- freely available
Viruses 2014, 6(3), 951-967; doi:10.3390/v6030951
Abstract: Due to novel, improved and high-throughput detection methods, there is a plethora of newly identified viruses within the genus Hantavirus. Furthermore, reservoir host species are increasingly recognized besides representatives of the order Rodentia, now including members of the mammalian orders Soricomorpha/Eulipotyphla and Chiroptera. Despite the great interest created by emerging zoonotic viruses, there is still a gross lack of in vitro models, which reflect the exclusive host adaptation of most zoonotic viruses. The usually narrow host range and genetic diversity of hantaviruses make them an exciting candidate for studying virus-host interactions on a cellular level. To do so, well-characterized reservoir cell lines covering a wide range of bat, insectivore and rodent species are essential. Most currently available cell culture models display a heterologous virus-host relationship and are therefore only of limited value. Here, we review the recently established approaches to generate reservoir-derived cell culture models for the in vitro study of virus-host interactions. These successfully used model systems almost exclusively originate from bats and bat-borne viruses other than hantaviruses. Therefore we propose a parallel approach for research on rodent- and insectivore-borne hantaviruses, taking the generation of novel rodent and insectivore cell lines from wildlife species into account. These cell lines would be also valuable for studies on further rodent-borne viruses, such as orthopox- and arenaviruses.
Emerging zoonotic viruses have received tremendous interest within recent years and are perceived as a major health risk for humans [1,2]. Among them are many RNA viruses from wildlife reservoirs, with recent examples including Severe Acute Respiratory Syndrome (SARS) and Middle East Respiratory Syndrome (MERS) Coronavirus (CoV) as well as Old- and New World hantaviruses [3,4,5,6,7,8,9,10]. In addition, recent “pathogen hunting” approaches resulted in the discovery of novel paramyxo-, hepe-, hepaci- and hepadnaviruses in bats and rodents [11,12,13,14,15,16,17].
Hantaviruses are enveloped viruses with a segmented RNA genome of negative polarity. Taxonomically, these viruses belong to the genus Hantavirus within the family Bunyaviridae . In contrast to other genera of the family Bunyaviridae, hantaviruses are harbored by small mammals, mainly rodents (order Rodentia). In general, each hantavirus species is thought to be carried and transmitted to humans by a single reservoir species. Thus, the prototype hantavirus species, the Hantaan virus, was exclusively detected in the striped field mouse Apodemus agrarius in Asia . Similarly, the European Puumala virus (PUUV), causing the majority of human infections in Northern, Western and Central Europe, seems to be adapted to the bank vole Myodes (Clethrionomys) glareolus [20,21]. For other rodent-borne hantaviruses, such as Dobrava-Belgrade virus, different genotypes have been identified, each harbored preferentially by a defined Apodemus species . In addition, Tula virus (TULV) was initially detected in the common vole Microtus arvalis representing the reservoir host, but was also molecularly detected in other vole species [23,24,25]. The multiple detection of TULV in different putative reservoirs underlines the problems of the identification of reservoir hosts and the necessity of comprehensive field studies in habitats with sympatrically occurring putative reservoir species [24,26].
Recently, a large number of shrews and moles (order Soricomorpha/Eulipotyphla) and bats (order Chiroptera) have been identified as reservoirs of additional hantaviruses [21,27,28,29,30,31,32]. The discovery of these highly divergent hantaviruses challenge the previous assumption of a strict virus-host coevolution over long time scales. Besides the virus-host coevolution hypothesis, alternative scenarios of host-switch events and adaptive evolution have been discussed recently [33,34,35,36,37,38]. Finally, recent findings of spillover infections of European hantaviruses, such as TULV and Dobrava-Belgrade virus, raise important questions on the host range of hantaviruses and the determinants of host specificity (see e.g., [24,39]). In humans, hantaviruses are known to cause a broad range of clinical disease, mainly affecting the renal tract: hemorrhagic fever with renal syndrome (HFRS), with its milder form, nephropathia epidemica (NE), or the respiratory tract: hantavirus cardiopulmonary syndrome (HCPS) caused by certain Old and New World hantaviruses, respectively [10,21,40]. Similarities in the clinical pictures of both syndromes and overlap of clinical presentation such as pulmonary symptoms in a subset of patients with NE and kidney involvement in some patients with HCPS suggest that the previously used dichotomy of clinical presentation might be not useful to describe the clinical outcome of human hantavirus infections and to understand its underlying pathological processes [41,42,43,44,45,46]. Therefore, the term “hantavirus disease” was proposed .
In contrast, in the reservoir host a hantavirus infection is usually believed to be persistent and not associated with (at least obvious) disease. However, field studies in bank voles indicated that hantavirus infection has a negative impact on over-winter survival, and histopathologic lesions in several organs have been observed in hantavirus-infected white-footed mice and in deer mice [48,49,50]. The causal relationship and the relevance of these observations remain, however, unknown.
With the discovery of hantaviruses in a broad spectrum of reservoirs and the identification of unexpected spillover and putative host-switch events, reservoir-host centered infection models become of immediate interest [10,51]. In addition, public health-related questions on the potential of these viruses to overcome species barriers and a rational-based risk assessment arise. This assessment is not only restricted to the field of hantavirus research but relevant in the context of many emerging virus species, such as members of the families Corona- or Paramyxoviridae. These research questions necessitate, however, novel tools and methods that allow comparative infection studies and immunological evaluation of virus-host interactions among a broad species context, not only including wildlife, but also livestock and companion animal species.
Until now, there is little knowledge on virus-host interaction in the natural reservoir; and currently available in vitro model systems do not reflect characteristics of reservoir specific virus-host interactions . Animal infection experiments with zoonotic viruses under laboratory conditions in the natural reservoir hosts are limited to a small number of species and to highly specialized laboratories. Currently available in vivo data on the immunology of hantavirus infection in their natural reservoir stem from animal experiments on Norway rats, deer mice, bank voles and cotton rats (for an overview see ). However, reservoir animal models for in vivo studies are not available for the majority of species that harbor hantaviruses. The main reasons are difficulties in breeding and keeping these species under laboratory conditions. Furthermore, many rodents as well as members of the orders Soricomorpha/Eulipotyphla and Chiroptera are protected species; therefore they are not available in large numbers for animal experiments or for in vivo studies in the laboratory at all. An overview on model systems for the study of zoonotic viruses is presented in Table 1.
Among all mammalian reservoir hosts, bats are most likely the order of mammals that has received the most attention from the virological research community in recent years [54,55,56]. A plethora of novel viruses have been identified in bats, among them many zoonotic viruses. However, most bat species, similar to rodents and insectivores, are not available for animal experiments, and this has stimulated the establishment of novel in vitro models such as bat cell lines. The generation of these cell lines across a broad range of species has already provided important insights into virus-host interaction on a cellular level and on innate immune functions, e.g., interferon response [57,58,59,60,61,62,63].
