Pathogenic potential and growth kinetics of Muko virus in mice and human-derived cells
© The Author(s) 2016
Received: 9 June 2016
Accepted: 17 August 2016
Published: 11 October 2016
Ticks have been long known as vectors of various pathogens, some of which can cause high fatality rates among infected individuals. Our enhanced tick surveillance around Nagasaki, Japan, led to the isolation and identification of a new strain of a recently identified Orbivirus, Muko virus (MUV). The orbiviruses have a wide host range, including humans, and is related to a spectrum of clinical outcomes. However, the zoonotic potential of some members of the genus, although reported, were not clearly elucidated. Hence, it is imperative to characterize newly isolated orbiviruses and investigate its ability to endanger public health.
In this study, we explored the in vivo pathogenicity of a newly isolated MUV strain (MUV-Hay) using a mouse model and demonstrated its growth kinetics in human-derived cells.
Our results showed the ability of MUV-Hay to propagate in human neuronal and renal cells with some cytopathic effect. Furthermore, intracerebral inoculation of our new isolate caused high mortality in adult A129 mice.
Our study provided a first step to experimentally test the hypothesis, that MUV can replicate and produce cytopathic effect in human cells and demonstrate virulence in adult mice.
KeywordsMuko virus Tick-borne virus Mouse model Human-derived cells
Ixodid ticks transmit a number of viruses, including those of the families Bunyaviridae, Flaviviridae, Reoviridae, Rhabdoviridae, and Orthomyxoviridae [1–3]. Tick-borne viruses include highly pathogenic agents such as the tick-borne encephalitis virus (TBEV), Crimean-Congo hemorrhagic fever virus (CCHFV), and severe fever with thrombocytopenia syndrome virus (SFTSV).
Of those mentioned, cases of tick-borne encephalitis (TBE) and severe fever with thrombocytopenia syndrome (SFTS) have been reported in Japan [4, 5]. A TBE case was confirmed in the southern area of Hokkaido, north island of Japan, and TBEV was isolated from Ixodes ovatus in the endemic area . On the other hand, more than 170 cases of SFTS have been identified in western Japan since 2005 (http://kanpoken.pref.yamaguchi.lg.jp/jyoho/page9/sfts_1.php). Although SFTSV has been detected in several species of ticks in China and Korea [7–13], we and another group were not able to isolate SFTSV from ticks collected by flagging during an epidemiological survey [14, 15].
To aid in the planning of public health measures such as early detection of cases and discrimination of viral from bacterial tick-borne infections, field studies are necessary in providing tick infection rates, species distribution, and level of endemicity. Our field collection of ticks aimed to identify viruses that are possible mammalian pathogens and obtain other data as part of tick surveillance in Japan.
Our efforts in the field sampling of ticks resulted to the identification of a new tick-borne virus, Tofla virus (TFLV), belonging to the genus Nairovirus, family Bunyaviridae, from Haemaphysalis flava and Haemaphysalis formsensis ticks . Although the infectivity and pathogenicity of TFLV in humans and animals remain unclear, the virus exhibited ability to propagate in both monkey and human-derived cultured cells. TFLV also produced lethal infection in interferon-α/β receptor knockout (IFNAR KO) mice with marked gastrointestinal pathology .
Our enhanced tick surveillance in Nagasaki, located on the Japanese island of Kyushu, isolated an infectious agent that produced fatal infection in IFNAR KO mice. Next-generation sequencing (NGS) identified the pathogen as a new strain of Muko virus (MUV) which was first reported by Ejiri et al. .
The recently identified virus, MUV, belongs to the genus Orbivirus of the family Reoviridae, initially isolated from Ixodes turdus collected in Hyogo within the Kansai region on the Honshu island of Japan. In the same study, they showed that their isolate (MUV-S1) could replicate and induce cytopathic effect in animal-derived cell lines such as BHK-21 (Syrian hamster kidney), Vero E6 (African green monkey kidney), and CCL-141 (duck embryo) and exhibit lethal infection in suckling mice after intracerebral inoculation. In addition, the genetic association of MUV to Kemerovo and Tribec viruses suggests that MUV may negatively impact human health and be a potential zoonotic agent. Collectively, their results raise the possibility that MUV may also cause disease among other animals including humans .
