key: cord-0014207-c15t5tsi
authors: Amimo, Joshua O.; Machuka, Eunice M.; Abworo, Edward O.; Vlasova, Anastasia N.; Pelle, Roger
title: Whole Genome Sequence Analysis of Porcine Astroviruses Reveals Novel Genetically Diverse Strains Circulating in East African Smallholder Pig Farms
date: 2020-11-05
journal: Viruses
DOI: 10.3390/v12111262
sha: fe8796e12972db26bf94881f504ad3372636f402
doc_id: 14207
cord_uid: c15t5tsi

Astroviruses (AstVs) are widely distributed and are associated with gastroenteritis in human and animals. The knowledge of the genetic diversity and epidemiology of AstVs in Africa is limited. This study aimed to characterize astroviruses in asymptomatic smallholder piglets in Kenya and Uganda. Twenty-four samples were randomly selected from a total of 446 piglets aged below 6 months that were initially collected for rotavirus study and sequenced for whole genome analysis. Thirteen (13/24) samples had contigs with high identity to genus Mamastrovirus. Analysis of seven strains with complete (or near complete) AstV genome revealed variable nucleotide and amino acid sequence identities with known porcine astrovirus (PoAstV) strains. The U083 and K321 strains had nucleotide sequence identities ranging from 66.4 to 75.4% with the known PoAstV2 strains; U460 strain had nucleotide sequence identities of 57.0 to 65.1% regarding the known PoAstV3; and K062, K366, K451, and K456 strains had nucleotide sequence identities of 63.5 to 80% with the known PoAstV4 strains. The low sequence identities (<90%) indicate that novel genotypes of PoAstVs are circulating in the study area. Recombination analysis using whole genomes revealed evidence of multiple recombination events in PoAstV4, suggesting that recombination might have contributed to the observed genetic diversity. Linear antigen epitope prediction and a comparative analysis of capsid protein of our field strains identified potential candidate epitopes that could help in the design of immuno-diagnostic tools and a subunit vaccine. These findings provide new insights into the molecular epidemiology of porcine astroviruses in East Africa.

Porcine astroviruses (PoAstVs) belong to the family Astroviridae consisting of two genera, Avastrovirus and Mamastrovirus, based on the host ranges of avian and mammalian species, respectively [1] . Astroviruses (AstVs) have been isolated from fecal samples of a wide variety of mammals and birds [1] [2] [3] [4] . AstVs are known to be the second most prevalent cause (after rotaviruses) of viral gastroenteritis in infants

The sample and library preparation and sequencing of samples used in this study have been described in detail by Amimo et al., 2016 [2] . Briefly, fecal suspensions were filtered using 0.22 µm membrane filters to remove eukaryotic and bacterial cell debris. Fecal filtrate was treated with DNases and RNases (Takara, Japan) and incubated for 2 h at 37 • C to destroy free unprotected nucleic acids. Extraction of viral RNA was performed using the QIAamp Viral RNA Mini Kit (Qiagen, USA) according to the manufacturer's instructions. Total RNA was used in library construction using the TruSeq™ RNA library preparation kit v2 (Illumina ® , USA) according to the manufacturer's instructions. The final size and concentration of each library were estimated using a Bioanalyzer (Agilent, Santa Clara, CA, USA) and the Qubit, respectively. A ten (10 nm) library pool was prepared by mixing the 24 samples to achieve an equal molar concentration for each library. Pooled libraries were sequenced by the MiSeq (Illumina ® ) platform using sequencing runs of 2 × 150 paired-end reads at the BecA-ILRI Hub genomics laboratory facility in Nairobi, Kenya.

