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Simple Summary: Avipoxvirus, the causative agent of avian pox disease, can infect more than 278 species of wild and domestic birds. It causes multiple negative consequences for both the economy and the ecosystem. These include reduced egg production, reduced mating success, growth retardation, and occasionally death. Several diagnostic methods are currently available, and prevention is mainly performed by implementing sanitary measures and vaccination. In order to evaluate and characterize the Avipoxviruses circulating in Portugal between 2017 and 2023, ten samples positive for this virus were analyzed. They were then compared with other isolates from other hosts, countries, and years of collection. As a result, it was possible to understand that certain variants of the virus continued to circulate over the years despite the introduction of new viruses. Avipoxvirus (APV), a linear dsDNA virus belonging to the subfamily Chordopoxvirinae of the family Poxviridae, infects more than 278 species of domestic and wild birds. It is responsible for causing avian pox disease, characterized by its cutaneous and diphtheric forms. With a high transmission capacity, it can cause high economic losses and damage to the ecosystem. Several diagnostic methods are available, and bird vaccination can be an effective preventive measure. Ten APV-positive samples were analyzed to update the molecular characterization and phylogenetic analysis of viruses isolated in Portugal between 2017 and 2023. A P4b gene fragment was amplified using a PCR, and the nucleotide sequence of the amplicons was determined using Sanger sequencing. The sequences obtained were aligned using ClustalW, and a maximum likelihood phylogenetic tree was constructed. With this study, it was possible to verify that the analyzed sequences are distributed in subclades A1, A2, B1, and B3. Since some of them are quite similar to others from different countries and obtained in different years, it is possible to conclude that there have been several viral introductions in Portugal. Finally, it was possible to successfully update the data on Avipoxviruses in Portugal. [ABSTRACT FROM AUTHOR]

Feline herpesvirus-1 (FeHV-1) is classified within the Varicellovirus genus and is frequently seen in cats. Ocular complications, such as conjunctivitis, keratitis, and corneal ulcers, are common and have the potential to result in latency and permanent visual loss if not appropriately diagnosed and monitored. This study aimed to isolate FeHV-1 from cats with ocular lesions using the CRFK cell line. This study included a total of ten cats that tested positive for FeHV-1 using PCR and showed symptoms, including ocular and nasal discharge (8/10), conjunctivitis (6/10), and keratitis (5/10). Conjunctival samples were collected and processed for nucleic acid extraction. The CRFK cell line was propagated, and all positive samples were inoculated in 6-well plates. Interestingly, no CPE was observed in the CRFK cell cultures during the observation period. Following post-inoculation in cell culture, the PCR analysis conducted on the supernatants obtained from the cultures found negative for FeHV-1. This study points out the challenges faced in isolating FeHV-1 in the CRFK from ocular samples of naturally infected cats. This highlights the requirement for future comprehensive in vitro studies to enhance the efficacy of FeHV-1 isolation techniques and explore potential approaches for FeHV-1 diagnosis. [ABSTRACT FROM AUTHOR]

In the study, alterations in antibody titers, proinflammatory and antiinflammatory cytokine levels were determined in serum samples collected at various periods before and after administration of inactive IBR and iPPVO to cattle. It was aimed to investigate the immunomodulatory effects of inactivated parapoxvirus ovis (iPPVO) in cattle vaccinated with inactivated-IBR vaccine. In the study, 40 unvaccinated, clinically healthy cattle of different breeds aged older than 3 months were used. Three groups of cattle were formed as control group 1 (n=10), control group 2 (n=10) and experimental group (n=20). iPPVO was applied to the cattle in the control group 1 and experimental groups on the 0, 2nd, and 4th days. Blood samples were collected from all the animals after 6th hours of the injections applied on 0th and 4th days of the study. Commercially available ELISA kits were used to determine serum levels of of IL-2, IL-6, IL-12 and IFN-γ. Furthermore, virus neutralization test was also performed to detect virus neutralizing antibody titres. In the present study, serum levels of IL-2, IL-6 IL-12, and IFN-γ levels were found to be significantly higher in the experimental group compared to that of the control group 1 and control group 2 (p<0,05). The differences between control group 1 and control group 2 groups were not statistically significant. In conclusion, iPPVO increased the levels of cytokines in IBR vaccinated cattle due to its immunomodulatory effects. In addition, virüs neutralizing antibody titers were found to be significantly higher in cattle that received vaccine and iPPVO. [ABSTRACT FROM AUTHOR]

Crocodilepox virus (CRV) belongs to the Poxviridae family and mainly infects hatchling and juvenile Nile crocodiles. Most poxviruses encode inhibitors of the host antiviral protein kinase R (PKR), which is activated by viral double-stranded (ds) RNA formed during virus replication, resulting in the phosphorylation of eIF2α and the subsequent shutdown of general mRNA translation. Because CRV lacks orthologs of known poxviral PKR inhibitors, we experimentally characterized one candidate (CRV157), which contains a predicted dsRNA-binding domain. Bioinformatic analyses indicated that CRV157 evolved independently from other poxvirus PKR inhibitors. CRV157 bound to dsRNA, co-localized with PKR in the cytosol, and inhibited PKR from various species. To analyze whether CRV157 could inhibit PKR in the context of a poxvirus infection, we constructed recombinant vaccinia virus strains that contain either CRV157, or a mutant CRV157 deficient in dsRNA binding in a strain that lacks PKR inhibitors. The presence of wild-type CRV157 rescued vaccinia virus replication, while the CRV157 mutant did not. The ability of CRV157 to inhibit PKR correlated with virus replication and eIF2α phosphorylation. The independent evolution of CRV157 demonstrates that poxvirus PKR inhibitors evolved from a diverse set of ancestral genes in an example of convergent evolution.

Since smallpox vaccination was discontinued in 1980, there has been a resurgence of poxvirus infections, particularly the monkeypox virus. Without a global recommendation to use the smallpox vaccine, the population is not immune, posing a severe threat to public health. Given these circumstances, it is crucial to understand the relationship between poxviruses and their hosts. Therefore, this study focuses on the ectromelia virus, the causative agent of mousepox, which serves as an excellent model for studying poxvirus pathogenesis. Additionally, we investigated the role of mitochondria in innate antiviral immunity during ECTV infection, focusing specifically on mitochondrial antiviral signaling protein. The study used a Moscow strain of ECTV and L929 mouse fibroblasts. Cells were treated with ECTV and chemical modulators of mitochondrial network: Mdivi-1 and CCCP. Our investigation revealed that an elongated mitochondrial network attenuates the suppression of MAVS-dependent immunity by ECTV and reduces ECTV replication in L929 fibroblasts compared to cells with an unaltered mitochondrial network. Conversely, a fragmented mitochondrial network reduces the number of progeny virions while increasing the inhibition of the virus-induced immune response during infection. In conclusion, our study showed that modifications of mitochondrial network morphology alter MAVS-dependent immunity in ECTV-infected mouse L929 fibroblasts.

