3-Amino-4-aminoximidofurazan derivatives: small molecules possessing antimicrobial and antibiofilm activityagainst Staphylococcus aureus and Pseudomonas aeruginosa

被引:31
作者
Das, M. C. [1 ]
Paul, S. [2 ]
Gupta, P. [1 ]
Tribedi, P. [3 ]
Sarkar, S. [1 ]
Manna, D. [2 ]
Bhattacharjee, S. [1 ]
机构
[1] Tripura Univ, Dept Mol Biol & Bioinformat, Agartala 799004, Tripura, India
[2] Indian Inst Technol Guwahati, Dept Chem, Gauhati 781039, Assam, India
[3] Assam Don Bosco Univ, Dept Microbiol, Azara, Assam, India
关键词
3-amino-4-aminoximidofurazan; antimicrobials; biofilm; haemolysis; motility; BIOFILM FORMATION; BACTERIAL BIOFILMS; INHIBITION;
D O I
10.1111/jam.13063
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
AimThe therapeutic treatment of microbial infections involving biofilm becomes quite challenging because of its increasing antibiotic resistance capacities. Towards this direction, in the present study we have evaluated the antibiofilm property of synthesized 3-amino-4-aminoximidofurazan compounds having polyamine skeleton. These derivatives were synthesized by incorporating furazan and biguanide moieties. Methods and ResultsDifferent 3-amino-4-aminoximidofurazan derivatives (PI1-4) were synthesized via protic acid catalysis and subsequently characterized by H-1 NMR and C-13 NMR spectra, recorded at 400 and 100MHz respectively. We have tested the antimicrobial and antibiofilm activities of these synthetic derivatives (PI1-4) against both Staphylococcus aureus and Pseudomonas aeruginosa. The compounds so tested were also compared with standard antibiotics namely Tobramycin (Ps.aeruginosa) and Azithromycin (Staph.aureus) which were used as a positive control in all experimental sets. All these compounds (PI1-4) exhibited moderate to significant antimicrobial activities against both micro-organisms wherein compound PI3 showed maximum activity. Biofilm inhibition of both micro-organisms was then evaluated by crystal violet and safranin staining, estimation of biofilm total protein and microscopy methods using sub-MIC dose of these compounds. Results showed that all compounds executed anti biofilm activity against both Staph.aureus and Ps.aeruginosa wherein compound PI3 exhibited maximum activity. In relation with microbial biofilm inhibition, we have observed reduction in bacterial motility, proteolytic activity and secreted exo-polysaccharide (EPS) from both Staph.aureus and Ps.aeruginosa when they were grown in presence of these compounds. While addressing the issue of toxicity on host, we have observed that these molecules exhibited minimum level of R.B.C degradation. ConclusionThese findings establish the antibacterial and anti biofilm properties of 3-amino-4-aminoximidofurazan derivatives (PI1-4). Significance and Impact of the StudyTherefore, our current findings demonstrate that 3-amino-4-aminoximidofurazan derivatives (PI1-4) may hold promise to be effective biofilm and microbial inhibitors that may be clinically significant.
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收藏
页码:842 / 859
页数:18
相关论文
共 54 条
  • [1] Mixed species biofilms of Candida albicans and Staphylococcus epidermidis
    Adam, B
    Baillie, GS
    Douglas, LJ
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 2002, 51 (04) : 344 - 349
  • [2] Inhibition of quorum sensing-controlled virulence factor production in Pseudomonas aeruginosa by south Florida plant extracts
    Adonizio, Allison
    Kong, Kok-Fai
    Mathee, Kalai
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (01) : 198 - 203
  • [3] [Anonymous], 1997, M2A7 NCCLS
  • [4] Gender differences in the immune system activities of sea urchin Paracentrotus lividus
    Arizza, Vincenzo
    Vazzana, Mirella
    Schillaci, Domenico
    Russo, Debora
    Giaramita, Francesca Tiziana
    Parrinello, Nicolo
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 2013, 164 (03): : 447 - 455
  • [5] Chelator-induced dispersal and killing of Pseudomonas aeruginosa cells in a biofilm
    Banin, E
    Brady, KM
    Greenberg, EP
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (03) : 2064 - 2069
  • [6] BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
  • [7] Synthesis and Activity of Biomimetic Biofilm Disruptors
    Boettcher, Thomas
    Kolodkin-Gal, Ilana
    Kolter, Roberto
    Losick, Richard
    Clardy, Jon
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (08) : 2927 - 2930
  • [8] The antimicrobial armamentarium: Evaluating current and future treatment options
    Bosso, JA
    [J]. PHARMACOTHERAPY, 2005, 25 (10): : 55S - 62S
  • [9] The Globalization of Traditional Medicine in Northern Peru: From Shamanism to Molecules
    Bussmann, Rainer W.
    [J]. EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2013, 2013
  • [10] Inhibition of Pseudomonas aeruginosa and Escherichia coli O157:H7 Biofilm Formation by Plant Metabolite ε-Viniferin
    Cho, Hyun Seob
    Lee, Jin-Hyung
    Ryu, Shi Yong
    Joo, Sang Woo
    Cho, Moo Hwan
    Lee, Jintae
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2013, 61 (29) : 7120 - 7126