Ambiguous role of CCR5 in Y-pestis infection

被引:47
作者
Elvin, SJ [1 ]
Williamson, ED
Scott, JC
Smith, JN
de Lema, GP
Chilla, S
Clapham, P
Pfeffer, K
Schlöndorff, D
Luckow, B
机构
[1] Def Sci & Technol Labs, Salisbury SP4 0JQ, Wilts, England
[2] Klinikum Univ Munchen, Med Poliklin Innenstadt, D-80336 Munich, Germany
[3] Univ Massachusetts, Worcester, MA 01605 USA
[4] Univ Dusseldorf, D-40225 Dusseldorf, Germany
关键词
D O I
10.1038/nature02822
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Arising from: J. Mecsas et al. Nature427, 606 (2004) Mecsas and colleagues suggest that a deficiency in the chemokine receptor CCR5 in humans is unlikely to confer protection against plague, based on their study of Yersinia pestis infection in Ccr5-deficient mice1. They were testing the hypothesis that a mutation in the CCR5 gene, frequently found in Caucasians, may have been selected for in the past because it provided protection against (bubonic) plague2,3,4,5,6,7; the mutation, called CCR5Δ32, is characterized by a 32-base-pair deletion. We have also tested this hypothesis by using Y. pestis infection in mice and, in addition, we have done phagocytosis experiments with macrophages from wild-type and Ccr5-deficient mice. Although, like Mecsas et al., we did not see any difference in the survival of the two groups of mice, we did find that there was a significantly reduced uptake of Y. pestis by Ccr5-deficient macrophages in vitro. Our results indicate that the role of Ccr5 in Y. pestis infection may therefore be more complex than previously thought.
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收藏
页码:417 / 417
页数:1
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