Since the prevention and control of pathogenic orbiviruses depend on current information, critical gaps in knowledge need to be addressed. The identification of host range susceptible to specific Orbivirus species and the molecular determinants involved in host specificity needs to be understood . However, the pathogenicity in adult animals and infectivity in human cells were not elucidated in the previous study. Our study, therefore, has focused on in vitro infectivity of MUV in cells of human origin and demonstrates its in vivo virulence among adult mice.
MUV isolation from ticks
MUV genome sequence
RNA was extracted from the homogenized mouse spleen using RNeasy Lipid Tissue Mini Kit (Qiagen, Hilden, Germany). Next-generation sequencing (NGS) was performed using GS Junior 454 (Roche Diagnostic Cooperation, Branford, CT, USA). The full-length sequences were determined using the primers designed from the sequence previously reported .
Phylogenetic analyses of the VP region of selected tick-borne Orbivirus proteins and amino acid sequences were aligned using the DIALIGN-TX v1.0.2 and TrimAl v1.2 [19–21]. The substitution models were determined by ProtTest v3.4.1 while the phylogenetic trees were reconstructed by the maximum likelihood model using PhyML v3.0.1 [22, 23]. The following accession codes were obtained for phylogenetic analyses from GenBank: Baku virus (AHW57716.1), Colorado tick fever virus (NP_690891.1), Great Island virus (YP_003896058.1), Kemerovo virus (AGG68141.1), Lipovnik virus (ADM88603.1), Muko virus (BAT21343.1), Okhotskiy virus (AHL27158.1), Tribec virus (ADZ96219.1), and Wad Medani virus (YP_009158877.1).
Virus and cells
The homogenized spleen sample of mouse that was previously inoculated with tick homogenate was inoculated into BHK-21 cells. The infectious culture fluid was harvested 6 days post-inoculation, aliquoted, and kept as master virus stocks.
BHK-21, T98-G (human glioblastoma multiforme), SK-N-SH (human neuroblastoma), and HEK-293 (human embryonic kidney) cells were maintained in EMEM containing 10 % FBS.
The IFNAR KO (A129) mice were purchased from B & K Universal Limited and were mated in the facility at Nagasaki University. The B6 mice were purchased from CLEA Japan, Inc. B6 was chosen since it is known to be a standard mouse model in infection research.
Infection of mice with MUV
Adult (>8 weeks old) A129 mice were assigned into one of the six dosage groups (n = 6 per group) prior to subcutaneous inoculation of 10−2 to 103 plaque-forming units (pfu) of MUV in EMEM containing 2 % FBS. On the other hand, adult B6 mice were inoculated with a single dose of MUV at 103 pfu (n = 6). The mice were weighed daily and observed for clinical signs of disease for 14 days. Weight and mortality ratios were calculated to demonstrate MUV in vivo pathogenicity.
To assess any difference in viral replication within the different organs, A129 mice were subcutaneously infected with 102 pfu of MUV, with three mice per group sacrificed at 1 and 3 days post-inoculation (pi). The thymus, lungs, spleen, liver, kidneys, small intestine, colon, cecum, brain, and spinal cord were removed following perfusion with cold phosphate-buffered saline (PBS). The small intestine, colon, and cecum were washed with cold PBS to remove fecal matter. Brain tissue was further classified and divided into two fractions, the brain cortex and non-cortex. The tissue segments were immediately submerged in RNAlater (Ambion, CA, USA) and stored at −80 °C until they were used.
