| Parvoviridae | |
|---|---|
 | |
| Electron micrograph ofcanine parvovirus | |
Virus classification | |
| (unranked): | Virus |
| Realm: | Monodnaviria |
| Kingdom: | Shotokuvirae |
| Phylum: | Cossaviricota |
| Class: | Quintoviricetes |
| Order: | Piccovirales |
| Family: | Parvoviridae |
| Genera | |
Parvoviruses are a family ofanimal viruses that constitute the familyParvoviridae. They have linear, single-strandedDNA (ssDNA)genomes that typically contain two genes encoding for a replication initiator protein, called NS1, and the protein the viralcapsid is made of. The coding portion of the genome is flanked bytelomeres at each end that form intohairpin loops that are important during replication. Parvovirus virions are small compared to most viruses, at 23–28 nanometers in diameter, and contain the genome enclosed in an icosahedral capsid that has a rugged surface.
Parvoviruses enter a host cell byendocytosis, travelling to the nucleus where they wait until the cell enters its replication stage. At that point, the genome is uncoated and the coding portion is replicated. Viralmessenger RNA (mRNA) is thentranscribed andtranslated, resulting in NS1 initiating replication. During replication, the hairpins repeatedly unfold, are replicated, and refold to change the direction of replication to progress back and forth along the genome in a process calledrolling hairpin replication that produces a molecule containing numerous copies of the genome. Progeny ssDNA genomes are excised from this concatemer and packaged into capsids. Mature virions leave the cell byexocytosis orlysis.
Parvoviruses are believed to be descended from ssDNA viruses that have circular genomes that form a loop because these viruses encode a replication initiator protein that is related to NS1 and have a similar replication mechanism. Another group of viruses calledbidnaviruses appear to be descended from parvoviruses. Within the family, three subfamilies and 28 genera are recognized.Parvoviridae is the sole family in the orderPiccovirales, which is the sole order in the classQuintoviricetes. This class is assigned to the phylumCossaviricota, which also includespapillomaviruses,polyomaviruses, and bidnaviruses.
A variety of diseases in animals are caused by parvoviruses. Notably, thecanine parvovirus andfeline parvovirus cause severe disease in dogs and cats, respectively. In pigs, theporcine parvovirus is a major cause of infertility. Human parvoviruses are less severe, the two most notable beingparvovirus B19, which causes a variety of illnesses includingfifth disease in children, andhuman bocavirus 1, which is a common cause of acute respiratory tract illness, especially in young children. In medicine, recombinantadeno-associated viruses (AAV) have become an important vector for delivering genes to the cell nucleus duringgene therapy.
Animal parvoviruses were first discovered in the 1960s, including minute virus of mice, which is frequently used to study parvovirus replication. Many AAVs were also discovered during this time period and research on them over time has revealed their benefit as a form of medicine. The first pathogenic human parvovirus to be discovered was parvovirus B19 in 1974, which became associated with various diseases throughout the 1980s. Parvoviruses were first classified as the genus Parvovirus in 1971 but were elevated to family status in 1975. They take their name from the Latin word parvum, meaning 'small' or 'tiny', referring to the small size of the virus's virions.
Parvoviruses have linear, single-stranded DNA (ssDNA) genomes that are about 4–6 kilobases (kb) in length. The parvovirus genome typically contains two genes, termed the NS/rep gene and the VP/cap gene.[1] The NS gene encodes the non-structural (NS) protein NS1, which is the replication initiator protein, and the VP gene encodes the viral protein (VP) that the viral capsid is made of. NS1 contains anHUH superfamilyendonuclease domain near itsN-terminus, containing both site-specific binding activity and site-specific nicking activity, and a superfamily 3 (SF3)helicase domain toward theC-terminus. Most parvoviruses contain a transcriptional activation domain near the C-terminus thatupregulates transcription from viralpromoters as well as alternate or overlappingopen reading frames that encode a small number of supporting proteins involved in different aspects of the viral life cycle.[2]
The coding portion of the genome is flanked at each end by terminal sequences about 116–550 nucleotides (nt) in length that consist of imperfect palindromes folded intohairpin loop structures. These hairpin loops contain most of thecis-acting information required for DNA replication and packaging and act as hinges during replication to change the direction of replication. When the genome is converted to double-stranded forms, replication origin sites are created involving sequences in and adjacent to the hairpins.[2][3]
