- Open Access
Replication of West Nile virus, Rabensburg lineage in mammalian cells is restricted by temperature
© Aliota and Kramer; licensee BioMed Central Ltd. 2012
Received: 9 November 2012
Accepted: 11 December 2012
Published: 14 December 2012
The genus Flavivirus currently consists of approximately 80 single-strand positive-sense RNA viruses. These replicate in a range of hosts including myriad vertebrate, insect, and tick species. As a consequence of this broad host range, the majority of flaviviruses can be propagated in most vertebrate and insect cell cultures. This ability to infect arthropods and vertebrates usually is essential for maintenance of these viruses in nature. But recently, there has been the discovery of a number of flaviviruses that infect mosquitoes but not vertebrates. It remains largely unknown why certain flaviviruses infect vertebrates and mosquitoes while others infect mosquitoes or vertebrates exclusively.
Here, we initiated in vitro host range studies of Rabensburg virus (RABV), an intermediate between the mosquito-specific and horizontally transmitted flaviviruses, to provide information on the factor(s) that underlie the varying host range of flaviviruses. RABV is an intermediate between the mosquito-specific and horizontally transmitted flaviviruses because it does not infect mammalian or avian cell cultures, house sparrows, or chickens, but it does share genetic characteristics with the Japanese Encephalitis serogroup of flaviviruses.
In vitro growth kinetic assays revealed the complete abrogation of RABV growth on Vero and E6 cells incubated at temperatures 35°C and higher, but surprisingly RABV infected, replicated efficiently, and displayed overt cytopathic effects (CPE) on Vero and E6 cell cultures incubated below 35°C. In contrast, RABV was fully viable, replicated efficiently, and displayed overt CPE on C6/36 cells incubated at 28°C or 37°C, thus implicating temperature as an important factor limiting the host range of RABV.
These data are critical for further study to more fully identify the determinants that mediate the evolution of biological transmission among flaviviruses. It also will be useful for studies that look to provide a comprehensive molecular definition of flavivirus-host cell interactions. And it will provide a cadre of information to design wet lab experiments to investigate the genetic changes that facilitate host switching, which may lead to new vertebrate pathogens or transmission pathways.
The genus Flavivirus (family Flaviviridae) presently comprises approximately 80 single-strand positive-sense RNA viruses, and consists of four groups, each with a distinct host range. The four groups include insect (mosquito) viruses without the capacity to replicate in vertebrates, vertebrate viruses without a vector (no known vector, NKV), tick-borne viruses that replicate in ticks and vertebrates, and mosquito-borne viruses that replicate in mosquitoes and vertebrates. Despite the presence of host-restricted groups within the genus, the majority of flaviviruses are transmitted horizontally between vertebrate hosts and hematophagous arthropods, such as mosquitoes and ticks. In fact, theoretical studies have estimated the existence of over 2000 undiscovered mosquito-borne flaviviruses. And several members of the genus, such as Dengue virus (DENV), Yellow fever virus (YFV), West Nile virus (WNV), Japanese encephalitis virus (JEV), and Tick-borne encephalitis virus (TBEV), are human pathogens that represent significant global health problems. Recently, there has been an upsurge in the discovery of ‘insect-specific’ flaviviruses and/or their related sequences in natural mosquito populations. Examples include Culex flavivirus (CxFV), Cell fusing agent virus (CFAV), Quang Binh virus, Kamiti River virus (KRV), and Aedes flavivirus, among others[4–7]. Yet, our understanding of the significance of the ‘insect-specific’ flaviviruses and the implications for the evolution and transmission of viruses belonging to the genus Flavivirus currently is limited.
Current dogma suggests that the ‘insect specific’ and ‘traditional’ vector-borne flaviviruses form sister groups which are both highly divergent from the other members of the family Flaviviridae. Several studies have hypothesized that the vector-borne group of flaviviruses evolved from a group of vertebrate viruses (NKV group), i.e., the absence of a vector is the ancestral condition for this family of viruses[8–12]. In contrast, it has been hypothesized that the NKV group evolved from insect-specific viruses (e.g., CFAV and KRV) or from a no-vector vertebrate virus (e.g., Tamana bat virus), although this is somewhat controversial and surely requires further study. Regardless, it would be reasonable to hypothesize that at least some of the current group of horizontally transmitted flaviviruses evolved from insect-specific viruses and it also would be reasonable to assume that some of these newly discovered mosquito-specific viruses have the potential to emerge and adapt to new host environments, i.e., humans or other vertebrates.
