- Open Access
Genetic characterization of the cell-adapted PanAsia strain of foot-and-mouth disease virus O/Fujian/CHA/5/99 isolated from swine
© Bai et al; licensee BioMed Central Ltd. 2010
- Received: 9 July 2010
- Accepted: 31 August 2010
- Published: 31 August 2010
According to Office International Des Epizooties (OIE) Bulletin, the PanAsia strain of Foot-and-Mouth Disease Virus (FMDV) was invaded into the People's Republic of China in May 1999. It was confirmed that the outbreaks occurred in Tibet, Hainan and Fujian provinces. In total, 1280 susceptible animals (68 cattle, 1212 swine) were destroyed for the epidemic control.
To investigate the distinct biological properties, we performed plaque assay, estimated the pathogenicity in suckling mice and determined the complete genomic sequence of FMDV swine-isolated O/Fujian/CHA/5/99 strain. In addition, a molecular modeling was carried out with the external capsid proteins.
The pathogenicity study showed that O/Fujian/CHA/5/99 had high virulence with respect to infection in 3-day-old suckling-mice (LD50 = 10-8.3), compared to O/Tibet/CHA/1/99 (LD50 = 10-7.0) which isolated from bovine. The plaque assay was distinguishable between O/Fujian/CHA/5/99 and O/Tibet/CHA/1/99 by their plaque phenotypes. O/Fujian/CHA/5/99 formed large plaque while O/Tibet/CHA/1/99 formed small plaque.
The 8,172 nucleotides (nt) of O/Fujian/CHA/5/99 was sequenced, and a phylogenetic tree was generated from the complete nucleotide sequences of VP1 compared with other FMDV reference strains. The identity data showed that O/Fujian/CHA/5/99 is closely related to O/AS/SKR/2002 (94.1% similarity). Based on multiple sequence alignments, comparison of sequences showed that the characteristic nucleotide/amino acid mutations were found in the whole genome of O/Fujian/CHA/5/99.
Our finding suggested that C275T substitution in IRES of O/Fujian/CHA/5/99 may induce the stability of domain 3 for the whole element function. The structure prediction indicated that most of 14 amino acid substitutions are fixed in the capsid of O/Fujian/CHA/5/99 around B-C loop and E-F loop of VP2 (antigenic site 2), and G-H loop of VP1 (antigenic site 1), respectively. These results implicated that these substitutions close to heparin binding sites (E136G in VP2, A174 S in VP3) and at antigenic site 1 (T142A, A152T and Q153P in VP1) may influence plaque size and the pathogenicity to suckling mice.
The potential of genetic characterization would be useful for microevolution and viral pathogenesis of FMDV in the further study.
- Internal Ribosome Entry Site
- Antigenic Site
- East Asia
- Internal Ribosome Entry Site Element
- Heparin Binding Site
Foot-and-mouth disease (FMD) is an acute, highly contagious viral disease of cloven-hoofed animals, mostly cattle, swine, sheep and goats, leading to severe economic losses due to reduction in livestock production and restriction of trade on animals and animal products. The etiological agent, foot-and-mouth disease virus (FMDV), belongs to the genus Aphthovirus of the Picornaviridae family. Seven distinct serotypes of FMDV (O, A, C, Asia1 and SAT1-3), with numerous subtypes in each serotype, are not distributed equally around the world [1–3].
