VirusDiseasePub Date : 2023-09-01Epub Date: 2023-09-17DOI: 10.1007/s13337-023-00838-7
Ganesh Kumar Sarvesan, Krupakar Parthasarathy, Chirayu Padhiar, HariBalaji V
{"title":"Genotypic characterization of HPV serotypes in cervical samples from Indian women: a multi centric study.","authors":"Ganesh Kumar Sarvesan, Krupakar Parthasarathy, Chirayu Padhiar, HariBalaji V","doi":"10.1007/s13337-023-00838-7","DOIUrl":"10.1007/s13337-023-00838-7","url":null,"abstract":"<p><p>Human papilloma virus (HPV infection) plays a important role in causing cervical cancer. Out of 184 different HPV genotypes, 40 diverse types only can cause anogenital infection. HPV present in >99% of cervical cancers with high risk types (16, 18) associated with cancer and Low risk types (6, 11) are associated with genital warts. Aim of the study is to determine the epidemiology of HPV infection in Indian women's population. Three hundred and thirty four liquid based cytology (LBC) samples were collected across India from the different age groups of Indian women. Pap smear, PCR and gene sequencing tests were performed for the collected LBC samples. Low risk serotype 6 (16.7%) were detected compared to other high risk serotypes. Majority of positive cases were observed in the age group between 19 and 39 groups. Northern part of India contributes high (7.1%) in HPV infection compared to other regions of India. Reports from these studies covered few regions of India showing a wide range in the prevalence of HPV infection and serotype distribution due to diversified socio economic and geo climatic conditions. This study aims to identify the epidemiology of HPV in the Indian population and concludes that early and periodic screening of women for HPV can avoid the risk of cervical cancer at the early stage of infection.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 3","pages":"395-401"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533473/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41154832","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}
VirusDiseasePub Date : 2023-09-01Epub Date: 2023-09-08DOI: 10.1007/s13337-023-00837-8
S Naveen Nayaka, Oinam Washington Singh, Pradeep Kumar, Anirban Roy, Bikash Mandal
{"title":"Geographical distribution of tomato-infecting begomoviruses in major cucurbits in India: a diagnostic analysis using begomovirus species specific PCR.","authors":"S Naveen Nayaka, Oinam Washington Singh, Pradeep Kumar, Anirban Roy, Bikash Mandal","doi":"10.1007/s13337-023-00837-8","DOIUrl":"10.1007/s13337-023-00837-8","url":null,"abstract":"<p><p>Cucurbits are an essential summer-season vegetable crops, but they are highly vulnerable from a range of abiotic and biotic factors. One of the significant biotic factors posing a growing menace to the production of major cucurbits in India is the emergence of tomato-infecting begomoviruses. In this study, we utilized PCR-based species-specific primers, developed earlier in our laboratory for the detection of begomoviruses infecting tomato and chilli plants, to identify begomoviruses in cucurbits across various regions of India. Leaf samples from major cucurbits were collected from different regions of Haryana, Delhi, Uttar Pradesh, Chhattisgarh, Maharashtra, Telangana and Karnataka, during the year 2020-2021. Total nucleic acid (TNA) was extracted from the samples and subjected to PCR using a generic primer specific to begomoviruses. The samples that exhibited positive amplification were further tested using six different species-specific primers targeting specific begomovirus species, namely <i>Tomato leaf curl New Delhi virus</i> (ToLCNDV), <i>Tomato leaf curl Palampur virus</i> (ToLCPalV), <i>Tomato leaf curl Bangalore virus</i> (ToLCBV), <i>Tomato leaf curl Joydebpur virus</i> (ToLCJoV), <i>Tomato leaf curl Gujarat virus</i> (ToLCGuV), and <i>Chilli leaf curl virus</i> (ChiLCV). The PCR analysis revealed that among the 551 plant samples tested, a total of 124 samples exhibited positive amplification using the universal begomovirus PCR. Specifically, 47 samples tested positive for ToLCNDV, 73 samples were positive for ToLCPalV and only one sample showed positive amplification for ChiLCV. However, none of the samples tested positive for ToLCJoV, ToLCGuV and ToLCBV. These findings from our study indicate the prevalence of ToLCNDV and ToLCPalV in major cucurbits across India. Furthermore, the study highlights the varied distribution of begomoviruses in major cucurbits between northern and southern regions of India.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 3","pages":"421-430"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533461/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41140985","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}
VirusDiseasePub Date : 2023-09-01Epub Date: 2023-09-19DOI: 10.1007/s13337-023-00840-z
Houda Boukhrissa, Salah Mechakra, Abbes Mahnane, Abdelmadjid Lacheheb
