Characterizations of individual mouse red blood cells parasitized by Babesia microti using 3-D holographic microscopy

Scientific Reports

Volumn 5, Issue , 2015, Pages

  Park, HyunJoo ^a   Hong, Sung Hee ^b   Kim, Kyoohyun ^a   Cho, Shin Hyeong ^b   Lee, Won Ja ^b   Kim, Youngchan ^a   Lee, Sang Eun ^b   Park, YongKeun ^a  

^a Korea Advanced Institute of Science and Technology (KAIST)   (South Korea)

^b Korea Centers for Disease Control and Prevention   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; BABESIA MICROTI; BLOOD; ERYTHROCYTE; ERYTHROCYTE DEFORMABILITY; HOLOGRAPHY; MEAN CORPUSCULAR VOLUME; MICROSCOPY; MOUSE; PARASITOLOGY; PATHOLOGY; PHYSIOLOGY; PIROPLASMOSIS; PROCEDURES;

ANIMALS; BABESIA MICROTI; BABESIOSIS; ERYTHROCYTE DEFORMABILITY; ERYTHROCYTE INDICES; ERYTHROCYTES; HOLOGRAPHY; MICE; MICROSCOPY;

EID: 84930648237     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep10827     Document Type: Article

References (47)

1. Hunfeld, K. P., Hildebrandt, A. & Gray, J. S. Babesiosis: recent insights into an ancient disease. International journal for parasitology 38, 1219-1237, doi: 10.1016/j.ijpara.2008.03.001 (2008
2. Krause, P. J. et al. Concurrent Lyme disease and babesiosis. Evidence for increased severity and duration of illness. Jama 275, 1657-1660 (1996
3. Pruthi, R. K., Marshall, W. F., Wiltsie, J. C. & Persing, D. H. Human babesiosis. Mayo Clinic proceedings 70, 853-862, doi: 10.1016/ S0025-6196(11)63943-8 (1995
4. Borggraefe, I. et al. Babesia microti primarily invades mature erythrocytes in mice. Infection and immunity 74, 3204-3212, doi: 10.1128/IAI.01560-05 (2006
5. Goethert, H. K. & Telford, S. R., 3rd. What is Babesia microti? Parasitology 127, 301-309 (2003
6. Ike, K. et al. High susceptibility of Djungarian hamsters (Phodopus sungorus) to the infection with Babesia microti supported by hemodynamics. The Journal of veterinary medical science/the Japanese Society of Veterinary Science 67, 515-520 (2005
7. Homer, M. J., Aguilar-Delfin, I., Telford, S. R., 3rd, Krause, P. J. & Persing, D. H. Babesiosis. Clinical microbiology reviews 13, 451-469 (2000
8. Kjemtrup, A. M. & Conrad, P. A. Human babesiosis: an emerging tick-borne disease. International journal for parasitology 30, 1323-1337 (2000
9. Rudzinska, M. A., Trager, W., Lewengrub, S. J. & Gubert, E. An electron microscopic study of Babesia microti invading erythrocytes. Cell and tissue research 169, 323-334 (1976
10. Gohil, S., Kats, L. M., Sturm, A. & Cooke, B. M. Recent insights into alteration of red blood cells by Babesia bovis: moovin' forward. Trends in parasitology 26, 591-599, doi: 10.1016/j.pt.2010.06.012 (2010
11. Popescu, G. Quantitative Phase Imaging of Cells and TIssues. (McGraw-Hill Professional, 2011
12. Lee, K. et al. Quantitative phase imaging techniques for the study of cell pathophysiology: from principles to applications. Sensors (Basel) 13, 4170-4191, doi: 10.3390/s130404170 (2013
13. Kim, Y. et al. Common-path diffraction optical tomography for investigation of three-dimensional structures and dynamics of biological cells. Opt Express 22, 10398-10407, doi: 10.1364/OE.22.010398 (2014
14. Kim, Y. et al. Profiling individual human red blood cells using common-path diffraction optical tomography. Sci Rep 4, 6659, doi: 10.1038/srep06659 (2014
15. Kim, K. et al. High-resolution three-dimensional imaging of red blood cells parasitized by Plasmodium falciparum and in situ hemozoin crystals using optical diffraction tomography. Journal of biomedical optics 19, 011005, doi: 10.1117/1.JBO.19.1.011005 (2014
16. Park, Y. et al. Refractive index maps and membrane dynamics of human red blood cells parasitized by Plasmodium falciparum. Proceedings of the National Academy of Sciences of the United States of America 105, 13730-13735, doi: 10.1073/pnas.0806100105 (2008
17. Schuster, F. L. Cultivation of Babesia and Babesia-like blood parasites: agents of an emerging zoonotic disease. Clin Microbiol Rev 15, 365-373 (2002
18. Park, Y. et al. Metabolic remodeling of the human red blood cell membrane. Proceedings of the National Academy of Sciences of the United States of America 107, 1289-1294, doi: 10.1073/pnas.0910785107 (2010
19. Sheetz, M. P. & Singer, S. J. On the mechanism of ATP-induced shape changes in human erythrocyte membranes. I. The role of the spectrin complex. The Journal of cell biology 73, 638-646 (1977
20. Park, Y., Popescu, G., Badizadegan, K., Dasari, R. R. & Feld, M. S. Diffraction phase and fluorescence microscopy. Opt Express 14, 8263-8268 (2006
21. Popescu, G. et al. Optical measurement of cell membrane tension. Physical review letters 97, 218101 (2006
