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      Salmonella typhimurium Persists within Macrophages in the Mesenteric Lymph Nodes of Chronically Infected Nramp1 + / + Mice and Can Be Reactivated by IFNγ Neutralization

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          Abstract

          Host-adapted strains of Salmonella are capable of establishing a persistent infection in their host often in the absence of clinical disease. The mouse model of Salmonella infection has primarily been used as a model for the acute systemic disease. Therefore, the sites of long-term S. typhimurium persistence in the mouse are not known nor are the mechanisms of persistent infection clearly understood. Here, we show that S. typhimurium can persist for as long as 1 yr in the mesenteric lymph nodes (MLNs) of 129sv Nramp1 + / + ( Slc11a1 + / +) mice despite the presence of high levels of anti– S. typhimurium antibody. Tissues from 129sv mice colonized for 60 d contain numerous inflammatory foci and lesions with features resembling S. typhi granulomas. Tissues from mice infected for 365 d have very few organized inflammatory lesions, but the bacteria continue to persist within macrophages in the MLN and the animals generally remain disease-free. Finally, chronically infected mice treated with an interferon-γ neutralizing antibody exhibited symptoms of acute systemic infection, with evidence of high levels of bacterial replication in most tissues and high levels of fecal shedding. Thus, interferon-γ, which may affect the level of macrophage activation, plays an essential role in the control of the persistent S. typhimurium infection in mice.

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          Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18.

          Salmonella enterica serovar Typhi (S. typhi) is the aetiological agent of typhoid fever, a serious invasive bacterial disease of humans with an annual global burden of approximately 16 million cases, leading to 600,000 fatalities. Many S. enterica serovars actively invade the mucosal surface of the intestine but are normally contained in healthy individuals by the local immune defence mechanisms. However, S. typhi has evolved the ability to spread to the deeper tissues of humans, including liver, spleen and bone marrow. Here we have sequenced the 4,809,037-base pair (bp) genome of a S. typhi (CT18) that is resistant to multiple drugs, revealing the presence of hundreds of insertions and deletions compared with the Escherichia coli genome, ranging in size from single genes to large islands. Notably, the genome sequence identifies over two hundred pseudogenes, several corresponding to genes that are known to contribute to virulence in Salmonella typhimurium. This genetic degradation may contribute to the human-restricted host range for S. typhi. CT18 harbours a 218,150-bp multiple-drug-resistance incH1 plasmid (pHCM1), and a 106,516-bp cryptic plasmid (pHCM2), which shows recent common ancestry with a virulence plasmid of Yersinia pestis.
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            Neurotransmitter synthesis and uptake by isolated sympathetic neurones in microcultures.

            Assays of isolated single sympathetic neurones show that their transmitter functions can be either adrenergic or cholinergic depending on growth conditions. The data suggest that the number of transmitters made by most mature individual neurones is restricted.
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              Neuroscience. Developmental refining of neuroglial signaling?

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                Author and article information

                Journal
                J Exp Med
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                19 January 2004
                : 199
                : 2
                : 231-241
                Affiliations
                [1 ]Department of Microbiology and Immunology, Stanford School of Medicine, Stanford University, Stanford, CA 94305
                [2 ]Department of Comparative Medicine, Stanford School of Medicine, Stanford University, Stanford, CA 94305
                Author notes

                Address correspondence to D.M. Monack, Dept. of Microbiology and Immunology, Stanford University School of Medicine, Stanford University, Stanford, CA 94305. Phone: (650) 723-2671; Fax: (650) 723-1837; email: dmonack@ 123456leland.stanford.edu

                Article
                20031319
                10.1084/jem.20031319
                2211772
                14734525
                15b96009-1abe-4c8a-a55d-9266e379c353
                Copyright © 2004, The Rockefeller University Press
                History
                : 1 August 2003
                : 17 November 2003
                Categories
                Article

                Medicine
                slc11a1,interferon-γ,monocytes,persistence,carriage
                Medicine
                slc11a1, interferon-γ, monocytes, persistence, carriage

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