Academic literature on the topic 'Adenovirus 40/41'

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Journal articles on the topic "Adenovirus 40/41"

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Arcangeletti, Maria-Cristina, Diego Germini, Davide Martorana, et al. "High frequency of cultivable human subgroup F adenoviruses in stool samples from a paediatric population admitted to hospital with acute gastroenteritis." Journal of Medical Microbiology 63, no. 6 (2014): 812–18. http://dx.doi.org/10.1099/jmm.0.072413-0.

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The family Adenoviridae consists of five genera of which the genus Mastadenovirus includes human viruses classified into 57 serotypes clustered into seven subgroups (A–G). Serotypes 40 and 41 (subgroup F) are specifically associated with childhood gastroenteritis and are the most common cause of acute gastroenteritis in young children after rotaviruses and noroviruses. Standard methods for laboratory diagnosis of adenovirus infection include electron microscopy (EM) and conventional cell culture (CCC), although it is widely considered that adenoviruses 40 and 41 are difficult to cultivate, suc
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Moore, P. L., A. D. Steele, and J. J. Alexander. "Relevance of Commercial Diagnostic Tests to Detection of Enteric Adenovirus Infections in South Africa." Journal of Clinical Microbiology 38, no. 4 (2000): 1661–63. http://dx.doi.org/10.1128/jcm.38.4.1661-1663.2000.

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The prevalence of enteric adenoviruses detected by an in-house enzyme-linked immunosorbent assay (the RIVM-ELISA) ranged from 13 to 38%, and subgroup F adenoviruses comprised 86%. All subgroup F adenoviruses reacted with both RIVM anti-adenovirus type 40 (Ad40) and anti-adenovirus type 41 (Ad41) monoclonal antibodies but were not detected by Adenoclone Type 40/41 enzyme immunoassay (EIA). The correlation between the Biotrin EIA and RIVM-ELISA results was low (26%). Immunospecific tests suggest that a significant proportion of enteric adenoviruses, possibly comprising previously unidentified or
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Jothikumar, Narayanan, Theresa L. Cromeans, Vincent R. Hill, Xiaoyan Lu, Mark D. Sobsey, and Dean D. Erdman. "Quantitative Real-Time PCR Assays for Detection of Human Adenoviruses and Identification of Serotypes 40 and 41." Applied and Environmental Microbiology 71, no. 6 (2005): 3131–36. http://dx.doi.org/10.1128/aem.71.6.3131-3136.2005.

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ABSTRACT A quantitative real-time TaqMan PCR assay for detection of human adenoviruses (HAdV) was developed using broadly reactive consensus primers and a TaqMan probe targeting a conserved region of the hexon gene. The TaqMan assay correctly identified 56 representative adenovirus prototype strains and field isolates from all six adenovirus species (A to F). Based on infectious units, the TaqMan assay was able to detect as few as 0.4 and 0.004 infectious units of adenovirus serotype 2 (AdV2) and AdV41, respectively, with results obtained in less than 90 min. Using genomic equivalents, the bro
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Jiang, Sunny C., Jijun Han, Jian-Wen He, and Weiping Chu. "Evaluation of four cell lines for assay of infectious adenoviruses in water samples." Journal of Water and Health 7, no. 4 (2009): 650–56. http://dx.doi.org/10.2166/wh.2009.088.

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Human viral contamination in drinking and recreational waters poses health risks. The application of PCR-based molecular technology has advanced our knowledge of the occurrence and prevalence of human viruses in water; however, it has provided no information on viral viability and infectivity. Four human cell lines were compared for their sensitivity to different serotypes of human adenoviruses using the TCID50 test. The sensitivity of each cell line varied with different serotypes of adenovirus. Human embryonic kidney cell line 293A and human lung carcinoma cell line A549 were the most sensit
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Santos, F. M., M. J. Vieira, P. Garrafa, et al. "Discrimination of adenovirus types circulating in urban sewage and surface polluted waters in São Paulo city, Brazil." Water Supply 4, no. 2 (2004): 79–85. http://dx.doi.org/10.2166/ws.2004.0031.