The many similarities between bat-, insectivore- and rodent-borne viruses could stimulate a synergistic approach for reservoir host-derived in vitro models to study hantaviruses.
|Model||Advantages||Disadvantages||Value for zoonosis research|
|Animal model, conventional (e.g., laboratory mouse, rat)||Easy to maintain and breed||Heterologous pathogen-host relationship||Limited|
|Species-specific reagents available||Transfer of results to humans or reservoir host limited|
|Animal model, reservoir host (natural reservoir host species)||Homologous pathogen-host relationship||Husbandry and breeding limited to few species||High, but limited to few species|
|Species-specific reagents rarely available|
|Cell culture, conventional (e.g., Vero E6, tumor cell lines, HUVECs, monocytes, dendritic cells)||Easy to culture||Heterologous pathogen-host relationship||Suitable as a basic model, but less useful for more complex questions on pathogen-host interaction|
|Assays, reagents and methods available||Accumulation of mutations/deregulation of important cellular pathways due to high passage numbers possible|
|Cell culture, reservoir host-derived||Homologous pathogen-host relationship||Very few reservoir-derived cell lines available so far||High|
|Thorough characterization necessary|
|Species-specific reagents rarely available|
2. What Have We Learned from Reservoir-Derived Cell Lines in the Field of Bat-Borne Viruses?
2.1. Virus Isolation Studies
Cell culture is the mainstay of classical virology and even in times of highly sensitive and high-throughput detection methods, isolation of a virus in cell culture enables its thorough phenotypical characterization. While in the early era of virology, isolation by cell culture was routinely performed; it has become something of an outdated method for many years. Cell lines such as Vero cells, derived from the kidney of an African green monkey, are widely used for virus isolation and especially the subclone Vero E6 provides an excellent environment for RNA viruses to replicate due to an impaired IFN response [64,65].
Vero E6 cells have enabled the isolation of a variety of hantaviruses [29,66,67,68,69,70], but most novel identified bat-, insectivore- and rodent-borne viruses remain uncultured. Therefore, primary and immortalized cell lines derived from reservoir hosts could provide a benefit for virus isolation. Several examples provide evidence that reservoir-derived cells can be beneficial over conventional cell lines to isolate reservoir-borne viruses: The henipa-related paramyxovirus Cedar virus was firstly isolated in primary kidney cells derived from a flying fox (Pteropus alecto), the species which naturally harbors this virus . In this study, only primary bat cells showed a cytopathic effect while several other cell lines, including Vero cells, did not. This cell line was also used for successful isolation of Menangle virus, another zoonotic paramyxovirus . In addition, Zhang et al. showed isolation and replication of a bat herpesvirus derived from the bat Miniopterus schreibersii in primary bat cells after unsuccessful isolation attempts in 14 other mammalian cell lines .
Although hantaviruses are not as hard to isolate as other zoonotic viruses (i.e., members of the family Coronaviridae), the number of hantavirus isolates of reservoir or human origin is still rather small . Therefore, the use of reservoir-derived cell lines might be also beneficial for the generation of a more comprehensive collection of hantavirus isolates.
2.2. Virus Evolution and Adaptation during Cell Culture Propagation
Many hantavirus isolates have been obtained a long time ago and were propagated on conventional cell lines such as Vero E6 cells. Therefore, they might have accumulated adaptations to the cell lines on which they have been propagated and do not fully display all characteristics of the viruses found in the reservoir. One example that supports this consideration is the report of the attenuation of a PUUV strain which subsequently lost its ability to infect the natural reservoir animal after passaging due to the accumulation of mutations in the S segment. Here, a wild-type variant that was passaged in bank voles was well adapted for reproduction in the reservoir host but not in cell culture, while the strains propagated on Vero E6 replicated to much higher efficiency in cell culture but did not reproducibly infect bank voles . It was further observed that hantavirus strains evolve during multiple cell culture passages. For example, Sundström et al. isolated PUUV strains which differed from the corresponding parental strain by plaque size, the ability to replicate in interferon-defective versus interferon-competent cell lines and the potential to induce innate immune responses .
The emergence of a stop codon within the coding sequence of the NSs open reading frame of TULV may represent also an adaptation of the virus to the IFN-deficient Vero E6 cell line . Similarly, the PUUV prototype strain passaged in Vero E6 cells was demonstrated to contain two sequence variants, an NSs-intact variant and a stop codon containing NSs variant . In contrast, the vole reservoir-derived PUUV and TULV strains were found to contain a conserved intact NSs open reading frame which might be functional in the reservoir .
2.3. Deciphering Replicative Capacity of Reservoir-Associated Viruses in Reservoir-Host Cell Lines
Reservoir-derived cell lines are not only a suitable tool for the study of evolutionary closely linked virus-host combinations, but they can also be used for deciphering cross-species transmission, hinting at a certain species as animal reservoir or estimating replicative capacity. Examples include assessment of the replicative capacity of the newly emerged MERS-CoV in bat cell lines not only originating from the presumed reservoir host, bats of the family Vespertilionidae, but across several other bat families and ungulates [80,81] and identification of the MERS-CoV receptor . Further, New World bat and cotton rat-derived cell lines were successfully used for the characterization of a sylvatic isolate of St. Louis encephalitis virus . Bat cell lines obtained from Pipistrellus ceylonicus allowed propagation of a rhabdovirus pathogenic to humans, Chandipura virus, and a bat adenovirus isolated from Rousettus leschenaulti from India, while the cells did not support replication of a number of bunya-, alpha- and flaviviruses . As bats have recently been identified as hosts of influenza viruses [85,86], bat cells were shown to be susceptible to influenza A virus infection, and importantly, to allow re-assortment during co-infection of two influenza viruses .
On the other hand, reservoir-derived cell lines from bats could provide hints to a wildlife origin of human viruses that are already circulating in the human population for some time: For example, Huynh and coworkers showed replication of the human coronavirus HCoV-NL63 in immortalized lung cells from the North American tri-colored bat (Perimyotis subflavus) for multiple passages, suggesting an origin of the virus in bats .
2.4. In Vitro Studies on Virus-Host Interaction
A main application of reservoir-derived cell lines is the investigation of virus-host interactions upon controlled infection experiments. Bat cell lines have already served as a valuable tool to study virus entry and replication among a broad range of zoonotic viruses in models representing the natural reservoir host. For example, two filoviruses, Ebola virus (EBOV) and Marburg virus which are harbored by bats in the wild, were shown to enter and replicate efficiently in a bat cell line derived from the Egyptian fruit bat (Rousettus aegyptiacus), indicating that this model is highly suitable to investigate the biology of filoviruses in cells derived from their presumed reservoir . Furthermore, it has been shown that the glycoprotein of EBOV can interact in fruit bat and human cells in a similar manner and does not limit EBOV tropism to certain bat species . Further, the glycoprotein of Lloviu virus, a filovirus from bats that has not been isolated so far, was found to mediate cellular entry in similar manner to other filoviruses with a tropism for bat cells derived from multiple species . Surface glycoproteins of African henipaviruses could induce syncytium formation in a cell line derived from an African fruit bat, indicating a similar strategy of virus entry for both Asian and African henipaviruses, and providing a cell culture model for isolation of these emerging viruses .
Besides entry studies, reservoir-derived cell lines from bats could also provide insights into the reservoir host innate immune response to paramyxoviruses. By the use of reservoir-derived cell lines, it was shown that interferon production and signaling pathways are antagonized during henipavirus infection of fruit bat cell lines . Further insight into the interferon system of bats was gained by characterization of the type I interferon reaction to viral infection in interferon-competent, immortalized cell lines from the African fruit bat Eidolon helvum .
