Viral RNA kinetics is associated with changes in trace elements in target organs of Coxsackie virus B3 infection

被引:11
作者
Molin, Ylva [1 ]
Frisk, Peter [2 ]
Ilback, Nils-Gunnar [1 ,3 ]
机构
[1] Univ Uppsala Hosp, Dept Med Sci, S-75185 Uppsala, Sweden
[2] Uppsala Univ, Rudbeck Lab, S-75185 Uppsala, Sweden
[3] Natl Food Adm Toxicol Lab, Div Toxicol, S-75126 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
CVB3; Infection; Mice; Tissues; Trace elements; DEFICIENCY INCREASES; ARSENIC TRIOXIDE; MICE; MYOCARDITIS; DISEASE; TYPE-1; PANCREATITIS; REPLICATION; INHIBITION; METABOLISM;
D O I
10.1016/j.micinf.2009.02.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Trace elements are pivotal for the host defense, as well as potentially important for viral replication and virulence. Studies of sequential changes in viral replication in target organs of infection are sparse and a possible association with changes in specific trace elements is unknown. In this study Balb/c mice were infected with Coxsackie virus B3 (CVB3). Results indicated that sequential changes in viral replication (RT-PCR) were related to changes in trace element (arsenic, copper, iron, selenium and zinc) concentrations (as determined by ICP-MS) on days 3, 5 and 7 of the infection in serum, heart, lung, liver, pancreas, kidney, spleen, intestine and brain. After an initial viral peak oil day 3, viral load drastically decreased in all organs, i.e. by >99% (serum), 97% (lung), 98% (liver), 60% (pancreas), 95% (kidney) and 93% (spleen), except in the heart, intestine and brain in which viral load increased after clay 3. Selenium decreased in all organs except the heart while arsenic decreased in all organs except the kidney, spleen and brain. Moreover, selenium was negatively correlated to viral load in serum, liver, pancreas and intestine. To conclude. these findings give evidence that trace elements are directly involved in the replication of CVB3. (C) 2009 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:493 / 499
页数:7
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