Viral replication in the different organs was assessed in A129 mice by quantitation of viral copy numbers using real-time RT-PCR. The total RNA was extracted from the previously prepared tissue segments using an RNeasy Lipid Tissue Mini Kit (Qiagen, Hilden, Germany). The MUV-specific primers and probes were designated based on viral segment 1 using Primer3web version 4.0.0 (http://primer3.ut.ee) [24, 25]. Primers used included forward primer MUV1_0745F20: 5′-GGCCAGCTATTCATGGTTCG-3′ and the reverse primer MUV1_0865R20: 5′-CGTCTCCAGCTCCGATATGT-3′, and the PrimeTime® qPCR probe was MUV1_A_int: 5′-/56-FAM/TTATCTCGG/ZEN/AGGGAGGGGAT/3IABkFQ/-3′ (Integrated DNA Technologies, IA, USA). The real-time RT-PCR reactions were performed using a One Step PrimeScript RT-PCR Kit (Takara Bio, Inc., Tokyo, Japan) detected by 7500 Real-time PCR System (Applied Biosystems, CA, USA). The copy numbers were calculated as ratio of the copy numbers of a standard control.
Determination of MUV infectious titers
Infectious titers of MUV-Hay were determined using a plaque-forming assay. Confluent BHK-21 cells were inoculated with serial dilutions of MUV culture fluid. The virus was allowed to adsorb for 1 h prior to the addition of an overlay medium (MEM with 1 % methylcellulose (Sigma-Aldrich), 2 % FBS). After an incubation of 4 days at 37 °C with 5 % CO2, the overlay was carefully removed and washed with PBS. Fixation of cells was done using 4 % paraformaldehyde in PBS at room temperature for at least 30 min. Crystal violet was used to visualize plaques after staining overnight at room temperature. The viral titers were expressed as plaque-forming unit per milliliter.
Inoculation of MUV into human-derived cell lines
A primary master stock of MUV was used to inoculate T98-G, SK-N-SH, and HEK-293 cells at multiplicity of infection (MOI) of 0.001 and incubated at 37 °C with 5 % CO2. After 1 h adsorption, supernatants were removed and fresh EMEM were added. The experiment was performed in triplicate. The culture fluids were harvested daily for 3 days pi and were kept at −80 °C until analysis. Infectious titers of MUV were determined using a plaque-forming assay.
Isolation of MUV
Amino acid and nucleotide sequence comparison between MUV-S1 and MUV-Hay strains
Pathogenicity of MUV in adult immunocompetent mice
A previous study has shown that intracerebral inoculation with 103 pfu of MUV-S1 caused fatal infection in suckling mice of outbred ddY mice . However, the pathogenic potential in adult mice is not known. Thus, we subcutaneously inoculated MUV-Hay into adult B6 mice. However, no mice exhibited apparent clinical signs and mortality was not observed (data not shown).
Pathogenicity of MUV in adult A129 mice
MUV infectivity and replication in human-derived cell lines
This study revealed the potential of MUV of infecting mammals including humans. MUV is a newly identified virus isolated from I. turdus in Japan; nonetheless, it is not clear whether MUV can cause any obvious pathology among humans and other animals. The main host of I. turdus is birds; thus, they may be the primary host of MUV. In support of that statement, the previous report on MUV showed infection and replication of the virus in avian cell culture. In addition, they also demonstrated MUV infectivity in rodent and primate cells . The results of our study strengthen the hypothesis that MUV can infect and replicate on a wide range of hosts, including humans. The observed difference in infectious virus titers between the neuronal and the embryonic kidney-derived cells at time 0 provides an interesting avenue for further research. It is likely that cell-specific receptors and factors, specifically during the initial stages of viral replication, contributed to this phenomenon.
MUV exhibited lethal infection in A129 mice, although the mechanism of death in the MUV-infected A129 mice was unclear. On the other hand, MUV infection did not show any apparent clinical signs in adult B6 mice. This indicates that IFN-I responses are likely to be important for protection against MUV in mice. IFNAR KO mice such as A129 mice are useful animal models for in vivo infections with tick-borne Bunyaviruses such as CCHFV, Hazara virus, and TFLV, even though these viruses do not exhibit apparent pathogenicity in immunocompetent mice [16, 26–28]. Therefore, evaluation of antiviral effect of candidate compounds on in vivo viral replication in IFNAR KO mice can be a solution. Since these mice have minimal interferon-mediated immune response, any observed effect can be attributed to the compound administered. These suggest that A129 mice may be used as an alternative model for testing antiviral agents against tick-borne Bunyaviruses as well as Orbiviruses.