{"title":"Viral hepatitis E, zoonotic transmission in Algeria.","authors":"Houda Boukhrissa, Salah Mechakra, Abbes Mahnane, Abdelmadjid Lacheheb","doi":"10.1007/s13337-023-00840-z","DOIUrl":"10.1007/s13337-023-00840-z","url":null,"abstract":"<p><p>Viral hepatitis E, a major cause of acute viral hepatitis in adults, is a global public health problem. The zoonotic potential of the virus is currently accepted in developed countries. In developing countries, where transmission is mainly enteric, data on the animal reservoir are very limited. Our objective was to identify a possible risk of zoonotic transmission in our region (eastern Algeria). Four hundred and thirty four sera from blood donors were analysed by an-ti-HEV IgG antibodies detection using a commercial ELISA kit. Study participants were asked about demographics, contact with farm animals, pets, rats, and with live or shot game during a hunting activity. The anti-HEV IgG seroprevalence was 17.05%. Two risk factors were identified; rat contact with a seroprevalence rate at 51.2% (<i>p</i> < 1p.1000), OR = 6.736 [95% CI 3, 42-13.26] and game contact with a seroprevalence at 33% (<i>p</i> = 0.003), OR = 2.76 [95% CI 1.37-5.56]. In summary, zoonotic transmission is possible in our region. Rats and game should be investigated for a probable animal reservoir.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 3","pages":"389-394"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533760/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41154833","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}
VirusDiseasePub Date : 2023-09-01Epub Date: 2023-08-09DOI: 10.1007/s13337-023-00833-y
Manesh Kumar Panner Selvam, Vijayrani Kanagaraj, Kumanan Kathaperumal, Ruth H Nissly, Janet M Daly, Suresh V Kuchipudi
{"title":"Comparative transcriptome analysis of spleen of Newcastle Disease Virus (NDV) infected chicken and Japanese quail: a potential role of NF-κβ pathway activation in NDV resistance.","authors":"Manesh Kumar Panner Selvam, Vijayrani Kanagaraj, Kumanan Kathaperumal, Ruth H Nissly, Janet M Daly, Suresh V Kuchipudi","doi":"10.1007/s13337-023-00833-y","DOIUrl":"10.1007/s13337-023-00833-y","url":null,"abstract":"<p><p>Newcastle disease (ND) affects a few hundred avian species including chicken and several species of domestic and wild birds. The clinical outcome of Newcastle disease virus (NDV) infection ranges from mild to severe fatal disease depending on the NDV pathotype and the host species involved. Japanese quails serve as natural reservoirs of NDV and play important role in NDV epidemiology. While infection of chicken with velogenic NDV results in severe often fatal illness, the same infection in Japanese quails results in inapparent infection. The molecular basis of this contrasting clinical outcomes of NDV infection is not yet clearly known. We compared global gene expression in spleen of chicken and Japanese quails infected with lentogenic and velogenic NDVs. We found contrasting regulation of key genes associated with NF-κB pathway and T-cell activation between chicken and Japanese quails. Our data suggests association of NDV resistance in Japanese quails to activation of NF-κB pathway and T cell proliferation.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13337-023-00833-y.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 3","pages":"402-409"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533468/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41136733","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}
VirusDiseasePub Date : 2023-09-01Epub Date: 2023-09-17DOI: 10.1007/s13337-023-00842-x
El-Shaymaa El-Nahass, Mohamed Kamal Abdelhamid, Ahmed Ali, Adel A Shalaby, Mohamed Shaalan
{"title":"Pathological assessment and tissue tropism of two different Egyptian infectious bronchitis strains.","authors":"El-Shaymaa El-Nahass, Mohamed Kamal Abdelhamid, Ahmed Ali, Adel A Shalaby, Mohamed Shaalan","doi":"10.1007/s13337-023-00842-x","DOIUrl":"10.1007/s13337-023-00842-x","url":null,"abstract":"<p><p>Avian infectious bronchitis is one of the most common viral infections in chickens affecting all ages. The tropism of infectious bronchitis virus (IBV) strains became broader and more variable posing major implications for the effective control of IBV infection. In this study, two IBV viruses representing classic and variant strains were inoculated intranasally into day-old SPF chicks (10<sup>5</sup> EID<sub>50</sub>/0.2 ml/bird). Clinical signs were observed for 15 days post-infection (DPI). Five chicks from each group were euthanized at 2, 4, 6, 8, 10, 12, and 15 DPI for histopathology and virus antigen detection by IHC and quantitative rRT-PCR. Results revealed that both classic and variant IBV strains induced mild clinical signs with no mortalities and fewer various histopathological lesions in infected SPF chickens. Although the viruses were detected by rRT-PCR up to 12 DPI, the affected tissues showed regeneration after 10 DPI with IHC revealing no IBV antigen. In summary, no differences were found in the behaviour of both IBV isolates in chickens. The broad tissue tropism for both IBV strains as indicated by viral antigen detection in various organs with no clinical or gross lesion suggest that the main cause of death in IBV infection under field conditions occurs as a result of complication with secondary infections rather single IBV infection. Due to positive immunostaining in the bursa, it is thought that IBV infection has immunosuppressive consequences, hence further study is required to validate this impact.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 3","pages":"410-420"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533428/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41155560","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}
