Species-independent bioassay for sensitive quantification of antiviral type I interferons
© Kuri et al. 2010
Received: 19 August 2009
Accepted: 26 February 2010
Published: 26 February 2010
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© Kuri et al. 2010
Received: 19 August 2009
Accepted: 26 February 2010
Published: 26 February 2010
Studies of the host response to infection often require quantitative measurement of the antiviral type I interferons (IFN-α/β) in biological samples. The amount of IFN is either determined via its ability to suppress a sensitive indicator virus, by an IFN-responding reporter cell line, or by ELISA. These assays however are either time-consuming and lack convenient readouts, or they are rather insensitive and restricted to IFN from a particular host species.
An IFN-sensitive, Renilla luciferase-expressing Rift Valley fever virus (RVFV-Ren) was generated using reverse genetics. Human, murine and avian cells were tested for their susceptibility to RVFV-Ren after treatment with species-specific IFNs. RVFV-Ren was able to infect cells of all three species, and IFN-mediated inhibition of viral reporter activity occurred in a dose-dependent manner. The sensitivity limit was found to be 1 U/ml IFN, and comparison with a standard curve allowed to determine the activity of an unknown sample.
RVFV-Ren replicates in cells of several species and is highly sensitive to pre-treatment with IFN. These properties allowed the development of a rapid, sensitive, and species-independent antiviral assay with a convenient luciferase-based readout.
Type-I interferons (IFN-α/β) are potent cytokines that can be released from virtually all vertebrate cells following viral infection. They comprise a large number of IFN-α subspecies and a single IFN-β, and their actions reflect an important part of the innate immune system . Upon infection, viruses are detected by one or several different pattern recognition receptors and production of IFN is induced. Newly synthesized IFNs are secreted in order to bind to their specific receptor (which is common for IFN-α and IFN-β) in an autocrine and paracrine manner. Receptor signaling via the Jak/Stat pathway leads to the up-regulation of a set of IFN-stimulated genes (ISGs), some of which having antiviral activity. As a consequence, neighbouring cells establish an antiviral state to prevent viral spread in the organism .
A wide variety of assays has been developed to determine the presence and activity of antiviral IFNs . One type of assay is based on the upregulation of ISGs, either directly by measuring enzymatic ISG products , or indirectly by using cells containing a reporter gene under control of an IFN-responsive promoter. Often, the promoter of the Mx gene is used [5–8] due to the sensitivity and the low background expression of this ISG . Although cell-line based ISG/reporter assays are rather convenient, a major drawback is their restriction to a particular host organism since IFNs bind to their receptor in a species-specific manner. In a similar vein, commercially available ELISAs are limited to a particular type of IFN and a single host species.
The historically oldest and still widely used assay to determine IFN activity are assays of antiviral activity. Here, IFN-mediated protection of cells is directly analyzed after infection with a sensitive challenge virus. The presence of IFNs is reflected by reduced cytopathic effects or diminished viral growth [10, 11]. Some recent modifications of this assay take advantage of green fluorescent protein (GFP)-expressing viruses. These viruses allow to determine the reduction in virus titers by counting GFP-positive cells, either manually or by flow cytometry [12–14].
Rift Valley fever virus (RVFV) is a highly pathogenic member of the family Bunyaviridae. RVFV encodes a non-structural gene termed NSs which is mainly responsible for the pathogenicity of this virus [15, 16]. Mutant RVFV lacking the NSs gene are thus highly sensitive to IFN-induced antiviral proteins such as MxA and PKR [17–20]. Here, we applied our recently developed reverse genetics system for RVFV  and replaced the NSs gene with the Renilla luciferase reporter gene, resulting in an attenuated, IFN-sensitive virus. We used this virus to establish a bioassay for quantification of IFN that combines the advantages of the classical antiviral assay with the convenience of luciferase reporter assays.
Similar to the conventional virus inhibition or GFP-virus-based IFN bioassays, it can not be excluded a priori that material derived from e.g. infected dendritic cells or clinical samples may contain antiviral cytokines other than type I IFNs which could inhibit RVRV-Ren. Depending on the species material, IFNAR -/- MEFs, other mutant cell lines, acid treatment, or IFNAR-neutralizing antisera could be employed to verify that only type I IFNs are causing RVFV-Ren inhibition. However, in many cases supernatants from tissue cells are used, a system in which apparently type I IFNs are the dominant antiviral cytokine.