The above-mentioned differences in the host range of hantaviruses might be driven by polymorphisms in the receptor molecules. Thus, closely related Microtus species (M. arvalis, M. agrestis) may have a similar hantavirus entry receptor, although they are phylogenetically a long time separated as reflected in their morphological features . In addition, the tissue tropism of hantaviruses in their natural reservoirs might be determined by the receptor repertoire, cellular cofactors of virus replication and transcription, and innate immunity mechanisms. Recently, it has been shown that pathogenic hantaviruses in contrast to non-pathogenic hantaviruses display a different induction of microRNAs, essential regulators of host immune response genes, in human endothelial cells, macrophages and epithelial cells . To study these immunological regulators in the reservoir host as well would be an interesting option. Therefore, bat-, insectivore- and rodent-derived cell lines would represent a valuable tool for identification of host factors. Moreover, such cell lines would help to understand innate immunity escape mechanisms that are linked to the activity of the putative NSs protein, exclusively identified in arvicoline, sigmodontine- and neotomine-associated hantaviruses .
3. What Are the Obstacles to Overcome? — A Research Agenda for Reservoir-Derived Rodent and Insectivore Cell Lines
It has been shown that hantaviruses can infect multiple cell types, but have a tropism to endothelial cells in human infection, a reason why human umbilical vein endothelial cells (HUVECs) are the main cell culture model for hantavirus disease in humans . Further, hantaviruses can infect dendritic cells which are suggested to significantly contribute to hantavirus pathogenesis in humans . In rodents, which shed the virus in saliva, urine and feces, the highest amount of hantaviral RNA is consistently found in the lungs [96,97,98]. As transmission of hantaviruses between rodents and also during zoonotic transmission from rodents to humans is mainly through the respiratory route, the lung is of interest for hantavirus infection. Indeed, we could observe PUUV hantavirus infection in human primary airway epithelial cells as well as in an airway epithelial cell line derived from a bank vole  Further, as the viruses are shed in the urine, renal epithelial cells could be of interest for the study of virus-host interactions in the natural reservoir host. One of the few reservoir-derived cell lines that are already available from a hantavirus reservoir host is a spontaneously immortalized cell line derived from the kidney of an adult bank vole . Although this cell line was permissive to several arthropod- and rodent-borne viruses such as Vesicular stomatitis virus, vaccinia virus, cowpox virus, Sindbis virus, Pixuna virus, Usutu virus, Inkoo virus, and Borna disease virus, it failed to allow productive infection with PUUV strain Vranica, a strain that is adapted to and passaged in Vero E6 cells. Another group isolated bank vole embryonic fibroblasts and showed that these primary cells were susceptible for PUUV-infection, including a wild‑type PUUV strain that was only passaged in bank voles . However, this approach is dependent on the availability of embryonic organ material of bank voles, which requires a successful bank vole breeding colony to continuously obtain embryos for the preparation of primary cells. In case of the existence of a breeding colony of a given rodent or insectivore species, this approach might be especially useful for studies on selected cell types, e.g., dendritic cells, but might be not a general option for most hantavirus-harboring species.
To ensure the continuous availability of a cell culture model system, immortalization is an option to create infinite cell lines from primary cells. While in primary rodent cells spontaneous immortalization can occur, it is not known if bat or insectivore cells behave in the same way. Other methods of immortalization include retroviral systems such as lentiviral transduction of the coding sequence of large T antigen of SV40 or introduction and stable expression of telomerase reverse transcriptase protein, both attempts which have been already successfully applied for the generation of bat cell lines [57,81,102]. For an overview of advantages and disadvantages of primary vs. spontaneously vs. artificially immortalized cells, see Table 2.
To obtain suitable tissue of reservoir hosts, ongoing research projects on small mammals can be of use for collection of organ material to isolate primary cells. While it is not possible to generate cell lines from the plethora of rodent and insectivore species in which hantaviruses are found, a pragmatic approach is to focus on representative species. Selection criteria for these representative species could be: the overall importance of the associated virus, availability of breeding colonies, and representation of certain families/genera.
|Cell characteristics||Primary cells||Spontaneously immortalized cells||Artificially immortalized cells|
|Immortalization||None||Occurs only after multiple passages||Possible at low passage number|
|Genetic background||Close to in vivo situation||Artificial (severe changes can occur upon immortalization)||Artificial (severe changes can occur upon immortalization)|
|Proliferative capacity||Mostly low *||High||High|
|Life span||Limited, finite||Not limited, infinite||Not limited, infinite|
|Biological properties||Close to in vivo situation||Dedifferentiation, more distant from in vivo situation||Dedifferentiation depends on immortalization methods|
|Selection of distinct cell types possible, conditional immortalization strategy feasible|
|Selection of distinct cell types difficult|
|Preferred culture medium||Specialized medium (expensive) **||Standard medium||Standard medium|
|Properties of cell population||Close to in vivo cell types||Loss of distinct cell types during subcultivation||Selection of distinct cell types possible|
|Standardization and reproducibility||Limited cell number, standardization only possible for some cell types ***||Standardization possible due to unlimited amount of cells||Standardization possible due to unlimited amount of cells|
* Exceptions of primary cells that have a high proliferative capacity are primary fibroblasts and HUVECs. They are, however, limited in their passage number. ** Exceptions include primary fibroblasts and HUVECs for which affordable media are widely available. *** Standardization of primary cells is possible to some extent given the case that cells of a low passage number can be sufficiently expanded after initial isolation, i.e., HUVECs.
Natural reservoir host species that are available as laboratory animals, in breeding colonies or in enclosures (such as Norway rats, deer mice, bank voles, common voles, cotton rats or Asian house shrews) are of special interest: cell lines derived from these animals could be compared to the in vivo infection in an animal model with the associated virus species. Further, laboratory-bred populations are less likely to be infected with unwanted pathogens, and in most instances, stem from a genetically characterized background.
If cell lines are generated from feral animals, a thorough screening for contaminants from the field is necessary (contaminants include bacteria and parasites such as mycoplasma or trypanosomes as well as viruses that might be cultured along with primary cells). Animals from which tissue material was obtained should be either directly tested for contamination with known pathogens or alternatively sentinel animals, i.e., laboratory mice are an option. Thorough screening, for example by next generation sequencing of organ material, can provide further assessment to ensure high-quality cell lines without contaminants, even for as yet unknown pathogens. Furthermore, thorough characterization of the cell lines is obligatory for their use in virus infection studies. This characterization should focus on the following questions: Do these cells still express relevant receptors, are interferon signaling pathways still intact, do these cells still represent important characteristics of their cell type of origin (i.e., in the case of epithelial cells: are cell-cell contacts intact, do cells still form a monolayer, do they retain their ability to form a polarized monolayer?). Although complex, this characterization ensures a valid cell culture model, which can then easily be shared between different research groups and lead to novel insights into the highly conserved hantavirus-host interaction in the context of their natural reservoir. As seen in the field of bat-borne zoonoses, reservoir-derived cell lines can serve as a valuable in vitro tool and therefore this approach should also be used in the field of rodent- and insectivore-borne zoonotic viruses. Furthermore, synergistic approaches of bat-, rodent- and insectivore-borne viruses and their reservoirs might enable the identification of general mechanisms of virus persistence, conserved across a broad range of mammalian reservoir hosts. Protocols for the generation of bat cell lines have been established and could be adapted to the rodent and insectivore host [57,81,102]; an exemplary approach is presented in Figure 1. In order to mimic the natural infection as close as possible, generation of cell lines should focus on cell types which are a target during natural infection or stem from organs that are involved in virus entry, spread or shedding, such as epithelial cells from the respiratory or renal tract.
