Literature DB >> 33504602

Contact-dependent transmission of Langat and tick-borne encephalitis virus in type I interferon receptor-1 deficient mice.

Sarah Schreier1, Kristin Cebulski1, Andrea Kröger2,3.   

Abstract

Tick-borne encephalitis virus (TBEV) is primarily transmitted to humans through tick bites or oral consumption of accordingly contaminated unpasteurized milk or milk products. The detection of TBEV RNA in various body fluids in immunosuppressed human patients is documented. However, the risk of direct contact exposure remains unclear. Interferon-alpha receptor-1 deficient (Ifnar1-/- ) mice, which are lacking the interferon-α/β responses, develop neurologic manifestations after infection with TBEV and Langat virus (LGTV). We showed that subcutaneous, intranasal, and peroral infection of LGTV lead to disease, whereas mice with intragastric application of LGTV showed no disease signs. With LGTV infected mice exhibit seroconversion and significant viral RNA levels was detected in saliva, eye smear, feces and urine. As a result, TBEV and LGTV are transmitted between mice from infected to naïve co-caged sentinel animals. Although intranasal inoculation of LGTV is entirely sufficient to establish the disease in mice, the virus is not transmitted by aerosols. These pooled results from animal models highlight the risks of exposure to TBEV contaminants and the possibility for close contact transmission of TBEV in interferon-alpha receptor-1 deficient laboratory mice.Importance Tick-borne encephalitis is a severe disease of the central nervous system caused by the tick-borne encephalitis virus (TBEV). Every year between 10,000-12,000 people become infected with this flavivirus. The TBEV is usually transmitted to humans via the bite of a tick, but infections due to consumption of infectious milk products are increasingly being reported. Since there is no therapy for an TBEV infection and mechanisms of virus persistence in reservoir animals are unclear, it is important to highlight the risk of exposure to TBEV contaminants and know possible routes of transmission of this virus. The significance of our research is in identifying other infection routes of TBEV and LGTV, and the possibility of close contact transmission.
Copyright © 2021 American Society for Microbiology.

Entities:  

Year:  2021        PMID: 33504602      PMCID: PMC8103697          DOI: 10.1128/JVI.02039-20

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  54 in total

1.  CD8+ T-cells mediate immunopathology in tick-borne encephalitis.

Authors:  Daniel Růzek; Jirí Salát; Martin Palus; Tamara S Gritsun; Ernest A Gould; Iva Dyková; Anna Skallová; Jirí Jelínek; Jan Kopecký; Libor Grubhoffer
Journal:  Virology       Date:  2008-12-13       Impact factor: 3.616

2.  Detection of tick-borne encephalitis virus RNA in urine.

Authors:  Malin Veje; Marie Studahl; Peter Norberg; Anette Roth; Ulrike Möbius; Magnus Brink; Tomas Bergström
Journal:  J Clin Microbiol       Date:  2014-08-27       Impact factor: 5.948

3.  Monoclonal antibodies directed against tick-borne encephalitis virus with neutralizing activity in vivo.

Authors:  M Niedrig; U Klockmann; W Lang; J Roeder; S Burk; S Modrow; G Pauli
Journal:  Acta Virol       Date:  1994-06       Impact factor: 1.162

Review 4.  The role of particular tick developmental stages in the circulation of tick-borne pathogens affecting humans in Central Europe. 1. The general pattern.

Authors:  Grzegorz Karbowiak; Beata Biernat; Tomasz Szewczyk; Hubert Sytykiewicz
Journal:  Ann Parasitol       Date:  2015

5.  Tick-borne encephalitis virus delays interferon induction and hides its double-stranded RNA in intracellular membrane vesicles.

Authors:  Anna K Overby; Vsevolod L Popov; Matthias Niedrig; Friedemann Weber
Journal:  J Virol       Date:  2010-06-16       Impact factor: 5.103

Review 6.  Tick-borne encephalitis: Clinical findings and prognosis in adults.

Authors:  Reinhard Kaiser
Journal:  Wien Med Wochenschr       Date:  2012-06-14

7.  Tick-bone encephalitis in Sweden in relation to aseptic meningo-encephalitis of other etiology: a prospective study of clinical course and outcome.

Authors:  G Günther; M Haglund; L Lindquist; M Forsgren; B Sköldenberg
Journal:  J Neurol       Date:  1997-04       Impact factor: 4.849

8.  Tickborne encephalitis in an area of high endemicity in lithuania: disease severity and long-term prognosis.

Authors:  Aukse Mickiene; Alvydas Laiskonis; Göran Günther; Sirkka Vene; Ake Lundkvist; Lars Lindquist
Journal:  Clin Infect Dis       Date:  2002-08-20       Impact factor: 9.079

9.  Zika Virus Targets Different Primary Human Placental Cells, Suggesting Two Routes for Vertical Transmission.

Authors:  Takako Tabata; Matthew Petitt; Henry Puerta-Guardo; Daniela Michlmayr; Chunling Wang; June Fang-Hoover; Eva Harris; Lenore Pereira
Journal:  Cell Host Microbe       Date:  2016-07-18       Impact factor: 21.023

10.  Cell-type- and region-specific restriction of neurotropic flavivirus infection by viperin.

Authors:  Richard Lindqvist; Chaitanya Kurhade; Jonathan D Gilthorpe; Anna K Överby
Journal:  J Neuroinflammation       Date:  2018-03-15       Impact factor: 8.322

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  1 in total

1.  The Role of IFITM Proteins in Tick-Borne Encephalitis Virus Infection.

Authors:  Alicja M Chmielewska; Maria Gómez-Herranz; Paulina Gach; Marta Nekulova; Małgorzata A Bagnucka; Andrea D Lipińska; Michał Rychłowski; Weronika Hoffmann; Ewelina Król; Borivoj Vojtesek; Richard D Sloan; Krystyna Bieńkowska-Szewczyk; Ted Hupp; Kathryn Ball
Journal:  J Virol       Date:  2021-10-06       Impact factor: 6.549

  1 in total

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