Relevant bibliographies by topics / Virus detection method

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Virus detection method'

Author: Grafiati
Published: 28 May 2022
Last updated: 31 July 2025

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Journal articles on the topic "Virus detection method"

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Liu, Yanbing, Shousheng Jia, and Congcong Xing. "A Novel Behavior-Based Virus Detection Method for Smart Mobile Terminals." Discrete Dynamics in Nature and Society 2012 (2012): 1–12. http://dx.doi.org/10.1155/2012/262193.

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The security of smart mobile terminals has been an increasingly important issue in recent years. While there are extensive researches on virus detections for smart mobile terminals, most of them share the same framework of virus detection as that for personal computers, and few of them tackle the problem from the standpoint of detection methodology. In this paper, we propose a behavior-based virus detection method for smart mobile terminals which signals the existence of malicious code through identifying the anomaly of user behaviors. We first propose a model to collect and analyze user behav
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Abdellatif, Berkat. "Metamorphic computer virus detection by Case-Based Reasoning (CBR) methods." International Journal of Software Engineering & Applications (IJSEA) 2, no. 4 (2021): 1–10. https://doi.org/10.5281/zenodo.4730062.

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Metamorphic virus employs code obfuscation techniques to mutate itself. It absconds from signature based detection system by modifying internal structure without compromising original functionality. -In this paper, we propose a new method, for detecting metamorphic computer viruses, that is based on the technique of Case-Based Reasoning (CBR). In this method: -Can detect similar viruses with high probability. - The updating of the virus database is done automatically without connecting to the Internet. Whenever a new virus is detected, it will be automatically added to the database used by our
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САВЕНКО, БОГДАН. "WORM-VIRUS DETECTION METHOD ACCORDING TO MULTI-CLASS CLASSIFICATION." Herald of Khmelnytskyi National University. Technical sciences 331, no. 1 (2024): 18–28. http://dx.doi.org/10.31891/2307-5732-2024-331-2.

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The work presents the results of research on worm viruses and methods of their detection. Malware distribution happens all the time. The analyzed modern tools and systems for prevention, detection and countermeasures against malicious software and computer attacks are quite effective, provide a high percentage of detection and function at an adequate level. But criminals constantly study the capabilities of such tools and systems, improve malicious software and computer attacks, and achieve certain results. Therefore, developers of tools and systems for prevention, detection and countermeasure
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Tyumentseva, M. A., A. I. Tyumentsev, A. N. Prelovskaya, and V. G. Akimkin. "Optimization of a Method for Detecting Single copies of Hepatitis B Virus DNA using CRISPR/Cas systems." Epidemiology and Vaccinal Prevention 23, no. 6 (2025): 114–28. https://doi.org/10.31631/2073-3046-2024-23-6-114-128.

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Relevance. Hepatitis B virus (HBV) is the etiologic agent of acute and chronic hepatitis B in humans. WHO recommends the use of sensitive laboratory assays based on nucleic acid amplification methods to detect HBV DNA. A method for detecting single copies of hepatitis B virus DNA using CRISPR/Cas systems was previously developed for ultrasensitive detection of HBV DNA.Aims. The aim of present study was to optimize the method for detecting single copies of hepatitis B virus DNA using CRISPR/Cas systems.Materials and methods. To obtain amplified fragments of the hepatitis B virus genome, 22 olig
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Lee, Brian W., Russell F. Bey, Mary J. Baarsch, and Randy R. Simonson. "ELISA Method for Detection of Influenza A Infection in Swine." Journal of Veterinary Diagnostic Investigation 5, no. 4 (1993): 510–15. http://dx.doi.org/10.1177/104063879300500402.