In conclusion, investing in a large range of reservoir-derived cell culture models will be a promising tool to reveal novel aspects of the hantavirus-host relationship. Further, experience and model systems from the field of bat-borne zoonosis can serve as a blueprint for the hantavirus research community.
We thank Christian Drosten and Marcel Müller for critical reading of the manuscript and helpful comments.
The authors are partners in the project “Establishment and characterization of airway and renal epithelial cell cultures from rodents and insectivores (EpiZell)” which is funded by the German Research Platform for Zoonoses (grant 01KI1308).
IE and RGU reviewed the literature; IE, ML and RGU wrote the manuscript.
Conflicts of Interest
The authors declare no conflict of interest
References and Notes
- Jones, K.E.; Patel, N.G.; Levy, M.A.; Storeygard, A.; Balk, D.; Gittleman, J.L.; Daszak, P. Global trends in emerging infectious diseases. Nature 2008, 451, 990–993. [Google Scholar] [CrossRef]
- Johnson, N. A short introduction to disease emergence. In The Role of Animals in Emerging Viral Diseases; Johnson, N., Ed.; Academic Press: Boston, MA, USA, 2014; Chapter 1; pp. 1–19. [Google Scholar]
- Peiris, J.S.; Guan, Y.; Yuen, K.Y. Severe acute respiratory syndrome. Nat. Med. 2004, 10, S88–S97. [Google Scholar] [CrossRef]
- Drosten, C.; Gunther, S.; Preiser, W.; van der Werf, S.; Brodt, H.R.; Becker, S.; Rabenau, H.; Panning, M.; Kolesnikova, L.; Fouchier, R.A.; et al. Identification of a novel coronavirus in patients with severe acute respiratory syndrome. N. Engl. J. Med. 2003, 348, 1967–1976. [Google Scholar] [CrossRef]
- Zaki, A.M.; van Boheemen, S.; Bestebroer, T.M.; Osterhaus, A.D.; Fouchier, R.A. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N. Engl. J. Med. 2012, 367, 1814–1820. [Google Scholar] [CrossRef]
- Corman, V.M.; Eckerle, I.; Bleicker, T.; Zaki, A.; Landt, O.; Eschbach-Bludau, M.; van Boheemen, S.; Gopal, R.; Ballhause, M.; Bestebroer, T.M.; et al. Detection of a novel human coronavirus by real-time reverse-transcription polymerase chain reaction. Euro. Surveill. 2012, 17. pii=20285. [Google Scholar]
- Drosten, C. Is MERS another SARS? Lancet Infect. Dis. 2013, 13, 727–728. [Google Scholar] [CrossRef]
- Nichol, S.T.; Spiropoulou, C.F.; Morzunov, S.; Rollin, P.E.; Ksiazek, T.G.; Feldmann, H.; Sanchez, A.; Childs, J.; Zaki, S.; Peters, C.J. Genetic identification of a hantavirus associated with an outbreak of acute respiratory illness. Science 1993, 262, 914–917. [Google Scholar]
- Ettinger, J.; Hofmann, J.; Enders, M.; Tewald, F.; Oehme, R.M.; Rosenfeld, U.M.; Ali, H.S.; Schlegel, M.; Essbauer, S.; Osterberg, A.; et al. Multiple synchronous outbreaks of Puumala virus, Germany, 2010. Emerg. Infect. Dis. 2012, 18, 1461–1464. [Google Scholar] [CrossRef]
- Vaheri, A.; Strandin, T.; Hepojoki, J.; Sironen, T.; Henttonen, H.; Makela, S.; Mustonen, J. Uncovering the mysteries of hantavirus infections. Nat. Rev. Microbiol. 2013, 11, 539–550. [Google Scholar] [CrossRef]
- Drexler, J.F.; Corman, V.M.; Muller, M.A.; Maganga, G.D.; Vallo, P.; Binger, T.; Gloza-Rausch, F.; Rasche, A.; Yordanov, S.; Seebens, A.; et al. Bats host major mammalian paramyxoviruses. Nat. Commun. 2012, 3, 796. [Google Scholar] [CrossRef]
- Drexler, J.F.; Seelen, A.; Corman, V.M.; Fumie Tateno, A.; Cottontail, V.; Melim Zerbinati, R.; Gloza-Rausch, F.; Klose, S.M.; Adu-Sarkodie, Y.; Oppong, S.K.; et al. Bats worldwide carry hepatitis E virus-related viruses that form a putative novel genus within the family Hepeviridae. J. Virol. 2012, 86, 9134–9147. [Google Scholar] [CrossRef]
- Johne, R.; Heckel, G.; Plenge-Bonig, A.; Kindler, E.; Maresch, C.; Reetz, J.; Schielke, A.; Ulrich, R.G. Novel hepatitis E virus genotype in Norway rats, Germany. Emerg. Infect. Dis. 2010, 16, 1452–1455. [Google Scholar] [CrossRef]
- Drexler, J.F.; Corman, V.M.; Muller, M.A.; Lukashev, A.N.; Gmyl, A.; Coutard, B.; Adam, A.; Ritz, D.; Leijten, L.M.; van Riel, D.; et al. Evidence for novel hepaciviruses in rodents. PLoS Pathog. 2013, 9, e1003438. [Google Scholar] [CrossRef]
- Quan, P.L.; Firth, C.; Conte, J.M.; Williams, S.H.; Zambrana-Torrelio, C.M.; Anthony, S.J.; Ellison, J.A.; Gilbert, A.T.; Kuzmin, I.V.; Niezgoda, M.; et al. Bats are a major natural reservoir for hepaciviruses and pegiviruses. Proc. Natl. Acad. Sci. USA 2013, 110, 8194–8199. [Google Scholar] [CrossRef]
- Kapoor, A.; Simmonds, P.; Scheel, T.K.; Hjelle, B.; Cullen, J.M.; Burbelo, P.D.; Chauhan, L.V.; Duraisamy, R.; Sanchez Leon, M.; Jain, K.; et al. Identification of rodent homologs of hepatitis C virus and pegiviruses. MBio 2013, 4, e00216-13. [Google Scholar]
- Drexler, J.F.; Geipel, A.; Konig, A.; Corman, V.M.; van Riel, D.; Leijten, L.M.; Bremer, C.M.; Rasche, A.; Cottontail, V.M.; Maganga, G.D.; et al. Bats carry pathogenic hepadnaviruses antigenically related to hepatitis B virus and capable of infecting human hepatocytes. Proc. Natl. Acad. Sci. USA 2013, 110, 16151–16156. [Google Scholar] [CrossRef]
- Plyusnin, A.; Beaty, B.J.; Elliott, R.M.; Goldbach, R.; Kormelink, R.; Lundkvist, A.; Schmaljohn, C.S.; Tesh, R.B. Bunyaviridae. In Virus Taxonomy: Ninth Report of the International Committee on Taxonomy of Viruses; King, M.Q., Adams, M.J., Carstensen, E.B., Lefkowitz, E.J., Eds.; Elsevier Inc.: San Diego, CA, USA, 2011. [Google Scholar]