Yaba monkey tumor virus (YMTV) and Tanapox virus (TPV) are members of the Yatapoxvirus genus and can infect humans and other primates. Despite the threat posed by yatapoxviruses, the factors determining their host range are poorly understood. In this study, we analyzed the ability of YMTV and TPV orthologs of vaccinia virus K3 (called 012 in YMTV and TPV), which share 75% amino acid identity with one another, to inhibit PKR from 15 different primate species. We first used a luciferase-based reporter, and found that YMTV and TPV K3 orthologs inhibited PKR in a species-specific manner and showed distinct PKR inhibition profiles. TPV 012 inhibited PKR from 11 primates, including humans, substantially better than YMTV 012. In contrast, both K3 orthologs inhibited the other four primate PKRs comparably well. Using YMTV 012 and TPV 012 hybrids, we mapped the region responsible for the differential PKR inhibition to the C- terminus of the K3 orthologs. Next, we generated chimeric vaccinia virus strains to investigate whether TPV K3 and YMTV K3 orthologs could rescue the replication of a vaccinia virus strain that lacks PKR inhibitors K3L and E3L. Virus replication in primate-derived cells generally correlated with the patterns observed in the luciferase-based assay. Together, these observations demonstrate that yatapoxvirus K3 orthologs have distinct PKR inhibition profiles and inhibit PKR in a species-specific manner, which may contribute to the differential susceptibility of primate species to yatapoxvirus infections.

Members of the eukaryotic translation initiation complex are co-opted in viral infection, leading to susceptibility in many crop species, including stone fruit trees (Prunus spp.). Therefore, modification of one of those eukaryotic translation initiation factors or changes in their gene expression may result in resistance. We searched the crop and wild Prunus germplasm from the Armeniaca and Amygdalus taxonomic sections for allelic variants in the eIF4E and eIFiso4E genes, to identify alleles potentially linked to resistance to Plum pox virus (PPV). Over one thousand stone fruit accessions (1397) were screened for variation in eIF4E and eIFiso4E transcript sequences which are in single copy within the diploid Prunus genome. We identified new alleles for both genes differing from haplotypes associated with PPV susceptible accessions. Overall, analyses showed that eIFiso4E is genetically more constrained since it displayed less polymorphism than eIF4E. We also demonstrated more variations at both loci in the related wild species than in crop species. As the eIFiso4E translation initiation factor was identified as indispensable for PPV infection, a selection of ten different eIFiso4E haplotypes along 13 accessions were tested by infection with PPV and eight of them displayed a range of reduced susceptibility to resistance, indicating new potential sources of resistance to sharka. [ABSTRACT FROM AUTHOR]

A plum pox virus (PPV) susceptible traditional cultivar (Besztercei Bt.2) and a clone of a PPV resistant autochthonous landrace, Nemtudom (Nábrád) of the hexaploid European plum (Prunus domestica) were used to identify and characterize an isoform of the eukaryotic translation initiation factor, eIF(iso)4E, a host susceptibility factor required for PPV infection in plum. The cDNA and intron sequences of the eIF(iso)4E gene and the modeled 3D structure of the encoded proteins revealed sequence alterations that are not expected to critically influence the structure and function of the protein. The introns shared the canonical GT-AG splice sites, although they showed base substitutions and indels among alleles, and were different in intron phases. However, none of the sequence variations seem to challenge the splicing efficiency of the introns. The expression rates of the gene were similar in the leaves of the PPV susceptible Besztercei Bt.2 and the tolerant Nábrád cultivars, suggesting the eIF(iso)E4 gene is not responsible for differences in the reaction of those cultivars to PPV. Our results indicate natural differences in the PPV-tolerance of Besztercei Bt.2 and Nábrád were not induced by the eIF(iso)4E gene and hence the PPV tolerant Nábrád and other Nemtudom accessions might be valuable donors of PPV resistance in breeding programs. By providing the first information on the allelic variations, exon-intron structure, and expression of the eIF(iso)4E gene in P. domestica, our results will help in both conventional and molecular breeding of the studied and other European plum cultivars. [ABSTRACT FROM AUTHOR]

Genus Avipoxvirus, an important member of the family Poxviridae, has 12 species which have been recognized by the International Committee on Taxonomy of Viruses (ICTV). Fowlpox virus and pigeonpox virus are two important species that may affect other species of birds, besides chicken and fowl. Hence, accurately identifying species, clades and subclades of Avipoxvirus is vital to design and implement adequate control strategies. The present study was carried out in a pigeon colony showing symptoms of pox. A fragment of viral Pan-genus 4b (P4b) gene was amplified and sequenced. As an equivocal and prototype species, sequence information of fowlpox virus isolated from an infected bird was also generated. The generated sequence information was compared with those of previously reported strains. It was found that both fowlpox and pigeonpox viruses belonged to clade A, and there was circulation of A1 and A2 subclades in chicken and pigeon respectively. From India, one report showed the circulation of A1 and A3 subclades in Indian chickens and pigeons respectively, since the other reports were based on clinical symptoms, histopathological examination and comparison of sequence information with those available without distinct demarcation of clade and subclade of Avipoxvirus. This study describes the findings of the novel A2 subclade of Avipoxvirus and the existence of pigeonpox in the Andaman and Nicobar Islands, India. [ABSTRACT FROM AUTHOR]

Introduction: Trans-grafting could be a strategy to transfer virus resistance from a transgenic rootstock to a wild type scion. However contradictory results have been obtained in herbaceous and woody plants. This work was intended to determine if the resistance to sharka could be transferred from transgenic plum rootstocks to wild-type apricot scions grafted onto them. Methods: To this end, we conducted grafting experiments of wild-type apricots onto plum plants transformed with a construction codifying a hairpin RNA designed to silence the PPV virus and studied if the resistance was transmitted from the rootstock to the scion. Results: Our data support that the RNA-silencing-based PPV resistance can be transmitted from PPV-resistant plum rootstocks to non-transgenic apricot scions and that its efficiency is augmented after successive growth cycles. PPV resistance conferred by the rootstocks was robust, already occurring within the same growing cycle and maintained in successive evaluation cycles. The RNA silencing mechanism reduces the relative accumulation of the virus progressively eliminating the virus from the wild type scions grafted on the transgenic resistant PPV plants. There was a preferential accumulation of the 24nt siRNAs in the scions grafted onto resistant rootstocks that was not found in the scions grafted on the susceptible rootstock. This matched with a significantly lower relative accumulation of hpRNA in the resistant rootstocks compared with the susceptible or the tolerant ones. Discussion: Using transgenic rootstocks should mitigate public concerns about transgenes dispersion and eating transgenic food and allow conferring virus resistance to recalcitrant to transformation cultivars or species. [ABSTRACT FROM AUTHOR]

Plum pox virus (PPV) is considered the most detrimental viral pathogen of stone fruits, causing important economic losses. Exhaustive studies revealed that D, M and Rec are the prevalent strains of PPV in Europe. While different experimental reports revealed that PPV-M is more aggressive than PPV-D, limited information is available about the competitiveness of PPV-Rec under field conditions. Also, symptoms developed by PPV-Rec infection are scarcely documented. To increase this knowledge, we selected and monitored an experimental plum orchard already contaminated by both PPV-D and PPV-Rec. The disease spread was monitored by visual observation and ELISA testing each year along five consecutive vegetative periods. The dynamic of single and mixed infections was assessed by molecular strain typing (IC-RT-PCR) of all newly and single-infected trees. While the disease prevalence increased almost linearly, the number of single PPV infected trees (either by PPV-Rec or by PPV-D) remained relatively stable during the five-year period of monitoring, which is explainable by the continual increase of the number of trees infected with both strains together. No significant difference in the progression rate between D and Rec strains was found when considering their presence in both single and mixed infections. Although the types of PPV symptoms developed on leaves and fruits varied among cultivars, no clear-cut D or Rec strain-specific symptoms were developed within the same cultivar. Overall results revealed that PPV-D and PPV-Rec strains had similar behaviour in terms of competitiveness and symptoms developed under our experimental field conditions. [ABSTRACT FROM AUTHOR]