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An antigen-capture enzyme-linked immunosorbent assay (ELISA) was developed to monitor virus shedding associated with experimental infection with a field strain of swine influenza in pigs. The assay consisted of a monoclonal anti-nucleoprotein capture antibody and a biotinylated rabbit anti-influenza A (H1N1) sandwich antibody. The antigen-capture system was capable of detecting as little as 1 ng/ml purified virus. The ELISA system surpassed egg cultivation procedures in the detection of low levels of shedding virus. Egg cultivation procedures indicated that most viral shedding had ceased by da
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Komínek, P. "Selection of RNA isolation method for molecular detection of grapevine viruses." Plant Protection Science 38, SI 2 - 6th Conf EFPP 2002 (2017): 267–70. http://dx.doi.org/10.17221/10463-pps.

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Grapevines infected with Grapevine leafroll-associated virus-1 (GLRaV-1) and Grapevine leafroll-associated virus-3 (GLRaV-3) were selected. Total RNA was isolated from grapevine phloem tissue scrapped from dormant canes by three different methods: extraction with urea buffer followed with phenol-chloroform extraction, method using Concert<sup>TM</sup> reagent (Invitrogen) followed with chloroform-isopropylalcohol extraction, and procedure using RNeasy Plant Mini Kit (Qiagen). The highest yield of RNA was obtained using Concert<sup>TM</sup> reagent. If this RNA was used
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Ilyas, Syafruddin. "Human Papillomavirus: Detection Method and Infection." International Journal of Ecophysiology 4, no. 1 (2023): 82–91. http://dx.doi.org/10.32734/ijoep.v4i1.11153.

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The Human Papilloma Virus (HPV) is a small non-enveloped DNA virus, around 8000 bp in size and only humans become its host by infecting skin epithelial tissue, human oral mucosa and anogenital epithelium. Human Papillomavirus is often found in patients and is ranked as the second most malignant disease in women, belonging to the Alphapapillomavirus genus. HPV infection can be identified through the structure of the HPV virus itself and the particles contained therein which initiate the carcinogenic process of its host. The research methods used in this study are literature studies. The literat
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Rowhani, Adib, Lenka Biardi, Geoffrey Routh, Steve D. Daubert, and Deborah A. Golino. "Development of a Sensitive Colorimetric-PCR Assay for Detection of Viruses in Woody Plants." Plant Disease 82, no. 8 (1998): 880–84. http://dx.doi.org/10.1094/pdis.1998.82.8.880.

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Diagnostic methods employing the polymerase chain reaction (PCR) provide the most sensitive means currently available for detecting viruses in woody plants. A new technique has been tested that does not rely on gel electrophoresis or molecular hybridization to detect virus-specific PCR products. This colorimetric method for detection of PCR products from woody plants was demonstrated to be at least as sensitive as gel analysis. When combined with immunocapture of virions from plant sap, colorimetric detection provides a means to apply PCR technology to a large number of samples. Here, we repor
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Moeis, Maelita Ramdani, Anis Puji Rahayu, Nisa Ihsani, and Wulan Pertiwi. "Coronavirus-SARS-CoV-2: Biology and Problems in rRT-PCR Detection." Borneo Journal of Pharmacy 3, Special-1 (2020): 136–45. http://dx.doi.org/10.33084/bjop.v3ispecial-1.1429.

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Coronavirus disease 2019 (COVID-19) first appeared in China in December 2019 and was declared a pandemic by the World Health Organization. COVID-19 is caused by Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2), a new virus previously unknown to humans. Here we look at what is known about this virus, the main method for detecting the presence of this virus in a person who is used as a golden standard, and the problems that could arise in this detection method. Understanding the biology of the virus and the strengths and weaknesses of the detection method are important for patient m
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Cheremiskina, A. A., D. V. Shanshin, V. M. Generalov, et al. "Method for rapid detection of recombinant protein E of West Nile virus." Izmeritel`naya Tekhnika, no. 10 (December 9, 2024): 57–64. https://doi.org/10.32446/0368-1025it.2024-10-57-64.