- Lee, H.W.; Lee, P.W.; Johnson, K.M. Isolation of the etiologic agent of Korean Hemorrhagic fever. J. Infect. Dis. 1978, 137, 298–308. [Google Scholar] [CrossRef]
- Brummer-Korvenkontio, M.; Vaheri, A.; Hovi, T.; von Bonsdorff, C.H.; Vuorimies, J.; Manni, T.; Penttinen, K.; Oker-Blom, N.; Lahdevirta, J. Nephropathia epidemica: Detection of antigen in bank voles and serologic diagnosis of human infection. J. Infect. Dis. 1980, 141, 131–134. [Google Scholar] [CrossRef]
- Schlegel, M.; Jacob, J.; Krüger, D.H.; Rang, A.; Ulrich, R.G. Hantavirus emergence in rodents, insectivores and bats: What comes next? In The Role of Animals in Emerging Viral Diseases; Johnson, N., Ed.; Academic Press: Boston, MA, USA, 2014; Chapter 10; pp. 235–292. [Google Scholar]
- Klempa, B.; Avsic-Zupanc, T.; Clement, J.; Dzagurova, T.K.; Henttonen, H.; Heyman, P.; Jakab, F.; Kruger, D.H.; Maes, P.; Papa, A.; et al. Complex evolution and epidemiology of Dobrava-Belgrade hantavirus: Definition of genotypes and their characteristics. Arch. Virol. 2013, 158, 521–529. [Google Scholar] [CrossRef]
- Plyusnin, A.; Vapalahti, O.; Lankinen, H.; Lehvaslaiho, H.; Apekina, N.; Myasnikov, Y.; Kallio-Kokko, H.; Henttonen, H.; Lundkvist, A.; Brummer-Korvenkontio, M.; et al. Tula virus: A newly detected hantavirus carried by European common voles. J. Virol. 1994, 68, 7833–7839. [Google Scholar]
- Schmidt-Chanasit, J.; Essbauer, S.; Petraityte, R.; Yoshimatsu, K.; Tackmann, K.; Conraths, F.J.; Sasnauskas, K.; Arikawa, J.; Thomas, A.; Pfeffer, M.; et al. Extensive host sharing of central European Tula virus. J. Virol. 2010, 84, 459–474. [Google Scholar] [CrossRef]
- Schlegel, M.; Kindler, E.; Essbauer, S.S.; Wolf, R.; Thiel, J.; Groschup, M.H.; Heckel, G.; Oehme, R.M.; Ulrich, R.G. Tula virus infections in the Eurasian water vole in Central Europe. Vector Borne Zoonotic Dis. 2012, 12, 503–513. [Google Scholar] [CrossRef]
- Hjelle, B.; Yates, T. Modeling hantavirus maintenance and transmission in rodent communities. Curr. Top. Microbiol. Immunol. 2001, 256, 77–90. [Google Scholar]
- Radosa, L.; Schlegel, M.; Gebauer, P.; Ansorge, H.; Heroldova, M.; Janova, E.; Stanko, M.; Mosansky, L.; Fricova, J.; Pejcoch, M.; et al. Detection of shrew-borne hantavirus in Eurasian pygmy shrew (Sorex minutus) in Central Europe. Infect. Genet. Evol. 2013, 19, 403–410. [Google Scholar] [CrossRef]
- Kang, H.J.; Bennett, S.N.; Sumibcay, L.; Arai, S.; Hope, A.G.; Mocz, G.; Song, J.W.; Cook, J.A.; Yanagihara, R. Evolutionary insights from a genetically divergent hantavirus harbored by the European common mole (Talpa europaea). PLoS One 2009, 4, e6149. [Google Scholar] [CrossRef]
- Song, J.W.; Kang, H.J.; Gu, S.H.; Moon, S.S.; Bennett, S.N.; Song, K.J.; Baek, L.J.; Kim, H.C.; O'Guinn, M.L.; Chong, S.T.; et al. Characterization of Imjin virus, a newly isolated hantavirus from the Ussuri white-toothed shrew (Crocidura lasiura). J. Virol. 2009, 83, 6184–6191. [Google Scholar] [CrossRef]
- Arai, S.; Ohdachi, S.D.; Asakawa, M.; Kang, H.J.; Mocz, G.; Arikawa, J.; Okabe, N.; Yanagihara, R. Molecular phylogeny of a newfound hantavirus in the Japanese shrew mole (Urotrichus talpoides). Proc. Natl. Acad. Sci. USA 2008, 105, 16296–16301. [Google Scholar] [CrossRef]
- Sumibcay, L.; Kadjo, B.; Gu, S.H.; Kang, H.J.; Lim, B.K.; Cook, J.A.; Song, J.W.; Yanagihara, R. Divergent lineage of a novel hantavirus in the banana pipistrelle (Neoromicia nanus) in Cote d'Ivoire. Virol. J. 2012, 9, 34. [Google Scholar] [CrossRef]
- Weiss, S.; Witkowski, P.T.; Auste, B.; Nowak, K.; Weber, N.; Fahr, J.; Mombouli, J.V.; Wolfe, N.D.; Drexler, J.F.; Drosten, C.; et al. Hantavirus in bat, Sierra Leone. Emerg. Infect. Dis. 2012, 18, 159–161. [Google Scholar] [CrossRef]
- Hughes, A.L.; Friedman, R. Evolutionary diversification of protein-coding genes of hantaviruses. Mol. Biol. Evol. 2000, 17, 1558–1568. [Google Scholar] [CrossRef]
- Plyusnin, A.; Morzunov, S.P. Virus evolution and genetic diversity of hantaviruses and their rodent hosts. Curr. Top. Microbiol. Immunol. 2001, 256, 47–75. [Google Scholar]
- Sironen, T.; Vaheri, A.; Plyusnin, A. Molecular evolution of Puumala hantavirus. J. Virol. 2001, 75, 11803–11810. [Google Scholar] [CrossRef]
- Morzunov, S.P.; Rowe, J.E.; Ksiazek, T.G.; Peters, C.J.; St Jeor, S.C.; Nichol, S.T. Genetic analysis of the diversity and origin of hantaviruses in Peromyscus leucopus mice in North America. J. Virol. 1998, 72, 57–64. [Google Scholar]
- Ramsden, C.; Holmes, E.C.; Charleston, M.A. Hantavirus evolution in relation to its rodent and insectivore hosts: No evidence for codivergence. Mol. Biol. Evol. 2009, 26, 143–153. [Google Scholar]
- Guo, W.P.; Lin, X.D.; Wang, W.; Tian, J.H.; Cong, M.L.; Zhang, H.L.; Wang, M.R.; Zhou, R.H.; Wang, J.B.; Li, M.H.; et al. Phylogeny and origins of hantaviruses harbored by bats, insectivores, and rodents. PLoS Pathog. 2013, 9, e1003159. [Google Scholar] [CrossRef]
- Schlegel, M.; Klempa, B.; Auste, B.; Bemmann, M.; Schmidt-Chanasit, J.; Buchner, T.; Groschup, M.H.; Meier, M.; Balkema-Buschmann, A.; Zoller, H.; et al. Dobrava-Belgrade virus spillover infections, Germany. Emerg. Infect. Dis. 2009, 15, 2017–2020. [Google Scholar] [CrossRef]
- Jonsson, C.B.; Figueiredo, L.T.; Vapalahti, O. A global perspective on hantavirus ecology, epidemiology, and disease. Clin. Microbiol. Rev. 2010, 23, 412–441. [Google Scholar] [CrossRef]
