{"title":"Antimicrobial Resistance Among Gram-Negative Bacteria Isolated in the Newborn Intensive Care Unit at Abderrezak-Bouhara Hospital of Skikda, Algeria.","authors":"Asma Labid, Sarah Benouagueni, Aida Mehainaoui, Djamila Gacemi Kirane, Abdelaziz Touati","doi":"10.1089/mdr.2022.0254","DOIUrl":null,"url":null,"abstract":"<p><p><b><i>Background:</i></b> This study aimed to determine the epidemiology of gram-negative bacteria (GNB) isolated in the newborn intensive care unit (NICU) population, to assess their antibiotic susceptibility patterns and possible associated risk factors. <b><i>Methods:</i></b> All neonates admitted to the NICU of Abderrezak-Bouhara hospital (Skikda, Algeria) with a clinical diagnosis of neonatal infections from March to May 2019 were included in the study. The extended-spectrum β-lactamase <b>(</b>ESBLs), plasmidic cephalosporinase (pAmpC), and carbapenemases genes were screened by polymerase chain reaction (PCR) and sequencing. PCR amplification of <i>oprD</i> among carbapenem-resistant <i>Pseudomonas aeruginosa</i> isolates was also performed. The clonal relatedness of the ESBLs isolates was studied using multilocus sequence typing <i>(</i>MLST). <b><i>Results:</i></b> Among 148 clinical specimens, 36 (24.3%) GNB strains were isolated from urine (<i>n</i> = 22), wound (<i>n</i> = 8), stool (<i>n</i> = 3), and blood (<i>n</i> = 3) samples. The bacterial species identified were <i>Escherichia coli</i> (<i>n</i> = 13), <i>Klebsiella pneumoniae</i> (<i>n</i> = 5), <i>Enterobacter cloacae</i> (<i>n</i> = 3), <i>Serratia marcescens</i> (<i>n</i> = 3), <i>Salmonella</i> spp. (<i>n</i> = 3), <i>Proteus mirabilis</i> (<i>n</i> = 1), <i>P. aeruginosa</i> (<i>n</i> = 5), and <i>Acinetobacter baumannii</i> (<i>n</i> = 3). PCR and sequencing showed that eleven <i>Enterobacterales</i> isolates harbored the <i>bla</i><sub>CTX-M-15</sub> gene, two <i>E. coli</i> isolates harbored the <i>bla</i><sub>CMY-2</sub> gene, and three <i>A. baumannii</i> isolates harbored both <i>bla</i><sub>OXA-23</sub> and <i>bla</i><sub>OXA-51</sub> genes. Also, five strains of <i>P. aeruginosa</i> were found to harbor mutations in the <i>oprD</i> gene. MLST showed that the <i>K. pneumoniae</i> strains belonged to ST13 and ST189, <i>E. coli</i> belonged to ST69, and <i>E. cloacae</i> belonged to ST214. Different risk factors that could predict positive GNB cultures were found, including female sex, Apgar score <8 at 5 min of life, enteral nutrition, antibiotic use, and extended length of hospitalization. <b><i>Conclusion:</i></b> Our study highlights the importance of determining the epidemiology of pathogens causing neonatal infections, their sequence types (ST), and their antibiotic susceptibility patterns to address rapidly a correct antibiotic treatment regimen.</p>","PeriodicalId":18701,"journal":{"name":"Microbial drug resistance","volume":"29 6","pages":"229-238"},"PeriodicalIF":2.3000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial drug resistance","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/mdr.2022.0254","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: This study aimed to determine the epidemiology of gram-negative bacteria (GNB) isolated in the newborn intensive care unit (NICU) population, to assess their antibiotic susceptibility patterns and possible associated risk factors. Methods: All neonates admitted to the NICU of Abderrezak-Bouhara hospital (Skikda, Algeria) with a clinical diagnosis of neonatal infections from March to May 2019 were included in the study. The extended-spectrum β-lactamase (ESBLs), plasmidic cephalosporinase (pAmpC), and carbapenemases genes were screened by polymerase chain reaction (PCR) and sequencing. PCR amplification of oprD among carbapenem-resistant Pseudomonas aeruginosa isolates was also performed. The clonal relatedness of the ESBLs isolates was studied using multilocus sequence typing (MLST). Results: Among 148 clinical specimens, 36 (24.3%) GNB strains were isolated from urine (n = 22), wound (n = 8), stool (n = 3), and blood (n = 3) samples. The bacterial species identified were Escherichia coli (n = 13), Klebsiella pneumoniae (n = 5), Enterobacter cloacae (n = 3), Serratia marcescens (n = 3), Salmonella spp. (n = 3), Proteus mirabilis (n = 1), P. aeruginosa (n = 5), and Acinetobacter baumannii (n = 3). PCR and sequencing showed that eleven Enterobacterales isolates harbored the blaCTX-M-15 gene, two E. coli isolates harbored the blaCMY-2 gene, and three A. baumannii isolates harbored both blaOXA-23 and blaOXA-51 genes. Also, five strains of P. aeruginosa were found to harbor mutations in the oprD gene. MLST showed that the K. pneumoniae strains belonged to ST13 and ST189, E. coli belonged to ST69, and E. cloacae belonged to ST214. Different risk factors that could predict positive GNB cultures were found, including female sex, Apgar score <8 at 5 min of life, enteral nutrition, antibiotic use, and extended length of hospitalization. Conclusion: Our study highlights the importance of determining the epidemiology of pathogens causing neonatal infections, their sequence types (ST), and their antibiotic susceptibility patterns to address rapidly a correct antibiotic treatment regimen.
期刊介绍:
Microbial Drug Resistance (MDR) is an international, peer-reviewed journal that covers the global spread and threat of multi-drug resistant clones of major pathogens that are widely documented in hospitals and the scientific community. The Journal addresses the serious challenges of trying to decipher the molecular mechanisms of drug resistance. MDR provides a multidisciplinary forum for peer-reviewed original publications as well as topical reviews and special reports.
MDR coverage includes:
Molecular biology of resistance mechanisms
Virulence genes and disease
Molecular epidemiology
Drug design
Infection control.