scholarly journals Pseudomonas aeruginosa as a priority group representative of bacteria with multiple antibiotic resistance

2021 ◽  
pp. 33-40
Author(s):  
Yevheniia Vashchyk ◽  
Dmytro Morozenko ◽  
Nataliia Seliukova ◽  
Andriy Zakhariev ◽  
Roman Dotsenko ◽  
...  
Keyword(s):  
Antibiotic Resistance ◽  
Scientific Literature ◽  
Multiple Drug Resistance ◽  
The Body ◽  
Source Analysis ◽  
Antibiotics Resistance ◽  
Multiple Drug ◽  
Positive Contribution ◽  
Priority Group ◽  
A Priority

The aim: the aim of the research is an analytical review of the scientific literature on Рseudomonas aeruginosa as a priority group representative of bacteria with multiple antibiotics resistance. Materials and methods. The research was conducted by the method of scientific literature open source analysis: PubMed, Elsevier, electronic resources of the National Library named after V. I. Vernadsky and others. Results. The problem of antibiotic resistance is rightly called the “apocalypse of the XXI century”. P. aeruginosa bacteria are characterized by a very high natural ability to form resistant forms to antimicrobial drugs due to the formation of specific resistance genes, the ability to resist the entry of antibiotics into the cell or remove antibiotics from the cell, and form biofilms. A characteristic feature of the epidemic and epizootic processes of P. aeruginosa, as an opportunistic ubiquitous microorganism is host-pathogenic interaction - the interaction of the pathogen with the host organism. The peculiarity of this bacterium is opportunism and long-term persistence in the body of the host and in the environment. The global trend towards the spread of antibiotic-resistant gram-negative bacteria, including P. aeruginosa, underscores the need to develop comprehensive response strategies targeting all sectors of health. Conclusions. Bacteria P. aeruginosa is classified in 1th Critical Group of the WHO list of resistant to antibiotics "priority pathogens". Among the main reasons that contribute to the emergence of resistance are irrational antibiotic therapy in both humans and animals, and the use of antibiotics as growth stimulants in animal husbandry. While more R&D is vital, alone, it cannot solve the problem. To address resistance, there must also be better prevention of infections and appropriate use of existing antibiotics in humans and animals, as well as rational use of any new antibiotics that are developed in future. New methods of combating antibiotic resistance and antibacterial substances, alternatives to antibiotics (biofilm-destroying drugs, antimicrobial peptides (AMP), bacteriophages, nanopreparations, etc.) can make a positive contribution to overcoming the multiple drug resistance of gram-negatives

scholarly journals Antibiotic Resistance Profile and Chemical Quality Assessment of Groundwater Sources from Periurban Area of Bucharest, Romania

2019 ◽  
Vol 70 (10) ◽  
pp. 3549-3554
Author(s):  
Florica Marinescu ◽  
Mihaela Ilie ◽  
Gina Ghita ◽  
Ioana Savin ◽  
Carmen Tociu ◽  
...  
Keyword(s):  
Antibiotic Resistance ◽  
Multiple Drug Resistance ◽  
Microbiological Quality ◽  
Shallow Groundwater ◽  
Total Coliform ◽  
Multiple Drug ◽  
Maximum Admissible Concentration ◽  
Antibiotic Resistance Profile ◽  
Physico Chemical ◽  
Resistance Rates