- Rasmuson, J.; Andersson, C.; Norrman, E.; Haney, M.; Evander, M.; Ahlm, C. Time to revise the paradigm of hantavirus syndromes? Hantavirus pulmonary syndrome caused by European hantavirus. Eur. J. Clin. Microbiol. Infect. Dis. 2011, 30, 685–690. [Google Scholar] [CrossRef]
- Eckerle, I.; Heussel, C.P. Fever, acute renal failure and pulmonary edema. NDT Plus 2011, 4, 130–132. [Google Scholar] [CrossRef]
- Braun, N.; Haap, M.; Overkamp, D.; Kimmel, M.; Alscher, M.D.; Lehnert, H.; Haas, C.S. Characterization and outcome following Puumala virus infection: A retrospective analysis of 75 cases. Nephrol. Dial. Transplant. 2010, 25, 2997–3003. [Google Scholar] [CrossRef]
- Kanerva, M.; Paakkala, A.; Mustonen, J.; Paakkala, T.; Lahtela, J.; Pasternack, A. Pulmonary involvement in nephropathia epidemica: Radiological findings and their clinical correlations. Clin. Nephrol. 1996, 46, 369–378. [Google Scholar]
- Passaro, D.J.; Shieh, W.J.; Hacker, J.K.; Fritz, C.L.; Hogan, S.R.; Fischer, M.; Hendry, R.M.; Vugia, D.J. Predominant kidney involvement in a fatal case of hantavirus pulmonary syndrome caused by Sin Nombre virus. Clin. Infect. Dis. 2001, 33, 263–264. [Google Scholar] [CrossRef]
- Zaki, S.R.; Greer, P.W.; Coffield, L.M.; Goldsmith, C.S.; Nolte, K.B.; Foucar, K.; Feddersen, R.M.; Zumwalt, R.E.; Miller, G.L.; Khan, A.S.; et al. Hantavirus pulmonary syndrome. Pathogenesis of an emerging infectious disease. Am. J. Pathol. 1995, 146, 552–579. [Google Scholar]
- Clement, J.; Maes, P.; Lagrou, K.; Van Ranst, M.; Lameire, N. A unifying hypothesis and a single name for a complex globally emerging infection: Hantavirus disease. Eur. J. Clin. Microbiol. Infect. Dis. 2012, 31, 1–5. [Google Scholar] [CrossRef]
- Kallio, E.R.; Voutilainen, L.; Vapalahti, O.; Vaheri, A.; Henttonen, H.; Koskela, E.; Mappes, T. Endemic hantavirus infection impairs the winter survival of its rodent host. Ecology 2007, 88, 1911–1916. [Google Scholar] [CrossRef]
- Lyubsky, S.; Gavrilovskaya, I.; Luft, B.; Mackow, E. Histopathology of Peromyscus leucopus naturally infected with pathogenic NY-1 hantaviruses: Pathologic markers of HPS viral infection in mice. Lab. Invest. 1996, 74, 627–633. [Google Scholar]
- Netski, D.; Thran, B.H.; St Jeor, S.C. Sin Nombre virus pathogenesis in Peromyscus maniculatus. J. Virol. 1999, 73, 585–591. [Google Scholar]
- Schonrich, G.; Rang, A.; Lutteke, N.; Raftery, M.J.; Charbonnel, N.; Ulrich, R.G. Hantavirus-induced immunity in rodent reservoirs and humans. Immunol. Rev. 2008, 225, 163–189. [Google Scholar] [CrossRef]
- Bean, A.G.; Baker, M.L.; Stewart, C.R.; Cowled, C.; Deffrasnes, C.; Wang, L.F.; Lowenthal, J.W. Studying immunity to zoonotic diseases in the natural host—Keeping it real. Nat. Rev. Immunol 2013, 13, 851–861. [Google Scholar] [CrossRef]
- Easterbrook, J.D.; Klein, S.L. Immunological mechanisms mediating hantavirus persistence in rodent reservoirs. PLoS Pathog. 2008, 4, e1000172. [Google Scholar] [CrossRef]
- Smith, I.; Wang, L.F. Bats and their virome: An important source of emerging viruses capable of infecting humans. Curr. Opin. Virol. 2013, 3, 84–91. [Google Scholar] [CrossRef]
- Wang, L.F.; Walker, P.J.; Poon, L.L. Mass extinctions, biodiversity and mitochondrial function: Are bats 'special' as reservoirs for emerging viruses? Curr. Opin. Virol. 2011, 1, 649–657. [Google Scholar] [CrossRef]
- Luis, A.D.; Hayman, D.T.; O'Shea, T.J.; Cryan, P.M.; Gilbert, A.T.; Pulliam, J.R.; Mills, J.N.; Timonin, M.E.; Willis, C.K.; Cunningham, A.A.; et al. A comparison of bats and rodents as reservoirs of zoonotic viruses: Are bats special? Proc. Biol. Sci. 2013, 280, 20122753. [Google Scholar] [CrossRef]
- Biesold, S.E.; Ritz, D.; Gloza-Rausch, F.; Wollny, R.; Drexler, J.F.; Corman, V.M.; Kalko, E.K.; Oppong, S.; Drosten, C.; Muller, M.A. Type I interferon reaction to viral infection in interferon-competent, immortalized cell lines from the African fruit bat Eidolon helvum. PLoS One 2011, 6, e28131. [Google Scholar] [CrossRef]
- Virtue, E.R.; Marsh, G.A.; Baker, M.L.; Wang, L.F. Interferon production and signaling pathways are antagonized during henipavirus infection of fruit bat cell lines. PLoS One 2011, 6, e22488. [Google Scholar]
- Cowled, C.; Baker, M.L.; Zhou, P.; Tachedjian, M.; Wang, L.F. Molecular characterisation of RIG-I-like helicases in the black flying fox, Pteropus alecto. Dev. Comp. Immunol. 2012, 36, 657–664. [Google Scholar] [CrossRef]
- Hagmaier, K.; Stock, N.; Goodbourn, S.; Wang, L.F.; Randall, R. A single amino acid substitution in the V protein of Nipah virus alters its ability to block interferon signalling in cells from different species. J. Gen. Virol. 2006, 87, 3649–3653. [Google Scholar] [CrossRef]
- Janardhana, V.; Tachedjian, M.; Crameri, G.; Cowled, C.; Wang, L.F.; Baker, M.L. Cloning, expression and antiviral activity of IFNgamma from the Australian fruit bat, Pteropus alecto. Dev. Comp. Immunol. 2012, 36, 610–618. [Google Scholar] [CrossRef]
- Zhou, P.; Cowled, C.; Marsh, G.A.; Shi, Z.; Wang, L.F.; Baker, M.L. Type III IFN receptor expression and functional characterisation in the pteropid bat, Pteropus alecto. PLoS One 2011, 6, e25385. [Google Scholar]