The Orbiviruses have a wide range of hosts, from ruminants to humans and exhibiting varied clinical outcomes. In fact, Bluetongue virus, the prototype Orbivirus, has caused devastating outbreaks in livestock leading to high economic losses while another member, Epizootic hemorrhagic disease virus, causes a hemorrhagic disease of deer [18, 29, 30]. The phylogenetic analysis revealed that MUV clustered with Lipovnik virus and Tribec virus and therefore suggests the possibility of MUV to be a zoonotic agent.
MUV-S1 and MUV-Hay were isolated from ticks in Nishinomiya and Nagasaki, respectively . The distance between Nishinomiya and Nagasaki is approximately 550 km. I. turdus is distributed over a large area of Japan. Therefore, MUV may be distributed throughout Japan and may naturally circulate within ticks and animals including birds. Thus, further investigations such as seroepidemiological surveys of human and animal samples are an important priority to determine the level of infectivity among humans and other animals. In addition, further in vitro experiments using other cell lines originating from tissues of both human and nonhuman mammals will provide useful information in understanding the infectivity and tissue tropism of MUV.
Although our results do not strongly point out that MUV directly associated with pathogenicity to humans, we also cannot rule out the possibility of MUV to be an important human pathogen. Our work provided a first step to experimentally test the hypothesis that MUV can replicate and produce CPE in human cells, which was not included in the previous study .
We described in this study the growth characteristics of a newly isolated strain of MUV using human cell lines and also demonstrated its pathogenicity using a mouse model. Our isolation of a new MUV strain from ticks at a location far from the initial report warrants further investigation. Seroepidemiological surveys of human and animal samples throughout the region are of importance to determine the level of infectivity among humans and other animals. The possible role of interferon during the course of MUV infection should also be further elucidated. Thus, further in vitro experiments using other cell lines originating from tissues of both human and nonhuman mammals will provide useful information in understanding the infectivity and tissue tropism of MUV.
Tick-borne encephalitis virus
Crimean-Congo hemorrhagic fever virus
Severe fever with thrombocytopenia syndrome
Severe fever with thrombocytopenia syndrome virus
- IFNAR KO:
Interferon-α/β receptor knockout
Eagle’s minimum essential medium
Fetal bovine serum
We thank Kazuhiro Takeda (Nagasaki University) for the tick collection and the members of the Department of Virology, Institute of Tropical Medicine, Nagasaki University, for their various support extended during this work.
This work was financially supported by a Health and Labor Sciences Research Grant on Emerging and Re-emerging Infectious Diseases from the Japanese Ministry of Health, Labor, and Welfare and Health and Labor Sciences Research Grants and also by KAKENHI (Grant-in-Aid for Scientific Research (B) (25304045) and Grant-in-Aid for Challenging Exploratory Research (15K15126)) from the Japan Society for the Promotion of Science and the Joint Usage/Research Center on Tropical Disease, Institute of Tropical Medicine, Nagasaki University.
Availability of data and materials
Sequences of MUV-Hay were uploaded to GenBank® awaiting its assigned accession number.
GELU performed the experiments of tick collection, sequencing of viral genome, titration of virus, and cell culture experiment and drafted the manuscript. SS performed the experiments of tick collection, sequencing of viral genome, animal experiments, titration of virus, and cell culture experiment. NTMM helped the animal experiments. TN helped to analyze the viral sequence data. KM helped to draft the manuscript. DH performed the experiments of tick collection and animal experiments, conceived and designed the study, and drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
The animal experiments were performed in accordance with the recommendations in the Fundamental Guidelines for the Proper Conduct of Animal Experiments and Related Activities in Academic Research Institutions under the jurisdiction of the Ministry of Education, Culture, Sports, Science, and Technology. The Animal Care and Use Committee of the Nagasaki University approved all of the experimental protocols (approval number: 1408051166, 1602031280).
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