Twenty-two groundwater sources mainly used for drinking purpose in Bucharest peri-urban area were investigated for assessment of physico-chemical and microbiological quality with a view to determining its potential risk to public health. Results of chemical analysis revealed that nitrites, sulphates and chlorides were below the permissible levels, while 63.64% of the analysed groundwater sources exceeded the maximum admissible concentration for nitrates, with concentration variations ranging from 67.27 to 523.19 mg/L. The bacteriological analysis showed that in about 63% of groundwater sources total coliform, faecal coliform and enterococci have exceeded the threshold limits recommended by the Drinking Water Directive 98/83/EC and the Romanian Law. Another aim of the study was to investigate the prevalence of antibiotic resistance among Gram-negative strains isolated from groundwater sources. There observed the resistance to many antibiotics, particularly: ticarcillin (80%), aztreonam (29%), gentamicin (11%), imipenem (9%), ceftriaxone (9%), ceftazidime (3%) and ciprofloxacin (3%). Significant higher resistance rates were observed in strains isolated from shallow groundwater sources as compared with strains isolated from deep groundwater sources. Pseudomonas sp. (26%) isolates with multiple-drug resistance (MDR) were encountered. The results of the study revealed a bacteriological contamination and high levels of nitrate concentrations in most of the groundwater samples, which could pose an important risk to human health.

scholarly journals Isolation, Molecular Identification and Multidrug Resistance Profiling of Bacteria Causing Clinical Mastitis in Cows

2020 ◽  
Author(s):  
D.J. Vatalia ◽  
B.B. Bhanderi ◽  
V.R. Nimavat ◽  
M.K. Jhala
Keyword(s):  
Drug Resistance ◽  
Antibiotic Resistance ◽  
Multiple Drug Resistance ◽  
Bacterial Species ◽  
Research Work ◽  
Resistance Index ◽  
Diffusion Method ◽  
Multiple Drug ◽  
Milk Samples ◽  
Sensitivity Pattern

Background: Mastitis, the inflammation of parenchyma of mammary gland is frequently considered to be costliest and complex disease prevalent in India. Mastitis is caused by pathogens like Staphylococcus spp., Streptococcus spp., Mycoplasma bovis, E. coli, Klebsiella spp., Citrobacter spp., Enterobacter spp. and Entercoccus. The treatment of mastitis in animals is carried out using antibiotics. Treatment failure in mastitis is due to increased antibiotic resistance of mastitis pathogens and also due to indiscriminate use of antibiotics without testing in vitro antibiotic sensitivity test against causal organisms. In comparison to cultural method, PCR assays takes less time for detection of bacteria from the mastitis milk samples. Present research work was carried out regarding isolation, identification and multiple drug resistance profile of clinical bovine mastitis associated pathogens using conventional as well as molecular approach. Methods: In the present study, 73 mastitis milk samples were collected from Anand and Panchmahal district of Gujarat. The milk samples were subjected for cultural isolation and DNA extraction for identification of bacteria by cultural and PCR method. Antimicrobial sensitivity pattern of the isolates were carried by disc diffusion method and isolates were categorized in multiple drug resistant. Result: In the present study, Out of 73 mastitis milk samples collected from cows 48 (65.75%) cows were positive for bacterial isolation and S. aureus was the most predominant bacterial species. PCR from the mastitis milk additionally detected bacteria in culturally negative milk samples. Most sensitive drug was gentamicin and most of the isolates (90.19%) showed the multiple drug resistance for the two to nine drugs with 0.1 to 0.6 multiple antibiotic resistance index.

scholarly journals Multiple drug resistance patterns and plasmid profiles of non-typhi salmonellae in Turkey

1998 ◽  
Vol 121 (2) ◽  
pp. 303-307 ◽  
Author(s):  
T. YILDIRMAK ◽  
A. YAZGAN ◽  
G. OZCENGIZ
Keyword(s):  
Antibiotic Resistance ◽  
Multiple Drug Resistance ◽  
Multiple Drug ◽  
Frequent Patterns ◽  
Drug Resistant ◽  
Plasmid Profiles ◽  
Resistance Patterns ◽  
Amoxicillin Clavulanic Acid ◽  
Almost All ◽  
Antibiotic Resistance Patterns

