Use of aqueous compositions of polyacrylamide with zinc and copper cations as a possible way to reduce the risks of microbial contamination in objects in the hospital environment
M.V. Kuznetsova1,2, E.V. Afanasievskaya2, N.V. Nikolaeva2, E.S. Gorovitz2, A.S. Averkina3, I.N. Feklistova4, V.A. Valtsifer3
1Institute of Ecology and Genetics of Microorganisms of Ural Branch of Russian Academy of Sciences – affiliation of Perm Federal Research Centre of Ural Branch of RAS, 13 Goleva Str., Perm, 614081, Russian Federation
2Perm State Medical University named after Academician E.A. Wagner, 26 Petropavlovskaya Str., Perm, 614990, Russian Federation
3Institute of Technical Chemistry of Ural Branch of Russian Academy of Sciences – affiliation of Perm Federal Research Centre of Ural Branch of RAS, 3 Akademika Koroleva Str., Perm, 613013, Russian Federation
4Belarusian State University, 4 Nezavisimosti Ave., Minsk, 220030, Belarus
Microbial contamination means that infectious agents are identified on objects in the hospital environment. This serious issue is the most significant for healthcare organizations. Covering abiotic surfaces with a thin polymer film can be a promising way to fight against microbial adhesion and colonization. This film acts as a depot of an antibacterial substance.
In this study, our aim was to investigate antimicrobial effects of new water compositions of polyacrylamides (PAM) with CuSO4 and ZnSO4.
We examined antibacterial activity of 5%-solutions of CuSO4 and ZnSO4 and their compositions with various PAM types in a concentration equal to 0.075 % against such reference cultures as Escherichia coli, Klebsiella pneumoniaе, Pseudomonas aeruginosa, and Staphylococcus aureus. We estimated use of PAM as a growth substrate as well as antimicrobial activity of the analyzed solutions and compositions in agar and liquid nutrient media.
As a result, we established that bacterial cultures did not use PAM as sole nutrition source when growing in a liquid mineral medium and on PAM-films covering glass and plastic surfaces. More apparent inhibitory effects were produced on microorganisms cultivated on solid and liquid nutrient media by 5%-solution of ZnSO4. When PAM Praestol 857 and PAM Praestol were added to solutions of Cu2+ and Zn2+ cations, it resulted in an authentic increase in a diameter of a zone with inhibited bacterial growth in the agar medium. In the liquid medium, salts of both metals inhibited the growth and viability of all the analyzed microorganisms already in a concentration equal to 0.16 % or lower. Adding PAM Praestol 2530 led to a slight decrease in antibacterial efficiency of the examined metal salts whereas PAM Praestol 857 had practically no influence on bacteriostatic and bactericidal effects produced by them.
Therefore, use of the obtained composite solutions where CuSO4 or ZnSO4, immobilized on a PAM matrix act as an antibacterial component seems a promising way to disinfect objects in the hospital environment. This can significantly reduce risks of hospital-acquired infections.
- Thakali А., MacRae J.D. A review of chemical and microbial contamination in food: What are the threats to a circular food system? Environ. Res., 2021, vol. 194, pp. 110635. DOI: 10.1016/j.envres.2020.110635
- Khan H.A., Baig F.K., Mehboob R. Nosocomial infections. Epidemiology, prevention, control and surveillance. Asian Pac. J. Trop. Biomed., 2017, vol. 7, no. 5, pp. 478–482. DOI: 10.1016/j.apjtb.2017.01.019
- Otter J.A., Yezli S., Salkeld J.A.G., French G.L. Evidence that contaminated surfaces contribute to the transmission of hospital pathogens and an overview of strategies to address contaminated surfaces in hospital settings. Am. J. Infect. Control., 2013, vol. 41, no. 5, pp. S6–S11. DOI: 10.1016/j.ajic.2012.12.004
- Prevention of hospital-acquired infections: a practical guide, 2nd ed. In: G. Ducel, J. Fabry, L. Nicolle eds. Geneva, WHO, 2002, 64 p. Available at: https://apps.who.int/iris/bitstream/handle/10665/67350/WHO_CDS_CSR_EPH_2...?