VirusDiseasePub Date : 2023-09-01Epub Date: 2023-09-07DOI: 10.1007/s13337-023-00834-x
Shagun Sharma, Surabhi Shrivastava, Shankar B Kausley, Beena Rai
{"title":"Integrated point-of-care RT-PCR methods during and after COVID-19 pandemic.","authors":"Shagun Sharma, Surabhi Shrivastava, Shankar B Kausley, Beena Rai","doi":"10.1007/s13337-023-00834-x","DOIUrl":"10.1007/s13337-023-00834-x","url":null,"abstract":"<p><p>The COVID-19 pandemic has taken the world by surprise and people and organisations worldwide worked in some way or the other to combat the spread; isolate from the infected and get back to normal life, as it was before the pandemic hit. In this regard, the diagnosis of COVID-19 was at the centre of control and prevention and have seen a vehement change in every aspect, especially development of point-of-care testing for better and quick diagnosis. Among different types of techniques developed, the most important was the RT-PCR method of detection which detects nucleic acid of the virus in samples. RT-PCR is a laboratory-based method requiring trained professionals and precise steps for accurate testing. With the advent and spread of the pandemic, number of RT-PCR diagnostic centres rose significantly, and the detection process became less cumbersome, easy to use, ability to handle large volume of samples, more accurate, less time-consuming, and cost-effective. Different industries developed RT-PCR kits, reducing the efforts to prepare laboratory samples. Machines were employed for labour-driven tasks in PCR testing. In addition, new age technologies such as artificial intelligence, IoT, digital systems were combined with RT-PCR for accurate and easy testing. In this review, point-of-care RT-PCR methods, when the COVID-19 started, and the methods now, has been compared on the basis of technological advancements.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 3","pages":"356-364"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533447/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41147109","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}
{"title":"Molecular characterization suggests kinetic modulation of expression of accessory viral protein, W, in Newcastle disease virus infected DF1 cells.","authors":"B Nagaraj Nayak, Kalaimagal Rajagopal, Revathi Shunmugasundaram, Pachineella Lakshmana Rao, Saraswathy Vaidyanathan, Madhuri Subbiah","doi":"10.1007/s13337-023-00813-2","DOIUrl":"10.1007/s13337-023-00813-2","url":null,"abstract":"<p><p>Viruses adopt strategies to efficiently utilize their compact genome. Members of the family <i>Paramyxoviridae</i>, exhibit a cotranscriptional RNA editing mechanism wherein polymerase stuttering generates accessory proteins from Phosphoprotein (<i>P</i>) gene. Newcastle disease virus (NDV), an avian paramyxovirus, expresses two accessory proteins, V and W, by RNA editing. While P and V proteins are well studied, very little is known about W protein. Recent studies confirmed W protein expression in NDV and the unique subcellular localization of W proteins of virulent and avirulent NDV. We characterized the W protein of NDV strain Komarov, a moderately virulent vaccine strain. W mRNA expression ranged between 7 and 9% of total <i>P</i> gene transcripts similar to virulent NDV. However, W protein expression, detectable by 6 h, peaked at 24 h and dropped by 48 h post infection in DF1 cells indicating a kinetically regulated expression by the virus. The W protein localized in the nucleus and by mutations, a strong nuclear localization signal was identified in the C-terminal region of W protein. The viral growth kinetics study suggested neither supplementation of W protein nor subcellular localization pattern of the supplemented W protein influenced viral replication in vitro similar to that noticed in avirulent NDV. A cytoplasmic mutant of W protein localized in cytoplasm unlike specific mitochondrial colocalization as recorded in velogenic NDV strain SG10 indicating a possible role of W protein in determining the viral pathogenicity. This study describes for the first time, the distinct features of W protein of moderately virulent NDV.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13337-023-00813-2.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 2","pages":"236-247"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317930/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9800652","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}
