Inactivation Methods for Experimental Nipah Virus Infection

被引:12
作者
Widerspick, Lina [1 ,2 ]
Vazquez, Cecilia Alejandra [3 ]
Niemetz, Linda [1 ,2 ]
Heung, Michelle [1 ,2 ]
Olal, Catherine [1 ,2 ]
Bencsik, Andras [1 ,2 ]
Henkel, Christoph [1 ,2 ]
Pfister, Anneke [1 ,2 ]
Brunetti, Jesus Emanuel [1 ,2 ]
Kucinskaite-Kodze, Indre [4 ]
Lawrence, Philip [5 ]
Fontela, Cesar Munoz [1 ,2 ]
Diederich, Sandra [6 ]
Escudero-Perez, Beatriz [1 ,2 ]
机构
[1] Bernhard Nocht Inst Trop Med, WHO Collaborating Ctr Arbovirus & Haemorrhag Feve, D-20359 Hamburg, Germany
[2] German Ctr Infect Res DZIF, Partner Site Hamburg Luebeck Borstel Reims, D-38124 Braunschweig, Germany
[3] Univ Buenos Aires, Inst Quim Biol, Fac Ciencias Exactas & Nat IQUIBICEN, Consejo Nacl Invest Cient & Tecn, Ciudad Univ, RA-1428 Buenos Aires, DF, Argentina
[4] Vilnius Univ, Life Sci Ctr, Sauletekio 7, LT-10257 Vilnius, Lithuania
[5] Catholic Univ Lyon UCLy, Sci & Humanities Confluence Res Ctr EA 1598, F-69002 Lyon, France
[6] Friedrich Loeffler Inst, Inst Novel & Emerging Infect Dis, D-17493 Greifswald, Germany
来源
VIRUSES-BASEL | 2022年 / 14卷 / 05期
关键词
Nipah virus; inactivation; syncytia; BSL-4; immunofluorescence; RT-qPCR; plaque assay; POPULATION BIOLOGY; EBOLA-VIRUS; HENDRA; DESIGN;
D O I
10.3390/v14051052
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nipah virus (NiV) is an emerging zoonotic paramyxovirus that causes severe disease in humans and livestock. Due to its high pathogenicity in humans and the lack of available vaccines and therapeutics, NiV needs to be handled in biosafety level 4 (BSL-4) laboratories. Safe inactivation of samples containing NiV is thus necessary to allow further processing in lower containment areas. To date, there is only limited information available on NiV inactivation methods validated by BSL-4 facilities that can be used as a reference. Here, we compare some of the most common inactivation methods in order to evaluate their efficacy at inactivating NiV in infected cells, supernatants and organs. Thus, several physical and chemical inactivation methods, and combinations thereof, were assessed. Viral replication was monitored for 3 weeks and NiV presence was assessed by RT-qPCR, plaque assay and indirect immunofluorescence. A total of nineteen methods were shown to reduce NiV infectious particles in cells, supernatants and organs to undetectable levels. Therefore, we provide a list of methods for the safe and efficient inactivation of NiV.
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页数:14
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