GENTAMICIN MODULATES THE GENE EXPRESSION OF HLA IN METHICILLIN RESISTANCE STAPHYLOCOCCUS AUREUS BIOFILM

Nihad Taha Mohammed Jaddoa, Harith Jabbar Fahad Al-Mathkhury

Abstract

Objective: The present work was undertaken to investigate the impact of sub inhibitory concentration of gentamicin on hla gene expression in methicillin resistant Staphylococcus aureus isolates. Methods: The bacterial isolates used in this study represent 33 MRSA strains, previously isolated form patients visiting several hospitals in Baghdad. Gentamicin, vancomycin, and oxacillin MIC were determined using broth dilution method. Microtiter plate method was adopted to investigate the biofilm forming capacity. Alpha hemolysin was detected by culturing MRSA isolates on rabbit blood agar. Furthermore, hla gene was detected in MRSA isolates using conventional PCR technique; while, qRT-PCR method was performed to assay the hla expression in planktonic and biofilm cells in presence and absence of gentamicin. Results: the present results demonstrated that 12 (36.36%) isolates were gentamicin-resistant; whereas, all isolates were resistant to oxacillin and sensitive to vancomycin. Out of 33 MRSA, 3, 23, and 7 isolates formed a weak, moderate, and strong biofilm, respectively. Phenotypically, 30 isolates produced alpha hemolysin on rabbit blood agar plates; nevertheless, hla gene was located in 29 isolates. Of considerable interest, the addition of gentamicin significantly (P < 0.05) reduced the hemolysis activity; while, insignificant fold change (less than two) of hla gene was observed in all tested isolates in the presence of sub MIC of gentamicin (16 µg/ml). Conclusion: gentamicin upregulated the hla gene expression in biofilm cells; hitherto, this increment was isolate specific.

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Muhammad HAO. A comparative study on biofilm forming capacity in Methicillin Resistant Staphylococcus aureus and Methicillin Resistant Staphylococcus epidermidis by using different techniques [MSc. Thesis]. Baghdad, Iraq: Biology, University of Baghdd; 2013.

Shalá AA, Restrepo S, Barrios AFG. A network model for biofilm development in Escherichia coli K-12. Bio. Med. 2011;8:34-40.

Henry-Stanley M, Hess D, Wells C. Aminoglycoside inhibition of Staphylococcus aureus biofilm formation is nutrient dependent. J. Med. Microbiol. 2014;63:861-869.

Vandenesch F, Lina G, Henry T. Staphylococcus aureus hemolysins, bi-component leukocidins, and cytolytic peptides: a redundant arsenal of membrane-damaging virulence factors? Frontiers in cellular and infection microbiology. 2012;2:12.

Worlitzsch D, Kaygin H, Steinhuber A, Dalhoff A, Botzenhart K, Doring G. Effects of amoxicillin, gentamicin, and moxifloxacin on the hemolytic activity of Staphylococcus aureus in vitro and in vivo. Antimicrobial agents and chemotherapy. Jan 2001;45(1):196-202.

Al-Dahbi A, Al-Mathkhury HJ. Distribution of Methicillin Resistant Staphylococcus aureus in Iraqi patients and Healthcare Workers. Iraqi Journal of Science. 2013;54:293-300.

Muhammad HAO, Al-Mathkhury HJF. The Prevalence of methicillin resistant Staphylococcus aureus and methicillin resistant Staphylococcus epidermidis in AL-Sulaimania city. Iraqi Journal of Science. 2014;55:386-393.

Karam NJ, Al-Mathkhury HJF. Staphylococcus epidermidis Prevails Staphylococcus aureus in Multispecies Biofilm under Gentamicin Stress. International Journal of Science and Research (IJSR). 2017;6(7):528-539.

Nawaz A, Razzaq A, S. I, Nawaz A, Ali A, Kaleem A. Characterization of antibiotic resistant gene in Staphylococcus aureus isolated from surgical wounds. Adv. Life Sci. 2016;3:83-88.

