Cooperative Vaccinia Infection Demonstrated at the Single-Cell Level Using FluidFM

被引:48
作者
Stiefel, Philipp [3 ]
Schmidt, Florian I. [2 ]
Doerig, Pablo [1 ]
Behr, Pascal [1 ]
Zambelli, Tomaso [1 ]
Vorholt, Julia A. [3 ]
Mercer, Jason [2 ]
机构
[1] Swiss Fed Inst Technol, Inst Biomed Engn, Lab Biosensors & Bioelect, Zurich, Switzerland
[2] Swiss Fed Inst Technol, Inst Biochem, Zurich, Switzerland
[3] Swiss Fed Inst Technol, Inst Microbiol, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Poxvirus; virus entry; cooperative infection; fluidFM; VIRUS; MICROSCOPY; MACROPINOCYTOSIS; REACTIVATION; POXVIRUSES; PROTEIN;
D O I
10.1021/nl3018109
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The mechanisms used by viruses to enter and replicate within host cells are subjects of intense investigation. These studies are ultimately aimed at development of new drugs that interfere with these processes. Virus entry and infection are generally monitored by dispensing bulk virus suspensions on layers of cells without accounting for the fate of each virion. Here, we take advantage of the recently developed FluidFM to deposit single vaccinia virions onto individual cells in a controlled manner. While the majority of virions were blocked prior to early gene expression, infection of individual cells increased in a nondeterministic fashion with respect to the number of viruses placed. Microscopic analyses of several stages of the virus lifecycle indicated that this was the result of cooperativity between virions during early stages of infection. These findings highlight the importance of performing controlled virus infection experiments at the single cell level.
引用
收藏
页码:4219 / 4227
页数:9
相关论文
共 24 条
[1]   MULTIPLICITY REACTIVATION AND MARKER RESCUE WITH VACCINIA VIRUS [J].
ABEL, P .
VIROLOGY, 1962, 17 (04) :511-&
[2]  
Berry G. P., 1936, J BACTERIOL, V31, P1
[3]   Compact, synthetic, vaccinia virus early/late promoter for protein expression [J].
Chakrabarti, S ;
Sisler, JR ;
Moss, B .
BIOTECHNIQUES, 1997, 23 (06) :1094-1097
[4]   Force-controlled spatial manipulation of viable mammalian cells and micro-organisms by means of FluidFM technology [J].
Doerig, Pablo ;
Stiefel, Philipp ;
Behr, Pascal ;
Sarajlic, Edin ;
Bijl, Daniel ;
Gabi, Michael ;
Voeroes, Janos ;
Vorholt, Julia A. ;
Zambelli, Tomaso .
APPLIED PHYSICS LETTERS, 2010, 97 (02)
[5]   REACTIVATION OF HEAT-INACTIVATED POXVIRUSES - GENERAL PHENOMENON WHICH INCLUDES THE FIBROMA-MYXOMA VIRUS TRANSFORMATION OF BERRY AND DEDRICK [J].
FENNER, F ;
HOLMES, IH ;
JOKLIK, WK ;
WOODROOFE, GM .
NATURE, 1959, 183 (4671) :1340-1341
[6]   STUDIES ON HOST-VIRUS INTERACTIONS IN THE CHICK EMBRYO-INFLUENZA VIRUS SYSTEM .6. EVIDENCE FOR MULTIPLICITY REACTIVATION OF INACTIVATED VIRUS [J].
HENLE, W ;
LIU, OC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1951, 94 (04) :305-322
[7]   A novel cellular protein, VPEF, facilitates vaccinia virus penetration into HeLa cells through fluid phase endocytosis [J].
Huang, Cheng-Yen ;
Lu, Tsai-Yi ;
Bair, Chi-Horng ;
Chang, Yuan-Shau ;
Jwo, Jeng-Kuan ;
Chang, Wen .
JOURNAL OF VIROLOGY, 2008, 82 (16) :7988-7999
[8]   PURIFICATION OF FOUR STRAINS OF POXVIRUS [J].
JOKLIK, WK .
VIROLOGY, 1962, 18 (01) :9-&
[10]  
Knipe D. M., 2007, FIELDS VIROLOGY, V5