Detection of whole cells using reflectometric interference spectroscopy
The detection of clinically relevant bacteria as whole cells is subject of intense research. Besides established methods like ELISAs, even optical biosensors as surface plasmon resonance spectroscopy (SPR) have been proven to be applicable for such purposes. However, detection limit seems to be only...
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Published in | Physica status solidi. A, Applications and materials science Vol. 211; no. 6; pp. 1416 - 1422 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Blackwell Publishing Ltd
01.06.2014
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1862-6300 1862-6319 |
DOI | 10.1002/pssa.201330436 |
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Abstract | The detection of clinically relevant bacteria as whole cells is subject of intense research. Besides established methods like ELISAs, even optical biosensors as surface plasmon resonance spectroscopy (SPR) have been proven to be applicable for such purposes. However, detection limit seems to be only at 105 cells mL−1, which is not sufficient for many applications. A possible reason for this limitation is that particles like bacteria could only immerse to a very restricted degree into the evanescent field. As an alternative to SPR, reflectometric interference spectroscopy (RIfS) can be used for whole cell detection. It is expected that this method can overcome the aforementioned limitation because the space for detection is only, theoretically, limited to the dimensions of the flow cell. Experiments were conducted using Legionella pneumophila as model organism. In this work, preliminary results are presented demonstrating that detection of whole cells using a RIfS‐device combined with a flow‐through system is generally possible. Legionella cells were either captured on the sensor surface by hydrophobic interaction or alternatively by specific antibodies. However, the results indicate that the detection limit is in the same range as observed for SPR. |
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AbstractList | The detection of clinically relevant bacteria as whole cells is subject of intense research. Besides established methods like ELISAs, even optical biosensors as surface plasmon resonance spectroscopy (SPR) have been proven to be applicable for such purposes. However, detection limit seems to be only at 105 cells mL−1, which is not sufficient for many applications. A possible reason for this limitation is that particles like bacteria could only immerse to a very restricted degree into the evanescent field. As an alternative to SPR, reflectometric interference spectroscopy (RIfS) can be used for whole cell detection. It is expected that this method can overcome the aforementioned limitation because the space for detection is only, theoretically, limited to the dimensions of the flow cell. Experiments were conducted using Legionella pneumophila as model organism. In this work, preliminary results are presented demonstrating that detection of whole cells using a RIfS‐device combined with a flow‐through system is generally possible. Legionella cells were either captured on the sensor surface by hydrophobic interaction or alternatively by specific antibodies. However, the results indicate that the detection limit is in the same range as observed for SPR. The detection of clinically relevant bacteria as whole cells is subject of intense research. Besides established methods like ELISAs, even optical biosensors as surface plasmon resonance spectroscopy (SPR) have been proven to be applicable for such purposes. However, detection limit seems to be only at 10 super(5)cellsmL super(-1), which is not sufficient for many applications. A possible reason for this limitation is that particles like bacteria could only immerse to a very restricted degree into the evanescent field. As an alternative to SPR, reflectometric interference spectroscopy (RIfS) can be used for whole cell detection. It is expected that this method can overcome the aforementioned limitation because the space for detection is only, theoretically, limited to the dimensions of the flow cell. Experiments were