Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis

Background: Cystic fibrosis (CF) is an autosomal recessive disorder due to genetic defect resulting cilliary function impairment. So that these patients are inclined to recurrent infection with opportunistic microorganism such as Pseudomonas aeruginosa. This organism is most important pathogen in cy...

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Main Authors: Hossein Fazeli, Reza Akbari, Sharaeh Moghim, Asadollah Asadian, Jamal Faghihinia, Hossein Saneeyan, Tahmineh Narimani
Format: Article
Language:fas
Published: Isfahan University of Medical Sciences 2012-03-01
Series:مجله دانشکده پزشکی اصفهان
Subjects:
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/1481
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author Hossein Fazeli
Reza Akbari
Sharaeh Moghim
Asadollah Asadian
Jamal Faghihinia
Hossein Saneeyan
Tahmineh Narimani
author_facet Hossein Fazeli
Reza Akbari
Sharaeh Moghim
Asadollah Asadian
Jamal Faghihinia
Hossein Saneeyan
Tahmineh Narimani
author_sort Hossein Fazeli
collection DOAJ
description Background: Cystic fibrosis (CF) is an autosomal recessive disorder due to genetic defect resulting cilliary function impairment. So that these patients are inclined to recurrent infection with opportunistic microorganism such as Pseudomonas aeruginosa. This organism is most important pathogen in cystic fibrosis (CF) which intend to colonize and form biofilm to confront immunsystem and therapeutic dosage of antimicrobial drug. These bacteria can mutate to survive and adapted to new to new condition. Colony morphotyping and antimicrobial drug resistant detecting in Pseudomonas aeruginosa can help treat of CF patient and prevent patient form being resource of resistant strain bacteria. The aim of this assay is detection of colony morphotype, antimicrobial resistant in Pseudomonas aeruginosa isolated form CF and urinary tract infection (UTI) patient, hospital personnel and environment. Methods: It is a cross sectional study. Samples wet were taken with swab in 59 CF patients (between 82-87 years), 27 UTI patient, 113 sample from hospital environment, 123 sample from 91 personnel (throat, hand, lab uniform) in Alzahra Hospital, Isfahan, Iran. Isolated Pseudomonas aeruginosa form these samples were identified bacteriologic standard method. The isolates were investigated for morphotyping and antimicrobial drug resistance. Findings: 21 cases form 59 patients (35.5%), 25 cases 27 UTI patient (92.5%) were infected with Pseudomonas aeruginosa. Pseudomonas aeruginosa were isolated from 11 of 113 sample taken from hospital environment and 4 of the (123 sample) were taken 91 hospital personnel. From 21 Pseudomonas aeruginosa isolated from CF patient (35 male, 24 female and the ages between 2 month to 24 years), 9 isolates had mucoid form (42%) and the rate antibiotic resistance to Gentamicin, Amikacin, ciprofloxacin, piperacillin and ceftazidime were 9.5%, 9.5%, 14.2%, 19% and 86% respectively. Conclusion: The mucoid form of Pseudomonas aeruginosa was seen most frequently in CF patients comparing with other samples. In all groups, antimicrobial resistance to Ceftazidime and antimicrobial sensitivity to Amikacin were most frequent.
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spelling doaj.art-2be9fff6e05941f8adafa81eefdde0b42023-09-03T02:11:06ZfasIsfahan University of Medical Sciencesمجله دانشکده پزشکی اصفهان1027-75951735-854X2012-03-0129171877Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic FibrosisHossein Fazeli0Reza Akbari1Sharaeh Moghim2Asadollah Asadian3Jamal Faghihinia4Hossein Saneeyan5Tahmineh Narimani6Assistant Professor, Department of Microbiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranMSc Student, Department of Microbiology, School of Medicine And Student Research Committee, Isfahan University of Medical Sciences, Isfahan, IranAssistant Professor, Department of Microbiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranAssistant Professor, Department of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranAssociate Professor, Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranAssistant Professor, Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranDepartment of Microbiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranBackground: Cystic fibrosis (CF) is an autosomal recessive disorder due to genetic defect resulting cilliary function impairment. So that these patients are inclined to recurrent infection with opportunistic microorganism such as Pseudomonas aeruginosa. This organism is most important pathogen in cystic fibrosis (CF) which intend to colonize and form biofilm to confront immunsystem and therapeutic dosage of antimicrobial drug. These bacteria can mutate to survive and adapted to new to new condition. Colony morphotyping and antimicrobial drug resistant detecting in Pseudomonas aeruginosa can help treat of CF patient and prevent patient form being resource of resistant strain bacteria. The aim of this assay is detection of colony morphotype, antimicrobial resistant in Pseudomonas aeruginosa isolated form CF and urinary tract infection (UTI) patient, hospital personnel and environment. Methods: It is a cross sectional study. Samples wet were taken with swab in 59 CF patients (between 82-87 years), 27 UTI patient, 113 sample from hospital environment, 123 sample from 91 personnel (throat, hand, lab uniform) in Alzahra Hospital, Isfahan, Iran. Isolated Pseudomonas aeruginosa form these samples were identified bacteriologic standard method. The isolates were investigated for morphotyping and antimicrobial drug resistance. Findings: 21 cases form 59 patients (35.5%), 25 cases 27 UTI patient (92.5%) were infected with Pseudomonas aeruginosa. Pseudomonas aeruginosa were isolated from 11 of 113 sample taken from hospital environment and 4 of the (123 sample) were taken 91 hospital personnel. From 21 Pseudomonas aeruginosa isolated from CF patient (35 male, 24 female and the ages between 2 month to 24 years), 9 isolates had mucoid form (42%) and the rate antibiotic resistance to Gentamicin, Amikacin, ciprofloxacin, piperacillin and ceftazidime were 9.5%, 9.5%, 14.2%, 19% and 86% respectively. Conclusion: The mucoid form of Pseudomonas aeruginosa was seen most frequently in CF patients comparing with other samples. In all groups, antimicrobial resistance to Ceftazidime and antimicrobial sensitivity to Amikacin were most frequent.http://jims.mui.ac.ir/index.php/jims/article/view/1481Cystic fibrosisPseudomonas aeruginosaMorphotyping
spellingShingle Hossein Fazeli
Reza Akbari
Sharaeh Moghim
Asadollah Asadian
Jamal Faghihinia
Hossein Saneeyan
Tahmineh Narimani
Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis
مجله دانشکده پزشکی اصفهان
Cystic fibrosis
Pseudomonas aeruginosa
Morphotyping
title Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis
title_full Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis
title_fullStr Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis
title_full_unstemmed Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis
title_short Detection of Morphotyping Characteristics Identification Antibiotic Resistance of Pseudomonas aeruginosa Isolated from Patients with Cystic Fibrosis
title_sort detection of morphotyping characteristics identification antibiotic resistance of pseudomonas aeruginosa isolated from patients with cystic fibrosis
topic Cystic fibrosis
Pseudomonas aeruginosa
Morphotyping
url http://jims.mui.ac.ir/index.php/jims/article/view/1481
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