Poxviruses belong to the Poxviridae family, a group of pathogens known for their high infectivity in humans, posing significant health threats. One of the most well‐known representatives of poxvirus infections is smallpox, which has been successfully eradicated. However, in recent years, there has been a resurgence in cases of mpox, another member of the Poxviridae family, raising concerns about the potential for a global pandemic or a worldwide health crisis. While the typical clinical presentation of mpox and other poxvirus infections often involves cutaneous lesions, there have been reports of various atypical and non‐classic clinical manifestations. Dermoscopy has emerged as a crucial diagnostic tool, aiding dermatologists in clinical practice to make informed decisions. In this summary, we provide an overview of the clinical and dermoscopic features of representative cutaneous lesions associated with human poxvirus infections, including mpox, orf, milker's nodule, and molluscum contagiosum. [ABSTRACT FROM AUTHOR]

Capripox viruses (CaPVs), including sheep pox virus (SPV), goat pox virus (GPV), and lumpy skin disease virus (LSDV), are the cause of sheep pox (SPP), goat pox (GTP), and lumpy skin disease (LSD) in cattle. These diseases are of great economic significance to farmers, as they are endemic on farms and are a major constraint to international trade in livestock and their products. Capripoxvirus (CaPV) infections produce similar symptoms in sheep and goats, and the three viruses cannot be distinguished serologically. In this study, we developed a real-time quantitative polymerase chain reaction (qPCR) method for identifying CaPV in goats, sheep, and cattle. Clinical samples were tested and verified. The developed assay was highly specific for target viruses, including GPVSPV and LSDV, which had no cross-reaction with other viruses causing similar clinical symptoms. An artificially synthesized positive control plasmid using the CaPV 32 gene inserted into the vector pMD19-T was used as a template, and the correlation coefficient of the linear regression curve (R2) was 0.9916, the estimated amplification efficiency (E) was 96.06%, and the sensitivity (limit of detection, LOD) was 3.80 copies per reaction. Using the clinical samples as a template, the limit of detection (LOD) was 4.91 × 10−5 ng per reaction (1.60 × 10−5–2.13 × 10−3 ng, 95% confidence interval (CI)), which means that this method was one of the most sensitive detection assays for CaPVs. A total of 85 clinical samples from CaPV-infected animals (goats, sheep, and cattle) and 50 clinical samples from healthy animals were used to test and compare the diagnostic results using the Synergy Brands (SYBR) Green-based PCR method recommended by the World Organization of Animal Health (WOAH). Both diagnostic sensitivity (DSe) (95.8–100%, 95% CI) and diagnostic specificity (DSp) (92.9–100%, 95% CI) results of the real-time quantitative PCR (qPCR) and SYBR Green PCR were 100%, and the kappa value (κ) was 1.0 (1-1, 95% CI). In summary, the assay established based on TaqMan probes was advantageous in high specificity, sensitivity, and general applicability and could be a competitive candidate tool for the diagnosis of CaPV in clinically suspected animals. [ABSTRACT FROM AUTHOR]

The present study focused on trees of Tuscany autochthonous plum cv. Coscia di Monaca in order to evaluate the presence of viruses and elucidate the physiological and biochemical responses to virus infections under real field conditions. Among the several investigated viruses, plums tested positive only to plum pox virus (PPV) and plum bark necrosis steam pitting associated virus (PBNSPaV), occurring as both singular and co-infections. This is the first report of PBNSPaV in a Tuscany orchard. Furthermore, the present study not only confirmed the detrimental effects of PPV on the carbon dioxide assimilation rate due to both stomatal limitations and mesophyll impairments, but also showed that although PBNSPaV did not induce such photosynthetic impairments when occurring as singular infection, it enhanced this damaging effect when present as a co-infection with PPV, as confirmed by a severe decrease in the chlorophyll content. Infection-specific responses in terms of accessory pigments (i.e., carotenoids and xanthophylls), as well as sugars and organic acids, were also reported, these being likely related to photoprotective mechanisms and osmotic regulations under virus-induced oxidative stress. Overall, the results here presented represent an important step to fill knowledge gaps about the interaction of plant viruses and autochthonous Prunus cultivars. [ABSTRACT FROM AUTHOR]

The complete genome of plum pox virus strain T isolates from five different Prunus spp., including almond (P. dulcis) and sour cherry (P. ceracus) isolates, was fully sequenced using the primer pairs designed in this study. The five isolates were aligned with other 50 PPV-T isolates whose complete genome sequences were available in GenBank and then subjected to phylogenetic and diversity analyses. Recombination analysis showed no significant signal detected in the five newly sequenced isolates while confirming four recombinant isolates reported in a previous study. Nucleotide and amino acid phylogenetic trees clustered the tested isolates into three major groups: Balkan 1, 2, and 3. Strain T isolates shared high nucleotide and amino acid identities among them. Diversity analysis applied different parameters to found that the sequences of P3 and 6K1 genes were more conserved over other genes. In accordance, the highly variable P1 and CP genes were found to experience weaker purifying pressures, ω = 0.127 and 0.219, respectively, than other genes. The three neutrality tests gave negative values to all genes, suggesting that strain T populations have expanding or bottleneck selections. Genetic make-up of the only known sour cherry isolate is highly identical to isolates from other Prunus spp. Therefore, this study has updated our knowledge of T strain diversity in new hosts and provided a clear picture of genetic variation and host relationships. [ABSTRACT FROM AUTHOR]

Background: The camel pox virus (CMLV) is a widespread infectious viral disease of camels. It is necessary to conduct research on new strains for the development of vaccines. Aim: The research aims to characterize a novel strain isolated from the CMLV used to produce a CMLV vaccine. Methods: The objects of the study were the "M-0001" strain isolated from a sample of animals infected with the CMLV during the epidemic. The cultural and reproductive properties of the virus isolate were studied using primary cell lines from primary trypsinized lamb kidney and testicular cell cultures (LK and LT). Other samples included kidney cell lines from transplanted sheep as well as a kidney cell line from transplanted cattle, Vero (transplanted green monkey kidney cell line), and calf trachea. The strain was polymerase chain reaction (PCR)-tested and sequenced for characterization purposes. Results: The PCR results show that the study sample is species specific and corresponds to the CMLV by the size of the cumulative amplifications, which is 241 bp. Given the maximum percentage of a sequence match analyzed by the BLAST algorithm based on the international database and the results of phylogenetic analysis, the M0001 sample was determined to belong to the CMLV (gene bank inventory number KP768318.1). Conclusion: The sample "M0001" is located on the same branch with a representative from CMLV. Among the cell cultures tested, the LK and LT cell lines were the most sensitive to the isolated CMLV isolate. Reproducing the virus in these cell cultures remains stable even after 15 consecutive passes. The cytopathic effect of the virus was less pronounced and low in transplanted cell lines, and the cytopathic effect was no longer apparent in the third passage. A genome alignment of the virus has identified potentially conserved sites, and analysis of loci in different virus types revealed one maximally conserved locus. An epizootic strain of the camelina virus "M-0001" candidate to produce vaccines for the camels was obtained. An experimental vaccine sample based on an isolated and charred camellia virus will be created in the future. [ABSTRACT FROM AUTHOR]

