TY - JOUR
T1 - Proteomic expression profiles of virulent and avirulent strains of Listeria monocytogenes isolated from macrophages
AU - Donaldson, Janet R.
AU - Nanduri, Bindu
AU - Pittman, Joseph R.
AU - Givaruangsawat, Sumalee
AU - Burgess, Shane C.
AU - Lawrence, Mark L.
N1 - Funding Information:
This project was supported by USDA NIFA grant number # 2007-35201-17732 and USDA Agricultural Research Service (Agreement No. 58-6202-5-083 ). We would like to thank Michelle Banes, Susan Bridges, Christopher Clark, Patrick Peavy, Ranjit Kumar, and Chamali Thanthiriwatte for their assistance with this project. We would also like to thank Tibor Pechan and Ken Pendarvis for their technical assistance with mass spectrometry.
PY - 2011/9/6
Y1 - 2011/9/6
N2 - Listeria monocytogenes is able to survive and proliferate within macrophages. In the current study, the ability of three L. monocytogenes strains (serovar 1/2a strain EGDe, serovar 4b strain F2365, and serovar 4a strain HCC23) to proliferate in the murine macrophage cell line J774.1 was analyzed. We found that the avirulent strain HCC23 was able to initiate an infection but could not establish prolonged infection within the macrophages. By contrast, strains EGDe and F2365 proliferated within macrophages for at least 7. h. We further analyzed these strains by comparing their protein expression profiles at 0. h, 3. h, and 5. h post-infection using multidimensional protein identification technology coupled with electrospray ionization tandem mass spectrometry. Our results indicated that similar metabolic and cell wall associated proteins were expressed by all three strains at 3. h post-infection. However, increased expression of stress response and DNA repair proteins was associated with the ability to proliferate in macrophages at 5. h post-infection. By comparing the protein expression patterns of these three L. monocytogenes strains during intracellular growth in macrophages, we were able to detect biological differences that may determine the ability of L. monocytogenes to survive in macrophages.
AB - Listeria monocytogenes is able to survive and proliferate within macrophages. In the current study, the ability of three L. monocytogenes strains (serovar 1/2a strain EGDe, serovar 4b strain F2365, and serovar 4a strain HCC23) to proliferate in the murine macrophage cell line J774.1 was analyzed. We found that the avirulent strain HCC23 was able to initiate an infection but could not establish prolonged infection within the macrophages. By contrast, strains EGDe and F2365 proliferated within macrophages for at least 7. h. We further analyzed these strains by comparing their protein expression profiles at 0. h, 3. h, and 5. h post-infection using multidimensional protein identification technology coupled with electrospray ionization tandem mass spectrometry. Our results indicated that similar metabolic and cell wall associated proteins were expressed by all three strains at 3. h post-infection. However, increased expression of stress response and DNA repair proteins was associated with the ability to proliferate in macrophages at 5. h post-infection. By comparing the protein expression patterns of these three L. monocytogenes strains during intracellular growth in macrophages, we were able to detect biological differences that may determine the ability of L. monocytogenes to survive in macrophages.
KW - Intracellular
KW - Listeria monocytogenes
KW - Macrophages
KW - Proteomics
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U2 - 10.1016/j.jprot.2011.05.008
DO - 10.1016/j.jprot.2011.05.008
M3 - Article
C2 - 21605710
AN - SCOPUS:80052029934
SN - 1874-3919
VL - 74
SP - 1906
EP - 1917
JO - Journal of Proteomics
JF - Journal of Proteomics
IS - 10
ER -