{"title":"Computational studies on rep and capsid proteins of CRESS DNA viruses","authors":"Yagavi Yadhav, Karthiga Selvaraj, Selvarajan Ramasamy, Sangita Venkataraman","doi":"10.1007/s13337-024-00858-x","DOIUrl":"https://doi.org/10.1007/s13337-024-00858-x","url":null,"abstract":"","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"2011 28","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140416630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-02DOI: 10.1007/s13337-023-00857-4
Iman Owliaee, Mehran Khaledian, Shahab Mahmoudvand, Razieh Amini, Sarah E. Abney, Farzad Beikpour, F. Jalilian
{"title":"Global investigation of the presence of adenovirus in different types of water resources: a systematic review","authors":"Iman Owliaee, Mehran Khaledian, Shahab Mahmoudvand, Razieh Amini, Sarah E. Abney, Farzad Beikpour, F. Jalilian","doi":"10.1007/s13337-023-00857-4","DOIUrl":"https://doi.org/10.1007/s13337-023-00857-4","url":null,"abstract":"","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"48 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139683612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-01DOI: 10.1007/s13337-023-00856-5
G. A. S. Tubalinal, Lawrence P. Belotindos, C. Mingala
{"title":"High positivity rate of caprine arthritis encephalitis virus in Luzon, the Philippines revealed by nested-polymerase chain reaction assay","authors":"G. A. S. Tubalinal, Lawrence P. Belotindos, C. Mingala","doi":"10.1007/s13337-023-00856-5","DOIUrl":"https://doi.org/10.1007/s13337-023-00856-5","url":null,"abstract":"","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"1 2","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139685790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-20DOI: 10.1007/s13337-023-00853-8
Mousumi Bora
{"title":"From pigs to wild boars, the rise of African swine fever in India","authors":"Mousumi Bora","doi":"10.1007/s13337-023-00853-8","DOIUrl":"https://doi.org/10.1007/s13337-023-00853-8","url":null,"abstract":"","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"48 20","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138955552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-19DOI: 10.1007/s13337-023-00854-7
P. Raja, K. S. Mallika, V. Y. Viva, M. Parthiban, G. Sathish, V. Vinitha, S. Parthiban, G. D. Raj
{"title":"Complete genome sequence and phylogenetic analysis of feline panleukopenia virus from India","authors":"P. Raja, K. S. Mallika, V. Y. Viva, M. Parthiban, G. Sathish, V. Vinitha, S. Parthiban, G. D. Raj","doi":"10.1007/s13337-023-00854-7","DOIUrl":"https://doi.org/10.1007/s13337-023-00854-7","url":null,"abstract":"","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":" 884","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138960321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The outbreak of novel SARS-CoV-2 virion has wreaked havoc with a high prevalence of respiratory illness and high transmission due to a vague understanding of the viral antigenicity, augmenting the dire challenge to public health globally. This viral member necessitates the expansion of diagnostic and therapeutic tools to track its transmission and confront it through vaccine development. Therefore, prophylactic strategies are mandatory. Virulent spike proteins can be the most desirable candidate for the computational design of vaccines targeting SARS-CoV-2, followed by the meteoric development of immune epitopes. Spike protein was characterized using existing bioinformatics tools with a unique roadmap related to the immunological profile of SARS-CoV-2 to predict immunogenic virulence epitopes based on antigenicity, allergenicity, toxicity, immunogenicity, and population coverage. Applying in silico approaches, a set of twenty-four B lymphocyte-based epitopes and forty-six T lymphocyte-based epitopes were selected. The predicted epitopes were evaluated for their intrinsic properties. The physico-chemical characterization of epitopes qualifies them for further in vitro and in vivo analysis and pre-requisite vaccine development. This study presents a set of screened epitopes that bind to HLA-specific allelic proteins and can be employed for designing a peptide vaccine construct against SARS-CoV-2 that will confer vaccine-induced protective immunity due to its structural stability.
Supplementary information: The online version contains supplementary material available at 10.1007/s13337-023-00852-9.