Comprehensive sequence data quality check, de novo contig assembly, and contig classification have been described by Amimo et al., 2016 [2] . Briefly, 27,260,153 raw reads were processed by trimming the adapters based on Phred quality scores, followed by removal of duplicate reads. Reads that passed quality check were used for de novo contig assembly using Trinity software by applying criteria of >50% overlap and >90 % overlap identity [31] . Assembled contigs (185,827) were classified by BLASTx search against the NCBI non-redundant protein database (NR), with an e-value cutoff of 10 −10 . The contigs with significant BLASTx hits were additionally classified using a second BLASTx search with an e-value cutoff of 10 −4 . Of the 185,827 contigs assembled, 98.8% (183,532) matched the sequences in the GenBank while 1.2% were unassigned. Using preliminary results, the contigs from 13 samples, having hits with high similarity to astroviruses, were analyzed with the Metavir2 beta version, the Web-based tool for virome analysis [32] ; the taxonomic composition was computed from a BLAST comparison with the Refseq complete viral genomes protein sequences database from NCBI using BLASTp and threshold of 10 −3 on the e-value. Additionally, to confirm that the 7 complete genomes of astroviruses from the seven individual samples were true astrovirus genomes, all the reads in a respective sample that were classified belonging to the Astroviridae family were aligned to long contigs using BWA. The contig quality was further checked based on this alignment to ensure all positions of the consensus contigs were filled with consensus nucleotide for the position.

Multiple sequence alignment was performed using Clustal Omega (ClustalO) Web server (http:// www.ebi.ac.uk/Tools/msa/clustalo/) to analyze the percentage identity with other genomes at nucleotide and amino acid levels. Phylogenetic analyses of assembled genomes and predicted proteins were performed in MEGA X [33] after building alignment by ClustalW algorithm and subsequent tree generation using the neighbor-joining method [34] with 1000 bootstrap replicates.

A nucleotide alignment was created by using ClustalW on the full genome sequences of 28 mamastroviruses, including the seven porcine astroviruses from this study and 21 known astroviruses from swine, bovines, camels, and humans. The representative whole genome sequences of the known astroviruses from the NCBI GenBank were selected based on the initial BLASTn search results of each of our seven field strains and phylogenetic analysis. Potential recombination patterns were screened by using RDP, GENECONV, MaxChi, Chimaera, SiScan, 3Seq, and Bootscan in the Recombination Detection Program (RDP4, Version 4.94) while following the instruction manual [35] , using the step-down correction for multiple comparisons and a p-value cutoff of 0.01. Regions of potential recombinant interest were also checked by the above methods. Recombination events were considered only when involving at least one of our 7 newly generated sequences and when supported by highest acceptable p-value of 0.05 with all of the above methods.

SVMTriP Web-based software [36] , which predict linear antigen epitopes based on a support vector machine to integrate tri-peptide similarity and propensity, was used to predict potential linear antigen epitopes with the capsid protein sequences of our PoAstVs. The astrovirus capsid gene is responsible for viral attachment and entry into host cells; therefore, realistic prediction of antigenic epitopes could help with the design of vaccine components and immuno-diagnostic reagents. The epitopes predicted by SVMTrip software were further analyzed with the IEDB analysis resource and the immuno-medicine group tool-Web-based programs which predict segments from within a protein sequence that are likely to be antigenic via eliciting antibody responses [37, 38] . Antigenicity of predicted candidate epitopes was determined using VaxiJen v2.0, protective antigen, tumor antigens, and subunit vaccines prediction server [39] . This server uses auto cross covariance (ACC) transformation of selected protein sequences based on unique amino acid properties. Each sequence is used to find out 100 known antigens and 100 non-antigens. The identified sequences are tested for antigenicity by leave-one-out cross-validation and overall external validation. The prediction accuracy is up to 89%. Thereafter, Swiss model was used for modelling the 3D structures of capsid proteins, as it is fully automated and provides complete stoichiometry and the overall structures of the complexes as inferred by homology modelling [40] . Conformational B-cell epitopes from the 3D models of detected PoAstV proteins were predicted by ElliPro, a Web tool designed by Thornton's method together with MODELLER program of a residue clustering algorithm and Jmol viewer [41] .

