9 research outputs found
INCIDENCE AND VIRULENCE TRAITS OF CANDIDA DUBLINIENSIS ISOLATED FROM CLINICALLY SUSPECTED PATIENTS
       Objective: Fungal infections are caused by Candida species are increasing mainly in immunocompromised patients. Among Candida species, Candida dubliniensis has recently increasing opportunistic pathogenic yeast. The present study was aimed to assess the incidence and virulence factors of C. dubliniensis isolated from urine samples of various hospitalized clinically suspected patients. Methods: Totally 1,406 urine samples were processed, among that 9(0.64%) were identified as C. dubliniensis by germ tube production, biochemical test (Candida identification kit), CHROM agar Candida differential medium and growth at 45°C. Virulence factors of the C. dubliniensis viz., phospholipase, proteinase, esterase, lipase, haemolysin and biofilm production were detected by standard procedures. Results: Maximum number of C.dubliniensis have ability to produce protienase 6(66.66%), followed by esterase 5(55.55%), biofilm formation 4(44.44%), haemolysin 2(22.22%) and phospholipase, lipase 1(11.1%) respectively. Conclusion: The result revealed that these enzymes are potential virulence factors are the most important thing to realize pathogenesis of C. dubliniensis.Â
DETECTION AND ANTIMICROBIAL SUSCEPTIBILITY PATTERN OF ESBL PRODUCING GRAM NEGATIVE BACTERIA
Objective: The ESBL producing organisms has been steadily increasing over the past years. The detection and treatment of these ESBL organisms are extremely limited. In the present study, to determine the Extended Spectrum Beta Lactamases producing organism which were isolated from various samples of Multispeciality hospital in Salem, India. Methods: A total of 278 gram negative isolates were received from various samples were used to detect the ESBL production by using double disk approximation test and Phenotypic confirmatory test with combination disc. The susceptibility of ESBL producers were analysed by antibiotic susceptibility test by using 4 commercially available beta-lactamase inhibitors combinations (Piperacillin/ tazobactam, Ampicillin/Sulbactam, Ticarcillin/Clavulanic acid and Amoxycillin/Clavulanic acid). Results: A total of 351 samples were received, from that 53 Escherichia coli, 73 Klebsiella spp, 37 Pseudomonas aeruginosa, 58 Salmonella spp, 31 Enterobacter spp and 26 Proteus spp were isolated and tested; from the 278 isolates 151 were found to be ESBL producers. From the 151 ESBL producers, P/T exhibited best activity against 134(88.74percent) followed by A/C 128(84.76percent) and A/S 126(83.44percent). T/C 108(71.52percent) shown the poor activity against all the organisms compare to other combination antibiotics. P/T exhibited significantly greater inhibitory activity against Klebsiella spp (96.15percent), E. coli (92.68percent), P. aeruginosa (90.47percent), whereas, A/C exhibited considerable antimicrobial activity against Klebsiella spp (92.30percent) and P. aeruginosa (90.47percent). The A/S exhibited greater inhibitory activity against P. aeruginosa (90.38percent) and Klebsiella spp (90.38percent). P/T, A/C and A/S exhibited better activity against rest of the organisms. All the four agents show good activity against Proteus spp. Conclusion: These data suggest that Amoxycillin/Clavulanic acid and Ampicillin/Sulbactam combination antibiotics showed maximum inhibitory activity against ESBL producers. So, it can be used for the treatment of ESBL infection.Â
ANTIMICROBIAL EFFICACY AND PHYTOCHEMICAL ANALYSIS OF INDIGOFERA TRITA LINN.
An in vitro antimicrobial activity and phytochemical analysis of various extracts of Indigofera trita L. viz. petroleum ether, chloroform, acetone, ethanol and aqueous extracts were carried out. A total of 21 microorganisms (19 bacteria and 2 fungal strains) were used for antimicrobial activity by disc diffusion method and a standard procedure was used to identify the phytochemical constituents. Petroleum ether extract showed moderate inhibitory activity against Staphylococcus aureus (14.40 mm), S. epidermidis (14.20 mm), Salmonella paratyphi A (12.80 mm), Streptococcus mutans (12.20 mm), Escherichia coli, Proteus vulgaris, S. typhi and Burkholderia cepacia (12.00 mm). The chloroform extract also showed antimicrobial activity against S. epidermidis (14.20 mm), S. typhimurium (12.60 mm), S. paratyphi A, S. brunei and Yersinia enterocolitica (12.00 mm). The acetone extract of I. trita showed considerable inhibitory activity against S. epidermidis (18.20 mm), S. typhimurium (14.60 mm), S. infantis (13.80 mm), S. aureus (13.40 mm), Y. enterocolitica (13.00 mm) and Enterobacter aerogenes (12.00 mm) were documented. Ethanol extract showed significant antimicrobial activity against S. epidermidis (18.60 mm), S. paratyphi A (14.60 mm), Y. enterocolitica (13.40 mm), S. typhi (12.40 mm), S. aureus, E. aerogenes, S. typhimurium and S. infantis (12.00 mm). Aqueous extract of I. trita considerably inhibited S. epidermidis (13.80 mm), S. paratyphi A and Y. enterocolitica (12.20 mm), E. aerogenes and Haemophilus parahaemolyticus (12.00 mm). All the five extracts showed a minimal antifungal activity when compared to antibacterial activity. The result revealed that the antimicrobial properties of I. trita might be associated with the presence of phenolic compounds, flavonoids, tannins, glycosides, saponins, phytosterols and alkaloids