Recently, we characterized an intermediate between the mosquito-specific and horizontally transmitted flaviviruses, Rabensburg virus (RABV; prototype strain 97–103). RABV is a Flavivirus with ~76% nucleotide and 90% amino acid identity with representative members of lineage one and two WNV. However, RABV97-103 did not infect mammalian or avian cell cultures, house sparrows or chickens, but the virus efficiently infected mosquito cells. In addition, mosquitoes within the Culex pipiens complex supported replication of RABV but displayed poor peroral vector competence for this virus as compared to wild type WNV, and the same mosquitoes vertically transmitted the virus at a much higher rate than what had been reported for wild type WNV. Therefore, RABV could be used as a model to provide significant insight into the determinants of flavivirus attenuation in vertebrates and could increase our understanding of the link between the ‘insect-specific’ flaviviruses and those that are transmitted between mosquitoes and vertebrates, further clarifying the evolution of flaviviruses.
Accordingly, we initiated in vitro host range studies of RABV97-103 and the most recent isolate, RABV strain 06–222, to provide information on the factor(s) that underlie the varying host range of flaviviruses. It remains largely unknown which viral determinants are responsible for host cell tropism and vector specificity, i.e., why do certain flaviviruses infect mosquitoes and vertebrates and why are other flaviviruses not able to infect vertebrates or vertebrates exclusively? Here, we demonstrate that the factor limiting the ability of RABV to infect mammalian cell culture is temperature, and to our knowledge, this is the first demonstration of a member of the genus Flavivirus exhibiting a narrow host range as a result of temperature sensitivity.
African Green Monkey kidney cells (Vero; ATCC #CCL-81) and a clone of standard Vero cells (E6; ATCC #CRL-1586) were grown in minimal essential medium (MEM; Gibco, Carlsbad, CA) supplemented with 10% fetal bovine serum (FBS; Hyclone, Logan, UT), 2 mM L-glutamine, 1.5 g/l sodium bicarbonate, 100 U/ml of penicillin, 100 μg/ml of streptomycin, and incubated at 37°C in 5% CO2. Aedes albopictus mosquito cells, (C6/36; ATCC #CRL-1660) were maintained in MEM supplemented with 10% FBS, 2 mM L-glutamine, 1.5 g/l sodium bicarbonate, 0.1 mM non-essential amino acids, 100 U/ml of penicillin, 100 μg/ml of streptomycin, and incubated at 28°C in 5% CO2. Culex tarsalis mosquito cells (CxT; courtesy of Aaron Brault, Centers for Disease Control and Prevention, Ft. Collins, CO, USA) were maintained in Schneider’s Insect Media (Sigma-Aldrich Inc., St. Louis, MO) supplemented with 10% FBS, and incubated at 28°C in 5% CO2.
RABV isolate 97–103 [GenBank AY765264], originally isolated from Cx. pipiens in the Czech Republic, and RABV isolate 06–222 [GenBank:GQ421359], originally isolated from Aedes rossicus in the Czech Republic, were obtained from Zdenek Hubalek (Institute of Vertebrate Biology, Academy of Sciences, Brno, Czech Republic). Virus stocks were prepared by inoculation onto a confluent monolayer of C6/36 mosquito cells and a clarified harvest of the culture medium was collected after six days of incubation at 28°C. These stocks were titered by plaque assay on Vero cells at 28°C. The titers by plaque assay on Vero cells for RABV97-103 and RABV06-222 were log10 7.34 plaque forming units (PFU)/ml) and log106.30 PFU/ml, respectively. WNV isolate WN02-1956 [GenBank:AY590210] was isolated from the kidney of an American Crow collected in New York State and isolated on Vero cells, followed by a single round of amplification on C6/36 cells. The titer by plaque assay on Vero cells was log108.6 PFU/ml.
In vitro viral replication
Six-well plates containing confluent monolayers of C6/36, CxT, Vero, or E6 cells were infected with virus (RABV97-103, RABV06-222, or WN02-1956), in triplicate, at multiplicity of infection (MOI) of 0.01 PFU/ml. After one hour of adsorption at 28°C or 37º, the inoculum was removed and the cultures were washed three times. Fresh media were added, the mosquito cell cultures were incubated for seven days at 28°C and 37°C, and Vero and E6 cell cultures were incubated for 14 days at 28°C and 37°C, with aliquots removed daily, diluted 1:10 in culture media, and stored at −80°C. Viral titers at each time point were determined by plaque titration on Vero cells. The absence of RABV growth also was confirmed by RT-PCR using RABV specific primers and the Qiagen one-step RT-PCR kit. Cytopathic effects (CPE) were observed using phase contrast optics on a Zeiss Axiovert 25 inverted microscope at 20X magnification, and phase contrast micrographs were taken of infected and uninfected C6/36 cell monolayers using AxioVision Software (Carl Zeiss Microscopy, Germany). RABV infection and replication also were assessed on Vero cells incubated at 32°C, 33°C, 34°C, and 35°C to identify the temperature threshold that blocks productive infection.