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It was noted that the detection time of West Nile virus protein E by standard methods – immunoenzyme assay for West Nile virus antigen, antibody seroconversion, polymerase chain reaction with reverse transcription, virus isolation and neutralization assay, is at least one hour. West Nile virus (genus Flavivirus) belongs to the Japanese encephalitis antigenic complex of the family Flaviviridae and is capable of causing West Nile fever or severe West Nile disease. To increase the detection rate of recombinant protein E of West Nile virus, an express detection method using the developed promising
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Dissertations / Theses on the topic "Virus detection method"

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Milne, Sarah Amelia. "The development of a sensitive and reliable molecular method for the detection of human pathogenic viruses in bivalve molluscs." Thesis, University of Aberdeen, 2002. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU159700.

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The overall aim of this project was to develop a sensitive, specific and reliable molecular assay for the detection of human pathogenic viruses in shellfish. In initial studies, 'viral surrogates' were used to evaluate two different assay formats, the reverse transcriptase-polymerase chain reaction-enzyme-linked immunosorbent assay (RT-PCR-ELISA) and the enzyme-labelled deoxynucleic acid-enzyme-linked coagulation assay (EDNA-ELCA). Each format was tested for ease of use, reliability and sensitivity, when compared with ethidium bromide gel detection. The RT-PCR-ELISA proved to be a successful a
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Gallegos, Karen M. "Characterization of Pathogens for Potential Diagnostic Tests." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367942509.

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PANDIAN, ARIVAZHAGAN. "Optimization of the Information Collection Rule’s Adsorption/Elution Method for Virus Detection and Enumeration." University of Cincinnati / OhioLINK, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=ucin975357716.

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Cha, Wonhee. "Application of multiplex branched DNA method for the detection and study of avian inlfuenza [i.e. influenza] virus." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1211475165.

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Walsh, Helen Ann. "Rapid Detection of Grapevine Leafroll-associated virus Type 3 using the reverse transcription loop-mediated amplification method." Diss., University of Pretoria, 2013. http://hdl.handle.net/2263/41018.

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Grapevine Leafroll disease (GLD), one of the most destructive diseases of grapevines, has been found in every country where grapevines are grown. Grapevine Leafroll associated virus type 3 (GLRaV-3), one of several viruses associated with GLD globally, is the most prevalent virus in South African grapevines and therefore control of GLRaV-3 takes high priority in any strategy aimed at control of GLD. GLD can be controlled through the use of an integrated strategy which includes using certified plant material, controlling insect vectors through use of systemic insecticides and the removal
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Payne, Holly Ann. "DEVELOPMENT OF A METHOD FOR POLIOVIRUS DETECTION IN FRESHWATER CLAMS (COLORADO RIVER, CORBICULA FLUMINEZ)." Thesis, The University of Arizona, 1985. http://hdl.handle.net/10150/275315.

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Musial, Cora Estabrook. "Development of a method for the detection of Cryptosporidium in water and selected studies on hepatitis A virus." Diss., The University of Arizona, 1985. http://etd.library.arizona.edu/etd/GetFileServlet?file=file:///data1/pdf/etd/azu_e9791_1985_343_sip1_w.pdf&type=application/pdf.

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Plante-Driscoll, Michelle L. "Development of a novel method for the rapid concentration and detection of norovirus and hepatitis A virus in foods." Thesis, University of Ottawa (Canada), 2008. http://hdl.handle.net/10393/27604.

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Noroviruses (NoV) and Hepatitis A viruses (HAV) are the most commonly implicated viruses in foodborne disease. Their transmission is mainly via the fecal-oral route and distribution of contaminated foods has lead to large outbreaks. Thus, it is crucial that contaminated foods be identified promptly. Detection by cell culture is not possible for these viruses so that researchers rely on the reverse transcription polymerase chain reaction (RT-PCR). Prior to detection, however, viruses must be isolated from foods and, as of yet, no one method has been found applicable to a large variety of food m
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Lemaire, Olivier. "Contribution a l'etude des proprietes biologiques des rna du virus de la rhizomanie (beet necrotic yellow vein virus) et de leur role dans l'etiologie de la maladie." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13115.