Smallpox caused by the variola virus (VARV) was one of the greatest infectious killers of mankind. Historical records trace back smallpox for at least a millennium while phylogenetic analysis dated the ancestor of VARV circulating in the 20th century into the 19th century. The discrepancy was solved by the detection of distinct VARV sequences first in 17th‐century mummies and then in human skeletons dated to the 7th century. The historical records noted marked variability in VARV virulence which scientists tentatively associated with gene losses occurring when broad‐host poxviruses narrow their host range to a single host. VARV split from camel and gerbil poxviruses and had no animal reservoir, a prerequisite for its eradication led by WHO. The search for residual pockets of VARV led to the discovery of the monkeypox virus (MPXV); followed by the detection of endemic smallpox‐like monkeypox (mpox) disease in Africa. Mpox is caused by less virulent clade 2 MPXV in West Africa and more virulent clade 1 MPXV in Central Africa. Exported clade 2 mpox cases associated with the pet animal trade were observed in 2003 in the USA. In 2022 a world‐wide mpox epidemic infecting more than 80,000 people was noted, peaking in August 2022 although waning rapidly. The cases displayed particular epidemiological characteristics affecting nearly exclusively young men having sex with men (MSM). In contrast, mpox in Africa mostly affects children by non‐sexual transmission routes possibly from uncharacterized animal reservoirs. While African children show a classical smallpox picture, MSM mpox cases show few mostly anogenital lesions, low‐hospitalization rates and 140 fatal cases worldwide. MPXV strains from North America and Europe are closely related, derived from clade 2 African MPXV. Distinct transmission mechanisms are more likely causes for the epidemiological and clinical differences between endemic African cases and the 2022 epidemic cases than viral traits. [ABSTRACT FROM AUTHOR]

Alternative lengthening of telomeres (ALTs) mechanism is activated in some somatic, germ cells, and human cancer cells. However, the key regulators and mechanisms of the ALT pathway remain elusive. Here we demonstrated that ZBTB40 is a novel telomere-associated protein and binds to telomeric dsDNA through its N-terminal BTB (BR-C, ttk and bab) or POZ (Pox virus and Zinc finger) domain in ALT cells. Notably, the knockout or knockdown of ZBTB40 resulted in the telomere dysfunction–induced foci and telomere lengthening in the ALT cells. The results also show that ZBTB40 is associated with ALT-associated promyelocytic leukemia nuclear bodies, and the loss of ZBTB40 induces the accumulation of the ALT-associated promyelocytic leukemia nuclear bodies in U2OS cells. Taken together, our results implicate that ZBTB40 is a key player of telomere protection and telomere lengthening regulation in human ALT cells. [ABSTRACT FROM AUTHOR]

Apricot has undergone an important cultivar renewal during the last years in response to productive and commercial changes in the crop. The impact of the sharka disease (plum pox virus) prompted the release of cultivars resistant/tolerant to this virus, leading to a major cultivar renewal worldwide. This has caused high variability in chilling requirements on new releases that remain unknown in many cases. In many apricot-growing areas, the lack of winter chilling is becoming a limiting factor in recent years. To deal with this situation, growers must choose cultivars well adapted to their areas. However, the information available on the agroclimatic requirements of the cultivars is very limited. To fill this gap, in this work, we have characterized the chilling requirements of 13 new apricot cultivars from Europe (France, Greece and Spain) and North America (USA) in two experimental collections in Aragón (Spain). We established the chilling period using male meiosis as a biomarker for endodormancy release over two years. Chilling requirements ranged from 51.9 Chill Portions (CP) to 70.9 CP. Knowing the chilling requirements of cultivars will help growers to select suitable cultivars adapted to the chill availability of their region. [ABSTRACT FROM AUTHOR]

Since ancient times, the fruits of the plum have occupied an important place on the table of the Bulgarians. To obtain high and stable yields an important condition is the proper organization and conduct of plant protection activities and the fast, the correct and accurate diagnosis of PPV - Stoneware. In our climate, Plum pattern manifests symptoms first on the first spring leaves. The described symptoms of flowers in different stone species are few and scarce, so we conducted the present study in two following years 2019 and 2020 to describe, differentiate and compare visual symptoms of flowering with the results of DAS-ELISA tests on the leaves of the studied stone species. From the surveyed PPV host species in two orchards 12 mather trees with color symptoms were selected and described in two regions of Bulgaria - the Sofia field (Vrajdebna (1,2 ha) and the Vratsa region (Roman Orchard Nursery (0,4 ha). In a total of 9 samples, PPV infection was confirmed. The established deviations were found only in fruit crops that bloom with white flowers. Based on the results and conclusions, the present study will contribute to the timely detection of the causative agent of pox virus in the earliest symptoms in nurseries and gardens and will provide the right and quick direction to overcome the damage through proper plant protection activities. [ABSTRACT FROM AUTHOR]

Host pattern recognition receptors (PRRs) sense pathogen-associated molecular patterns (PAMPs), which are molecular signatures shared by different pathogens. Recognition of PAMPs by PRRs initiate innate immune responses via diverse signaling pathways. Over recent decades, advances in our knowledge of innate immune sensing have enhanced our understanding of the host immune response to poxviruses. Multiple PRR families have been implicated in poxvirus detection, mediating the initiation of signaling cascades, activation of transcription factors, and, ultimately, the expression of antiviral effectors. To counteract the host immune defense, poxviruses have evolved a variety of immunomodulators that have diverse strategies to disrupt or circumvent host antiviral responses triggered by PRRs. These interactions influence the outcomes of poxvirus infections. This review focuses on our current knowledge of the roles of PRRs in the recognition of poxviruses, their elicited antiviral effector functions, and how poxviral immunomodulators antagonize PRR-mediated host immune responses.

Monkeypox is a natural focal zoonosis of rodents and monkeys living in the Congo Valley (clade CB) and West Africa (clade WA). The special interest in monkeypox is due to its pandemic spread, which began in May 2022. The aim of this article is to consider the danger of monkeypox due to the lack of knowledge about its nature, as well as existing achievements in the treatment and prevention of this disease. The information was collected mainly from English­language sources available through the PubMed and Google Scholar databases. The study was conducted in the following areas: the epidemiology of monkeypox outbreaks until May 2022; taxonomy and origin of monkeypox virus (MPV); morphology and life cycle of poxviruses; ecology and epidemiology of MPV; the clinical picture of monkeypox in humans with natural infection; monkeypox clinic in European homosexuals; clinical picture and pathomorphology of monkeypox in animals with artificial infection; immunoprophylaxis and therapy of monkeypox. It has been established that until May 2022 the appearance of MPV into non­endemic countries was limited to single cases of the disease. Because of that, the monkeypox pandemic that began in May 2022 looks atypical. The low­contagious MPV (WA) that caused it did not occur in Nigeria until 2017. Its spread was facilitated by a new mechanism of infection through organized homosexual contacts. Therefore, monkeypox should no longer be considered a rare disease geographically limited to the countries of West and Central Africa. It is also necessary to take into account the possibility of activating the natural reservoirs of other poxviruses, as well as the realization of their epidemic potential through immunodeficient human populations, which reach 20% of the total population in the developed countries. At present, there are no vaccines or drugs whose efficacy and safety have been confirmed in epidemic foci of MPV with immunodeficient populations. Serious efforts should be made to identify man­made outbreaks of monkeypox; to the identification of possible zoonotic hosts of MPV in Russia; factors that support MPV in ecosystems; host factors that determine the severity of the disease, as well as facilitating animal­to­human and human­to­human transmission.