Genomic DNA strands in mature virions may bepositive-sense or negative-sense. This varies from species to species as some have a preference for packaging strands of one polarity, others package varying proportions, and others package both sense strands at equal proportions. These preferences reflect the efficiency with which progeny strands are synthesized, which in turn reflects the efficiency of specific replication origin sites.[2] The 3′-end (usually pronounced "three prime end") of a negative sense strand, and the 5′-end (usually pronounced "five prime end") of a positive sense strand, is called the left end, and the 5′-end of the negative sense strand, and the 3′-end of a positive sense strand, is called the right end.[2][4][5]
Parvovirus virions are 23–28 nanometers (nm) in diameter and consist of the genome enclosed inside a capsid that isicosahedral in shape with a rugged surface. The capsid is composed of 60 structurally equivalent polypeptide chains derived from the C-terminal end of a VP protein's sequence, interlocking extensively to form an icosahedron with 60 asymmetric, superficial triangular units. These units have 3-foldradial symmetry at two vertices and 5-fold radial symmetry at one, with 2-fold radial symmetry at the line opposite of the 5-fold vertex and a 2/5 circular fold wall surrounding the point of the 5-fold vertex. Twenty 3-fold vertices, thirty 2-fold lines, and twelve 5-fold vertices exist per capsid, the latter corresponding to the 12 vertices of the icosahedron.[2]
Typical features of the capsid surface include depressions at each 2-fold axis, elevated protrusions surrounding the 3-fold axes, and raised cylindrical projections made of five beta-barrels[6] surrounded by canyon-like depressions at the 5-fold axes. Each of these cylinders potentially contains an opening to connect the exterior of the capsid to the interior, which mediates entry and exit of the genome. About 20 nucleotides from the 5′-end of the genome may remain exposed outside of the capsid carrying a copy of NS1 bound to the 5′-end, which is a result of how the genome is synthesized and packaged.[2]
Varying sizes of the VP protein are expressed for different parvoviruses, the smaller ones, VP2–5, being expressed at a higher frequency than the large size, VP1. The smaller VPs share a common C-terminus with different N-terminus lengths due to truncation. For VP1, the N-terminus is extended to contain regions important in the replication cycle, and it is incorporated into the capsid, typically 5–10 per capsid, with the common C-terminus responsible for assembling capsids.[1][2]
Each VP monomer contains a core beta-barrel structure called thejelly roll motif of eight strands arranged in two adjacent antiparallel beta sheets, labeled CHEF and BIDG after the individual strands, the latter forming the interior surface of the capsid. Individual beta strands are connected by loops that have varying length, sequence, and conformation, and most of these loops extend toward the exterior surface, giving parvoviruses their unique, rough surface. Related parvoviruses share their surface topologies and VP protein folds to a greater degree than their sequence identities, so the structure of the capsid and capsid protein are useful indicators of phylogeny.[1][2]
Parvoviruses enter cells byendocytosis, using a variety of cellular receptors to bind to the host cell. Inendosomes, many parvoviruses undergo a change in conformation so that thephospholipase A2 (PLA2) domain on the VP1 N-termini are exposed so the virion can penetrate lipid bilayer membranes. Intracellular trafficking of virions varies, but virions ultimately arrive to the nucleus, inside of which the genome is uncoated from the capsid. Based on studies of minute virus of mice (MVM), the genome is ejected from the capsid in a 3′-to-5′ direction from one of the openings in the capsid, leaving the 5′-end of the DNA attached to the capsid.[2]
Parvoviruses lack the ability to induce cells into theirDNA replication stage, called S-phase, so they must wait in the nucleus until the host cell enters S-phase on its own. This makes cell populations that divide rapidly, such as fetal cells, an excellent environment for parvoviruses. Adeno-associated viruses (AAV) are dependent on helper viruses, which may be anadenovirus or aherpesvirus, since coinfection alters the cellular environment to allow for replication.[2] In the absence of coinfection, AAV's genome is integrated into the host cell's genome until coinfection occurs.[7] Infected cells that enter S-phase are forced to synthesize viral DNA and cannot leave S-phase. Parvoviruses establish replication foci in the nucleus that grow progressively larger as infection progresses.[8]
Once a cell enters S-phase and the genome is uncoated, a hostDNA polymerase uses the 3′-end of the 3′ hairpin as a primer to synthesize a complementary DNA strand for the coding portion of the genome, which isconnected to the 5′-end of the 5′ hairpin.[3][7][9]Messenger RNA (mRNA) that encodes NS1 is then transcribed from the genome by the DNA polymerase, capped and polyadenylated, and translated by host ribosomes to synthesize NS1.[2][5][10] If proteins are encoded in multiple co-linear frames, then alternative splicing, suboptimal translation initiation, orleaky scanning may be used to translate different gene products.[2]