- Zhou, P.; Cowled, C.; Todd, S.; Crameri, G.; Virtue, E.R.; Marsh, G.A.; Klein, R.; Shi, Z.; Wang, L.F.; Baker, M.L. Type III IFNs in pteropid bats: Differential expression patterns provide evidence for distinct roles in antiviral immunity. J. Immunol. 2011, 186, 3138–3147. [Google Scholar] [CrossRef]
- Emeny, J.M.; Morgan, M.J. Regulation of the interferon system: Evidence that Vero cells have a genetic defect in interferon production. J. Gen. Virol. 1979, 43, 247–252. [Google Scholar] [CrossRef]
- Chew, T.; Noyce, R.; Collins, S.E.; Hancock, M.H.; Mossman, K.L. Characterization of the interferon regulatory factor 3-mediated antiviral response in a cell line deficient for IFN production. Mol. Immunol. 2009, 46, 393–399. [Google Scholar] [CrossRef]
- Gavrilovskaya, I.; LaMonica, R.; Fay, M.E.; Hjelle, B.; Schmaljohn, C.; Shaw, R.; Mackow, E.R. New York 1 and Sin Nombre viruses are serotypically distinct viruses associated with hantavirus pulmonary syndrome. J. Clin. Microbiol. 1999, 37, 122–126. [Google Scholar]
- Elliott, L.H.; Ksiazek, T.G.; Rollin, P.E.; Spiropoulou, C.F.; Morzunov, S.; Monroe, M.; Goldsmith, C.S.; Humphrey, C.D.; Zaki, S.R.; Krebs, J.W.; et al. Isolation of the causative agent of hantavirus pulmonary syndrome. Am. J. Trop. Med. Hyg. 1994, 51, 102–108. [Google Scholar]
- Puthavathana, P.; Lee, H.W.; Kang, C.Y. Typing of Hantaviruses from five continents by polymerase chain reaction. Virus Res. 1992, 26, 1–14. [Google Scholar] [CrossRef]
- Kitamura, T.; Morita, C.; Komatsu, T.; Sugiyama, K.; Arikawa, J.; Shiga, S.; Takeda, H.; Akao, Y.; Imaizumi, K.; Oya, A.; et al. Isolation of virus causing hemorrhagic fever with renal syndrome (HFRS) through a cell culture system. Jpn. J. Med. Sci. Biol. 1983, 36, 17–25. [Google Scholar]
- Song, J.W.; Baek, L.J.; Gavrilovskaya, I.N.; Mackow, E.R.; Hjelle, B.; Yanagihara, R. Sequence analysis of the complete S genomic segment of a newly identified hantavirus isolated from the white-footed mouse (Peromyscus leucopus): Phylogenetic relationship with other sigmodontine rodent-borne hantaviruses. Virus Genes 1996, 12, 249–256. [Google Scholar]
- Marsh, G.A.; de Jong, C.; Barr, J.A.; Tachedjian, M.; Smith, C.; Middleton, D.; Yu, M.; Todd, S.; Foord, A.J.; Haring, V.; et al. Cedar virus: A novel Henipavirus isolated from Australian bats. PLoS Pathog. 2012, 8, e1002836. [Google Scholar] [CrossRef]
- Barr, J.A.; Smith, C.; Marsh, G.A.; Field, H.; Wang, L.F. Evidence of bat origin for Menangle virus, a zoonotic paramyxovirus first isolated from diseased pigs. J. Gen. Virol. 2012, 93, 2590–2594. [Google Scholar] [CrossRef]
- Zhang, H.; Todd, S.; Tachedjian, M.; Barr, J.A.; Luo, M.; Yu, M.; Marsh, G.A.; Crameri, G.; Wang, L.F. A novel bat herpesvirus encodes homologues of major histocompatibility complex classes I and II, C-type lectin, and a unique family of immune-related genes. J. Virol. 2012, 86, 8014–8030. [Google Scholar] [CrossRef]
- Plyusnin, A.; Elliott, R. Concluding remarks. In Bunyaviridae: Molecular and Cellular Biology; Caister Academic Press: Poole, UK, 2011. [Google Scholar]
- Lundkvist, A.; Cheng, Y.; Sjolander, K.B.; Niklasson, B.; Vaheri, A.; Plyusnin, A. Cell culture adaptation of Puumala hantavirus changes the infectivity for its natural reservoir, Clethrionomys glareolus, and leads to accumulation of mutants with altered genomic RNA S segment. J. Virol. 1997, 71, 9515–9523. [Google Scholar]
- Sundstrom, K.B.; Stoltz, M.; Lagerqvist, N.; Lundkvist, A.; Nemirov, K.; Klingstrom, J. Characterization of two substrains of Puumala virus that show phenotypes that are different from each other and from the original strain. J. Virol. 2011, 85, 1747–1756. [Google Scholar] [CrossRef]
- Jaaskelainen, K.M.; Plyusnina, A.; Lundkvist, A.; Vaheri, A.; Plyusnin, A. Tula hantavirus isolate with the full-length ORF for nonstructural protein NSs survives for more consequent passages in interferon-competent cells than the isolate having truncated NSs ORF. Virol. J. 2008, 5, 3. [Google Scholar] [CrossRef]
- Rang, A.; Heider, H.; Ulrich, R.; Kruger, D.H. A novel method for cloning of non-cytolytic viruses. J. Virol. Methods 2006, 135, 26–31. [Google Scholar] [CrossRef]
- Jaaskelainen, K.M.; Kaukinen, P.; Minskaya, E.S.; Plyusnina, A.; Vapalahti, O.; Elliott, R.M.; Weber, F.; Vaheri, A.; Plyusnin, A. Tula and Puumala hantavirus NSs ORFs are functional and the products inhibit activation of the interferon-beta promoter. J. Med. Virol. 2007, 79, 1527–1536. [Google Scholar] [CrossRef]
- Muller, M.A.; Raj, V.S.; Muth, D.; Meyer, B.; Kallies, S.; Smits, S.L.; Wollny, R.; Bestebroer, T.M.; Specht, S.; Suliman, T.; et al. Human coronavirus EMC does not require the SARS-coronavirus receptor and maintains broad replicative capability in mammalian cell lines. MBio 2012, 3. [Google Scholar] [CrossRef]
- Eckerle, I.; Ehlen, L.; Kallies, R.; Wollny, R.; Corman, V.M.; Cottontail, V.M.; Tschapka, M.; Oppong, S.; Drosten, C.; Muller, M.A. Bat airway epithelial cells: A novel tool for the study of zoonotic viruses. PLoS One 2014, 9, e84679. [Google Scholar] [CrossRef]
- Raj, V.S.; Mou, H.; Smits, S.L.; Dekkers, D.H.; Muller, M.A.; Dijkman, R.; Muth, D.; Demmers, J.A.; Zaki, A.; Fouchier, R.A.; et al. Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature 2013, 495, 251–254. [Google Scholar] [CrossRef]