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BERNA, ANNE. "Les proteines non structurales du virus de la mosaique de la luzerne : immunodetection et role possible dans la multiplication du virus." Université Louis Pasteur (Strasbourg) (1971-2008), 1986. http://www.theses.fr/1986STR13039.

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Utilisation de la technique des immunoempreintes pour detecter les 3 proteines non structurales du virus de la mosaique de la luzerne dans des tabacs infectes. Ces proteines se trouvent dans la fraction membranaire contenant le complexe de replication viral. Les proteines p1 et p2 ont la meme cinetique d'apparition que la replicase au cours de la virose. Il est possique que p2 soit la polymerase virale; p1 ne participerait qu'a la synthese des brins. P3 pourrait etre impliquee dans la diffusion systemique du virus
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Books on the topic "Virus detection method"

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O, Myŏng-ju. Sikpʻum chung sikchungdok pairŏsŭ kŏmchʻulpŏp yŏnʼgu =: A study on detection method of food-borne virus. Sikpʻum Ŭiyakpʻum Anjŏnchʻŏng, 2007.

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L, Wiedbrauk Danny, and Farkas Daniel H, eds. Molecular methods for virus detection. Academic Press, 1995.

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service), SpringerLink (Online, ed. Hepatitis A Virus in Food: Detection and Inactivation Methods. Springer New York, 2013.

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D, Sobsey Mark, and AWWA Research Foundation, eds. Enteric virus detection in water by nucleic acid methods. AWWA Research Foundation and American Water Works Association, 1996.

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Liu, Dongyou. Molecular detection of human viral pathogens. CRC Press, 2011.

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Liu, Dongyou. Molecular detection of human viral pathogens. CRC Press, 2011.

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Melnick, Joseph L. Improved methods for hepatitis A virus and rotavirus concentration and detection in recreational, raw potable, and finished waters. U.S. Environmental Protection Agency, Environmental Monitoring and Support Laboratory, 1988.

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Molecular Methods for Virus Detection. Elsevier, 1995. http://dx.doi.org/10.1016/b978-0-12-748920-9.x5000-6.

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Farkas, Daniel H., and Danny L. Wiedbrauk. Molecular Methods for Virus Detection. Elsevier Science & Technology Books, 1995.

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Wick, Charles H. Integrated Virus Detection. Taylor & Francis Group, 2014.

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Book chapters on the topic "Virus detection method"

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Wick, Charles H. "Mass Spectrometry Proteomic (MSP) Method." In Virus Detection. CRC Press, 2023. http://dx.doi.org/10.1201/9781003106623-7.

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Nguyen, Nhu Tuan, Van Huong Pham, Ba Cuong Le, Duc Thuan Le, and Thi Hong Van Le. "A New Method of Virus Detection Based on Maximum Entropy Model." In Advanced Computational Methods for Knowledge Engineering. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17996-4_14.

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Wick, Charles H. "Indirect Methods of Detecting Viruses." In Virus Detection. CRC Press, 2023. http://dx.doi.org/10.1201/9781003106623-3.

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Wick, Charles H. "Molecular Methods for Detecting Viruses." In Virus Detection. CRC Press, 2023. http://dx.doi.org/10.1201/9781003106623-5.

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Wick, Charles H. "Direct Virus Counting Methods, Such as IVDS." In Virus Detection. CRC Press, 2023. http://dx.doi.org/10.1201/9781003106623-6.

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Okomo-Adhiambo, Margaret, Aeron C. Hurt, and Larisa V. Gubareva. "The Chemiluminescent Neuraminidase Inhibition Assay: A Functional Method for Detection of Influenza Virus Resistance to the Neuraminidase Inhibitors." In Methods in Molecular Biology. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-621-0_6.

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Hurt, Aeron C., Margaret Okomo-Adhiambo, and Larisa V. Gubareva. "The Fluorescence Neuraminidase Inhibition Assay: A Functional Method for Detection of Influenza Virus Resistance to the Neuraminidase Inhibitors." In Methods in Molecular Biology. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-621-0_7.

