Table of Contents Table of Contents
Previous Page  6 / 19 Next Page
Information
Show Menu
Previous Page 6 / 19 Next Page
Page Background

Page 26

N o v e m b e r 2 6 - 2 7 , 2 0 1 8 | M a d r i d , S p a i n

&

&

BIOTECHNOLOGY

Euro Congress on

GENOMICS AND MOLECULAR BIOLOGY

International Conference on

CANCER SCIENCE AND THERAPY

Global Congress on

Joint Event on

OF EXCELLENCE

IN INTERNATIONAL

MEETINGS

alliedacademies.com

YEARS

Euro Biotechnology 2018 & Genomics Congress 2018 & Cancer Congress 2018

Journal of RNA and Genomics

|

ISSN: 2591-7781

|

Volume 14

Anirban Banerjee et al., J RNA Genomics 2018, Volume 14

INTRACELLULAR, BIOFILM-INHIBITORY

AND MEMBRANE DAMAGING ACTIVITIES

OF NIMBOLIDE ISOLATED FROM

AZADIRACHTA INDICA A. JUSS (MELIACEAE)

AGAINST METICILLIN-RESISTANT

STAPHYLOCOCCUS AUREUS

Anirban Banerjee, Prodipta Sarkar, Saurabh Acharyya

Amarendra Patra, Karthika Thankamani, Hemanta Koley

and

Prasanta K Bag

University of Calcutta, India

S

taphylococcus aureus

is a leading aetiologic agent of nosocomial- and

community-acquired infectious diseases worldwide.

S. aureus

causes

several human diseases, ranging from minor skin and soft tissue infections

to more severe conditions such as toxic shock syndrome, glomerulonephri-

tis, pneumonia, meningitis, endocarditis, osteomyelitis and septicaemia. The

public health concern regarding staphylococcal infections is inflated by the

increasing occurrence of multidrug-resistant strains, e.g. multidrug- and

meticillin- resistant

S. aureus

(MDR MRSA). This study was designed to eval-

uate the intracellular bactericidal activity and

in vitro

membrane-damaging

and biofilm-inhibitory activities of nimbolide isolated from Azadirachta indi-

ca against MDR MRSA.

In vitro

antibacterial activity of nimbolide was deter-

mined by performing MIC, MBC and time-kill kinetic studies. It showed much

lower MIC (8 μg ml

-1

) and MBC (32 μg ml

-1

) values than other antibiotics.

Biofilm-inhibitory activities were determined by SEM. Cellular drug accumu-

lation and assessments of intracellular activities were performed using Vero

cell culture. SEM findings revealed that exposure to nimbolide at 1X MBC on

S. aureus

resulted in the disintegration of the bacterial cell envelope, severe

bacterial membrane perturbation, significant membrane damage, bursting of

cells and cell lysis. The biofilm structure was disrupted, and the biofilm forma-

tion was greatly reduced in the presence of nimbolide as examined by SEM.

The level of accumulation of nimbolide in Vero cells incubated for 24 h is

relatively higher than that of ciprofloxacin and nalidixic acid. The viable num-

ber of intracellular

S. aureus

was decreased [reduction of ~2 log10 c.f.u. (mg

Vero cell protein)

-1

] in a time-dependent manner in the presence of nimbolide

(4 X MBC) that was comparable to that of tetracycline and nalidixic acid. The

significant intracellular, biofilm-inhibitory and bacterial membrane-damaging

activities of nimbolide demonstrated here suggested that it has potential as

an effective antibacterial agent for the treatment of severe infections caused

by MDR MRSA.

Anirban Banerjee has completed his PhD at the age of 29

years from Visva Bharati Santiniketan, India. He is now

Post-Doctoral fellow in Department of Biochemistry, Uni-

versity of Calcutta, India. He is engaged in research in mi-

crobiology and parasitology and has many publications

in reputed Journals.

anibanerjee930@gmail.com

BIOGRAPHY