Smallpox was eradicated in less than 200 years after Edward Jenner's practice of cowpox variolation in 1796. The forty-three years of us living free of smallpox, beginning in 1979, never truly separated us from poxviruses. The recent outbreak of monkeypox in May 2022 might well warn us of the necessity of keeping up both the scientific research and public awareness of poxviruses. One of them in particular, the vaccinia virus (VACV), has been extensively studied as a vector given its broad host range, extraordinary thermal stability, and exceptional immunogenicity. Unceasing fundamental biological research on VACV provides us with a better understanding of its genetic elements, involvement in cellular signaling pathways, and modulation of host immune responses. This enables the rational design of safer and more efficacious next-generation vectors. To address the new technological advancement within the past decade in VACV research, this review covers the studies of viral immunomodulatory genes, modifications in commonly used vectors, novel mechanisms for rapid generation and purification of recombinant virus, and several other innovative approaches to studying its biology. [ABSTRACT FROM AUTHOR]

[ Objective] The ORFV FIL gene and marker genes were inserted at the 135 gene locus of goat virus by Cre/loxP system to provide a strategies for the design and development of a vaccine to prevent the infection of Orf virus in clinic. [ Method] Based on pDonor vector, about 500 bp fragments of the region sequence on both sides of 135 gene coding region were used as upper and lower recombination homologous arms. The expression cassette named pGTPV( 135 )-ORFV-FlL, which also included 135 gene, maker gene gpt and EGFP, early and late promoter, and loxp locus. PCR identification and sequencing were performed on the positive clone. The correct sequence bacterial fluid was inoculated into ampicillin LB liquid medium for overnight culture. The endotoxin was removed and the plasmid was extracted and identified by double enzyme digestion. The immortalized goat testicular cells were infected with low virulent goatpox virus at 2 hours, the recombinant plasmid was transfected into immortalized goat testicular cells by liposome method to observe the cytopathic effect and the expression of the marker gene EGFP. The virus solution was harvested 48 hours later, repeated freezing and thawing for 3 times, and then passed to 3 generations blindly. The integration of the target gene was identified by PCR. The ORFV positive serum was used as the first antibody, and the donkey anti goat IgG was used as the second antibody. The recombinant virus was identified by western blot analysis of the expression of the target gene. [Result] The recombinant plasmid of goat pox virus expressing Fl L gene of ORFV was identified by PCR and sequenced. The result of comparison with the target sequence is correct, which indicated that the recombinant plasmid was successfully constructed. The concentration of the recombinant plasmid was determined after endotoxin removal and extraction, and the results were correct. After the identified recombinant plasmid was transfected into immortalized goat testicular cells, green fluorescence was observed 48 hours later, and Fl L gene was integrated into the recombinant virus by PCR identification. The western blot analysis showed that the foreign gene Fl L inserted by the recombinant goat pox virus was successfully expressed. [ Conclusion]The FIL gene ofORFV was inserted into the 135 gene site of the attenuated strain of goatpox virus, and the recombinant virus was obtained in immortalized goat testicle cells. The target gene can be stably expressed, and a method for constructing a recombinant goatpox virus with the 135 gene site inserted into the FIL gene of goatpox virus was successfully established. [ABSTRACT FROM AUTHOR]

Plum pox virus (PPV) a potyvirus in the family Potyviridae, is the etiologic agent of sharka, the worldwide most important and detrimental viral disease of stone fruits (genus Prunus). Although PPV was identified in Italy already in the 1970s and it has been largely reported in almost all Italian regions, a broad investigation and genetic characterization of PPV isolates was lacking in most of them, including Tuscany (Central Italy). To address this knowledge gap, in 2020 and 2021, field surveys were carried out in 80 commercial Tuscany orchards and a total of 690 leaf samples were collected from different Prunus species. PPV was identified in 25 and 12 peach and plum samples, respectively (more than 5% of tested samples), whereas no positive samples were reported in apricot. Eighteen of the 37 PPV positive samples showed mixed infections with other viruses and viroids, mostly Prunus necrotic ringspot virus in plum and peach latent mosaic viroid in peach. Molecular typing of PPV infected samples generated NIb/CP amplicons corresponding to PPV-Marcus (M) or PPV-Recombinant (Rec) strains. Furthermore, starting from the identification of eight PPV nucleotide sequences (among which five and two new PPV-M and PPV-Rec isolates, respectively), this study firstly identified the PPV-Mb subgroup in Italy, which was even prevalent than PPV-Ma. Finally, PPV-Rec isolates resulted phylogenetically close to Italian and Turkish isolates previously detected. Overall, the results here presented represent an important step to fill knowledge gaps about PPV in Tuscany, and we believe it may encourage other similar research to achieve more accurate data on PPV populations at both national and international levels. [ABSTRACT FROM AUTHOR]

Background: The years 2022–2023 witnessed a monkeypox virus (mpox) outbreak in some countries worldwide, where it exists in an endemic form. However, the number of infectious cases is continuously on the rise, and there has been an unexpected, drastic increase in cases that result from sustained transmission in non-endemic regions of the world. Under this scenario, it is pertinent for the world to be aware of healthcare threats to mpox infection. This review aimed to compile advanced data regarding the different aspects of mpox disease. Methods: A comprehensive strategy for the compilation of recent data was adopted to add data regarding mpox, biology, viral pathology, immune response, and brief details on the antiviral strategies under trial; the search was limited to 2016–2023. The aim is to make the scientific community aware of diverse aspects of mpox. Results: Consequently, detailed insights have been drawn with regard to the nature, epidemiology, etiology, and biological nature of mpox. Additionally, its host interaction and viral infectious cycle and immune interventions have been briefly elaborated. This comprehensively drawn literature review delivers brief insights into the biological nature, immune responses, and clinical developments in the form of therapeutics against mpox. This study will help scientists understand the biological nature and responses in hosts, which will further help clinicians with therapeutic handling, diagnosis, and treatment options. Conclusions: This study will provide updated information on mpox's pathology, immune responses, and antiviral strategies. Moreover, it will also help the public to become educated on the healthcare-associated threat and take timely mitigation measures against expected mpox outbreaks in the future. [ABSTRACT FROM AUTHOR]

Apricot is one of the most important stone-fruit plants widely cultivated in Azerbaijan. SSR markers were used to evaluate the genetic diversity of 61 apricot genotypes representing the entire gene pool in Azerbaijan. A total of 138 alleles were produced based on 17 SSR markers with an average of 8.1 alleles per primer. The polymorphism information content (PIC) and expected (He) heterozygosity for individual loci were in the range of 0.42-0.8 (mean 0.68) and 0.52-0.82 (mean 0.72), respectively, indicating the abundant genetic variation in Azerbaijani apricot cultivars. The polymorphisms generated by SSRs were enough to differentiate 95% of genotypes, while 4 apricot cultivars exhibited complete similarity between them. NJ tree grouped the 61 genotypes into 7 clusters with 1000 bootstrap values, where the grouping of genotypes was not closely related to the geographic origin or collection site. STRUCTURE analysis identified 4 subpopulations in the collection and, in general, was in agreement with cluster analysis. (SEO)/Harlayne-type resistance alleles of three SSR (PGS1.21-240 bp, PGS1.23-161 bp, PGS1.24-119 bp) and one SSLP loci (ZP002-127 bp) were detected in 3, 15, 15, and 9 accessions, respectively. STRUCTURE analysis could separate genotypes with resistance alleles grouping them in the first two subpopulations. Of the 61 apricot genotypes, 28 had at least one resistance allele. The results demonstrate that Azerbaijani apricots are an important source for breeding PPV-resistant apricots. [ABSTRACT FROM AUTHOR]