A total of 259 clinical isolates of nonrepetitive non-typhi salmonellae (NTS) were examined for antibiotic resistance patterns and plasmid content. The antibiotics used were amoxicillin-clavulanic acid (AMC), ampicillin (AM), aztreonam (ATM), carbenicillin (CB), cefixime (CFM), cefotaxime (CTX), cefoxitin (FOX), ceftazidime (CAZ), ceftriaxone (CRO), chloramphenicol (C), ciprofloxacin (CIP), gentamicin (GM), imipenem (IPM), ofloxacin (OFX), tetracycline (TE), trimethoprim-sulfomethoxazole (SXT). Multi-drug resistant (MDR) strains comprised 19·3% of the total isolates (50/259) and almost all were S. typhimurium (49/50). Fifteen different patterns of resistance was observed, AM/CB/C/AMC/TE and AM/CB/C/AMC/SXT/GM/CTX/CRO/CAZ/CFM/ATM being the most frequent patterns. Twenty-eight out of 50 multiresistant isolates were found to contain at least one plasmid (mean five) and the size of the plasmids ranged between 1·7 and 158 kb. Plasmid profiles of multi-resistant NTS strains were heterogenous as 21 different profiles were detected in a total of 28 plasmid-bearing isolates. No direct correlation was established between antibiotic resistance patterns and plasmid profiles.

scholarly journals Detection of antibiotic resistance genes among multiple drug resistant Pseudomonas aeruginosa strains isolated from clinical sources in selected health institutions in Kwara State.

2021 ◽  
Vol 10 (1) ◽  
pp. 40-48
Author(s):  
O.C. Adekunle ◽  
A. Mustapha ◽  
G. Odewale ◽  
R.O. Ojedele
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Antibiotic Resistance ◽  
Resistance Genes ◽  
Multiple Drug Resistance ◽  
Antibiotic Resistance Genes ◽  
Clinical Samples ◽  
Multiple Drug ◽  
Antibiotic Resistant ◽  
Clinical Specimens ◽  
Health Institutions

Introduction: Pseudomonas aeruginosa (P. aeruginosa) is a frequent nosocomial pathogen that causes severe diseases in many clinical and community settings. The objectives were to investigate the occurrence of multiple antibiotic resistant P. aeruginosa strains among clinical samples and to detect the presence of antibiotic resistance genes in the DNA molecules of the strains.Methods: Clinical specimens were collected aseptically from various human anatomical sites in five selected health institutions within Kwara State, Nigeria. Multiple drug resistance patterns of isolated micro-organisms to different antibiotics were determined using the Bauer Kirby disc diffusion technique. The DNA samples of the multiple resistant P. aeruginosa strains were extracted and subjected to Polymerase Chain Reaction (PCR) for resistance gene determination.Results: A total of 145 isolates were identified as P. aeruginosa from the clinical samples. Absolute resistance to ceftazidime, gentamicin and ceftriaxone was observed while low resistance to ciprofloxacin, piperacillin and imipenem was documented. The prevalence of bla VIM , ,bla CTX-M and blaTEM were 34.4 %, 46.7 % and 16.7 % respectively.Conclusion: This study has shown that there is a high occurrence of metallo â-lactamase- producing and antibiotic-resistant strains of P. aeruginosa in clinical specimens from the studied area. Keywords: Metallo â-lactamase enzyme, P. aeruginosa, clinical samples, antibiotic-resistance genes

scholarly journals Molecular characterization of Vibrio cholerae O1 strains circulating in Assam: a north eastern state of India

2021 ◽  
Author(s):  
Ajanta Sharma ◽  
Bornali Sarmah Dutta ◽  
Debajit Rabha ◽  
Elmy Samsun Rasul ◽  
Naba Kumar Hazarika
Keyword(s):  
Antibiotic Resistance ◽  
Vibrio Cholerae ◽  
Virulence Genes ◽  
Multiple Drug Resistance ◽  
Public Health Problem ◽  
Amino Acid Sequences ◽  
Multiple Drug ◽  
Major Public Health Problem ◽  
Genotype 3 ◽  
El Tor