conducted using Legionella pneumophila as model organism. In this work, preliminary results are presented demonstrating that detection of whole cells using a RIfS-device combined with a flow-through system is generally possible. Legionella cells were either captured on the sensor surface by hydrophobic interaction or alternatively by specific antibodies. However, the results indicate that the detection limit is in the same range as observed for SPR. The detection of clinically relevant bacteria as whole cells is subject of intense research. Besides established methods like ELISAs, even optical biosensors as surface plasmon resonance spectroscopy (SPR) have been proven to be applicable for such purposes. However, detection limit seems to be only at 105cellsmL-1, which is not sufficient for many applications. A possible reason for this limitation is that particles like bacteria could only immerse to a very restricted degree into the evanescent field. As an alternative to SPR, reflectometric interference spectroscopy (RIfS) can be used for whole cell detection. It is expected that this method can overcome the aforementioned limitation because the space for detection is only, theoretically, limited to the dimensions of the flow cell. Experiments were conducted using Legionella pneumophila as model organism. In this work, preliminary results are presented demonstrating that detection of whole cells using a RIfS-device combined with a flow-through system is generally possible. Legionella cells were either captured on the sensor surface by hydrophobic interaction or alternatively by specific antibodies. However, the results indicate that the detection limit is in the same range as observed for SPR. [PUBLICATION ABSTRACT] |
Author | Merkl, Stefan Keusgen, Michael Dassinger, Nina Vornicescu, Doru |
Author_xml | – sequence: 1 givenname: Stefan surname: Merkl fullname: Merkl, Stefan organization: Institute of Pharmaceutical Chemistry, University of Marburg, Marbacher Weg 6, 35032, Marburg, Germany – sequence: 2 givenname: Doru surname: Vornicescu fullname: Vornicescu, Doru organization: Institute of Pharmaceutical Chemistry, University of Marburg, Marbacher Weg 6, 35032, Marburg, Germany – sequence: 3 givenname: Nina surname: Dassinger fullname: Dassinger, Nina organization: Institute of Pharmaceutical Chemistry, University of Marburg, Marbacher Weg 6, 35032, Marburg, Germany – sequence: 4 givenname: Michael surname: Keusgen fullname: Keusgen, Michael email: keusgen@staff.uni-marburg.de organization: Institute of Pharmaceutical Chemistry, University of Marburg, Marbacher Weg 6, 35032, Marburg, Germany |
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Cites_doi | 10.1016/j.bios.2009.04.002 10.1016/j.bios.2006.09.004 10.1093/oxfordjournals.aje.a113953 10.1016/j.bios.2003.11.009 10.1128/IAI.66.9.4151-4157.1998 10.1016/S0956-5663(99)00039-1 10.1023/A:1008872002336 10.1128/AEM.63.5.2047-2053.1997 10.1007/s00005-009-0035-8 10.1097/00001432-200304000-00011 10.1128/JCM.41.1.34-43.2003 10.1002/pssa.201100818 10.1001/jama.1985.03360040075028 10.1128/CMR.00052-09 10.1007/978-1-60327-567-5_8 10.1128/CMR.15.3.506-526.2002 |
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References_xml | – reference: G. Proll, G. Markovic, L. Steinle, and G. Gauglitz, Biosens. Biodetect. 503, 167-178 (2009). – reference: P. Leonard, S. Hearty, J. Quinn, and R. O'Kennedy, Biosens. Bioelectron. 19, 1331-1335 (2004). – reference: P. M. Fratamico, T. P. Strobaugh, M. B. Medina, and A. G. Gehring, Biotechnol. Technol. 12, 571-576 (1998). – reference: B. S. Fields, R. F. Benson, and R. E. Besser, Clin. Microbiol. Rev. 15, 506-526 (2002). – reference: S. D. Mazumdar, B. Barlen, P. Kämpfer, and M. Keusgen, Biosens. Bioelectron. 25, 967-971 (2010). – reference: B. Neumeister, M. Faigle, M. Sommer, U. Zähringer, F. Stelter, R. Menzel, C. Schütt, and H. Northoff, Infect. Immun. 66, 4151-4157 (1998). – reference: P. L. Garbe, B. J. Davis, J. S. Weisfeld, L. Markowitz, P. Miner, F. Garrity, J. M. Barbaree, and A. L. Reingold, J. Am. Med. Assoc. 254, 521-524 (1985). – reference: M. Steinert, L. Emödi, R. Amann, and J. Hacker, Appl. Environ. Microbiol. 63, 2047-2053 (1997). – reference: C. Cordevant, J. S. Tang, D. Cleland, and M. Lange, J. Clin. Microbiol. 