The genome of FMDV is composed of a positive-sense, single-stranded RNA that is approximately 8,200 nucleotides (nt) in length. The viral RNA contains 5'-untranslated region (5'-UTR), a single long open reading frame (ORF), and 3'-untranslated region (3'-UTR), followed by a poly(A) tail at its 3' end . There is a small viral protein, VPg (3B), covalently linked to the 5' end of the genomic RNA . The viral ORF encodes a single polyprotein, which is subsequently cleaved into multiple mature proteins (Lab/Lb; VP4, VP2, VP3, and VP1; 2A, 2B, 2C, 3A, 3B1-3, 3C, and 3D) by viral proteases (Lpro, 2A, and 3Cpro) [6, 7]. The viral capsid comprised of 60 copies of the four structural proteins termed VP4 (internal), VP2, VP3 and VP1, surrounds the RNA. The 5'-UTR, consists of the S-fragment, poly(C) tract, 2-4 pseudoknots (PKs), a cis-acting replication element (cre), and an internal ribosome entry site (IRES). This region is predicted to display complex secondary structures, and contains several genetic elements necessary to control essential function in viral replication and gene expression . The 3'-UTR, a region of about 90 nt of heterogeneous sequence, is a highly ordered structure, and stimulate the cap-independent translation and likely affect other aspects of viral infection cycle [9, 10].
During 1997-2002, outbreaks of FMD caused by FMDV serotype O, occurred in the countries and districts of East Asia (EA) and the Far East . The O/YUN/TAW/97 strain, a member of the Cathay topotype, containing the deletion of codons 93 to 102 in 3A coding region, is associated with the porcinophilic properties that caused a catastrophic outbreak of FMD in Taiwan [12–14]. The O/AS/SKR/2002 strain, a member of the PanAsia lineages, contains an intact 3A coding region of the virus that developed typical lesions of FMD with highly virulent and contagious in pigs but very limited in cattle . In addition, pigs infected experimentally with another PanAsia strain of FMDV (O/JPN/2000) showed typically clinical signs of FMD, but the disease in Japanese black cattle was atypical, no clinical signs in an infection of Holstein cattle, and sheep and goats were not susceptible . Comparison of amino acid sequence of structural proteins of two different plaque phenotypes in O/JPN/2000 strain, revealed that two substitutions existed in VP2 (133rd) and VP3 (56th) [17, 18]. These substitutions may influence heparin-binding feature and in the attenuation of this virus in the natural host. Unfortunately, these two mutations close to heparin interacting regions cannot account for the characteristics of the PanAsia strains isolated from China (as detailed in Results & Discussion).
Here, we first report the cell-adapted PanAsia strain (O/Fujian/CHA/5/99) of FMDV isolated from swine in Fujian province of China in 1999, perform plaque assay and estimate the pathogenicity in suckling mice, determine the complete genomic sequence for comparison with O/YUN/TAW/97 and 14 reference strains of PanAsia lineages. Furthermore, we model the three dimensional structure of the predominant conformation in the surface FMDV capsid proteins to mimic the probable altered receptor-ligand interactions, triggered by substitutions of residues in VP1, VP2 and VP3.
Comparison of plaque phenotypes and infectivity of O/Fujian/CHA/5/99, and O/Tibet/CHA/1/99 strain
The complete genomic sequence of O/Fujian/CHA/5/99 strain
Primers used for amplification of the complete genomic sequence of FMDV O/Fujian/CHA/5/99 strain[a]
Nucleotide sequence (5'-3')
Nucleotide sequence alignments and amino acids comparison
Amino acid differences in the whole genome of FMDV O/Fujian/CHA/5/99 as compared to O/Tibet/CHA/1/99
Amino acid substitution[b]
B-C loop, antigenic site 2
G-H loop, close to antigenic site 1
G-H loop, antigenic site 1
G-H loop, antigenic site 1
G-H loop, antigenic site 1
C terminus, antigenic site 1
The 3'-UTR of O/Fujian/CHA/5/99, a region of 92 nt with high tolerant changes (72.8%-95.7% similarity) following the ORF termination codon, contains a "Y" shape of RNA which is required for its function, where the nucleotide changes of C32T and A91G were observed (Table 2).