With a total remaining area of approximately five thousand hectares, after the existence of approximately 6900 ha with cherries was shown in 2013, Romania continues to be a country with relatively good productivity in terms of obtaining cherries. The cherry tree germplasm fund is part of the plant biodiversity that has developed over time in nature in a spontaneous and controlled way and that is the basis for the permanent improvement of cultivated varieties. The activity of collecting and preserving biological material in organized collections has a long tradition. The importance of this biological material is substantial, especially when we talk about the interaction of these genotypes with quarantine viruses, especially Plum pox virus, considered the most devastating. The pollination scheme used under SCDP Baneasa Bucharest conditions included one pollinating variety, Boambe de Cotnari, and four controlled pollinated varieties, Daria, Izverna, Superb and Severin. [ABSTRACT FROM AUTHOR]

Target double-stranded DNA (dsDNA) or single-stranded DNA (ssDNA) can activate the trans-cleavage activity of the CRISPR/Cas12a, cutting the surrounding non-target ssDNA arbitrarily. In a typical CRISPR/Cas12a system, this non-target ssDNA, with a fluorescent tag and its quencher incorporated at both ends (ssDNA-FQ), is usually used as the reporter. Here, a 2-aminopurine probe (T-pro 4), made by inserting four 2-APs in non-target ssDNA, was screened for using as a reporter in the CRISPR/Cas12a system. Compared with ssDNA-FQ, each 2-AP probe is cleaved by the activated CRISPR/Cas12a system, multi-unit signals are generated. Therefore, the CRISPR/Cas12a system using the 2-AP probe as a reporter may be more sensitive than the CRISPR/Cas12a system which uses ssDNA-FQ as the reporter. We achieved ssDNA detection at as little as 10−11 M using the 2-AP probe as the reporter in the CRISPR/Cas12a system. Compared to the CRISPR/Cas12a system using ssDNA-FQ as the reporter, its sensitivity increased by an order of magnitude. Furthermore, the method that combines PCR and the 2-AP-probe-mediated CRISPR/Cas12a system can detect goat pox virus (GTPV) down to 8.35 × 10−2 copies per μL, 10 times lower than the method that combines PCR and the ssDNA-FQ-mediated CRISPR/Cas12a system. These results indicate that the CRISPR/Cas12a system using the screened 2-AP probe as a reporter has potential in highly sensitive detection of viruses. [ABSTRACT FROM AUTHOR]

Plum pox virus (PPV) infects Prunus trees across the globe, causing the serious Sharka disease. Breeding programs in the past 20 years have been successful, generating plum varieties hypersensitive to PPV that show resistance in the field. Recently, a single tree displaying typical PPV symptoms was detected in an orchard of resistant plums. The tree was eradicated, and infected material was propagated under controlled conditions to study the new PPV isolate. Performing overlapping PCR analysis, the viral sequence was reconstructed, cloned and tested for infectivity in different 'Jojo'-based resistant plums. The results confirmed that the isolate, named PPV-D 'Herrenberg' (PPVD-H), was able to infect all these varieties. Analyses of chimeras between PPVD-H and a PPV-D standard isolate (PPVD) revealed that the NIa region of PPD-H, carrying three amino acid changes, was enough to break the resistance of these plums. Experiments with single and double mutants showed that all changes were essential to preserve the escaping phenotype. Additionally, one of the changes at the VPg-NIapro junction suggested the involvement of controlled endopeptidase cleavage in the viral response. Transient expression experiments in Nicotiana benthamiana confirmed that NIa cleavage in PPVD-H was reduced, compared to PPVD, linking the observed behavior to an NIa cleavage modulation. [ABSTRACT FROM AUTHOR]

Background: Smallpox-like symptoms are seen in the viral zoonotic illness known as monkeypox. In the current outbreaks being reported, the World Health Organization (WHO) claims that this is the first instance of chains of transmission being documented in Europe without known epidemiological connections to West or Central Africa. On August 7, 2022, the WHO reported a total of 27,815 confirmed cases in over 89 countries, with the majority of those affected experiencing monkeypox for the first time. The objective of this article is to provide a succinct overview of the monkey pox, its transmission mechanisms, and available preventative methods in adolescents. Materials and Methods: Several databases, including WHO guidelines, PubMed, Bentham Science, and Elsevier, were used to compile the data for the article following a thorough analysis of the various research findings connected to monkey pox infection, pathogenesis, and available treatments. Results: Monkeypox is a zoonotic orthopoxvirus that causes disease in humans similar to smallpox. Complications are more likely in children and the immunocompromised. Treatment is largely symptomatic. The first-line treatment for monkeypox, including in kids and teenagers, is tecovirimat. Conclusion: We came to the conclusion from this review that adolescents and adults both transmit the monkey pox virus. The most common sign of monkeypox in kids and teens is a rash that starts out as maculopapular lesions and turns into vesicles, pustules, and then scabs, just like diseases in adults. Children and adolescents who have been exposed to individuals with suspected or confirmed monkeypox may benefit from Post-Exposure Prophylaxis (PEP) with vaccination, immune globulin, or antiviral medicine. [ABSTRACT FROM AUTHOR]

Cherry Valley breeder ducks in Shandong province in northern China have experienced swollen eyes, lachrymation, pox scabs on glabrous or glabrous skin, depression and dysentery since 2021. The spread of this infectious disease has seriously affected the breeder ducks in major Cherry Valley duck farms in China. The virus causing clinical signs in Cherry Valley breeder ducks was isolated by chicken embryo inoculation. We successfully isolated a strain of duck pox virus from diseased breeder ducks by virus replication. We have also successfully conducted experiments for duck pox disease using the isolated strains to infect ducklings. By comparison with 22 pox viruses already published in GenBank, the virus strain obtained in this study was most homologous (about 99.7%) to the strain isolated from infected domestic ducks in Guangxi, China in 2014 (KJ192189), and belonged to the same A5 subtype. Since there were no previous cases of avian pox virus infecting white or Cherry Valley duck breeds, this study identified a new host for avian pox virus infection and provided theoretical support and data for the development of avian pox virus research. RESEARCH HIGHLIGHTS Avian pox virus can infect a new host type – Cherry Valley breeder ducks. The avian pox virus isolated from Cherry Valley breeder ducks showed highest identity with Guangxi hemp duck-derived avian pox virus. Cherry Valley breeder ducks were infected with avian pox virus of subtype A5. [ABSTRACT FROM AUTHOR]

Background: Monkeypox virus (MPXV) is a double-stranded DNA virus belonging to the orthopoxvirus genus in the family Poxviridae. Distinct clades are identified: the clade I belonging to the Central African (or Congo Basin) clade and the subclades IIa and IIb belonging to the West African clade. Here, a commercial droplet digital PCR (ddPCR) assay was evaluated for the quantification of the MPXV West Africa clade in clinical samples. Methods: The ddPCR reaction was assessed as a duplex assay using RPP30 as an internal amplification control. A total of 60 clinical specimens were tested, 40 positives (skin lesions, n=10; rectal swabs, n = 10; pharyngeal swabs, n = 10; and whole blood, n = 10), and 20 negatives (n = 5 for each biological matrix) were found at the routine molecular diagnostics (orthopoxvirus qPCR followed by confirmation with Sanger sequencing). To evaluate the analytical sensitivity, the ddPCR reaction was first analyzed on serial dilutions of synthetic DNA spiked in water and in negative biological matrices, achieving a limit of detection of 3.5 copy/µL. Results: Regarding the clinical samples, compared to routine molecular diagnostics, the ddPCR duplex assay showed 100% of specificity for all biological matrices and 100% sensitivity (10/10) for lesions, 100% (10/10) for rectal swabs, 90% (9/10) for pharyngeal swabs, and 60% (6/10) for whole blood. Conclusion: Overall, our data showed that the commercial ddPCR assay allowed the DNA detection of MPXV in 87.5% (35/40) of our cohort, highlighting useful technical indications for the different specimens with a potential greatest performance for skin lesions and rectal swabs. [ABSTRACT FROM AUTHOR]