Here we established a novel antiviral bioassay based on a recombinant RVFV encoding the gene for Renilla luciferase in place of the IFN-antagonistic NSs gene (RVFV-Ren). Growth of this virus is inhibited by IFN in a dose-dependent manner, which can easily be monitored by the measurement of luciferase activity in lysates of infected cells. Furthermore, IFN of at least three different species was reliably measured, indicating that RVFV-Ren not only infects cells of human or murine origin, as previously known, but also bird cells. The latter fact indicates that the RVFV-Ren assay could be used for other, less established species as well, e.g. bats. Our results show that these properties make this virus a useful tool for quantitative, species-independent measurement of IFN in biological samples, and that the use of luciferase and the 96-well plate format greatly facilitates readout. RVFV is classified as a BSL3 pathogen, and RVFV-Ren also needs to be handled under BSL3 conditions. The principle of our assay, however, namely the use of an IFN-sensitive virus expressing Renilla luciferase might as well be adapted for IFN-sensitive non-BSL3 viruses with a broad host range such as Vesicular stomatitis virus or Newcastle disease virus.
BHK-21, Vero E6 (ATCC; CRL-1586), 293T (ATCC; CRL-11268), human A549 (ATCC; CCL-185) cells, and murine L929 cells (ATCC; CCL-1) and IFNAR -/- MEFs (kindly provided from Jovan Pavlovic, University of Zurich, Switzerland) were cultivated in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal calf serum (FCS; Biochrom AG) and antibiotics. Chicken embryo fibroblasts (CEF) were prepared from 10-day-old chicken embryos and maintained in DMEM with 2% chicken serum (Invitrogen), 8% FCS and antibiotics. Viruses used in this study were recombinant Rift Valley fever virus (RVFV) expressing Renilla luciferase (see below), RVFV Clone 13 [15, 16], and recombinant La Crosse viruses expressing (wt) or lacking expression (mutant) of the NSs gene . Virus titers were determined by standard plaque assay on Vero E6 cells.
Recombinant pan-species IFN-α (IFN-α B/D BglII) was purchased from PBL Biomedical Laboratories, and Multiferon, a mix of natural human IFN-α subtypes, was from Viragen. Recombinant chicken interferon (chIFN) was purified from E. coli and calibrated as described previously [23, 24].
We used our plasmid-based rescue system for generation of recombinant RVFV. Expression of Renilla luciferase by RVFV-Ren was achieved by replacing the non-structural NSs gene on the genomic S segment with the Renilla gene. The corresponding S segment rescue plasmid pHH21-RVFV-vN_Ren was generated by inserting the Renilla luciferase open reading frame, amplified from plasmid pRL-SV40 (Promega), into the cloning site of pHH21-RVFV-vN_TCS . RVFV-Ren was rescued by transfecting cocultures of 293T and BHK-21 cells in six-well plates with 0.5 μg of helper plasmids (pI.18-RVFV-L and pI.18-RVFV-N), together with 1 μg each of pHH21-RVFV-vL, pHH21-RVFV-vM, and pHH21-RVFV-vN_Ren using Nanofectin transfection reagent (PAA Laboratories). Supernatants containing recombinant viruses were collected 5 days post transfection and used to grow virus stock on Vero E6 cells. All RVFV rescues were performed under biosafety level (BSL) 3 conditions.
Prior to measurement of IFN-containing samples, remaining virus was inactivated using β-propiolactone (Acros Organics) [11, 25]. Briefly, supernatants were first incubated in the presence of 0.05% β-propiolactone in plastic dishes overnight at 4°C, and then at 37°C for 2 hours for hydrolysis of β-propiolactone.
Approximately 10,000 cells were seeded into each well of a 96-well microtiter plate and incubated overnight in a humified incubator at 5% CO2 and 37°C. Cells were then treated either with different dilutions of standard IFN or serial ten-fold dilutions of IFN-containing samples in 100 μl of growth medium for 7 hours. Subsequently, cell culture medium was removed and 10,000 plaque forming units of RVFV-Ren in 100 μl of infection medium (DMEM with 2% FCS and 20 mM HEPES, pH 7.3) were added per well. After 16 hours of further incubation, supernatants were removed and cells lysed in 50 μl of 1 × Renilla lysis buffer (Promega). Luciferase activity in 10 μl of cell lysate was measured using the Renilla luciferase assay system (Promega), according to the manufacturer's instructions.
chicken embry fibroblast
Dulbecco's modified Eagle's medium
green fluorescent protein
mouse embryo fibroblast
relative light unit
Rift Valley fever virus.
We thank Jovan Pavlovic for providing cells which were essential for this study. Work in the authors' laboratories is supported by the grants We 2616/5-2 from the Deutsche Forschungsgemeinschaft and 01 KI 0705 of the Bundesministerium für Bildung und Forschung.
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