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Singh, Arun Pratap, Akanksha Soni, and Sanjay Sharma. "A Novel Method for Corona Virus Detection Based on Directional Emboss and SVM from CT Lung Images." In Algorithms for Intelligent Systems. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-4893-6_40.

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Nguyen, Vu Thanh, Vu Thanh Hien, Le Dinh Tuan, Mai Viet Tiep, Nguyen Hoang Anh, and Pham Thi Vuong. "A Computer Virus Detection Method Based on Information from PE Structure of Files Combined with Deep Learning Models." In Future Data and Security Engineering. Big Data, Security and Privacy, Smart City and Industry 4.0 Applications. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-33-4370-2_9.

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Nguyen, Vu Thanh, Cao Ngoc Tuan, Ly Tan Dung, Vo Minh Hai, and Toan Tan Nguyen. "Computer Virus Detection Method Using Feature Extraction of Specific Malicious Opcode Sets Combine with aiNet and Danger Theory." In Future Data and Security Engineering. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-48057-2_14.

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Conference papers on the topic "Virus detection method"

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D, Anil, Shreeshayana R, Kiran B, and Preethi. "Advanced Malware Detection Methods for Polymorphic Virus Identification." In 2024 5th International Conference on Communication, Computing & Industry 6.0 (C2I6). IEEE, 2024. https://doi.org/10.1109/c2i663243.2024.10895844.

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Chen, Dan-Wei, Jian-Ping Liu, Guo-Zi Sun, and Jun Han. "One Formalized Method of Virus Detection." In 2009 International Symposium on Computer Network and Multimedia Technology (CNMT 2009). IEEE, 2009. http://dx.doi.org/10.1109/cnmt.2009.5374539.

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Zhao, Xiaoyong, and Jingwei Wang. "Pathogenic virus detection method based on multi-model fusion." In 2020 International Conference on Computer, Information and Telecommunication Systems (CITS). IEEE, 2020. http://dx.doi.org/10.1109/cits49457.2020.9232598.

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Zhang, Han, Yumin Zhang, Pei-Ran Feng, Ruo-Yu Zheng, Yi-lin Luo, and Ze-Xiao Yang. "Establishment of RT-LAMP Detection Method for Bluetongue Virus." In 2018 9th International Conference on Information Technology in Medicine and Education (ITME). IEEE, 2018. http://dx.doi.org/10.1109/itme.2018.00178.

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Vasilijević, Bojana, Vera Katanić, Sanja Živković, Tanja Vasić, Stefan Kovačević, and Darko Jevremović. "APPLICATION OF MULTIPLEX RT-PCR FOR GRAPEVINE VIRUSES DETECTION." In 2nd International Symposium on Biotechnology. Faculty of Agronomy in Čačak, University of Kragujevac, 2024. http://dx.doi.org/10.46793/sbt29.18bv.

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Grapevine, a significant fruit crop globally, is a host of various viruses that negatively affect yield, plant vigor, and fruit quality. Multiplex polymerase chain reaction (mPCR) offers the ability to detect numerous viruses simultaneously. Our study aimed to evaluate the effectiveness of mRT-PCR for the detection of nine grapevine viruses in Serbia, including: grapevine fanleaf virus, grapevine leafroll-associated viruses 1, 2, and 3, grapevine rupestris stem pitting associated virus, grapevine virus A, grapevine virus B, grapevine fleck virus, and arabis mosaic virus. This study confirms mR
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Qin, Renchao, Tao Li, and Yu Zhang. "An Immunity Based Computer Virus Detection Method with GA-RVNS." In 2008 Second International Symposium on Intelligent Information Technology Application. IEEE, 2008. http://dx.doi.org/10.1109/iita.2008.258.

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Zeng, Jie, and Tao Li. "A Novel Computer Virus Detection Method from Ideas of Immunology." In 2009 International Conference on Multimedia Information Networking and Security. IEEE, 2009. http://dx.doi.org/10.1109/mines.2009.278.