Glycosylation is an important post-translational modification, and is known to influence protein folding, localization, trafficking, and solubility; antigenicity; biological activity and half-life; and cell-cell interactions. We investigated the spread of known and predicted N-glycosylation sites across the capsid protein of the 7 PoAstV field strains identified in this study using NetNglyc software [42] . This software uses artificial neural networks that examine the sequence context of Asn-X-Ser/Thr sequons (Asn = asparagine, Ser = serine, Thr = threonine, and X = any other amino acid except proline) and distinguishes glycosylated sequences from non-glycosylated ones. The predictions are only shown on Asn-X-Ser/Thr sequences, since only asparagine residues within Asn-X-Ser/Thr (and in some cases, Asn-X-Cys) are N-glycosylated in-vivo.

The lengths of RNA genome sequences of the seven newly identified field strains (U083, K321, U460, K456, K451, K366, K062), excluding the 30 adenines [poly(A) tail)] at the 3 end, varied from 5281 to 6649 nt, as shown in Table 1 . They had typical AstV genomic organization with the three predicted main ORFs (ORF1a, ORF1b, and ORF2) preceded by a 5' untranslated region (UTR) and ending with a 3' UTR, with ribosomal slippage site between ORF1a and ORF1b. The 5' UTR regions of K451 and U460 strains were not assembled. A frameshift heptamer, AAAAAAC, followed by a stem-loop structure, was present near the 3 end of ORF1a in all the strains, which is signal for a ribosomal frameshift during translation to generate the replicase polyprotein ORF1ab [43] . PoAstVs detected in this study showed the conserved tyrosine residue within the TEEEY motif in the viral protein genome-linked (VPg) putative protein at the 3 end of ORF1a (PoAstV3 contained SEEEY). Additionally, a typical YGDD motif was conserved in the middle of the predicted RNA-dependent RNA polymerase (RdRp) protein of all our strains [43] [44] [45] . All the strains also contained a conserved sequence located at the junction of RdRp and capsid region (UUUGGAGGGG(A/C)GGACCAAA(G/A) 8/11 AUGGC), which was proposed to be a regulatory element used as a promoter for sgRNA transcription [14, 43] . Finally, all our strains contained a trypsin-like peptidase domain in the nonstructural protein 1a and an astrovirus capsid protein precursor domain. 

Genome sequence comparison revealed that the complete genomes of K456, K451, K366, and K062 strains shared relatively moderate to high nucleotide sequence identities among themselves (64.5 to 88.4%) and with the known sequences for PoAstV4 in the GenBank (63.5 to 80%), while low identities (41 to 48%) were noted with other AstV types (Table S1 ). The U083 and K321 strains had nucleotide sequence identities of 82% among themselves and 66.4 to 75.4% identity with the known sequences for PoAstV2 in the GenBank. U460 strain had nucleotide sequence identities of 57.0 to 65.5% with the known sequences for PoAstV3. These data demonstrate a wide genetic divergence among the PoAstV strains circulating in the East Africa region, and therefore, significant serological differences are expected because of the < 95% identity at the nt sequence level [11, 46] . Further analysis of the nucleotide and deduced amino acid sequences of the capsid region revealed significant variation among the identified strains. Analysis of the nucleotide and deduced amino acid sequences of the capsid region revealed significant variations among East African field strains ranging from 51.7 to 77.8% and 49 to 76.4%, respectively, compared to other PoAstVs in the same group (Tables S2 and S3 ), suggesting that they are distinct/unusual PoAstVs within their respective genotypes; similar to reports has been documented in Japan [47] . We carried out phylogenetic analysis using the nucleotide and/or amino acid sequences of the complete genomes and capsid regions (ORF2) of the PoAstVs reported in this study and those available from GenBank, together with selected AstV sequences from other species to establish genetic relatedness (Figures 1 and 2 ). In the phylogenetic trees constructed, East African strains clustered with astroviruses of the PoAstV2 (U083 and K321), PoAstV3 (U460), and PoAstV4 (K456, K451, K366, and K062) lineages.