Lumpy skin disease is an emerging bovine viral disease which is endemic in most African countries and some Middle East ones and the elevated risk of the spread of disease into the rest of Asia and Europe should be considered. Understanding the restrictions and channels of distribution is crucial given the recent rapid spread of disease in nations that are currently disease-free. Capripoxvirus, the responsible agent, can also cause goatpox and sheeppox. Given that they pose a threat to worldwide trade and could be exploited as tools of economic bioterrorism, the economic impact of these diseases is a major worry. Due to poor conditions in farming communities and limited availability to efficient immunizations, the dissemination of Capripoxvirus appears to be spreading.This is mostly caused by the economic consequences of the Covid-19 pandemic, the enforcement of debilitating sanctions in endemic areas, a growth in the trading in live animals and animal products, both legally and illegally, as well as the repercussions of global climate change. The goal of the current review is to offer current knowledge on the different facets of the illness, including its clinicpathology, transmission, epidemiology, diagnostics, preventative and control strategies and the probable contribution of wildlife to the disease's spread. [ABSTRACT FROM AUTHOR]

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Human mpox is an emerging epidemic in the world. The monkey pox virus (MPXV) belongs to the same family of zoonotic Orthopoxviridae as that of the smallpox virus and exhibits similar clinical symptomology. Information regarding its diagnostics, disease epidemiology, surveillance, preventive methods, and treatment strategies are being collated with time. The purpose of this review is to trace the recent events in the scientific platform that have defined new preventive and treatment strategies against mpox. A methodological approach has been used to gather data from the latest literature to comprehensively overview the emerging treatment options. The results portion will cover details regarding the prevention of mpox. It will also shed light on a brief description of contemporary vaccines and antiviral agents that have been evaluated for their treatment potential since the emergence of the mpox threat. These treatment options are setting the pace for controlling the widespread monkeypox infection. However, the limitations attached to these treatment strategies need to be tackled quickly to increase their efficacy so that they can be deployed on a large scale for the prevention of this epidemic becoming another pandemic in this decade. [ABSTRACT FROM AUTHOR]

African swine fever virus (ASFV) belongs to the family of Asfarviridae, part of the group of nucleocytoplasmic large DNA viruses (NCLDV). Little is known about the internalization of ASFV in the host cell and the fusion membrane events that take place at early stages of the infection. Poxviruses, also members of the NCLDV and represented by vaccinia virus (VACV), are large, enveloped, double-stranded DNA viruses. Poxviruses were considered unique in having an elaborate entry-fusion complex (EFC) composed of 11 highly conserved proteins integrated into the membrane of mature virions. Recent advances in methodological techniques have again revealed several connections between VACV EFC proteins. In this study, we explored the possibility of an analogous ASFV EFC by identifying ten candidate proteins exhibiting structural similarities with VACV EFC proteins. This could reveal key functions of these ASFV proteins, drawing attention to shared features between the two virus families, suggesting the potential existence of an ASFV entry-fusion complex.

The genetic diversity and evolutionary history of the epidemic plum pox virus strain M (PPV‐M) have been poorly studied. We sequenced the genomes of 69 PPV‐M isolates selected from different Turkish regions. These new nearly full‐length genomic sequences were analysed together with 21 previously reported Turkish sequences of the PPV‐MIs clade and with 50 sequences of other PPV‐M isolates collected worldwide, including four sequences of Albanian isolates. Major genomic features were maintained in all new PPV‐M genomic sequences, with the highest divergence detected in the PIPO, P1 and CP proteins. Turkish PPV‐M isolates displayed a high genetic diversity and grouped into two sister clades, one formed by PPV‐MIs isolates only and a second clade consisting of the previously described PPV‐Ma and PPV‐Mb subclades. The combined diversity for PPV‐M isolates (Europe, Japan and Turkey) reached to 0.022 ± 0.001, which is slightly higher than the diversity of the globally distributed PPV‐D strain (0.017 ± 0.001). Likewise, the genetic diversity of PPV‐M (0.020 ± 0.001) in Turkey was found to be comparable to that observed for PPV‐M isolates from other countries (0.021 ± 0.001) and even marginally higher if considering partial genomic sequences that allow the inclusion of a much larger number of isolates and countries. Overall, the original distribution of PPV‐MIs, which seems to be almost specific to Turkey, and the high genetic diversity of PPV‐MIs and other Turkish PPV‐M isolates suggest a long evolutionary history of M isolates in Turkey and position this country as a centre of diversity of PPV‐M. [ABSTRACT FROM AUTHOR]

Objective: Foot-and-mouth disease (FMD) and Peste des petits ruminant disease (PPR) are acute and severe infectious diseases of sheep and are listed as animal diseases for compulsory immunization. However, there is no dual vaccine to prevent these two diseases. The Modified Vaccinia virus Ankara strain (MVA) has been widely used in the construction of recombinant live vector vaccine because of its large capacity of foreign gene, wide host range, high safety, and immunogenicity. In this study, MVA-GFP recombinant virus skeleton was used to construct dual live vector vaccines against FMD and PPR. Methods: The recombinant plasmid pUC57-FMDV P1-2A3CPPRV FH was synthesized and transfected into MVA-GFP infected CEF cells for homologous recombination. Results: The results showed that a recombinant virus without fluorescent labeling was obtained after multiple rounds of plaque screening. The recombinant virus successfully expressed the target proteins, and the empty capsid of FMDV could be observed by transmission electron microscope (TME), and the expression levels of foreign proteins (VP1 and VP3) detected by ELISA were like those detected in FMDV-infected cells. This study laid the foundation for the successful construction of a live vector vaccine against FMD and PPR. Key points: • A recombinant MVA expressing FMDVP12A3C and PRRV HF proteins • Both the FMDV and PRRV proteins inserted into the virus were expressed • The proteins expressed by the recombinant poxvirus were assembled into VLPs [ABSTRACT FROM AUTHOR]

Mpox is caused by the mpox virus, which belongs to the Orthopoxvirus genus and Poxviridae family. Animal hosts, such as African rodents, mice, prairie dogs, and non‐human primates, play important roles in the development and transmission of outbreaks. Laboratory animal infection experiments have demonstrated that some animals are susceptible to mpox virus. This review summarizes the current progress on the animal hosts for mpox virus. The surveillance of mpox virus in animal hosts will provide important insights into virus tracing, analysis of mutation evolutionary patterns, transmission mechanisms, and development of control measures. [ABSTRACT FROM AUTHOR]