sequence=1&isAllowed=y (December 07, 2022). - Robakowska M., Bronk M., Tyrańska-Fobke A., Ślęzak D., Kraszewski J., Balwicki Ł. Patient Safety Related to Microbiological Contamination of the Environment of a Multi-Profile Clinical Hospital. Int. J. Environ. Res. Public Health, 2021, vol. 18, no. 7, pp. 3844. DOI: 10.3390/ijerph18073844
- Rozman U., Pušnik M., Kmetec S., Duh D., Šostar Turk S. Reduced Susceptibility and Increased Resistance of Bacteria against Disinfectants: A Systematic Review. Microorganisms, 2021, vol. 9, no. 12, pp. 2550. DOI: 10.3390/microorganisms9122550
- Cheknev S.B., Vostrova E.I., Apresova M.A., Piskovskaya L.S., Vostrov A.V. Deceleration of bacterial growth in Staphylococcus aureus and Pseudomonas aeruginosa cultures in the presence of copper and zinc cations. Zhurnal mikrobiologii, epidemiologii i immunobiologii, 2015, no. 2, рр. 9–17 (in Russian).
- Ning C., Wang X., Li L., Zhu Y., Li M., Yu P., Zhou L., Zhou Z. [et al.]. Concentration ranges of antibacterial cations for showing the highest antibacterial efficacy but the least cytotoxicity against mammalian cells: implications for a new antibacterial mechanism. Chem. Res. Toxicol., 2015, vol. 28, no. 9, pp. 1815–1822. DOI: 10.1021/acs.chemrestox.5b00258
- Casey A.L., Adams D., Karpanen T.J., Lambert P.A., Cookson B.D., Nightingale P., Miruszenko L., Shillam R. [et al.]. Role of copper in reducing hospital environment contamination. J. Hosp. Infect., 2010, vol. 74, no. 1, pp. 72–77. DOI: 10.1016/j.jhin.2009.08.018
- Jaiswal S., McHale P., Duffy B. Preparation and rapid analysis of antibacterial silver, copper and zinc doped sol-gel surfaces. Colloids Surf. B Biointerfaces, 2012, vol. 94, pp. 170–176. DOI: 10.1016/j.colsurfb.2012.01.035
- Guezennec A.-G., Michel C., Bru K., Touzé S., Desroche N. Transfer and degradation of polyacrylamide-based floccu-lants in hydrosystems: a review. Environ. Sci. Pollut. Res., 2015, vol. 22, no. 9, pp. 6390–6406. DOI: 10.1007/s11356-014-3556-6
- Fahmy A., Jácome L.A., Schönhals A. Effect of Silver Nanoparticles on the Dielectric Properties and the Homogeneity of Plasma Polyacrylic Acid Thin Films. J. Phys. Chem., 2020, vol. 124, no. 41, pp. 22817–22826. DOI: 10.1021/acs.jpcc.0c06712
- Singh A., Mishra M., Tripathi P., Sachan S. Resistance of heavy metals on some pathogenic bacterial species. Afr. J. Microbiol. Res., 2015, vol. 9, no. 16, pp. 1162–1164. DOI: 10.5897/AJMR2014.7344
- Alsaadi L.A.S. Heavy metals tolerance and antibiotics susceptibility profiles of Staphylococcus aureus strains isolated from clinical sources in Baquba city. Diyala Journal for Pure Science, 2017, vol. 13, no. 1, pp. 130–144. DOI: 10.24237/djps.1301.136A
- Kay-Shoemake J.L., Watwood M.E., Lentz R.D., Sojka R.E. Polyacrylamide as an organic nitrogen source for soil microorganisms with potential effects on inorganic soil nitrogen in agricultural soil. Soil Biol. Biochem., 1998, vol. 30, no. 8/9, pp. 1045–1052.
- Kay-Shoemake J.L., Watwood M.E., Sojka R.E., Lentz R.D. Polyacrylamide as a substrate for microbial amidase in culture and soil. Soil Biol. Biochem., 1998, vol. 30, no. 13, pp. 1647–1654.
- Wen Q., Chen Z., Zhao Y., Zhang H., Feng Y. Biodegradation of polyacrylamide by bacteria isolated from activated sludge and oil-contaminated soil. J. Hazard. Mater., 2010, vol. 175, no. 1–3, pp. 955–959. DOI: 10.1016/j.jhazmat.2009.10.102
- Maksimova Yu.G., Gorshkova A.A., Demakov V.A. Polyacrylamide biodegradation by soil microflora and bacteria containing amidase. Vestnik Permskogo universiteta. Seriya: Biologiya, 2017, no. 2, pp. 200–204 (in Russian).