Background and Objectives: Information on the genetic epidemiology of cholera in Assam, a northeastern state of India is lacking despite cholera being a major public health problem. The study aimed to determine the virulence genes and genes encoding antibiotic resistance in Vibrio cholerae isolates and to determine the prevalent genotypes based on the presence or absence of the virulence genes and ctxB genotype. Materials and Methods: Twenty-five V. cholerae strains were subjected to conventional biotyping and serotyping followed by multiplex PCR to detect ctxA, ctxB, zot, ace, O1rfb, tcpA, ompU, ompW, rtxC, hly and toxR and antibiotic resistance genes. Cholera toxin B (ctxB) gene was amplified followed by sequencing. Results: All the V. cholerae O1 isolates were El Tor Ogawa and showed the presence of the core toxin region representing the genome of the filamentous bacteriophage CTXø. The complete cassette of virulence genes was seen in 48% of the isolates which was the predominant genotype. All the isolates possessed amino acid sequences identical to the El Tor ctxB subunit of genotype 3. sulII gene was detected in 68% of the isolates, dfrA1 in 88%, strB in 48% and SXT gene was detected in 36% of the isolates. Conclusion: Toxigenic V. cholerae O1 El Tor Ogawa strains of ctxB genotype 3 carrying a large pool of virulence genes are prevailing in Assam. Presence of a transmissible genetic element SXT in 36% of the strains is of major concern as it indicates the emergence of multiple drug resistance among the V. cholerae isolates.  

scholarly journals Advanced molecular characterization of enteropathogenic Escherichia coli isolated from diarrheic camel neonates in Egypt

2021 ◽  
Vol 14 (1) ◽  
pp. 85-91
Author(s):  
Momtaz A. Shahein ◽  
Amany N. Dapgh ◽  
Essam Kamel ◽  
Samah F. Ali ◽  
Eman A. Khairy ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Drug Resistance ◽  
Antibiotic Resistance ◽  
Resistance Genes ◽  
Multiple Drug Resistance ◽  
Microbial Pathogens ◽  
Multiple Drug ◽  
Gastrointestinal Infections ◽  
Fecal Samples ◽  
E Coli

Background and Aim: Camels are important livestock in Egypt on cultural and economic bases, but studies of etiological agents of camelid diseases are limited. The enteropathogen Escherichia coli is a cause of broad spectrum gastrointestinal infections among humans and animals, especially in developing countries. Severe infections can lead to death. The current study aimed to identify pathogenic E. coli strains that cause diarrhea in camel calves and characterize their virulence and drug resistance at a molecular level. Materials and Methods: Seventy fecal samples were collected from diarrheic neonatal camel calves in Giza Governorate during 2018-2019. Samples were cultured on a selective medium for E. coli, and positive colonies were confirmed biochemically, serotyped, and tested for antibiotic susceptibility. E. coli isolates were further confirmed through detection of the housekeeping gene, yaiO, and examined for the presence of virulence genes; traT and fimH and for genes responsible for antibiotic resistance, ampC, aadB, and mphA. The isolates in the important isolated serotype, E. coli O26, were examined for toxigenic genes and sequenced. Results: The bacteriological and biochemical examination identified 12 E. coli isolates from 70 fecal samples (17.1%). Serotyping of these isolates showed four types: O26, four isolates, 33.3%; O103, O111, three isolates each, 25%; and O45, two isolates, 16.7%. The isolates showed resistance to vancomycin (75%) and ampicillin (66.6%), but were highly susceptible to ciprofloxacin, norfloxacin, and tetracycline (100%). The structural gene, yaiO (115 bp), was amplified from all 12 E. coli isolates and traT and fimH genes were amplified from 10 and 8 isolates, respectively. Antibiotic resistance genes, ampC, mphA, and aadB, were harbored in 9 (75%), 8 (66.6%), and 5 (41.7%), respectively. Seven isolates (58.3%) were MDR. Real-time-polymerase chain reaction of the O26 isolates identified one isolate harboring vt1, two with vt2, and one isolate with neither gene. Sequencing of the isolates revealed similarities to E. coli O157 strains. Conclusion: Camels and other livestock suffer various diseases, including diarrhea often caused by microbial pathogens. Enteropathogenic E. coli serotypes were isolated from diarrheic neonatal camel calves. These isolates exhibited virulence and multiple drug resistance genes.

