Журнал микробиологии, эпидемиологии и иммунобиологии. 2018; : 3-9
МЕХАНИЗМЫ БАКТЕРИЦИДНОГО ДЕЙСТВИЯ В РЕАЛИЗАЦИИ ОБЩИХ АНТИБАКТЕРИАЛЬНЫХ ЭФФЕКТОВ КАТИОНОВ МЕТАЛЛОВ В КУЛЬТУРЕ STREPTOCOCCUS PYOGENES
Чекнев С. Б., Вострова Е. И., Кисиль С. В., Сарычева М. А., Востров А. В.
https://doi.org/10.36233/0372-9311-2018-2-3-9Аннотация
Список литературы
1. Бузолева Л.С., Кривошеева А.М. Влияние тяжелых металлов на размножение патогенных бактерий. Успехи соврем. естествознания. 2013, 7: 30-33.
2. Савченко О.И., Кравчук Т.Н., Тапальский Д.В., Филиппова В.А. Антибактериальное действие катионов тяжелых металлов. Пробл. здоровья и экологии. 2014, 2 (40): 104109.
3. Чекнев С.Б., Вострова Е.И., Апресова М.А., Писковская Л.С., Востров А.В. Торможение роста бактерий в культурах Staphylococcus aureus и Pseudomonas aeruginosa в присутствии катионов меди и цинка. Журн. микробиол. 2015, 2: 9-17.
4. Чекнев С.Б., Вострова Е.И., Сарычева М.А., Кисиль С.В., Анисимов В.В., Востров А.В. Торможение роста бактерий в культурах Streptococcus pyogenes и Streptococcus agalac-tiae в присутствии катионов меди и цинка. Журн. микробиол. 2017, 3: 26-35.
5. Bayle L., Chimalapati S., Schoehn G. et al. Zinc uptake by Streptococcus pneumoniae depends on both AdcA and AdcAII and is essential for normal bacterial morphology and virulence. Molec. Microbiol. 2011, 82 (4): 904-916.
6. Botella H., Stadthagen G., Lugo-Villarino G. et al. Metallobiology of host-pathogen interactions: an intoxicating new insight. Trends Microbiol. 2012, 20 (3): 106-112.
7. Crane J.K., Byrd I.W., Boedeker E.C. Virulence inhibition by zinc of Shiga-toxigenic Escherichia coli. Infect. Immunity. 2011, 79 (4): 1696-1705.
8. Crane J.K., Naeher T.M., Shulgina I. et al. Effect of zinc on enteropathogenic Escherichia coli infection. Infect. Immunity. 2007, 75 (12): 5974-5984.
9. Dixon S.J., Lemberg K.M., Lamprecht M.R. et al. Ferroptosis: an iron-dependent form of non-apoptotic cell death. Cell. 2012, 149: 1060-1072.
10. Dupont D.P., Duhamel G.E., Carlson M.P., Mathiesen M.R. Effect of divalent cations on hemolysin synthesis by Serpulina (Treponema) hyodysenteriae: inhibition induced by zinc and copper. Vet. Microbiol. 1994, 41: 63-73.
11. Huynh C., Andrews N.W. Iron acquisition within host cells and the pathogenicity of Leishmania. Cell. Microbiol. 2008,10 (2): 293-300.
12. Kirsten A., Herzberg M., Voigt A. et al. Contributions of five secondary metal uptake systems to metal homeostasis of Cupriavidus metallidurans CH34. J. Bacteriol. 2011, 193 (18): 46524663.
13. Kloosterman T.G., Witwicki R.M., van der Kooi-Pol M.M. et al. Opposite effects of Mn2+ and Zn2+ on PsaR-mediated expression of the virulence genes pcpA, prtA, and psaBCA of Streptococcus pneumoniae. J. Bacteriol. 2008, 190 (15): 5382-5393.
14. Lensbouer J.J., Patel A., Sirianni J.P., Doyle R.P. Functional characterization and metal ion specificity of the metal-citrate complex transporter from Strepromyces coelicolor. J. Bacteriol. 2008, 190 (16): 5616-5623.
15. Nies D.H. Microbial heavy-metal resistance. Appl. Microbiol. Biotechnol. 1999, 51: 730750.
16. Ong C.-I.Y., Walker M.J., McEwan A.G. Zinc disrupts central carbon metabolism and capsule biosynthesis in Streptococcus pyogenes. Scientific Reports. 2015, 5: 10 p.
17. Remy L., Carriere M., Derre-Bobillot M. et al. The Staphylococcus aureus Opp1 ABC transporter impairs nickel and cobalt in zinc-depleted conditions and contributes to virulence. Molec. Microbiol. 2013, 87 (4): 730-743.
18. Waldron K.J., Robinson N.J. How do bacterial cells ensure that metalloproteins get the correct metal? Nature Reviews Microbiol. 2009, 7 (1): 25-35.
19. Wang P., Lutton A., Olesik J. et al. A novel iron- and copper-binding protein in the Lyme disease spirochaete. Molec. Microbiol. 2012, 86 (6): 1441-1451.