{"title":"Human papillomaviruses and bladder cancer risk: first report in south of Iran.","authors":"Fatemeh Farshadpour, Reza Taherkhani, Mohammadreza Farzaneh","doi":"10.1007/s13337-023-00819-w","DOIUrl":"10.1007/s13337-023-00819-w","url":null,"abstract":"<p><p>Information regarding the possible carcinogenicity of human papillomaviruses (HPVs) in bladder tissue might pave the way for the prevention of bladder cancer through improving HPV vaccination of the at-risk population. To address this, this study was conducted to detect HPVs in bladder cancer tissues in the South of Iran. Bladder biopsy samples of 181 patients with bladder cancer were included in this study. The detection of HPVs was performed by nested PCR assay, targeting the L1 region of the genome, and sequencing. HPV was detected in 0.55% of the bladder cancer samples, while the non-cancerous bladder samples were negative for HPV. HPV genotype 6 was detected in this study. The HPV-positive patient was a 55-year-old man with papillary urothelial neoplasms of low malignant in stage Ta-T1. This patient was resident of Dayer city. Overall, HPV prevalence among patients with bladder cancer was not statistically associated with place of residency, gender, age, stage, and grade of the tumor (<i>P </i>value > 0.05). The presence of HPV is extremely rare in bladder cancer biopsy specimens in the south of Iran. Therefore, the results of our study rule out the possible role of HPVs in the etiology of bladder cancer. Due to the increasing air pollution in this region and high-risk jobs, and habits such as cigarette smoking and hookah smoking, the role of these factors alongside genetic factors seems more prominent than the role of HPVs in causing bladder cancer in the south of Iran.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s13337-023-00819-w.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 2","pages":"257-262"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317924/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9794389","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}
VirusDiseasePub Date : 2023-06-01Epub Date: 2023-04-15DOI: 10.1007/s13337-023-00816-z
Muluken Kebede, Demsachew Guadie, Dawit Kidanemariam, Adane Abraham
{"title":"Serological, biological and molecular characterization of viruses causing mosaic diseases on cabbage (<i>Brassica</i> sp <i>L.)</i> in Central Ethiopia.","authors":"Muluken Kebede, Demsachew Guadie, Dawit Kidanemariam, Adane Abraham","doi":"10.1007/s13337-023-00816-z","DOIUrl":"10.1007/s13337-023-00816-z","url":null,"abstract":"<p><p>The productivity of cabbage (<i>Brassica oleracea</i> var<i>. capitata)</i> in Ethiopia has been generally low due to several biotic and abiotic constraints among which are several viral diseases. There is a recent report indicating that this economically important vegetable is seriously affected in Ethiopia by cauliflower mosaic virus (CaMV) and turnip mosaic virus (TuMV). However, little information exists on the incidence and distribution of these viruses as the previous report is based on samples only from Addis Ababa. In this study, a total of 370 leaf samples were collected from 75 cabbage growing fields in Central Ethiopia in two rounds of survey. Two cabbage varieties locally known as \"<i>Habesha gomen\"</i> and <i>\"Tikur gomen\"</i> with virus-like symptoms were collected and tested with Double Antibody Sandwich Enzyme-Linked Immunosorbent Assay (DAS-ELISA) using polyclonal antibodies specific to CaMV and TuMV. Results from serological diagnosis were confirmed with PCR and Sanger sequencing. The results indicated a high incidence and wide distribution of both viruses in Central Ethiopia with an average of 29.5% infection for CaMV and 40% for TuMV. Biological inoculation tests for CaMV or TuMV or both on healthy cabbage seedlings gave similar symptoms as those observed in the field. Symptom severity was higher with co-infection of CaMV and TuMV followed by TuMV single infection. BLAST analysis showed that TuMV and CaMV isolates from Ethiopia have nucleotide identity of 95-98% and 93-98%, respectively to previously reported isolates. Phylogenetic analysis revealed that CaMV isolates from Ethiopia are closely related to isolates from USA and Italy within Group II clade whereas TuMV isolates have close similarities with isolates from World B clade including isolates from Kenya, UK, Japan and the Netherlands. The identification of the causative agents of the mosaic disease observed on cabbage in Central Ethiopia may lay the foundation for future management studies.</p>","PeriodicalId":23708,"journal":{"name":"VirusDisease","volume":"34 2","pages":"213-220"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317906/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9807272","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}