scholarly journals Antimicrobial Resistance of Enterococcus Species Isolated from Produce

2004 ◽  
Vol 70 (5) ◽  
pp. 3133-3137 ◽  
Author(s):  
Lynette M. Johnston ◽  
Lee-Ann Jaykus
Keyword(s):  
Antibiotic Resistance ◽  
Multiple Drug Resistance ◽  
Fresh Produce ◽  
Clinical Importance ◽  
Multiple Drug ◽  
Human Populations ◽  
Intrinsic Resistance ◽  
Resistance Patterns ◽  
Low Prevalence ◽  
Susceptibility Profiles

ABSTRACT The purpose of this study was to characterize the antibiotic resistance profiles of Enterococcus species isolated from fresh produce harvested in the southwestern United States. Among the 185 Enterococcus isolates obtained, 97 (52%) were Enterococcus faecium, 38 (21%) were Enterococcus faecalis, and 50 (27%) were other Enterococcus species. Of human clinical importance, E. faecium strains had a much higher prevalence of resistance to ciprofloxacin, tetracycline, and nitrofurantoin than E. faecalis. E. faecalis strains had a low prevalence of resistance to antibiotics used to treat E. faecalis infections of both clinical and of agricultural relevance, excluding its intrinsic resistance patterns. Thirty-four percent of the isolates had multiple-drug-resistance patterns, excluding intrinsic resistance. Data on the prevalence and types of antibiotic resistance in Enterococcus species isolated from fresh produce may be used to describe baseline antibiotic susceptibility profiles associated with Enterococcus spp. isolated from the environment. The data collected may also help elucidate the role of foods in the transmission of antibiotic-resistant strains to human populations.

scholarly journals TYPING OF VIBRIO CHOLERAE NON O1/NON O139 STRAINS, ISOLATED IN ROSTOV REGION IN 2014

2016 ◽  
pp. 3-9 ◽  
Author(s):  
N. A. Selyanskaya ◽  
I. V. Arkhangelskaya ◽  
A. S. Vodopianov ◽  
S. O. Vodopianov ◽  
V. D. Kruglikov ◽  
...  
Keyword(s):  
Vibrio Cholerae ◽  
Multiple Drug Resistance ◽  
Antibiotics Resistance ◽  
Dilution Method ◽  
Multiple Drug ◽  
Genetic Characteristics ◽  
Rostov Region ◽  
Serial Dilution Method ◽  
Water Transmission ◽  
Resistance Data

Aim. Comparative study of antibiotics resistance and VNTR-typing of Vibrio cholerae non O1/ non O139 strains, isolated on the territory of Rostov region in 2014. Materials and methods. Antibioticogramms of strains were determined by serial dilution method in dense nutrient medium according to MG 4.2.2495-09 (2009). Pheno-, sero- and VNTR-typing was carried out by conventional methods. Results. The studied strains belonged to V. cholerae species, did not agglutinate with O1 and O139 sera, were atoxigenic, hemolysis-positive, did not contain genes of cholera toxin and toxin-coregulating pili ofadhesion, contained genes ofhemagglutinin/protease, protease PrtV, collagenase, cytotonic factor Cef, outer membrane protein OmpW, tol- and vps-clusters, regulatory genes toxR and hapR. Antibioticogramms of the strains have shown the presence of cultures, resistant to ampicillin, ceftazidime, furazolidone, trimethoprim/sulfamethoxazole with intermediate resistance to streptomycin, kanamycin, gentamycin, amikacin, netilmicin. Approximately 20% of isolates had multiple drug resistance. Data of VNTR- and geno-typing confirmed a possibility of water transmission route of the infection. Conclusion. Execution of monitoring of cultures from environmental samples is necessary for timely detection of genetic characteristics, antibiotics resistance.

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