41(1), 34-43 (2003). – reference: D. Ivnitzky, I. Abdel-Hamid, P. Atanasov, and E. Wilkins, Biosens. Bioelectron. 14, 599-624 (1999). – reference: H. J. Newton, D. K. Y. Ang, I. R. van Driel, and E. L. Hartland, Clin. Microbiol. Rev. 23, 274-298 (2010). – reference: D. W. Fraser, T. R. Tsai, W. Orenstein, W. E. Parkin, H. J. Beecham, R. G. Sharrar, J. Harris, G. F. Mallison, S. M. Martin, J. E. McDade, C. C. Shepard, P. S. Brachman, and N. Engl, J. Med. 297, 1189-1197 (1977). – reference: K. C. Spitalny, R. L. Vogt, L. A. Orciari, L. E. Witherell, P. Etkind, and L. F. Novick, Am. J. Epidemiol. 120(6), 809-817 (1984). – reference: J. Roig, M. Sabria, and M. L. Pedro-Botet, Curr. Opin. Infect. Dis. 16, 145-151 (2003). – reference: S. Merkl, D. Vornicescu, N. Dassinger, M. Kehrel, S. Harpel, and M. Keusgen, Phys. Status Solidi A 209, 864-870 (2012). – reference: M. Palusińska-Szysz and M. Cendrowska-Pinkosz, Arch. Immunol. Therm. Exp. 57, 279-290 (2009). – reference: S. D. Mazumdar, M. Hartmann, P. Kämpfer, and M. Keusgen, Biosens. Bioelectron. 22, 2040-2046 (2007). – volume: 25 start-page: 967 year: 2010 end-page: 971 publication-title: Biosens. Bioelectron. – volume: 63 start-page: 2047 year: 1997 end-page: 2053 publication-title: Appl. Environ. Microbiol. – volume: 503 start-page: 167 year: 2009 end-page: 178 publication-title: Biosens. Biodetect. – volume: 22 start-page: 2040 year: 2007 end-page: 2046 publication-title: Biosens. Bioelectron. – volume: 15 start-page: 506 year: 2002 end-page: 526 publication-title: Clin. Microbiol. Rev. – volume: 66 start-page: 4151 year: 1998 end-page: 4157 publication-title: Infect. Immun. – volume: 120 start-page: 809 issue: 6 year: 1984 end-page: 817 publication-title: Am. J. Epidemiol. – volume: 41 start-page: 34 issue: 1 year: 2003 end-page: 43 publication-title: J. Clin. Microbiol. – volume: 19 start-page: 1331 year: 2004 end-page: 1335 publication-title: Biosens. Bioelectron. – volume: 254 start-page: 521 year: 1985 end-page: 524 publication-title: J. Am. Med. Assoc. – volume: 23 start-page: 274 year: 2010 end-page: 298 publication-title: Clin. Microbiol. Rev. – volume: 297 start-page: 1189 year: 1977 end-page: 1197 publication-title: J. Med. – volume: 57 start-page: 279 year: 2009 end-page: 290 publication-title: Arch. Immunol. Therm. Exp. – volume: 209 start-page: 864 year: 2012 end-page: 870 publication-title: Phys. Status Solidi A – volume: 12 start-page: 571 year: 1998 end-page: 576 publication-title: Biotechnol. Technol. – volume: 16 start-page: 145 year: 2003 end-page: 151 publication-title: Curr. Opin. Infect. Dis. – volume: 14 start-page: 599 year: 1999 end-page: 624 publication-title: Biosens. Bioelectron. – ident: e_1_2_6_3_1 doi: 10.1016/j.bios.2009.04.002 – ident: e_1_2_6_2_1 doi: 10.1016/j.bios.2006.09.004 – volume: 297 start-page: 1189 year: 1977 ident: e_1_2_6_7_1 publication-title: J. Med. – ident: e_1_2_6_9_1 doi: 10.1093/oxfordjournals.aje.a113953 – ident: e_1_2_6_16_1 doi: 10.1016/j.bios.2003.11.009 – volume: 66 start-page: 4151 year: 1998 ident: e_1_2_6_18_1 publication-title: Infect. Immun. doi: 10.1128/IAI.66.9.4151-4157.1998 – ident: e_1_2_6_4_1 doi: 10.1016/S0956-5663(99)00039-1 – ident: e_1_2_6_17_1 doi: 10.1023/A:1008872002336 – ident: e_1_2_6_11_1 doi: 10.1128/AEM.63.5.2047-2053.1997 – ident: e_1_2_6_8_1 doi: 10.1007/s00005-009-0035-8 – ident: e_1_2_6_14_1 doi: 10.1097/00001432-200304000-00011 – ident: e_1_2_6_15_1 doi: 10.1128/JCM.41.1.34-43.2003 – ident: e_1_2_6_5_1 doi: 10.1002/pssa.201100818 – ident: e_1_2_6_10_1 doi: 10.1001/jama.1985.03360040075028 – ident: e_1_2_6_12_1 doi: 10.1128/CMR.00052-09 – ident: e_1_2_6_6_1 doi: 10.1007/978-1-60327-567-5_8 – ident: e_1_2_6_13_1 doi: 10.1128/CMR.15.3.506-526.2002 |
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SubjectTerms | Antibodies Bacteria ELISA Hydrophobicity immobilization Interference Legionella pneumophila Legionnaires' disease Organisms Plasmons reflectometric interference spectroscopy (RIfS) Spectroscopy Spectrum analysis whole cell detection |
Title | Detection of whole cells using reflectometric interference spectroscopy |
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