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Owing to frequent overflow of sewage-polluted creeks and rivers in São Paulo city, the population that lives in those surrounding areas is constantly exposed to a high risk of infection by many pathogens. Our aim was to evaluate the occurrence of human adenovirus, especially F species (HAdV-40 and HAdV-41), in sewage and creek water in São Paulo city. A total of 95 water samples were collected from July 1998 to June 1999 and from September 2000 to December 2001 at Sewage Pumping Station Edu Chaves and Creek Pirajussara. Four-litre samples were concentrated by a two-step procedure based on filt
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Ciruela, P., C. Izquierdo, M. Oviedo, and A. Domínguez. "Rotavirus y adenovirus 40–41 como causantes de gastroenteritis infantil." Vacunas 5, no. 1 (2004): 16–23. http://dx.doi.org/10.1016/s1576-9887(04)70351-9.

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Wigand, R. "Fast identification of adenovirus 40/41 in infants with enteritis." European Journal of Clinical Microbiology 6, no. 5 (1987): 606–7. http://dx.doi.org/10.1007/bf02014267.

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Karakus, Yasin Tugrul. "Incidence of rotavirus and adenovirus 40/41 in children and infants." European Journal of Medical Sciences 1, no. 1 (2014): 22–25. http://dx.doi.org/10.12973/ejms.2014.104p.

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Ali, Alyaa Younis, Areej Atiyah Hussein, and Najdat Shukur Mahmood. "Detection of human adenovirus 40/41 among children with some hematological disorders." Journal of Ideas in Health 2, no. 2 (2019): 81–86. http://dx.doi.org/10.47108/jidhealth.vol2.iss2.33.

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Background: Different parts of the world are witnessing a significant increase in the prevalence of human adenoviruses (HAdVs) diarrhea among children. This study aimed to assess the prevalence rate of HAdVs type 40 and type 41 (40/41) infections in children with diarrhea and to assess the relationship between viral infection and different socio-demographic and clinical parameters.
 Methods: A cross-sectional study was recruited to analyze a convenient sample of children presented with diarrhea. Data was collected from 8th August 2018 till 6th July 2019 at Al-Batool teaching hospital for
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Roy, Soumitra, David S. Clawson, Virginie S. Adam, Angelica Medina, and James M. Wilson. "Construction of gene transfer vectors based on simian adenovirus 7." Journal of General Virology 92, no. 8 (2011): 1749–53. http://dx.doi.org/10.1099/vir.0.032300-0.

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The complete nucleotide sequence of an isolate of simian adenovirus 7 (SAdV-7) was determined. The genome organization of this isolate was found to be similar to that of other primate adenoviruses with two principal notable points: severe truncation of the E1A and E1B 19K proteins and an E3 region encoding only the 12.5K homologue. The viral gene products of SAdV-7 are most closely related to simian adenovirus 1 (SAdV-1), and like SAdV-1, are related to the human adenovirus species HAdV-F, such as the enteric adenoviruses HAdV-40 and HAdV-41 and the recently defined HAdV-G (HAdV-52). Two kinds
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Dissertations / Theses on the topic "Adenovirus 40/41"

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BERNAIS, THIERRY. "Utilisation de la ligne cellulaire hepg2 pour l'isolement des adenovirus 40 et 41." Nice, 1990. http://www.theses.fr/1990NICE6825.

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Ledwaba, Solanka Ellen. "Prevalence of selected bacterial and viral entero-pathogens in children less than 5 years of age in Limpopo Province, South Africa." Diss., 2016. http://hdl.handle.net/11602/779.

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Books on the topic "Adenovirus 40/41"

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Wilson-Friesen, Heather Louise. Biological characterization of fastidious enteric adenoviruses types 40 and 41 in 293 and HeLa cell lines. National Library of Canada, 1995.

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Book chapters on the topic "Adenovirus 40/41"

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de Jong, J. C. "III, 2. Epidemiology of enteric adenoviruses 40 and 41 and other adenoviruses in immunocompetent and immunodeficient individuals." In Perspectives in Medical Virology. Elsevier, 2003. http://dx.doi.org/10.1016/s0168-7069(03)09025-6.

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