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Zhang, Yumin, Shsha Yang, Dan-yang Li, Pei-Ran Feng, Li-Jun Zhou, and Ze-Xiao Yang. "Preliminary Study of RT-LAMP Method for Detection of Ibaraki Virus." In 2018 9th International Conference on Information Technology in Medicine and Education (ITME). IEEE, 2018. http://dx.doi.org/10.1109/itme.2018.00204.

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Wang, Yi, Shuizhou Ke, Shaohong Wang, and ZhiBo Zheng. "A Grapevine Virus Disease Detection Method Based on Convolution Neural Network." In 2022 3rd International Conference on Computer Vision, Image and Deep Learning & International Conference on Computer Engineering and Applications (CVIDL & ICCEA). IEEE, 2022. http://dx.doi.org/10.1109/cvidliccea56201.2022.9825086.

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Singh, Prashant, Jay Prakash, Jyoti Srivastava, and Jyoti Srivastava. "Lumpy Skin Disease Virus Detection on Animals Through Machine Learning Method." In 2023 Third International Conference on Secure Cyber Computing and Communication (ICSCCC). IEEE, 2023. http://dx.doi.org/10.1109/icsccc58608.2023.10176394.

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Reports on the topic "Virus detection method"

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Osburn, Bennie I., Marius Ianconescu, C. A. Dangler, Rozalia Kaufman, Carlos de Mattos, and Cecilia de Mattos. Rapid Method for Detection of Bluetongue: Virus Infection Using Recombinant cDNA Probes. United States Department of Agriculture, 1987. http://dx.doi.org/10.32747/1987.7566878.bard.

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D’Agostino, Martin, Nigel Cook, Liam O’Connor, et al. Optimising extraction and RT-qPCR-based detection of hepatitis E virus (HEV) from pork meat and products. Food Standards Agency, 2023. http://dx.doi.org/10.46756/sci.fsa.ylv958.

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Hepatitis E is an infection of the liver caused by the hepatitis E virus (HEV). HEV infection usually produces a mild disease, hepatitis E. However, disease symptoms can vary from no apparent symptoms to liver failure. There are 4 main types (genotypes) of the virus that cause concern in humans. Genotypes 1 and 2 infections are mainly restricted to humans but 3 and 4 can be identified in numerous other animal species including pigs. Transmission routes of HEV genotypes 3 and 4 have been identified to include the consumption of food products derived from infected animals and shellfish, and via
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Osburn, Bennie, Marius Ianconescu, Geoffrey Akita, and Rozalia Kaufman. Rapid, Sensitive Bluetongue Virus Serogroup and Serotype Detection Using Polymerase Chain Reaction. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7612836.bard.

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The objectives of this proposal were to enhance animal health by 1) development of a BTV serogroup diagnostic assay using polymerase chain reaction (PCR) and 2) development of a BTV serotype specific diagnostic PCR assay. A PCR assay for diagnosis of bluetongue virus (BTV) serogroup from clinical samples meeting the criteria of objective 1 was developed. This PCR assay is more sensitive than virus isolation and has been adopted by both the U.S. and Israeli collaborating laboratories of this project, as well as at least one other U.S. laboratory for routine diagnosis of BTV infection in ruminan
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Perk, Simon, Egbert Mundt, Alexander Panshin, et al. Characterization and Control Strategies of Low Pathogenic Avian Influenza Virus H9N2. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7697117.bard.

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The avian influenza virus, subtype H9N2 subtype, defined as having a low pathogenicity, causes extensive economical losses in commercial flocks, probably due to management and synergism with other pathogens. AIV H9N2 was first identified in Israel in the year 2000, and since then it became endemic and widespread in Israel. Control by vaccination of commercial flocks with an inactivated vaccine has been introduced since 2007. In face of the continuous H9N2 outbreaks, and the application of the vaccination policy, we aimed in the present study to provide a method of differentiating naturally inf
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Gafny, Ron, A. L. N. Rao, and Edna Tanne. Etiology of the Rugose Wood Disease of Grapevine and Molecular Study of the Associated Trichoviruses. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7575269.bard.