- Sipulinov R.B., Karagaicheva Yu.V., Kozulina T.N., Rogacheva S.M., Otradnova M.I. Vydelenie i otsenka destruktivnoi aktivnosti mikroorganizmov, utiliziruyushchikh akrilovye polimery [Isolation and assessment of the destructive activity of microorganisms utilizing acrylic polymers]. Uchenye zapiski Tavricheskogo natsional'nogo universiteta imeni V.I. Vernadskogo. Seriya: Biologiya, khimiya, 2014, vol. 27 (66), no. 2, pp. 150–156 (in Russian).
- Yu F., Fu R., Xie Y., Chen W. Isolation and characterization of polyacrylamide-degrading bacteria from dewatered sludge. Int. J. Environ. Res. Public Health, 2015, vol. 12, no. 4, pp. 4214–4230. DOI: 10.3390/ijerph120404214
- Matsuoka H., Ishimura F., Takeda T., Hikuma M. Isolation of polyacrylamide-degrading microorganisms from soil. Biotech. Bioproc. Eng., 2002, vol. 7, no. 5, pp. 327–330. DOI: 10.1007/BF02932844
- Shanker R., Ramakrishna C., Seth P.K. Microbial degradation of acrylamide monomer. Arch. Microbiol., 1990, vol. 154, no. 2, pp. 192–198. DOI: 10.1007/BF00423332
- Nawaz M.S., Khan A.A., Bhattacharayya D., Siitonen P.H., Cerniglia C.E. Physical, biochemical, and immunological characterization of a thermostable amidase from Klebsiella pneumoniae NCTR 1. J. Bacteriol., 1996, vol. 178, no. 8, pp. 2397–2401. DOI: 10.1128/jb.178.8.2397–2401.1996
- Petka K., Tarko Т., Duda-Chodak А. Is Acrylamide as Harmful as We Think? A New Look at the Impact of Acrylamide on the Viability of Beneficial Intestinal Bacteria of the Genus Lactobacillus. Nutrients, 2020, vol. 12, no. 4, pp. 1157. DOI: 10.3390/nu12041157
- Büttner F.M., Zoll S., Nega M., Götz F., Stehle T. Structure-function analysis of Staphylococcus aureus amidase reveals the determinants of peptidoglycan recognition and cleavage. J. Biol. Chem., 2014, vol. 289, no. 16, pp. 11083–11094. DOI: 10.1074/jbc.M114.557306
- Wilson S.A., Drew R.E. Transcriptional analysis of the amidase operon from Pseudomonas aeruginosa. J. Bacteriol., 1995, vol. 177, no. 11, pp. 3052–3057. DOI: 10.1128/jb.177.11.3052-3057.1995
- Tuson H.H., Renner L.D., Weibel D.B. Polyacrylamide hydrogels as substrates for studying bacteria. Chem. Commun. (Camb.), 2012, vol. 48, no. 10, pp. 1595–1597. DOI: 10.1039/C1CC14705F
- Yazdankhah S., Skjerve E., Wasteson Y. Antimicrobial resistance due to the content of potentially toxic metals in soil and fertilizing products. Microb. Ecol. Health Dis., 2018, vol. 29, no. 1, pp. 1548248. DOI: 10.1080/16512235.2018.1548248
- Chudobova D., Dostalova S., Blazkova I., Michalek P., Ruttkay-Nedecky B., Sklenar M., Nejdl L., Kudr J. [et al.]. Effect of ampicillin, streptomycin, penicillin and tetracycline on metal resistant and non-resistant Staphylococcus aureus. Int. J. Environ. Res. Public Health, 2014, vol. 11, no. 3, pp. 3233–3255. DOI: 10.3390/ijerph110303233
- Xue H., Wu Z., Li L., Li F., Wang Y., Zhao X. Coexistence of heavy metal and antibiotic resistance within a novel composite staphylococcal cassette chromosome in a Staphylococcus haemolyticus isolate from bovine mastitis milk. Antimicrob. Agents Chemother., 2015, vol. 59, no. 9, pp. 5788–5792. DOI: 10.1128/AAC.04831-14
- Boyce J.M. Modern technologies for improving cleaning and disinfection of environmental surfaces in hospitals. Antimicrob. Resist. Infect. Control, 2016, vol. 5, pp. 10. DOI: 10.1186/s13756-016-0111-x