Journal of microbiology, epidemiology and immunobiology. 2018; : 3-9
THE MECHANISMS OF BACTERICIDAL ACTION IMPACT IN COMMON ANTIBACTERIAL EFFECTS OF METAL CATIONS IN CULTURE OF STREPTOCOCCUS PYOGENES
Cheknev S. B., Vostrova E. I., Kisil S. V., Sarycheva M. A., Vostrov A. V.
https://doi.org/10.36233/0372-9311-2018-2-3-9Abstract
References
1. Buzoleva L.S., Krivosheeva A.M. Vliyanie tyazhelykh metallov na razmnozhenie patogennykh bakterii. Uspekhi sovrem. estestvoznaniya. 2013, 7: 30-33.
2. Savchenko O.I., Kravchuk T.N., Tapal'skii D.V., Filippova V.A. Antibakterial'noe deistvie kationov tyazhelykh metallov. Probl. zdorov'ya i ekologii. 2014, 2 (40): 104109.
3. Cheknev S.B., Vostrova E.I., Apresova M.A., Piskovskaya L.S., Vostrov A.V. Tormozhenie rosta bakterii v kul'turakh Staphylococcus aureus i Pseudomonas aeruginosa v prisutstvii kationov medi i tsinka. Zhurn. mikrobiol. 2015, 2: 9-17.
4. Cheknev S.B., Vostrova E.I., Sarycheva M.A., Kisil' S.V., Anisimov V.V., Vostrov A.V. Tormozhenie rosta bakterii v kul'turakh Streptococcus pyogenes i Streptococcus agalac-tiae v prisutstvii kationov medi i tsinka. Zhurn. mikrobiol. 2017, 3: 26-35.
5. Bayle L., Chimalapati S., Schoehn G. et al. Zinc uptake by Streptococcus pneumoniae depends on both AdcA and AdcAII and is essential for normal bacterial morphology and virulence. Molec. Microbiol. 2011, 82 (4): 904-916.
6. Botella H., Stadthagen G., Lugo-Villarino G. et al. Metallobiology of host-pathogen interactions: an intoxicating new insight. Trends Microbiol. 2012, 20 (3): 106-112.
7. Crane J.K., Byrd I.W., Boedeker E.C. Virulence inhibition by zinc of Shiga-toxigenic Escherichia coli. Infect. Immunity. 2011, 79 (4): 1696-1705.
8. Crane J.K., Naeher T.M., Shulgina I. et al. Effect of zinc on enteropathogenic Escherichia coli infection. Infect. Immunity. 2007, 75 (12): 5974-5984.
9. Dixon S.J., Lemberg K.M., Lamprecht M.R. et al. Ferroptosis: an iron-dependent form of non-apoptotic cell death. Cell. 2012, 149: 1060-1072.
10. Dupont D.P., Duhamel G.E., Carlson M.P., Mathiesen M.R. Effect of divalent cations on hemolysin synthesis by Serpulina (Treponema) hyodysenteriae: inhibition induced by zinc and copper. Vet. Microbiol. 1994, 41: 63-73.
11. Huynh C., Andrews N.W. Iron acquisition within host cells and the pathogenicity of Leishmania. Cell. Microbiol. 2008,10 (2): 293-300.
12. Kirsten A., Herzberg M., Voigt A. et al. Contributions of five secondary metal uptake systems to metal homeostasis of Cupriavidus metallidurans CH34. J. Bacteriol. 2011, 193 (18): 46524663.
13. Kloosterman T.G., Witwicki R.M., van der Kooi-Pol M.M. et al. Opposite effects of Mn2+ and Zn2+ on PsaR-mediated expression of the virulence genes pcpA, prtA, and psaBCA of Streptococcus pneumoniae. J. Bacteriol. 2008, 190 (15): 5382-5393.
14. Lensbouer J.J., Patel A., Sirianni J.P., Doyle R.P. Functional characterization and metal ion specificity of the metal-citrate complex transporter from Strepromyces coelicolor. J. Bacteriol. 2008, 190 (16): 5616-5623.
15. Nies D.H. Microbial heavy-metal resistance. Appl. Microbiol. Biotechnol. 1999, 51: 730750.
16. Ong C.-I.Y., Walker M.J., McEwan A.G. Zinc disrupts central carbon metabolism and capsule biosynthesis in Streptococcus pyogenes. Scientific Reports. 2015, 5: 10 p.
17. Remy L., Carriere M., Derre-Bobillot M. et al. The Staphylococcus aureus Opp1 ABC transporter impairs nickel and cobalt in zinc-depleted conditions and contributes to virulence. Molec. Microbiol. 2013, 87 (4): 730-743.
18. Waldron K.J., Robinson N.J. How do bacterial cells ensure that metalloproteins get the correct metal? Nature Reviews Microbiol. 2009, 7 (1): 25-35.
19. Wang P., Lutton A., Olesik J. et al. A novel iron- and copper-binding protein in the Lyme disease spirochaete. Molec. Microbiol. 2012, 86 (6): 1441-1451.
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