Báo cáo y học: Use of different but overlapping determinants in a retrovirus receptor accounts for non-reciprocal interference between xenotropic and polytropic murine leukemia viruses
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Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học quốc tế cung cấp cho các bạn kiến thức về ngành y đề tài:Use of different but overlapping determinants in a retrovirus receptor accounts for non-reciprocal interference between xenotropic and polytropic murine leukemia viruses
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Báo cáo y học: " Use of different but overlapping determinants in a retrovirus receptor accounts for non-reciprocal interference between xenotropic and polytropic murine leukemia viruses"Retrovirology BioMed Central Open AccessResearchUse of different but overlapping determinants in a retrovirusreceptor accounts for non-reciprocal interference betweenxenotropic and polytropic murine leukemia virusesNeal S Van Hoeven1,2,3 and A Dusty Miller*1Address: 1Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA, 2Molecular and Cellular BiologyProgram, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA and 3Current address: Centers for Disease Control, Atlanta,Georgia 30333, USAEmail: Neal S Van Hoeven - nvanhoeven@cdc.gov; A Dusty Miller* - dmiller@fhcrc.org* Corresponding authorPublished: 15 December 2005 Received: 13 September 2005 Accepted: 15 December 2005Retrovirology 2005, 2:76 doi:10.1186/1742-4690-2-76This article is available from: http://www.retrovirology.com/content/2/1/76© 2005 Van Hoeven and Miller; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Retrovirus infection depends on binding of the retroviral envelope (Env) protein to specific cell-surface protein receptors. Interference, or superinfection resistance, is a frequent consequence of retroviral infection, and occurs when newly-synthesized Env binds to receptor proteins resulting in a block to entry by retroviruses that use the same receptors. Three groups of viruses demonstrate a non-reciprocal pattern of interference (NRI), which requires the existence of both a common receptor utilized by all viruses within the group, and a specific receptor that is used by a subset of viruses. In the case of amphotropic and 10A1 murine leukemia viruses (MLV), the common and specific receptors are the products of two related genes. In the case of avian sarcoma and leukosis virus types B, D, and E, the two receptors are distinct protein products of a single gene. NRI also occurs between xenotropic and polytropic MLV. The common receptor, Xpr1, has been identified, but a specific receptor has yet to be described. Results: Using chimeric receptor proteins and interference studies, we have identified a region of Xpr1 that is uniquely utilized by xenotropic MLV and show that this receptor domain is required for non-reciprocal interference. Conclusion: We propose a novel pattern of receptor usage by xenotropic and polytropic MLV to explain the NRI observed between these viruses. We propose that the specific and common receptor determinants for xenotropic and polytropic viruses are simultaneously present in discreet domains of a single Xpr1 protein. ing in fusion and delivery of the viral capsids into the hostBackgroundRetroviral infection of a host cell is initiated by interaction cell cytoplasm (reviewed in [1,2]). In addition to promot-of the retroviral Env protein surface (SU) subunit with a ing virus entry, the intracellular interaction of a viral Envspecific host cell receptor. This interaction triggers confor- and its cognate receptor can limit subsequent infection bymational changes within the Env protein that bring the subsequent viruses that bind the same receptor. This phe-virus and host cell membranes in close proximity, result- notype is referred to as interference or superinfection Page 1 of 12 (page number not for citation purposes)Retrovirology 2005, 2:76 http: ...
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Báo cáo y học: " Use of different but overlapping determinants in a retrovirus receptor accounts for non-reciprocal interference between xenotropic and polytropic murine leukemia viruses"Retrovirology BioMed Central Open AccessResearchUse of different but overlapping determinants in a retrovirusreceptor accounts for non-reciprocal interference betweenxenotropic and polytropic murine leukemia virusesNeal S Van Hoeven1,2,3 and A Dusty Miller*1Address: 1Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA, 2Molecular and Cellular BiologyProgram, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA and 3Current address: Centers for Disease Control, Atlanta,Georgia 30333, USAEmail: Neal S Van Hoeven - nvanhoeven@cdc.gov; A Dusty Miller* - dmiller@fhcrc.org* Corresponding authorPublished: 15 December 2005 Received: 13 September 2005 Accepted: 15 December 2005Retrovirology 2005, 2:76 doi:10.1186/1742-4690-2-76This article is available from: http://www.retrovirology.com/content/2/1/76© 2005 Van Hoeven and Miller; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Retrovirus infection depends on binding of the retroviral envelope (Env) protein to specific cell-surface protein receptors. Interference, or superinfection resistance, is a frequent consequence of retroviral infection, and occurs when newly-synthesized Env binds to receptor proteins resulting in a block to entry by retroviruses that use the same receptors. Three groups of viruses demonstrate a non-reciprocal pattern of interference (NRI), which requires the existence of both a common receptor utilized by all viruses within the group, and a specific receptor that is used by a subset of viruses. In the case of amphotropic and 10A1 murine leukemia viruses (MLV), the common and specific receptors are the products of two related genes. In the case of avian sarcoma and leukosis virus types B, D, and E, the two receptors are distinct protein products of a single gene. NRI also occurs between xenotropic and polytropic MLV. The common receptor, Xpr1, has been identified, but a specific receptor has yet to be described. Results: Using chimeric receptor proteins and interference studies, we have identified a region of Xpr1 that is uniquely utilized by xenotropic MLV and show that this receptor domain is required for non-reciprocal interference. Conclusion: We propose a novel pattern of receptor usage by xenotropic and polytropic MLV to explain the NRI observed between these viruses. We propose that the specific and common receptor determinants for xenotropic and polytropic viruses are simultaneously present in discreet domains of a single Xpr1 protein. ing in fusion and delivery of the viral capsids into the hostBackgroundRetroviral infection of a host cell is initiated by interaction cell cytoplasm (reviewed in [1,2]). In addition to promot-of the retroviral Env protein surface (SU) subunit with a ing virus entry, the intracellular interaction of a viral Envspecific host cell receptor. This interaction triggers confor- and its cognate receptor can limit subsequent infection bymational changes within the Env protein that bring the subsequent viruses that bind the same receptor. This phe-virus and host cell membranes in close proximity, result- notype is referred to as interference or superinfection Page 1 of 12 (page number not for citation purposes)Retrovirology 2005, 2:76 http: ...
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