The PanAsia strain of FMDV serotype O originated in India no later than 1982 . It has been the most dominant outbreak strain in the recent years and distributed around the world in over 24 countries . Towards the west, the virus spread into Saudi Aribia (1994), then emerged as the pandemic virus circulating in Middle East, Middle East-South Asia region and into European countries such as Turkey, Greece and Bulgaria (1996) [3, 11, 31]. Furthermore, the virus strain even invaded into South Africa (2000) . A catastrophic outbreak caused by the same viral lineage occurred in the United Kingdom in 2001, and subsequently spread into Ireland, France and the Netherlands within 1 mouth [3, 32]. Towards the east, the virus spread into Nepal (1993), Bangladesh (1996), Bhutan (1998), China (1999), Japan (2000), Korea (2000) and finally invaded countries of the Far East such as Mongolia (2000) and Russia (2000) [3, 11, 33].
The extent to the genetic diversity of these PanAsia virus isolates accumulating over the course of FMD outbreaks with infection of susceptible animals, is contributed to the understanding of the occurrence of phenotypic changes in cultured cells and alteration in host tropism. Here, a gradual accumulation of nucleotide/amino acid mutations were observed in O/Fujian/CHA/5/99 evolving in FMDV populations. The radical ambiguities of convergent evolution will potentially affect the functional and/or structural features involved in 5'-UTR and 3'-UTR of FMDV, respectively. The S-fragment located at the 5' terminus of the FMDV genome may play a role in the switch from translation to replication . The variable nature of PKs was documented that it can be used along with the 3A-based phylogenetic tree for genetic analysis of FMDVs (data not shown). Mutations in the AAACA motif and the stem region of the cre element significantly reduced replication of FMDV genome , suggesting that two substitutions (positions 30th, 33rd) located at the loop within this structure of O/Fujian/CHA/5/99 may induce decreasing for RNA replication in vivo. Deletion, insertion and substitutions (the majority of which were transitions) probably lead to changes in the organization of the IRES structure, resulting in modulated its activity for internal initiation of translation . The structure of 3'-UTR could affect the infectivity of FMDV due to RNA-RNA and RNA-protein interactions .
In the present study, George et al. (2001)  has discussed that few unusual variations in the L protein may reflect its role in either RNA-RNA or RNA-protein interactions that specifically enhanced IRES-dependent translation. By sequencing the structural proteins of O/Fujian/CHA/5/99, we have provided the first homology analysis of the plaque-purified PanAsia strain of FMDV isolated from swine in China. In spite of the evidence generated from O/JPN/2000  and studies determined by Sa-carvalho et al. (1997) , our analysis of O/Fujian/CHA/5/99 and 9 reference strains of FMDV indicated that all of these viruses display 133 D in VP2 (excluding D133 S in VP2 of O/YUN/TAW/97) and 56 H in VP3. Chinese Yellow cattle and native cattle infected experimentally with the FMDV O/Taiwan/99 strain showed no clinical signs. However, pigs infected with O/Taiwan/99 developed typical disease . In Korea, the isolated virus (O/SKR/2000) infected Holstein cattle caused typical vesicles in the field, but did not develop typical vesicular lesions on the foot in animal experiments (OIE, 2000). The 174th amino acid in VP3 substitution was presumably provided as a practical explanation for attenuated virulence of these viruses in cattle (Table 2). Meanwhile, Y79 H (O/JPN/2000 and O/YUN/TAW/97), E136G (O/AS/SKR/2002 and O/Fujian/CHA/5/99) and F214L (O/YUN/TAW/97, O/AS/SKR/2002 and O/Fujian/CHA/5/99) in VP2, T56I (O/YUN/TAW/97 and O/AS/SKR/2002), N85 D (O/YUN/TAW/97), T96A (O/AS/SKR/2002 and O/Fujian/CHA/5/99), T142N/A (O/YUN/TAW/97 and O/Fujian/CHA/5/99, respectively) and A152T (O/AS/SKR/2002 and O/Fujian/CHA/5/99) in VP1 may be associated with bovine attenuation of these viruses. Y79 H within βC strand and E136G within E-F loop of VP2, T142N/A and A152T within G-H loop of VP1 are exposed on the surface of the viral capsid. The direct induction of capsid alterations in the cell attachment sites may influence virus interaction with cellular receptor for FMDV adaptation to cells in culture and mild pathogenicity [38, 39].