{"title":"Immunodominant conserved moieties on spike protein of SARS-CoV-2 renders virulence factor for the design of epitope-based peptide vaccines.","authors":"Subhashree Mohapatra, Santosh Kumar, Shashank Kumar, Atul Kumar Singh, Bismita Nayak","doi":"10.1007/s13337-023-00852-9","DOIUrl":"10.1007/s13337-023-00852-9","url":null,"abstract":"<p><p>The outbreak of novel SARS-CoV-2 virion has wreaked havoc with a high prevalence of respiratory illness and high transmission due to a vague understanding of the viral antigenicity, augmenting the dire challenge to public health globally. This viral member necessitates the expansion of diagnostic and therapeutic tools to track its transmission and confront it through vaccine development. Therefore, prophylactic strategies are mandatory. Virulent spike proteins can be the most desirable candidate for the computational design of vaccines targeting SARS-CoV-2, followed by the meteoric development of immune epitopes. Spike protein was characterized using existing bioinformatics tools with a unique roadmap related to the immunological profile of SARS-CoV-2 to predict immunogenic virulence epitopes based on antigenicity, allergenicity, toxicity, immunogenicity, and population coverage. Applying <i>in silico</i> approaches, a set of twenty-four B lymphocyte-based epitopes and forty-six T lymphocyte-based epitopes were selected. The predicted epitopes were evaluated for their intrinsic properties. The physico-chemical characterization of epitopes qualifies them for further in vitro and in vivo analysis and pre-requisite vaccine development. This study presents a set of screened epitopes that bind to HLA-specific allelic proteins and can be employed for designing a peptide vaccine construct against SARS-CoV-2 that will confer vaccine-induced protective immunity due to its structural stability.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13337-023-00852-9.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 4","pages":"456-482"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686954/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138478719","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-11-20DOI: 10.1007/s13337-023-00850-x
V Venkataravanappa, K V Ashwathappa, Shridhar Hiremath, L Manjunatha, K S Shankarappa, M Krishna Reddy, C N Lakshminarayana Reddy
The numerous plants of Solanum nigrum L, and Physalis minima L, well-known weeds with medicinal properties in agriculture and horticulture crops exhibiting severe mosaic, enation and leaf curl symptoms, were collected from the Varanasi and Mirzapur districts of Uttar Pradesh, India. The begomovirus infection in S. nigrum and P. minima was validated by PCR using virus-specific primers. The whole genome of the represented isolate of S. nigrum (SN1), P. minima (PM1), and beta satellite was amplified, cloned and sequenced. The SDT analysis showed that the DNA-A of PM1 and SN1 isolate showed the highest nt identity of 87.4 to 99.1%, with several chilli leaf curl virus (ChiLCuV) isolates from India and Oman, respectively. The betasatellite sequence (PM1β) obtained from the PM1 isolate showed a very low identity of 83.1-84.5%. A demarcation threshold of 91% for betasatellite species delineation has led to identifying a new betasatellite in the PM1 sample. This unique betasatellite has been named "physalis minima leaf curl betasatellite," indicating its novelty with the plant. Whereas, betasatellite sequence (SN1β) obtained from the SN1 sample showed 86.8-91.2% nucleotide identity with ChiLCB isolates infecting several crops in Indian subcontinents. The RDP analysis of the viral genome and betasatellite of SN1 and PM1 isolates revealed recombination in substantial portions of their genetic makeup, which appeared to have originated from pre-existing begomoviruses known to infect diverse host species. The present research also highlights the potential role of these plants as significant reservoir hosts for ChiLCuV in chili plants.
Supplementary information: The online version contains supplementary material available at 10.1007/s13337-023-00850-x.
在印度北方邦的Varanasi和Mirzapur地区收集了大量的Solanum nigrum L和Physalis minima L,这两种在农业和园艺作物中具有药用价值的知名杂草,表现出严重的花叶、萎蔫和卷曲症状。采用病毒特异性引物,用PCR方法验证了血吸虫和小螺旋体的begomvirus感染。对具有代表性的SN1、PM1和β卫星分离株进行全基因组扩增、克隆和测序。SDT分析表明,PM1和SN1分离物的DNA-A与来自印度和阿曼的辣椒卷曲叶病毒(ChiLCuV)分离物的DNA-A同源性最高,分别为87.4 ~ 99.1%。从PM1分离物中获得的betasatsatellite序列(PM1β)的同源性很低,为83.1 ~ 84.5%。betasat卫星物种划分阈值为91%,从而在PM1样品中确定了一个新的betasat卫星。这种独特的betasatella被命名为“physalis minima leaf curl betasatella”,表明它与这种植物的新颖性。而从SN1样品中获得的betasatsatellite序列(SN1β)与感染印度次大陆几种作物的ChiLCB分离株核苷酸同源性为86.8-91.2%。对SN1和PM1分离株的病毒基因组和betasatsatellite的RDP分析显示,它们基因组成的大部分重组,似乎源于已知感染多种宿主物种的先前存在的begomovirus。本研究还强调了这些植物作为辣椒植物中ChiLCuV的重要宿主的潜在作用。补充信息:在线版本包含补充资料,提供地址为10.1007/s13337-023-00850-x。