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Rugose wood is a complex disease of grapevines, characterized by modification of the woody cylinder of affected vines. The control of rugose wood is based on the production of healthy propagation material. Detection of rugose wood in grapevines is difficult and expensive: budwood from tested plants is grafted onto sensitive Vitis indicators and the appearance of symptoms is monitored for 3 years. The etiology of rugose wood is complex and has not yet been elucidated. Several elongated clostero-like viruses are consistently found in affected vines; one of them, grapevine virus A (GVA), is close
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Gan, Charles, Melissa Pitton, Jolinda de Korne, et al. Wastewater-based poliovirus surveillance using digital PCR. Swiss Federal Institute of Aquatic Science and Technology, Eawag, 2025. https://doi.org/10.55408/eawag:34819.

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Poliovirus is the causative agent of poliomyelitis, a potentially debilitating disease that is a target for global eradication. Vaccination against poliomyelitis is an important tool in the eradication effort, but one of the available vaccines, the oral poliovirus vaccine, contains live, attenuated strains that can revert to virulent forms. Community transmission of so-called vaccine-derived polioviruses (VDPVs) can contribute to outbreaks, including in areas with no recently reported poliomyelitis cases. Wastewater-based surveillance (WBS) is a widely applied method to monitor communities for
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Jordan, Ramon L., Abed Gera, Hei-Ti Hsu, Andre Franck, and Gad Loebenstein. Detection and Diagnosis of Virus Diseases of Pelargonium. United States Department of Agriculture, 1994. http://dx.doi.org/10.32747/1994.7568793.bard.

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Abstract:
Pelargonium (Geranium) is the number one pot plant in many areas of the United States and Europe. Israel and the U.S. send to Europe rooted cuttings, foundation stocks and finished plants to supply a certain share of the market. Geraniums are propagated mainly vegetatively from cuttings. Consequently, viral diseases have been and remain a major threat to the production and quality of the crop. Among the viruses isolated from naturally infected geraniums, 11 are not specific to Pelargonium and occur in other crops while 6 other viruses seem to be limited to geranium. However, several of these v
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Hedrick, Ronald, and Herve Bercovier. Characterization and Control of KHV, A New Herpes Viral Pathogen of Koi and Common Carp. United States Department of Agriculture, 2004. http://dx.doi.org/10.32747/2004.7695871.bard.

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Abstract:
In this project we proposed to characterize the virus genome and the structural virion polypeptides to allow development of improved diagnostic approaches and potential vaccination strategies. These goals have been mostly achieved and the corresponding data were published in three papers (see below) and three more manuscripts are in preparation. The virion polypeptides of KHV strains isolated from USA (KHV-U) and Israel (KHV-I) were found to be identical. Purified viral DNA analyzed with a total of 5 restriction enzymes demonstrated no fragment length polymorphism between KHV-I and KHV-U but b
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Davidson, Irit, Hsing-Jien Kung, and Richard L. Witter. Molecular Interactions between Herpes and Retroviruses in Dually Infected Chickens and Turkeys. United States Department of Agriculture, 2002. http://dx.doi.org/10.32747/2002.7575275.bard.

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Abstract:
Tumors in commercial poultry are caused mainly by infection with avian herpes and retroviruses, the herpesvirus Marek's disease virus (MDV) and the retroviruses, reticuloendotheliosis (REV), lymphoid leukosis, subgroups A-I and J (ALV and ALV-J) in chickens, or Iymphoprolipherative disease (LPDV) in turkeys. Infection with one virus aggravates the clinical outcome of birds that are already infected by another oncogenic virus. As these viruses do not interfere for infection, MDV and one or more retroviruses can infect the same flock, the same bird and the same cell. While infecting the same cel
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