CLSI. Performance Standards for Antimicrobial Susceptibility Testing. M100S. 26th edition. Wayne: Clinical and Laboratory Standards Institute; 2016.

Atshan SS, Nor Shamsudin M, Sekawi Z, et al. Prevalence of adhesion and regulation of biofilm-related genes in different clones of Staphylococcus aureus. Journal of biomedicine & biotechnology. 2012;2012:976972.

Jarraud S, Mougel C, Thioulouse J, et al. Relationships between Staphylococcus aureus Genetic Background, Virulence Factors, agr Groups (Alleles), and Human Disease. Infection and Immunity. 2002;70:631–641.

Rasigade JP, Moulay A, Lhoste Y, et al. Impact of sub-inhibitory antibiotics on fibronectin-mediated host cell adhesion and invasion by Staphylococcus aureus. BMC Microbiol. Dec 14 2011;11:263.

Belbase A, Pant ND, Nepal K, et al. Antibiotic resistance and biofilm production among the strains of Staphylococcus aureus isolated from pus/wound swab samples in a tertiary care hospital in Nepal. Annals of clinical microbiology and antimicrobials. Mar 23 2017;16(1):15.

Gad GFM, El-Feky MA, El-Rehewy MS, Hassan MA, Abolella H, El-Baky RMA. Detection of icaA, icaD genes and biofilm production by Staphylococcus aureus and Staphylococcus epidermidis isolated from urinary tract catheterized patients. The Journal of Infection in Developing Countries. 2009;3(05).

Moghadam SO, Pourmand MR, Aminharat F. Biofilm formation and antimicrobial resistance in methicillin-resistant Staphylococcus aureus isolated from burn patients, Iran. J Infect Dev Ctries. 2014;8:1511-1517.

Croes S, Deurenberg RH, Boumans ML, Beisser PS, Neef C, Stobberingh EE. Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage. BMC Microbiol. Oct 28 2009;9:229.

Aarestrup FM, Larsen HD, Eriksen NH, Elsberg CS, Jensen NE. Frequency of alpha- and beta-haemolysin in Staphylococcus aureus of bovine and human origin. A comparison between pheno- and genotype and variation in phenotypic expression. 1999;107:425-430.

Möllby R, Wadström.T. Purification of staphylococcal beta-, gamma- and delta-hemolysins. In: Jeljaszewicz J, ed. Topics in Microbiology and Immunology. Vol 11. Basel: Karger Press; 1973:298-313.

Gray GS, Kehoe M. Primary sequence of the alpha-toxin gene from Staphylococcus aureus wood 46. Infect Immun. Nov 1984;46(2):615-618.

O’Reilly M, Kreiswirth BN, Foster TJ. Molecular analysis of a non-expressed a-toxin gene (hla) of clinical isolates of Staphylococcus aureus,. In: Novick RP, ed. Molecular biology of the staphylococci. New York: VCH Publishers Inc; 1990:439-443.

Bhakdi S, Muhly M, Fussle R. Correlation between toxin binding and hemolytic activity in membrane damage by staphylococal a-toxin. Infect. Immun. 1984;46:318-323.

Hildebr A, Pohl M, Bhakdi S. Staphylococcus aureus alpha-toxin. Dual mechanism of binding to target cells. J Biol Chem. 1991;266:17195-17200.

Ohlsen K, Ziebuhr W, Koller KP, Hell W, Wichelhaus TA, Hacker J. Effects of subinhibitory concentrations of antibiotics on alpha-toxin (hla) gene expression of methicillin-sensitive and methicillin-resistant Staphylococcus aureus isolates. Antimicrobial agents and chemotherapy. Nov 1998;42(11):2817-2823.

Ariyanti D, Salasia S, Tato S. Characterization of Haemolysin of Staphylococcus aureus Isolated from Food of Animal Origin. Indonesian J. biotech., : . 2011;16:32- 37.