- Kopp, A.; Gillespie, T.R.; Hobelsberger, D.; Estrada, A.; Harper, J.M.; Miller, R.A.; Eckerle, I.; Muller, M.A.; Podsiadlowski, L.; Leendertz, F.H.; et al. Provenance and geographic spread of St. Louis encephalitis virus. MBio 2013, 4, e00322-13. [Google Scholar]
- Mourya, D.T.; Lakra, R.J.; Yadav, P.D.; Tyagi, P.; Raut, C.G.; Shete, A.M.; Singh, D.K. Establishment of cell line from embryonic tissue of Pipistrellus ceylonicus bat species from India & its susceptibility to different viruses. Indian J. Med. Res. 2013, 138, 224–231. [Google Scholar]
- Tong, S.; Li, Y.; Rivailler, P.; Conrardy, C.; Castillo, D.A.; Chen, L.M.; Recuenco, S.; Ellison, J.A.; Davis, C.T.; York, I.A.; et al. A distinct lineage of influenza A virus from bats. Proc. Natl. Acad. Sci. USA 2012, 109, 4269–4274. [Google Scholar] [CrossRef]
- Tong, S.; Zhu, X.; Li, Y.; Shi, M.; Zhang, J.; Bourgeois, M.; Yang, H.; Chen, X.; Recuenco, S.; Gomez, J.; et al. New world bats harbor diverse influenza A viruses. PLoS Pathog. 2013, 9, e1003657. [Google Scholar] [CrossRef]
- Dlugolenski, D.; Jones, L.; Tompkins, S.M.; Crameri, G.; Wang, L.F.; Tripp, R.A. Bat cells from Pteropus alecto are susceptible to influenza A virus infection and reassortment. Influenza Other Respir. Viruses 2013, 7, 900–903. [Google Scholar] [CrossRef]
- Huynh, J.; Li, S.; Yount, B.; Smith, A.; Sturges, L.; Olsen, J.C.; Nagel, J.; Johnson, J.B.; Agnihothram, S.; Gates, J.E.; et al. Evidence supporting a zoonotic origin of human coronavirus strain NL63. J. Virol. 2012, 86, 12816–12825. [Google Scholar] [CrossRef]
- Krahling, V.; Dolnik, O.; Kolesnikova, L.; Schmidt-Chanasit, J.; Jordan, I.; Sandig, V.; Gunther, S.; Becker, S. Establishment of fruit bat cells (Rousettus aegyptiacus) as a model system for the investigation of filoviral infection. PLoS Negl. Trop. Dis. 2010, 4, e802. [Google Scholar] [CrossRef]
- Kuhl, A.; Hoffmann, M.; Muller, M.A.; Munster, V.J.; Gnirss, K.; Kiene, M.; Tsegaye, T.S.; Behrens, G.; Herrler, G.; Feldmann, H.; et al. Comparative analysis of Ebola virus glycoprotein interactions with human and bat cells. J. Infect. Dis. 2011, 204, S840–S849. [Google Scholar] [CrossRef]
- Maruyama, J.; Miyamoto, H.; Kajihara, M.; Ogawa, H.; Maeda, K.; Sakoda, Y.; Yoshida, R.; Takada, A. Characterization of the envelope glycoprotein of a novel filovirus, Lloviu virus. J. Virol. 2013, 88, 99–109. [Google Scholar]
- Kruger, N.; Hoffmann, M.; Weis, M.; Drexler, J.F.; Muller, M.A.; Winter, C.; Corman, V.M.; Gutzkow, T.; Drosten, C.; Maisner, A.; et al. Surface Glycoproteins of an African Henipavirus Induce Syncytium Formation in a Cell Line Derived from an African Fruit Bat, Hypsignathus monstrosus. J. Virol. 2013, 87, 13889–13891. [Google Scholar] [CrossRef]
- Shin, O.S.; Kumar, M.; Yanagihara, R.; Song, J.W. Hantaviruses induce cell type- and viral species-specific host microRNA expression signatures. Virology 2013, 446, 217–224. [Google Scholar] [CrossRef]
- Mackow, E.R.; Gavrilovskaya, I.N. Hantavirus regulation of endothelial cell functions. Thromb. Haemost. 2009, 102, 1030–1041. [Google Scholar]
- Raftery, M.J.; Kraus, A.A.; Ulrich, R.; Kruger, D.H.; Schonrich, G. Hantavirus infection of dendritic cells. J. Virol. 2002, 76, 10724–10733. [Google Scholar] [CrossRef]
- Botten, J.; Mirowsky, K.; Kusewitt, D.; Ye, C.; Gottlieb, K.; Prescott, J.; Hjelle, B. Persistent Sin Nombre virus infection in the deer mouse (Peromyscus maniculatus) model: Sites of replication and strand-specific expression. J. Virol. 2003, 77, 1540–1550. [Google Scholar] [CrossRef]
- Yanagihara, R.; Amyx, H.L.; Gajdusek, D.C. Experimental infection with Puumala virus, the etiologic agent of nephropathia epidemica, in bank voles (Clethrionomys glareolus). J. Virol. 1985, 55, 34–38. [Google Scholar]
- Hutchinson, K.L.; Rollin, P.E.; Peters, C.J. Pathogenesis of a North American hantavirus, Black Creek Canal virus, in experimentally infected Sigmodon hispidus. Am. J. Trop. Med. Hyg. 1998, 59, 58–65. [Google Scholar]
- Eckerle, I.; (Institute of Virology, University Hospital Bonn, Bonn, Germany); Rang, A.; (Institute of Medical Virology, University Hospital Berlin, Berlin, Germany). Unpublished work. 2014.
- Essbauer, S.S.; Krautkramer, E.; Herzog, S.; Pfeffer, M. A new permanent cell line derived from the bank vole (Myodes glareolus) as cell culture model for zoonotic viruses. Virol. J. 2011, 8, 339. [Google Scholar] [CrossRef]
- Stoltz, M.; Sundstrom, K.B.; Hidmark, A.; Tolf, C.; Vene, S.; Ahlm, C.; Lindberg, A.M.; Lundkvist, A.; Klingstrom, J. A model system for in vitro studies of bank vole borne viruses. PLoS One 2011, 6, e28992. [Google Scholar] [CrossRef]
- Crameri, G.; Todd, S.; Grimley, S.; McEachern, J.A.; Marsh, G.A.; Smith, C.; Tachedjian, M.; De Jong, C.; Virtue, E.R.; Yu, M.; et al. Establishment, immortalisation and characterisation of pteropid bat cell lines. PLoS One 2009, 4, e8266. [Google Scholar] [CrossRef]
- Eckerle, I.; Corman, V.M.; Muller, M.A.; Lenk, M.; Ulrich, R.G.; Drosten, C. Replicative capacity of MERS coronavirus in livestock cell lines. Emerg. Infect. Dis. 2014, 20, 2. [Google Scholar]
- Corman, V.M.; Kallies, R.; Philipps, H.; Gopner, G.; Muller, M.A.; Eckerle, I.; Brunink, S.; Drosten, C.; Drexler, J.F. Characterization of a novel betacoronavirus related to middle East respiratory syndrome coronavirus in European hedgehogs. J. Virol. 2014, 88, 717–724. [Google Scholar] [CrossRef]
© 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).