The phylogenetic analysis of complete (nearly) genome showed our PoAstV2 strains were closely related at the nucleotide level, while the PoAstV4s were very diverse, consistent with our comparative sequence analysis results. The sequence identity between these novel viruses was generally greater in the RdRp region than in the NSP1a and capsid regions (data not shown). Capsid proteins are naturally under intense positive selective pressure from the host immune reaction [48] ; hence they are likely to be more diverse, as shown in this study. According to the ICTV, the capsid protein encoded by the ORF2 is used to distinguish genotypes and species of astroviruses. They defined an amino acid sequence diversity in the capsid gene product of <0.312 and >0.378 within and between astrovirus species, respectively. Analysis of evolutionary divergence using the capsid region (ORF2) of our strains (Table S4) showed that PoAstV2 were 0.512 divergent among themselves and 0.418 to 0.579 with the known PoAstV2 strains in the same group. Similarly, PoAstV4 were diverse with 0.309-0.624 and 0.243-0.661 among themselves and with other known PoAstV4 strains, respectively. PoAstV3 was also diverse with 0.499-0.730 with known PoAstV3 strains. Thus, these results further confirm that our strains could be novel strains within their respective genotypes. Phylogenetic tree based on the nucleotide (a) and amino acid (b) sequences of the capsid proteins (ORF2) of the East African astrovirus field strains and the known astroviruses in the GenBank. Multiple sequence alignments were performed using the ClustalO program. The evolutionary history was inferred by using the maximum likelihood method on the GTR model for nucleotide and neighbor-joining method using the p-distance substitution model for amino acid sequences in MEGA X [33] . The scale bar is given in numbers of substitutions per site. Phylogeny was inferred following 1000 bootstrap replications, and the node values show percentage bootstrap support.

In this study, seven novel and genetically distinct PoAstVs have been described in fecal samples from apparently clinically healthy pig populations in East Africa. The phylogenetic analysis of nucleotides of complete genomes and ORF2 nucleotide and amino acid sequences of PoAstVs in our study revealed wider phylogenetic diversity than previously thought for the respective genotypes. These analyses confirmed that swine harbor phylogenetically diverse AstV strains, most likely derived from distinct ancestors, as has been report elsewhere [19] .

Viral recombination can affect phylogenetic groupings, increase the virulence/fitness of the virus, complicate molecular epidemiological studies, and have major implications in vaccine design [49, 50] . We further analyzed our strains for potential recombination, since our previous study identified multiple genotypes of PoAstV in same pigs and/or same farms [2, 23] . The complete sequences of the seven new strains of astrovirus sequences were analyzed together with selected known AstV strains for probable recombination events. Between the four PoAstV4 strains (K456, K451, K366, and K062), three recombination events were identified: one starting at position 2713 and ending at position 4089 (event 1), another starting at position 4244 and ending at position 6305 (event 2), and the last event starting at position 6346 and ending at position 6649 (event 3) in K062, K366, and K456 respectively ( Figure 3 ). Based on the recombination analysis, we concluded that all the four PoAstV4 strains may be of recombinant origin. Recombination event 1 (K062 recombinant) was predicted at the overlap between ORF1a and ORF1b, whereas recombination event 2 (K366 recombinant) was predicted from the junction of ORF1b-ORF2 and covered almost the entire ORF2. Event 3 (K456 recombinant) was predicted at the 3 end of the capsid region (ORF2). These recombination patterns were supported by RDP, GENECONV, MaxChi, Chimaera, SiScan, 3Seq, LARD, Phylpro, and Bootscan programs, as shown in Table 2 . Potential recombination event 2 reported in this study supports the previous suggestion that the ORF1b/ORF2 junction region is prone to the recombination region in AstVs [51, 52] . The co-occurrence of different strains within swine farms is certainly feasible due to the high incidence of PoAstV in swine farms [2, 43] , and this may promote co-infections of individual pigs with multiple strains at the same time, as observed in this study. Therefore, recombination events between different strains have been observed. As an immune-escape mechanism, viral recombination events may lead to the generation of novel virus strains, to which the affected host may have a lower immunity than to the parent strains. These novel viruses may potentially cross species barriers at some point. Previous studies have found evidence for recombination amongst astrovirus serotypes in humans, pigs, marine mammals, turkeys, small ruminants, and dogs [51, [53] [54] [55] [56] . 