Moraveji Z, Tabatabaei M, Shirzad Aski H, Khoshbakht R. Characterization of hemolysins of Staphylococcus strains isolated from human and bovine, southern Iran. Iran J Vet Res. Fall 2014;15(4):326-330.

Shukla SK, Karow ME, Brady JM, et al. Virulence genes and genotypic associations in nasal carriage, community-associated methicillin-susceptible and methicillin-resistant USA400 Staphylococcus aureus isolates. Journal of clinical microbiology. Oct 2010;48(10):3582-3592.

Kateete DP, Namazzi S, Okee M, et al. High prevalence of methicillin resistant Staphylococcus aureus in the surgical units of Mulago hospital in Kampala, Uganda. BMC research notes. Sep 7 2011;4:326.

Lorian V, Gemmell GC. Effect of low antibiotic concentrations on bacteria: effects on ultrastructure, virulence, and susceptibility to immune defenses. In: V L, ed. Antibiotics in Laboratory Medicine. Baltimore: Williams & Wilkins; 1991:493-555.

Drummond LJ, Smith DG, Poxton IR. Effects of sub-MIC concentrations of antibiotics on growth of and toxin production by Clostridium difficile. Journal of medical microbiology. Dec 2003;52(Pt 12):1033-1038.

Stevens DL, Ma Y, Salmi DB, McIndoo E, Wallace RJ, Bryant AE. Impact of antibiotics on expression of virulence-associated exotoxin genes in methicillin-sensitive and methicillin-resistant Staphylococcus aureus. The Journal of infectious diseases. Jan 15 2007;195(2):202-211.

Worlitzsch D, Kaygin H, Steinhuber A, Dalhoff A, Botzenhart K, Doring G. Effects of Amoxicillin, Gentamicin, and Moxifloxacin on the Hemolytic Activity of Staphylococcus aureus In Vitro and In Vivo. Antimicrobial agents and chemotherapy. 2001;45(1):196-202.

Otto MP, Martin E, Badiou C, et al. Effects of subinhibitory concentrations of antibiotics on virulence factor expression by community-acquired methicillin-resistant Staphylococcus aureus. The Journal of antimicrobial chemotherapy. Jul 2013;68(7):1524-1532.

Mun SH, Kong R, Seo YS, et al. Subinhibitory concentrations of punicalagin reduces expression of virulence-related exoproteins by Staphylococcus aureus. FEMS microbiology letters. Nov 2016;363(22).

DeLeo FR, Qiu J, Wang D, et al. Subinhibitory Concentrations of Thymol Reduce Enterotoxins A and B and α-Hemolysin Production in Staphylococcus aureus Isolates. PLoS ONE. 2010;5(3):e9736.

Dancer SJ. The effect of antibiotics on methicillin-resistant Staphylococcus aureus. The Journal of antimicrobial chemotherapy. Feb 2008;61(2):246-253.

Henry-Stanley MJ, Hess DJ, Wells CL. Aminoglycoside inhibition of Staphylococcus aureus biofilm formation is nutrient dependent. Journal of medical microbiology. Jun 2014;63(Pt 6):861-869.

Kolodkin-Gal I. Beyond the wall: can D-amino acids and small molecule inhibitors eliminate infections? Future medicinal chemistry. Jun 2017;9(9):843-846.

de Oliveira A, Cataneli Pereira V, Pinheiro L, Moraes Riboli DF, Benini Martins K, Ribeiro de Souza da Cunha Mde L. Antimicrobial Resistance Profile of Planktonic and Biofilm Cells of Staphylococcus aureus and Coagulase-Negative Staphylococci. International journal of molecular sciences. Sep 1 2016;17(9).

Schilcher K, Andreoni F, Dengler Haunreiter V, Seidl K, Hasse B, Zinkernagel AS. Modulation of Staphylococcus aureus Biofilm Matrix by Subinhibitory Concentrations of Clindamycin. Antimicrobial agents and chemotherapy. Oct 2016;60(10):5957-5967.

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