{"title":"Begomovirus and DNA-satellites association with mosaic and leaf curl disease of <i>Solanum nigrum</i> and <i>Physalis minima</i>: the new hosts for chilli leaf curl virus.","authors":"V Venkataravanappa, K V Ashwathappa, Shridhar Hiremath, L Manjunatha, K S Shankarappa, M Krishna Reddy, C N Lakshminarayana Reddy","doi":"10.1007/s13337-023-00850-x","DOIUrl":"10.1007/s13337-023-00850-x","url":null,"abstract":"<p><p>The numerous plants of <i>Solanum nigrum</i> L, and <i>Physalis minima</i> L, well-known weeds with medicinal properties in agriculture and horticulture crops exhibiting severe mosaic, enation and leaf curl symptoms, were collected from the Varanasi and Mirzapur districts of Uttar Pradesh, India. The begomovirus infection in <i>S. nigrum</i> and <i>P. minima</i> was validated by PCR using virus-specific primers. The whole genome of the represented isolate of <i>S. nigrum </i>(SN1), <i>P. minima</i> (PM1), and beta satellite was amplified, cloned and sequenced. The SDT analysis showed that the DNA-A of PM1 and SN1 isolate showed the highest nt identity of 87.4 to 99.1%, with several chilli leaf curl virus (ChiLCuV) isolates from India and Oman, respectively. The betasatellite sequence (PM1β) obtained from the PM1 isolate showed a very low identity of 83.1-84.5%. A demarcation threshold of 91% for betasatellite species delineation has led to identifying a new betasatellite in the PM1 sample. This unique betasatellite has been named \"physalis minima leaf curl betasatellite,\" indicating its novelty with the plant. Whereas, betasatellite sequence (SN1β) obtained from the SN1 sample showed 86.8-91.2% nucleotide identity with ChiLCB isolates infecting several crops in Indian subcontinents. The RDP analysis of the viral genome and betasatellite of SN1 and PM1 isolates revealed recombination in substantial portions of their genetic makeup, which appeared to have originated from pre-existing begomoviruses known to infect diverse host species. The present research also highlights the potential role of these plants as significant reservoir hosts for ChiLCuV in chili plants.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13337-023-00850-x.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 4","pages":"504-513"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686937/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138478718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-01Epub Date: 2023-11-15DOI: 10.1007/s13337-023-00851-w
G Tejaswi, R V Chandrasekhar Reddy, N M Ponnanna, L N Sarangi
Bovine alphaherpesvirus-1 (BoAHV-1) is an important viral pathogen that causes significant economic losses to the dairy industry. The present study aimed to determine the prevalence of BoAHV-1 in cases of bovine reproductive disorder. Clinical samples were collected from various villages in Gujarat using specialized FTA® cards and were tested using real-time PCR assay targeting the gB gene of BoAHV-1. Out of 401 animals, 18.20% (95% CI: 14.74-22.28%) tested positive for BoAHV-1 DNA. The percentage positivity of BoAHV-1 was 20.37% in abortion cases and 19.55% in retention of fetal membrane cases, while only one out of nine metritis cases screened in the study was positive for BoAHV-1 DNA. A higher percentage positivity in buffaloes (22.14%) compared to cattle (16.30%) was recorded, but this difference was not statistically significant (p = 0.169). The frequency of BoAHV-1 detection was higher among crossbreeds (16.76%) and exotics (19.61%) than among indigenous cattle (8.82%), although this difference was not statistically significant (p = 0.400). There was also no significant difference in frequency distribution among animals of varying parity, ranging from 15.20 to 33.33% (p = 0.540). This study confirms the widespread circulation of BoAHV-1 and highlights the need for its control and prevention.
{"title":"Molecular detection of bovine alphaherpesvirus-1 in cases of reproductive disorders among cattle and buffaloes in Gujarat.","authors":"G Tejaswi, R V Chandrasekhar Reddy, N M Ponnanna, L N Sarangi","doi":"10.1007/s13337-023-00851-w","DOIUrl":"10.1007/s13337-023-00851-w","url":null,"abstract":"<p><p>Bovine alphaherpesvirus-1 (BoAHV-1) is an important viral pathogen that causes significant economic losses to the dairy industry. The present study aimed to determine the prevalence of BoAHV-1 in cases of bovine reproductive disorder. Clinical samples were collected from various villages in Gujarat using specialized FTA<sup>®</sup> cards and were tested using real-time PCR assay targeting the <i>gB</i> gene of BoAHV-1. Out of 401 animals, 18.20% (95% CI: 14.74-22.28%) tested positive for BoAHV-1 DNA. The percentage positivity of BoAHV-1 was 20.37% in abortion cases and 19.55% in retention of fetal membrane cases, while only one out of nine metritis cases screened in the study was positive for BoAHV-1 DNA. A higher percentage positivity in buffaloes (22.14%) compared to cattle (16.30%) was recorded, but this difference was not statistically significant (<i>p</i> = 0.169). The frequency of BoAHV-1 detection was higher among crossbreeds (16.76%) and exotics (19.61%) than among indigenous cattle (8.82%), although this difference was not statistically significant (<i>p</i> = 0.400). There was also no significant difference in frequency distribution among animals of varying parity, ranging from 15.20 to 33.33% (<i>p</i> = 0.540). This study confirms the widespread circulation of BoAHV-1 and highlights the need for its control and prevention.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 4","pages":"526-530"},"PeriodicalIF":0.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686898/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138478720","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}