Virus titration was performed on freshly confluent Vero cell monolayers in six-well plates. Duplicate wells were infected with 0.1 ml aliquots from serial 10-fold dilutions in growth media and virus was adsorbed for one hour. Following incubation, the inoculum was removed, and monolayers were overlaid with 3 ml containing a 1:1 mixture of 1.2% oxoid agar and 2X MEM (Gibco, Carlsbad, CA) with 10% (vol/vol) FBS and 2% (vol/vol) penicillin/streptomycin. Cells were incubated at 28°C in 5% CO2 for 10 days for RABV plaque development and incubated at 37°C in 5% CO2 for two days for WNV plaque development. Cell monolayers then were stained with 3 ml of overlay containing a 1:1 mixture of 1.2% oxoid agar and 2X MEM with 2% (vol/vol) FBS, 2% (vol/vol) penicillin/streptomycin, and 0.33% neutral red (Gibco). Cells were incubated overnight at 28° (RABV) or 37°C (WNV), plaques were counted, and RABV plaque morphology did not differ from WNV plaque morphology.
Results and discussion
Influence of temperature on virus growth on mammalian cells
Previously, we reported that RABV97-103 was unable to infect mammalian or avian cell cultures, house sparrows or chickens, but the virus efficiently infected mosquito cells, i.e., it displayed characteristics of a host-restricted flavivirus. The basis for its host-restriction occurred at the point of entry into mammalian cells, as infectious RABV97-103 RNA was able to replicate in human cells following transfection. This was contradictory to a previous report that observed the production of overt CPE and replication of RABV97-103 on E6 and Xenopus laevis frog cells (XTC-2). It should be noted, however, that passage via intracranial inoculation of suckling mice had been required for RABV97-103 growth on E6 cells and that XTC-2 cells are cultured at 28°C. Subsequently, Hubalek et al. showed that a second isolate of RABV (strain 06–222) produced CPE and replicated after original inoculation of mosquito suspension on E6 cells. These data suggested that there may be varying host range even among strains of RABV, which is consistent with the fact that RABV97-103 was isolated from a pool of Cx. pipiens and RABV06-222 was isolated from a pool of Ae. rossicus[16, 17], yet no human isolate exists. This, in conjunction with the fact that RABV97-103 replicated on mosquito cell culture and reports of RABV replicating on vertebrate cell culture at 28°C (e.g., XTC-2) but not on vertebrate cell culture at 37°C (e.g., Vero, avian, human), led us to postulate that temperature was an important determinant for RABV infection of mammalian cells.
Influence of temperature on virus growth on mosquito cells
The factors that determine host restriction among flaviviruses are poorly understood, but the host range of any arbovirus unquestionably is governed by multiple abiotic and biologic factors including genetic traits of viruses and hosts for (review see[21, 22]). For biological transmission to evolve, the factors that favor appropriate encounters among virus, competent vector, and susceptible vertebrate are of fundamental importance. But, no matter how perfectly other basic requirements for the establishment of biological transmission are met, many viruses do not replicate sufficiently in certain hosts because of genetic constraints[13, 23, 24]. For example, available data suggest that mutations in the glycosylation patterns of the envelope and nonstructural protein 1 of certain flaviviruses can influence cell/tissue tropism, infectivity, and infection efficiency (e.g.,[25–27]). However, these mutations result in attenuation and do not completely abolish replication. Until now, temperature has not been identified as a factor that can restrict flavivirus host range, although previous studies have suggested that alphavirus host range can be restricted, at least in part, by temperature. For example, Sindbis virus can be cultured to high titers from 15°C to 40°C[28, 29]; whereas, Salmon pancreas disease virus has been demonstrated to have a narrow temperature range of 10°C to 15°C.
Regardless of the mechanism, understanding the factors involved in the maintenance and spread of an infectious organism are crucial for timely recognition of emerging infections. This becomes especially relevant when one considers that a large proportion of emerging viral infections are caused by multi-host zoonotic RNA viruses, because these viruses have a higher propensity to switch hosts[37–40]. Clearly, RABV is capable of replicating in vertebrate cells if conditions are appropriate, and it has not yet been excluded that RABV might circulate and be amplified in certain vertebrates, e.g., herptiles. Therefore, RABV provides a powerful tool to study the evolution and molecular determinants of flavivirus host range, as well as genetic changes in the pathogen that facilitate emergence. Identifying the mechanism(s) involved in mediating RABV temperature sensitivity will be the subject of future investigations. As such, reverse genetic tools currently are being developed for RABV and will be especially valuable in efforts to elucidate genetic changes that facilitate host switching, which will provide a comprehensive molecular portrait of flavivirus-host cell interactions.
The authors thank the Wadsworth Center Tissue Culture Core facility for providing C6/36, Vero, and E6 Cells; and Zdenek Hubalek of the Academy of Sciences of the Czech Republic for providing isolates of Rabensburg virus. Useful discussion with Alan Dupuis is greatly appreciated. MTA is supported by the Wadsworth Center Biodefense and Emerging Infectious Disease postdoctoral fellowship, NIH T32AI055429.
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