22. Park, Y. et al. Measurement of red blood cell mechanics during morphological changes. Proceedings of the National Academy of Sciences of the United States of America 107, 6731-6736, doi: 10.1073/pnas.0909533107 (2010
23. Popescu, G. et al. Imaging red blood cell dynamics by quantitative phase microscopy. Blood cells, molecules & diseases 41, 10-16, doi: 10.1016/j.bcmd.2008.01.010 (2008
24. Barer, R. Determination of dry mass, thickness, solid and water concentration in living cells. Nature 172, 1097-1098 (1953
25. Davies, H. G. & Wilkins, M. H. Interference microscopy and mass determination. Nature 169, 541 (1952
26. Popescu, G. et al. Optical imaging of cell mass and growth dynamics. American journal of physiology. Cell physiology 295, C538-544, doi: 10.1152/ajpcell.00121.2008 (2008
27. Barer, R. Interference microscopy and mass determination. Nature 169, 366-367 (1952
28. Barer, R. & Tkaczyk, S. Refractive index of concentrated protein solutions. Nature 173, 821-822 (1954
29. Park, Y., Yamauchi, T., Choi, W., Dasari, R. & Feld, M. S. Spectroscopic phase microscopy for quantifying hemoglobin concentrations in intact red blood cells. Optics letters 34, 3668-3670, doi: 10.1364/OL.34.003668 (2009
30. McClatchey, K. D., Amin, H. M. & Curry, J. L. Clinical laboratory medicine : self-Assessment and review. 2nd edn, (Lippincott Williams & Wilkins, 2002
31. Suresh, S. Mechanical response of human red blood cells in health and disease: Some structure-property-function relationships. J Mater Res 21, 1871 (2006
32. Park, Y. et al. Measurement of the nonlinear elasticity of red blood cell membranes. Physical review. E, Statistical, nonlinear, and soft matter physics 83, 051925 (2011
33. Johnson, R. M., Taylor, G. & Meyer, D. B. Shape and volume changes in erythrocyte ghosts and spectrin-Actin networks. The Journal of cell biology 86, 371-376 (1980
34. Gligorijevic, B., Bennett, T., McAllister, R., Urbach, J. S. & Roepe, P. D. Spinning disk confocal microscopy of live, intraerythrocytic malarial parasites. 2. Altered vacuolar volume regulation in drug resistant malaria. Biochemistry 45, 12411-12423, doi: 10.1021/ bi0610348 (2006
35. Kirk, K. Membrane transport in the malaria-infected erythrocyte. Physiological reviews 81, 495-537 (2001
36. Weed, R I., Reed, C. F. & Berg, G. Is hemoglobin an essential structural component of human erythrocyte membranes? The Journal of clinical investigation 42, 581-588, doi: 10.1172/JCI104747 (1963
37. Kahn, S. B., Cheung, T., Lodise, R. & Brodsky, I. Red blood cell metabolism in AKR mice in the prelymphomatous phase. Cancer research 36, 194-199 (1976
38. Diez-Silva, M. et al. Pf155/RESA protein influences the dynamic microcirculatory behavior of ring-stage Plasmodium falciparum infected red blood cells. Sci Rep 2, 614, doi: 10.1038/srep00614 (2012
39. Dondorp, A. M., Pongponratn, E. & White, N. J. Reduced microcirculatory flow in severe falciparum malaria: pathophysiology and electron-microscopic pathology. Acta Trop 89, 309-317 (2004
40. Mills, J. P. et al. Effect of plasmodial RESA protein on deformability of human red blood cells harboring Plasmodium falciparum. Proceedings of the National Academy of Sciences of the United States of America 104, 9213-9217, doi: 10.1073/pnas.0703433104 (2007
41. Hutchings, C. L. et al. New insights into the altered adhesive and mechanical properties of red blood cells parasitized by Babesia bovis. Molecular microbiology 65, 1092-1105, doi: 10.1111/j.1365-2958.2007.05850.x (2007
42. Chandramohanadas, R. et al. Biophysics of malarial parasite exit from infected erythrocytes. PloS one 6, e20869, doi: 10.1371/ journal.pone.0020869 (2011
43. Brasseur, P., Lecoublet, S., Kapel, N., Favennec, L. & Ballet, J. J. In vitro evaluation of drug susceptibilities of Babesia divergens isolates. Antimicrobial agents and chemotherapy 42, 818-820 (1998
44. Kim, K. et al. Diffraction optical tomography using a quantitative phase imaging unit. Optics letters 39, 6935-6938, doi: Doi 10.1364/Ol.39.006935 (2014
45. Lee, K. & Park, Y. Quantitative phase imaging unit. Optics letters 39, 3630-3633, doi: Doi 10.1364/Ol.39.003630 (2014
46. Tomaiuolo, G., Rossi, D., Caserta, S., Cesarelli, M. & Guido, S. Comparison of two flow-based imaging methods to measure individual red blood cell area and volume. Cytometry. Part A : the journal of the International Society for Analytical Cytology 81, 1040-1047, doi: 10.1002/cyto.a.22215 (2012
47. Waugh, R. E. et al. Rheologic properties of senescent erythrocytes: loss of surface area and volume with red blood cell age. Blood 79, 1351-1358 (1992