The degree of conservation was somewhat higher for 2A, 2B, 2C, 3B1-3 and 3C, and the impact of adaptive positive selection at the amino acid level on these non-structural proteins has been found by identified genome regions of 10 FMDV isolates involved in genetic diversity. To date, these included N1 S (O/JPN/2000), D3N(O/TAW/2/99) and S13P (O/AS/SKR/2002) in 2A; I18V (O/YUN/TAW/97 and O/AS/SKR/2002) in 2B; Q164 H (O/AS/SKR/2002) and I241T (O/Fujian/CHA/5/99) in 2C (nearly the conserved motifs D160DLG163 and N243KLD246, respectively); K18E (O/JPN/2000) in 3B1 and V17A (O/YUN/TAW/97 and O/AS/SKR/2002) in 3B2. 3A contains residues predicted to undergo positive selection with respect to infection in guinea pigs . Deletions in 3A have been associated with altered host range in the hepatoviruses , rhinoviruses , enteroviruses , and aphthoviruses [12–14, 44]. This deletion cannot be found in the 3A region of O/Fujian/CHA/5/99, which has high similarity with the other PanAsia strains (91.7%-92.6% in nucleotide sequences and 86.9%-89.5% in amino acid sequences, respectively). I61V and I76L (O/YUN/TAW/97), L69 M (O/AS/SKR/2002) and I72 M (O/Fujian/CHA/5/99) in transmembrane domain were observed (Fig. 3). The highly variable C-terminal half (positions 117 to 143) in the 3A coding region of O/YUN/TAW/97, form a short α-helix (Zhang et al., unpublished data, 2007). A previously described FMDV mutant 3Dpol with amino acid replacement D338A in the NTP-binding domain (the peptide motif Y336GDD339) destroyed the viral polymerase activity  suggesting that although 3Dpol is more tolerate of substitutions at most positions, conservation of the tertiary structure is likely to be necessary for its function. These observations implied that dramatic alteration in these regions contributed to properties of these proteins and the fitness of dynamic mutant distributions, though the pathogenicity of O/Fujian/CHA/5/99 in cattle is not clear.
Thus, further investigations should aim to O/Fujian/CHA/5/99 infected normal hosts in animal experiments and the finding of molecular basis for the derivation of genetic mutants by utilizing reverse genetics. These studies may help us to clarify how is it that the mutations responsible for genetic diversity and antigenic drift have a moderate effect on the interactions of FMDV to its cellular receptors and in responses to selective constraints.
Our studies found very different phenotypes and pathogenicities between FMDV O/Fujian/CHA/5/99 strain and O/Tibet/CHA/1/99. The distinct biological properties are the results of error-prone replication of genome during viral life cycles. Our findings indicate that nucleotide and amino acid mutations were present in the whole genome of O/Fujian/CHA/5/99, as compared to O/Tibet/CHA/1/99. The great majority of these mutations associated with the effect of viral fitness in physical and biological environment. Advantageous mutations fixed on the viral genome of O/Fujian/CHA/5/99 may be essential contributed to FMDV adaptation of susceptible animals in the field. Consequently, future study can be interested in these predictions for the understanding of viral populations, genetic variability and its biological implications.