Parvoviruses replicate their genome viarolling hairpin replication, a unidirectional, strand displacement form of DNA replication that is initiated by NS1. Replication begins once NS1 binds to and makes a nick in a replication origin site in the duplex DNA molecule at the end of one hairpin. Nicking releases the 3′-end of the nicked strand as a freehydroxyl (-OH) to prime DNA synthesis[2] with NS1 remaining attached to the 5′-end.[7] The nick causes the adjacent hairpin to unfold into a linear, extended form. At the 3′-OH, a replication fork is established using NS1's helicase activity, and the extended telomere is replicated by the DNA polymerase.[10][11] The two telomere strands then refold back in on themselves to their original configurations, which repositions the replication fork to switch templates to the other strand and move in the opposite direction toward the other end of the genome.[12][13]
Parvoviruses vary in whether the termini are similar or the same, called homotelomeric parvoviruses, or different, called heterotelomeric parvoviruses. In general, homotelomeric parvoviruses, such as AAV and B19, replicate both ends of their genome through the aforementioned process, called terminal resolution, and their hairpin sequences are contained within larger (inverted) terminal repeats. Heterotelomeric viruses, such as minute virus of mice (MVM), replicate one end by terminal resolution and the other end via an asymmetric process called junction resolution[2][14] so that the correct orientation of the telomere can be copied.[15]
During asymmetric junction resolution, the duplex extended-form telomeres refold in on themselves into a cruciform shape. A replication origin site on the lower strand of the right arm of the cruciform is nicked by NS1, leading to the lower arm of the cruciform unfolding into its linear extended form. A replication fork established at the nick site moves down the extended lower arm to copy the lower arm's sequence. The two strands of the lower arm then refold to reposition the replication fork to go back toward the other end, displacing the upper strand in the process.[16]
The back and forth, end-to-end pattern of rolling hairpin replication produces a concatemer containing multiple copies of the genome.[2][3] NS1 periodically makes nicks in this molecule and, through a combination of terminal resolution and junction resolution, individual strands of the genome are excised from the concatemer.[9][13] Excised genomes may either be recycled for further rounds of replication or packaged into progeny capsids.[7] Translation of mRNA containing VP proteins leads to the accumulation of capsid proteins in the nucleus that assemble into these empty capsids.[8]
Genomes are encapsidated at one of the capsid's vertices through a portal,[2] potentially the one opposite the portal used to expel the genome.[5] Once complete virions have been constructed, they may be exported from the nucleus to the exterior of the cell before disintegration of the nucleus. Disruption of the host cell environment may also occur later on in the infection. This results in celllysis vianecrosis orapoptosis, which releases virions to the outside of the cell.[2][8]
Parvoviruses are believed to be descended from ssDNA viruses that have a circular genome that forms a loop and which replicate viarolling circle replication, which is similar to rolling hairpin replication. These circular ssDNA viruses encode a replication initiator protein that is related to and possesses many of the same characteristics as the replication initiator protein of parvoviruses, such as the HUH endonuclease domain and the SF3 helicase domain.[17] In contrast to these other replication initiator proteins, NS1 shows only vestigial traces of being able to perform ligation, which is a key part of rolling circle replication.[8] TheBidnaviridae family, which are also linear ssDNA viruses, appear to be descended from a parvovirus that had its genome integrated into the genome of apolinton, a type of DNAtransposon related to viruses in the realmVaridnaviria.[17]
Based on phylogenetic analysis of the SF3 helicase, parvoviruses split into two branches early in their evolutionary history, one of which contains viruses assigned to the subfamilyHamaparvovirinae. The other branch split into two sublineages that constitute the other two subfamilies,Densovirinae andParvovirinae.[18] Parvoviruses in theHamaparvovirinae lineage are likely all heterotelomeric,Densovirinae are exclusively homotelomeric, andParvovirinae varies.[2] Telomere sequences have significant complexity and diversity, suggesting that many species have co-opted them to perform additional functions.[7][10] Parvoviruses are also considered to have high rates of geneticmutations andrecombinations.[2][9]
Parvoviruses constitute the familyParvoviridae. The family is the sole family in the orderPiccovirales, which is the sole order in the classQuintoviricetes. The classQuintoviricetes belongs to the phylumCossaviricota, which also includespapillomaviruses,polyomaviruses, and bidnaviruses.Cossaviricota is included in the kingdomShotokuvirae, which is assigned to the realmMonodnaviria.Parvoviridae belongs to Group II: ssDNA viruses in theBaltimore classification system, which groups viruses together based on their manner of mRNA synthesis. WithinParvoviridae, three subfamilies, 26 genera, and 126 species are recognized as of 2020 (-virinae denotes subfamily and -virus denotes genus):[18][19]
