enteroviruses</topic><topic>Genotype & phenotype</topic><topic>Glucose</topic><topic>Health services</topic><topic>Hypotheses</topic><topic>Immunohistochemistry</topic><topic>Infections</topic><topic>Insulin</topic><topic>Islets of Langerhans</topic><topic>Laboratories</topic><topic>Ljungan virus</topic><topic>Pathogenesis</topic><topic>Pathogens</topic><topic>picornavirus</topic><topic>Population</topic><topic>Pregnancy</topic><topic>Review</topic><topic>Rodents</topic><topic>T1D</topic><topic>T2D</topic><topic>Viral infections</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Klitz, William</creatorcontrib><creatorcontrib>Niklasson, Bo</creatorcontrib><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Microorganisms (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Klitz, William</au><au>Niklasson, Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extending the Enterovirus Lead: Could a Related Picornavirus be Responsible for Diabetes in Humans?</atitle><jtitle>Microorganisms (Basel)</jtitle><date>2020-09-10</date><risdate>2020</risdate><volume>8</volume><issue>9</issue><spage>1382</spage><pages>1382-</pages><issn>2076-2607</issn><eissn>2076-2607</eissn><abstract>We found an association between the abundance of rodents in the wild and onset of type 1 diabetes (T1D) in humans. A picornavirus named Ljungan virus (LV) was subsequently isolated from wild bank voles. Both picornavirus-like particles detected by electron microscopy and LV antigen visualized by immunohistochemistry was seen in islets of Langerhans in diabetic wild bank voles. LV antigen has also been found in islets of Langerhans in a patient with recent onset of T1D and in the commonly used Bio Breeding (BB) T1D rat model. We discuss the possibility of T1D and type 2 diabetes (T2D) as parts of a single disease entity. Antiviral compounds directed against picornavirus have been found to be an effective treatment of diabetes in BB rats. We propose using the same currently available antiviral compounds in clinical trials in humans. 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subjects | animal models Animals Antigens Clinical trials Cloning Diabetes Diabetes mellitus (insulin dependent) Diabetes mellitus (non-insulin dependent) Disease Electron microscopy Enteroviruses Genotype & phenotype Glucose Health services Hypotheses Immunohistochemistry Infections Insulin Islets of Langerhans Laboratories Ljungan virus Pathogenesis Pathogens picornavirus Population Pregnancy Review Rodents T1D T2D Viral infections Viruses |
title | Extending the Enterovirus Lead: Could a Related Picornavirus be Responsible for Diabetes in Humans? |
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