PREVALENCE OF EXTENDED-SPECTRUM BETA-LACTAMASE PRODUCING ENTEROBACTERIACEAE MEMBERS ISOLATED FROM CLINICALLY SUSPECTED PATIENTS
 Objective: Emergence of extended-spectrum beta-lactamases (ESBLs) production poses another clinical problem with Gram-negative bacterial infections. The present study was aimed to evaluate the ESBL producers among various clinical samples of clinically suspected patients.Methods: A total of 1279 samples (urine [918], pus [207] and stool [154]) were collected and 465 isolates (Escherichia coli [320], Enterobacter aerogenes [119] and Klebsiella pneumoniae [26]) were isolated and screened for the presence of ESBL producers using combination disc method and double disc synergy test.Results: Of the 465 culture positive isolates, 130 (E. coli 93 [29.06%], E. aerogenes 35 [29.41%] and K. pneumoniae 2 [7.69%]) were identified as ESBL producers. Among the three Enterobacteriaceae members, E. coli 93 (29.06%) was found to be predominant ESBL producer next in order E. aerogenes 35 (29.41%) and K. pneumoniae 2 (7.69%). Maximum number of ESBL producers were recovered from urine (n=111) followed by pus (n=14) and stool (n=5). All the ESBL-producing isolates were subjected to antibiotic sensitivity test using 10 different antibiotics. ESBL producers were chiefly resistance to ceftriaxone followed by ceftazidime and cefotaxime. Of 130 ESBL producers, 15 (E. coli (8), E. aerogenes (6) and K. pneumoniae (1)] strains were selected for genotypic identification. Among, only two strains of E. aerogenes were positive isolates for CTX-M type ESBL in polymerase chain reaction.Conclusion: This study concluded that among Enterobacteriaceae members, E. coli was the predominant ESBL producers and urine was noted as the prime source for the ESBL positive isolates when compared to other source. Genotypic identification was the best method to differentiate ESBL types which were essential to provide proper treatment
Prioritization of Drugs for Fungal Keratitis Eye Infections: An In-Silico Analysis
The fungal keratitis (FK) infections that cause cornea inflammations are more virulent than other bacterial keratitis infections and remain one of the most ethereal and challenging infections for ophthalmologists to diagnose and treat. Thus, the urgency in understanding the current perspectives of antifungal agents and their interactions with novel therapeutic targets and the identification of novel anti-fungal agents are at the frontline of studies in the pharmaceutical industry. In this study, DNA dependent RNA polymerase was modelled and virtually screened against eight antifungal agents, and it was found that Itraconazole (−22.0427 kJ/mol), Ketoconazole (−20.2194 kJ/mol), and Voriconazole (−12.6388 kJ/mol) exhibited better binding interactions. further, the structural and electronic properties of Itraconazole calculated through density functional theory studies revealed the sites of chemical reactivity that are vital in the compounds for possible interactions with RNA polymerase (RNAP). Hence, this study explores the binding efficacies of various anti-fungal agents through docking studies and their chemical entities, which might pave a significant path for the design of novel anti-fungal agents against hyalohyphomycetes causing keratitis
IN VITRO ANTIBACTERIAL ACTIVITY OF ESSENTIAL PLANT OILS AGAINST BIOFILM FORMING METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS
An alarming increase in biofilm forming methicillin-resistant Staphylococcus aureus (MRSA) possesses a serious problem in hospital environment demands a renewed effort to seek agents from natural system that are effective against pathogenic bacteria resistant to current antimicrobials. In the study, the distribution of biofilm forming MRSA and the antibacterial activity of essential oils (Eucalyptus, Mint, Turpentine, Neem and Amla) was studied in 58 strains of S. aureus isolated from pus samples. Out of 58 clinical samples 22 S. aureus were found to be methicillin-resistant and showed a dry black crystalline morphology indicating strong biofilm production and they were screened for the antibacterial activity of five different essential oils by using agar well diffusion method. The results from the agar well diffusion method showed that 4 essential oils could inhibit the growth of biofilm forming S. aureus isolates. Among those turpentine oil had strong inhibitory effects with a zone of inhibition ranging from 16.8 ± 1.77 mm to 32.0 ±2.12 mm. Eucalyptus oil shown moderate antibacterial activity against all tested isolates and followed by mint and neem with the average zones of inhibition. The oils at all concentrations showed potent inhibitory activity against the tested S. aureus with the exception of amla oil where there were no reports of inhibition. It is known that essential oils are composed of numerous different chemical compounds and their antimicrobial activity might be attributed to several different mechanisms, which could explain the variations in their mode of action. However, more studies are required to find the compounds of essential oils responsible for their antimicrobial activity, since little is known about essential oils and their medicinal property