Cells, sample collection and virus isolation
Baby hamster kidney (BHK-21) cells were maintained at 37°C in Dulbecco's modified Eagle's medium (DMEM, Gibco) containing 10% fetal bovine serum (FBS, Hyclone). The sample of vesicles on hoof was collected from swine, which showed clinical symptoms of FMD, in Fujian province of China (OIE, May 1999). The grinding suspension (1/10, w/v) was prepared in phosphate buffered saline (PBS) containing the antibiotics penicillin (100 U/ml) and streptomycin (0.1 mg/ml), overnight at 4°C, clarified by centrifugation at 2,000 × g for 10 min, sterilized by using 0.45 μm filter unit (Millipore), and the virus was propagated on BHK-21 cells as described previously . The isolated virus adapted to BHK-21 cells was designated O/Fujian/CHA/5/99 strain. The FMDV O/Tibet/CHA/1/99 strain isolated from bovine in Tibet of China was used in this work and conserved in national foot-and-mouth disease reference laboratory.
Plaque assay and the pathogenicity in suckling-mice
Confluent BHK-21 cell cultures in 6-well plates were prepared for plaque-forming assay. The serial 10-fold dilutions of viruses were inoculated 200 μl per well. After 1 h of incubation at 37°C in 5% CO2, 2 ml overlay medium containing 0.6% Gum and 1% FBS was added and cultured for 48 h under the same conditions. Subsequently, the BHK-21 cells were washed three times with PBS (pH 7.5), then fixed with cold acetone/methanol for 20 min at -20°C, and stained with 0.2% crystal violet for 30 min at room temperature. Finally, we were able to observe plaque morphology and calculate virus titres by plaque-forming units (PFU) from the infected BHK-21 cell cultures.
Serial ten-fold diluted viruses were prepared in DMEM containing 2% FBS, and the pathogenicities were titrated by intraperitoneal inoculation of 3-day-old suckling-mice in groups of five animals each with 0.2 ml of virus dilutions. The suckling mice were observed for 72 h after infection and the 50% lethal dose (LD50) was determined by the method of Reed and Muench (1938) .
Sequencing and genetic characterization
Rneasy Mini Kit (Qiagen) RNA extraction was performed as the manufacture's protocol. 4 μl 5 × AMV buffer, 4 μl 10 mM dNTP, 10 μl RNA, 1 μl 50 pmol/L anti-sense genome specific primers (Pan/S-, L3, NK61, P222, Pan/205, and Dnn-, respectively; Table 1), 1 μl AMV (TaKaRa) mix was incubated at 42°C for 1 h and then on ice for 3 min. After completion of the reverse transcript (RT) reaction, six overlapping PCR fragments covering the viral genome were amplified from each sample by using specific primer sets (set 1, S+ and Pan/S-; set 2, Pan/I+ and L3; set 3, Pan/204 and NK61; set 4, P211 and P222; set 5, Pan/201 and Pan/205; set 6, D3+ and Dnn-; Table 1) with LA Taq DNA polymerase (TaKaRa). The target PCR products were cleaned up using Wizard® Gel and PCR Clean-Up System (Promega) and cloned into pGEM®-T Vector (Promega). Cycle sequencing reaction were performed with fluorescent BigDye chain terminators (Applied Biosystems), followed by resolution on an ABI Prism 310 genetic analyzer (Applied Biosystems).
The complete genetic sequences were assembled using SeqMan (DNAStar). Multiple sequence alignment was analyzed using MegAlign (DNAStar) to construct a phylogenetic tree. MegAlign was also used for the genomic analysis of nucleotide mutations in 5'-UTR and 3'-UTR, and amino acid substitutions in leader (L) protein, structural proteins and non-structural proteins. The atomic coordinates of FMDV crystallized for O1BFS [48–51] were used to model the conformations, and the structures of FMDV O/Tibet/CHA/1/99 and O/Fujian/CHA/5/99 strains were optimized by placing substituted amino acids which exist in the external surface of capsid, in their standard conformations.
We thank National Foot-and-Mouth Disease Reference Laboratory of China, for providing FMDV isolates. This work was supported by the Chinese National Key Basic Research Program (Grant No. 2005CB523201) and National Key Technology R&D Program of China (Grant No. 2006BAD06A03).
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