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      Threat of infection: Microbes of high pathogenic potential – strategies for detection, control and eradication

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          Abstract

          Infectious diseases due to microbes of high pathogenic potential remain a constant and variable threat for human and animal health. The emergence of new diseases or the re-emergence of diseases that were previously under control complicates the situation to date. Infectious disease research, which has undergone a dramatic progress in understanding disease mechanisms such as host–pathogen interactions, is now focusing increasingly on new strategies for prevention and therapy. Significant progress has been achieved in the development of delivery systems for protective heterologous protein antigens and in veterinary vaccinology. A landmark of infectious diseases research is the chemical synthesis of genomes, a major new field of research referred to as “synthetic biology”, that to date has resulted in the chemical synthesis of the poliovirus and of phage φX174 genomes and their expression as infectious viruses. On the molecular level the evolution of pathogens and mechanisms of genome flexibility, which account for several pathogenic properties of infectious agents, have received increased attention. Bacterial toxins are an additional threat to human health and their interference with host cells and cellular functions is receiving more attention.

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          Most cited references64

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          Genomic islands in pathogenic and environmental microorganisms.

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            Chemical synthesis of poliovirus cDNA: generation of infectious virus in the absence of natural template.

            Full-length poliovirus complementary DNA (cDNA) was synthesized by assembling oligonucleotides of plus and minus strand polarity. The synthetic poliovirus cDNA was transcribed by RNA polymerase into viral RNA, which translated and replicated in a cell-free extract, resulting in the de novo synthesis of infectious poliovirus. Experiments in tissue culture using neutralizing antibodies and CD155 receptor-specific antibodies and neurovirulence tests in CD155 transgenic mice confirmed that the synthetic virus had biochemical and pathogenic characteristics of poliovirus. Our results show that it is possible to synthesize an infectious agent by in vitro chemical-biochemical means solely by following instructions from a written sequence.
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              Cellular receptor for poliovirus: molecular cloning, nucleotide sequence, and expression of a new member of the immunoglobulin superfamily.

              Restriction of poliovirus replication to a few sites in the infected primate host appears to be controlled by the expression of viral receptors. To learn more about these binding sites and their role in viral tissue tropism, cDNA clones encoding functional poliovirus receptors were isolated. The predicted amino acid sequence reveals that the human poliovirus receptor is an integral membrane protein with the conserved amino acids and domain structure characteristic of members of the immunoglobulin superfamily. Northern hybridization analysis indicates that poliovirus receptor transcripts are expressed in a wide range of human tissues, in contrast to the limited expression of virus binding sites, which suggests that additional factors or modifications of the receptor protein are required to permit poliovirus attachment.
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                Author and article information

                Contributors
                Journal
                Int J Med Microbiol
                Int. J. Med. Microbiol
                International Journal of Medical Microbiology
                Published by Elsevier GmbH
                1438-4221
                1618-0607
                26 April 2005
                28 June 2005
                26 April 2005
                : 295
                : 3
                : 141-151
                Affiliations
                [a ]Research Center for Infectious Diseases, University of Würzburg, Würzburg, Germany
                [b ]Institute of Molecular Infection Biology, University of Würzburg, Würzburg, Germany
                [c ]Institute for Virology, University of Marburg, Marburg, Germany
                Author notes
                [* ]Corresponding author. Tel.: +49 931 31 2153; fax: +49 931 31 2578. s.hammerschmidt@ 123456mail.uni-wuerzburg.de
                Article
                S1438-4221(05)00045-7
                10.1016/j.ijmm.2005.03.004
                7129083
                16044855
                06ef991a-997b-40c2-ba71-963e1ed47211
                © 2005

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

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                Microbiology & Virology
                infectious disease,vaccination strategies,eradication,bacterial evolution,synthetic biology,toxins

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