Additionally, the family contains one genus unassigned to a subfamily:Metalloincertoparvovirus.[19]
Parvoviruses are assigned to the same species if they share at least 85% of their protein sequence identities. Species are grouped together in a genus based on phylogeny of the NS1 and SF3 helicase domains, as well as similarity of NS1 sequence identity and coverage. If these criteria aren't satisfied, then genera can still be established provided that common ancestry is supported. The three subfamilies are distinguished based on phylogeny of the SF3 helicase domain, which corresponds to host range: viruses inDensovirinae infect invertebrates, viruses inHamaparvovirinae infect invertebrates and vertebrates, and viruses inParvovirinae infect vertebrates.[18]
In humans, the most prominent parvoviruses that cause disease areparvovirus B19 andhuman bocavirus 1. B19 infection is often asymptomatic but can manifest in a variety of ways, includingFifth disease with its characteristic rash in children, persistentanemia in immunocompromised persons and in people who have underlyinghemoglobinopathies,[20] transientaplastic crises,hydrops fetalis in pregnant women, andarthropathy. Human bocavirus 1 is a common cause of acute respiratory tract infection, especially in young children, wheezing being a common symptom. Other parvoviruses associated with different diseases in humans include human parvovirus 4 and human bufavirus, though the manner by which these viruses cause disease is unclear.[6]
Carnivore-infecting viruses in the genusProtoparvovirus, in contrast to human parvoviruses, are more life-threatening.[2]Canine parvovirus causes severe illness in dogs, the most common symptom being hemorrhagic enteritis, with up to a 70% mortality rate in pups but usually less than 1% in adults.[21]Feline parvovirus, a closely related virus,[22] likewise causes severe illness in cats along withpanleukopenia.[23][24] In pigs,porcine parvovirus is a major cause of infertility as infection frequently leads to death of the fetus.[25]
Adeno-associated viruses have become an important vector forgene therapy aimed at treating genetic diseases, such as those caused by a single mutation. The recombinant AAV (rAAV) contains a viral capsid but lacks a complete viral genome. Instead, the typical nucleic acid packaged into the capsid contains a promoter region, the gene of interest, and a terminator region, all contained within two inverted terminal repeats derived from the viral genome. rAAV essentially acts as a container that can traverse the cell membrane and deliver its nucleic acid cargo to the nucleus.[26][27]
Parvoviruses were discovered relatively late in comparison to other prominent virus families, potentially due to their small size. In the late 1950s[28] and 1960s,[29] a variety of animal parvoviruses were discovered, includingminute virus of mice,[30] which has since been used extensively to study rolling hairpin replication.[31] Many AAVs were also discovered during this time period[32] and research on them led to their first usage in gene therapy in the 1980s. Over time, improvements in aspects such as vector design led to certain AAV gene therapy products reaching clinical efficacy in 2008 and being approved in the following years.[27]
In 1974, the first pathogenic human parvovirus was discovered byTamim.k, N.I Urbi, et al. When testing for thehepatitis B virus's surface antigen, one serum sample gave anomalous results and withelectron microscopy was shown to contain a virus resembling animal parvoviruses. This virus was named B19 after the coding of the serum sample, number 19 in panel B.[20][33] B19 was later recognized as a species by theInternational Committee on Taxonomy of Viruses (ICTV) in 1985, and throughout the 1980s it increasingly became associated with various diseases.[33]
In the ICTV's first report in 1971, parvoviruses were grouped together in the genusParvovirus.[30][32] They were elevated to the rank of family in 1975 and remained unassigned to higher taxa until 2019, when they were assigned to higher taxa up to the highest rank, realm.[34] The family was reorganized in 2019, departing from the "traditional" invertebrate-vertebrate distinction betweenDensovirinae andParvovirinae and instead distinguishing the subfamilies based on helicase phylogeny, leading to the establishment of a new subfamily,Hamaparvovirinae.[18]
Parvoviruses take their name fromLatinparvus orparvum, meaningsmall ortiny, referring to the small size of parvovirus virions compared to most other viruses.[2][20] In the family nameParvoviridae, -viridae is the suffix used for virus families.[35] The orderPiccovirales takes the first part of its name from theItalian wordpiccolo, meaningsmall, and the second part is the suffix used for virus orders. The classQuintoviricetes takes the first part of its name from theGalician wordquinto, meaningfifth, referring tofifth disease (erythema infectiosum) caused by parvovirus B19, andviricetes, the suffix used for virus classes.[17]
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