AstVs are not easy to propagate in cell culture; hence, comparisons of their antigenic properties are difficult. However, since the capsid protein induces host immunity, serological property is speculated based on its sequence similarity. Since AstV's capsid protein is responsible for viral attachment and entry into host cells, we used capsid protein sequences of our strains to predict linear antigenic epitopes to generate information that could help in the design of vaccine components and immuno-diagnostic reagents. A total of 10 linear antigenic epitopes were identified in the capsid gene products of each of the seven field strains by SVMTrip Web-based software. The program-recommended antigenic linear epitopes predicted by SVMTrip tool for PoAstV4 strains were all antigenic in nature when analyzed by VaxiJen software; however, some of the recommended epitopes predicted by SVMTrip for PoAstV2 and PoAstV3 strains were non-antigenic in nature when analyzed by VaxiJen (Table S5) . Therefore, to narrow down on the potential linear antigenic epitope candidates, which could be used as immunological targets, we further analyzed our sequences using IEDB analysis resource software and the immune-medicine group tool, which uses different algorithms to predict antigenic epitopes. The antigenic properties of identified target sequences from these epitopes were predicted based on threshold value of 0.4 by VaxiJen software. The sequences with values below the threshold value were considered non-antigenic, while sequences with values above threshold were considered antigenic in nature. Importantly, using the three analytic pieces of software above (SVMTrip, IEDB, and immune-medicine), among all the epitopes, we determined three potential candidate motifs at the surface of the structure that were present at same position on all the capsid proteins of PoAstV2, PoAstV3, and PoAstV4 strains, as shown in Table 3 . The antigenicity of these predicted epitopes was further analyzed with VaxiJen software with a threshold of 0.4, which means the segments greater than the threshold were potentially antigenic in nature. Based on the results of the VaxiJen, we are proposing that the epitope at the amino acid position 126-161 is the best potential candidate epitope, since it contains a conserved motif in each genotype (Table 3) .

After predicting the potential linear B cell epitope, we constructed 3D models of the capsid protein of each of our strains using Swiss model [40] , to be able to predict potential conformational B-cell epitopes. We then predicted the conformational B-cell epitopes of our PoAstVs capsid protein models using Ellipro server [41] . The sequence identity between the capsid proteins of our PoAstV strains and the selected template (Q82452-human AstV 1 strain) ranged from 39.45 to 42.86%, which is more than the required 30% sequence similarity for generating useful models [57] . Our potential candidate epitopes predicted were identified in the capsid protein model by Ellipro software and visualized in Jmol to show their 3D structures or the relative orientations of protein and peptide molecules (Figure 4 ). The amino acid positions of each predicted epitope were also confirmed by Jmol viewer. The peptide was predicted to be highly antigenic (>1) and could be considered for effective immunization or immune diagnosis. Furthermore, all the selected epitopes were found at the surface of the structure, so could be used as the immunological targets for the proper diagnosis and treatment of PoAstVs in the study region. The generated information can be used to test the predicted functions of these peptides via in vitro and in vivo experiments. Table 3 . Predicted antigenic epitopes within capsid proteins (ORF2) of our field strains using three different pieces of software, and antigenicity of the predicted epitopes determined.