Simple Summary: Lumpy skin disease (LSD) is an economically important viral disease of cattle caused by the lumpy skin disease virus (LSDV) of the Poxviridae family. It was first reported in Armenia in 2015 when the disease was rapidly identified with no further spread from the initial outbreak. This was followed by a vaccination campaign to help keep the disease from returning. Vaccination can be a powerful tool for preventing the spread of transboundary diseases, but there is currently no single vaccine that protects cattle from all strains of LSD, with many vaccines providing various results. We sought to assess the quality of vaccination currently used in Armenia by evaluating the antibody response of a dry culture sheep pox virus-based vaccine against LSD in cattle. Cattle were able to produce protective antibodies >80%, which should protect against lumpy skin disease, based on previous observations, but suggests more work is needed. We have also observed no adverse side-effects in cattle following vaccination. In an area that is not suffering from continuous outbreaks, we suggest this vaccine could be a safe alternative for protection from LSD in cattle. Lumpy skin disease (LSD) is a highly infectious viral disease of cattle caused by LSD virus (LSDV), which was first reported in Armenia in late 2015. It was identified in pasture-raised cattle near the border with Iran. Currently, vaccination plays a key role in preventing further incursion of disease in high-risk areas. The purpose of this work was to assess the quality of vaccination currently used in Armenia by determining the immune response of the heterologous dry culture sheep pox virus-based vaccine against LSD in cattle. Seroprevalence and seroconversion testing was carried out using an ELISA to detect specific antibodies against LSD before and 30 days after vaccination in three adjacent regions of Armenia (Ararat, Armavir, Gegharkunik). Ixodes ticks were also examined for the presence of LSDV via real-time PCR. We found that the heterologous vaccine used in Armenia creates a high level of population immunity of 86.09% (83.83–87.97%) and no adverse side effects were observed in cattle. Of the 6 types of Ixodes ticks identified and tested, we found no evidence of LSDV circulating in these vectors. These results suggest that regular serological monitoring via ELISA and heterologous vaccination should continue in areas of Armenia at high risk for incursion of LSD to reduce the spread of this highly infectious transboundary disease. [ABSTRACT FROM AUTHOR]

Nucleus accumbens-associated 1 (NAC1) is a member of pox virus and zinc finger/bric-a-brac tramtrack broad complex (BTB/POZ) gene family. Overexpression of NAC1 is implicated in cancer development, recurrence and chemotherapy resistance. In our previous study, we found NAC1 was a potential small ubiquitin-like modifier (SUMO) substrate in prostate cancer cells. However, there was still lack of evidences to further support and validate the result. In this work, we found that NAC1 is a multi-SUMO-sites acceptor. The SUMO acceptor lysines were K167, K318, K368, K483 and K498. SUMOylation didn't alter the localization of NAC1, but facilitated the formation of NAC1 nuclear bodies. Compared with NAC1 wild type (NAC1 WT), the SUMO-sites mutant of NAC1 (NAC1 SM) suppressed cell proliferation and tumor growth in cellular and animal levels. This work uncovered the function of SUMOylation of NAC1 in prostate cancer cells. • NAC1 is a multi-SUMO-sites acceptor. • The SUMOylation of NAC1 facilitates the formation of NAC1 nuclear bodies. • The SUMOylation of NAC1 affects the growth of prostate cancer cells. [ABSTRACT FROM AUTHOR]

Cowpox is caused by a DNA virus known as the cowpox virus (CPXV) belonging to the Orthopoxvirus genus in the family Poxviridae. Cowpox is a zoonotic disease with the broadest host range among the known poxviruses. The natural reservoir hosts of CPXV are wild rodents. Recently, the cases of orthopoxviral infections have been increasing worldwide, and cowpox is considered the most common orthopoxviral infection in Europe. Cowpox is often a self-limiting disease, although cidofovir or anti-vaccinia gammaglobulin can be used in severe and disseminated cases of human cowpox. In this computational study, a molecular docking analysis of thymine- and arabinofuranosyl-thymine-related structures (1–21) on two cowpox-encoded proteins was performed with respect to the cidofovir standard and a 3D ligand-based pharmacophore model was generated. Three chemical structures (PubChem IDs: 123370001, 154137224, and 90413364) were identified as potential candidates for anti-cowpox agents. Further studies combining in vitro and in silico molecular dynamics simulations to test the stability of these promising compounds could effectively improve the future design of cowpox virus inhibitors, as molecular docking studies are not sufficient to consider a ligand a potential drug. [ABSTRACT FROM AUTHOR]

The monkeypox virus (MPXV) has become a major threat due to the increasing global caseload and the ongoing multi-country outbreak in non-endemic territories. Due to limited research in this avenue and the lack of intervention strategies, the present study was aimed to virtually screen bioactive phytochemicals against envelope proteins of MPXV via rigorous computational approaches. Molecular docking, molecular dynamic (MD) simulations, and MM/PBSA analysis were used to investigate the binding affinity of 12 phytochemicals against three envelope proteins of MPXV, viz., D13, A26, and H3. Silibinin, oleanolic acid, and ursolic acid were computationally identified as potential phytochemicals that showed strong binding affinity toward all the tested structural proteins of MPXV through molecular docking. The stability of the docked complexes was also confirmed by MD simulations and MM/PBSA calculations. Results from the iMODS server also complemented the findings from molecular docking and MD simulations. ADME analysis also computationally confirmed the drug-like properties of the phytochemicals, thereby asserting their suitability for consumption. Hence, this study envisions the candidature of bioactive phytochemicals as promising inhibitors against the envelope proteins of the MPXV, serving as template molecules that could further be experimentally evaluated for their efficacy against monkeypox. [ABSTRACT FROM AUTHOR]

The paper focuses on Influence of Librarians on curbing Monkey pox in Nigeria, it examines the concept of monkey pox and a brief history of it and how it got into Nigeria. Signs and symptom of monkey pox were also discussed as well as the mode of transmission which basically is through animals and from an infected person to the other. The paper further shows discussed the influence of librarians in curbing monkey pox in Nigeria. Four research objectives and four research questions were formulated for the study. Random sampling technique will be used to draw 250 health draws from the 3 senatorial zones were used as the population. The data collected use descriptive statistics analysis to generate frequencies and percentages to answer the research questions. Findings of the shows that monkey pox can be curbed in Benue State using various methods and strategies speculated. Monkey pox is a rare zoonotic viral infection caused by the monkey pox virus, a genus of Orthopoxvirus in the Pox family of viruses that includes smallpox, cowpox and vaccinia viruses. The clinical signs include enlarged lymph nodes, especially the sub-mental, submandibular, cervical, and inguinal nodes. Transmission is in two modes-animal to human and human to human. Prevention of contact with natural hosts of the virus will help to break the transmission from animal to human. Avoidance of contact with the body fluids and personal items of infected persons will prevent human-human transmission. [ABSTRACT FROM AUTHOR]

Plum pox virus (PPV) is a causal agent of the stone fruit tree sharka disease that often causes enormous economic losses. Due to its worldwide distribution and economic importance, rapid and reliable diagnostic technologies are becoming increasingly important for successful management of sharka disease. In this study, we have produced two super-sensitive and specific anti-PPV monoclonal antibodies (i.e., MAbs 13H4 and 4A11). Using these two MAbs, we have now developed a dot enzyme-linked immunosorbent assay (dot-ELISA) and a colloidal gold immunochromatographic strip (CGICS) assay. These two technologies can be used to quickly and reliably detect PPV. The results of these sensitivity assays confirmed that the dot-ELISA and CGICS assays could detect PPV infection in apricot tree leaf crude extracts diluted up to 1:5120 and 1:6400 (w/v), respectively. Further analyses using field-collected apricot tree leaf samples showed that the detection endpoint of the dot-ELISA was ~26 times above that obtained through RT-PCR, and the CGICS was as sensitive as RT-PCR. This present study is to broaden the knowledge about detection limits of dot-ELISA and CGICS for PPV monitoring. We consider that these newly developed dot-ELISA and CGICS are particularly useful for large scale PPV surveys in fields. [ABSTRACT FROM AUTHOR]