Amino 

Glycosylation is generally required for progeny formation and infectivity of many viruses [58] . High levels of glycosylation of various pathogens serve as a protective shield from the host's immune system, where during viral entry into host cells, glycans on the host cell represent viral receptors interacting with carbohydrate binding proteins on the viral surface [59, 60] . We observed glycosylation on the capsid proteins of PoAstV2, PoAstV3, and PoAstV4, and more glycosylation sites in PoAstV2 compared to PoAstV3 and PoAstV4 (Table 4 ). Studies have shown that N-and O-linked glycans shield immunodominant epitopes from immune recognition [59] [60] [61] . Our analysis of the predicted antigenic epitopes at position 126-161 common between PoAstV2, PoAstV3, and PoAstV4 showed that they had at least one glycosylation site. Therefore, in-depth studies of the glycosylation in AstVs would be an important step in designing suitable antigens for diagnostic tools and vaccine development. Based on these results, we suggest that any approach that is based on inhibition of the host mechanism to glycosylate astrovirus proteins may offer the best potential approach to developing therapeutics for astrovirus infections. ) + † = Any potential crossing the default threshold of 0.5 represents a predicted glycosylated site; + = N glycosylated; -= a negative site; * = proline occurs just after the asparagine residue, so is unlikely to be glycosylated; the jury agreement column indicates how many of the nine networks support the prediction; N = asparagine; S = serine; T = threonine. For picking up N-glycosylation sites with high specificity (asparagine residues very likely to be glycosylated), use only (++) predictions (and better) for asparagines that occur within the Asn-X-Ser/Thr triplet (no Proline at the X position).

To our knowledge, this is the first time that the complete genome sequence of a PoAstV from an African region has been determined and characterized. These data provide insights into the epidemiology and evolution of PoAstVs in the region and facilitate investigations on the genetic diversity of PoAstVs worldwide. The discovery of novel PoAstV strains described in this study provides an example of how diverse these viruses are in the smallholder pig population in the study region, where there is close contact between pigs and humans. Our data taken together would be helpful in the development of PoAstV immunodiagnostic tools and vaccines for African regions. However, it is important to note that the high genetic diversity among PoAstV strains (especially diversity at predicted potential antigenic epitopes) and high levels of glycosylation reported in the PoAstVs reported here may pose practical implications for virus detection methods, vaccine development, and epidemiological studies. Importantly, we have identified three potential linear antigenic epitopes which occurred at the surface of the structure of capsid protein, which could be used as the immunological targets for the proper diagnosis and treatment of PoAstVs in the study region. The generated information can be used to test the predicted functions of these peptides by conducting in vitro and in vivo experiments to confirm the immunogenicity and ultimately the vaccine properties to prevent PoAstV infections. Finally, understanding the genetic differences of these novel PoAstV variants that may emerge locally or globally through genetic drift or shift, in wild and domestic animals, could lead to early identification of the source of an emerging outbreak, leading to faster and more targeted interventions to control and/or limit the spread of such outbreaks.

Supplementary Materials: The following are available online at http://www.mdpi.com/1999-4915/12/11/1262/s1. Table S1 : Pairwise comparison of nucleotide sequence identities of the complete (near complete, U460) genomes of the seven (7) astrovirus field strains (bold) and with sequences of other astroviruses available in GenBank. Table S2 : Summary of nucleotide sequence identity matrix of the capsid protein (ORF2) among the seven (7) astrovirus field strains (bold) and the known reference strains in the GenBank using Clustal Omega. Table S3 : Summary of amino acid sequence identity matrix of the capsid protein (ORF2) among the 7 astrovirus field strains (bold) and the known reference strains in the GenBank using Clustal Omega. Table S4 : Estimates of evolutionary divergence between the East African PoAstVs and selected known AstV in the GenBank based on the amino acid sequences of complete ORF2 protein. The number of amino acid differences per site from between sequences is shown. Standard error estimate(s) are shown above the diagonal for our strains. Table S5 : Recommended potential linear antigenic epitopes predicted inside capsid protein (ORF2) of our field strains by SVMTriP Web-based tool and corresponding antigenicity predicted by VaxiJen software. Data Availability: The sequences of the strains discussed in this study have been deposited in GenBank under accession numbers KY940075-KY940077, KY933398, KY933399, MT451917, and MT451918. Additional data are presented in the supplementary files. 

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We thank smallholder pig farmers in the study region for allowing us to sample their pigs for this study.

The authors declare no conflict of interest.