1H-nuclear magnetic resonance spectroscopy for identifying and quantifying common uropathogens

A metabolic approach to the urinary tract infection

Ashish Gupta, Mayank Dwivedi, Abbas Ali Mahdi, G. A Nagana Gowda, Chunni Lal Khetrapal, Mahendra Bhandari

Research output: Contribution to journalArticle

Abstract

OBJECTIVE To address the shortcomings of urine culture for the diagnosis of urinary tract infection (UTI), we used 1H-nuclear magnetic resonance (NMR) spectroscopy for identifying and quantifying Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia and Proteus mirabilis. PATIENTS, SUBJECTS AND METHODS Urine samples from patients with suspected UTI (617), healthy volunteers (50) and commercially available standard strains of E. coli, K. pneumonia, P. aeruginosa, Enterobacter, Acinobacter, Pr. mirabilis, Citrobacter frundii, Streptococcus saprophyticus and Enterococcus faecalis were assessed between 2003 and 2006. 1H-NMR spectra were recorded on a 400 MHz spectrophotometer; to quantify the bacteria we estimated the areas under the spectral peaks of the specific metabolic product compared with the known concentration of trimethyl silyl propionic acid. All urine specimens were cultured in addition to an assessment by NMR spectroscopy. RESULTS Preliminary urinary spectroscopy of the unprocessed samples showed peaks of nonspecific metabolites such as succinate, acetate, lactate and ethanol, indicating infected samples. Based on the results from processed samples, 93% (240/256) of E. coli, 92% (101/110) of K. pneumoniae, 93% (56/60) of P. aeruginosa and eight of 10 Pr. mirabilis could be diagnosed with NMR (numerator) and urine culture (denominator). The remaining samples were sterile and/or had a bacterial population of 3 colony-forming units (CFU)/mL. The NMR method diagnosed bacterial densities of >103 CFU. CONCLUSIONS The identification of the common uropathogens E. coli, K. pneumoniae, P. aeruginosa and Pr. mirabilis by NMR spectroscopy has a shorter reporting time and can be used to differentiate between infected, contaminated and sterile specimens.

Original languageEnglish (US)
Pages (from-to)236-244
Number of pages9
JournalBJU International
Volume104
Issue number2
DOIs
StatePublished - Jul 2009
Externally publishedYes

Fingerprint

Proteus mirabilis
Urinary Tract Infections
Magnetic Resonance Spectroscopy
Pseudomonas aeruginosa
Urine
Escherichia coli
Enterococcus faecalis
Klebsiella pneumoniae
Pneumonia
Stem Cells
Citrobacter
Enterobacter
Succinic Acid
Lactic Acid
Spectrum Analysis
Healthy Volunteers
Acetates
Ethanol
Bacteria
Population

Keywords

  • Metabolic approach
  • NMR
  • Urinary tract infection

ASJC Scopus subject areas

  • Urology

Cite this

1H-nuclear magnetic resonance spectroscopy for identifying and quantifying common uropathogens : A metabolic approach to the urinary tract infection. / Gupta, Ashish; Dwivedi, Mayank; Mahdi, Abbas Ali; Gowda, G. A Nagana; Khetrapal, Chunni Lal; Bhandari, Mahendra.

In: BJU International, Vol. 104, No. 2, 07.2009, p. 236-244.

Research output: Contribution to journalArticle

Gupta, Ashish ; Dwivedi, Mayank ; Mahdi, Abbas Ali ; Gowda, G. A Nagana ; Khetrapal, Chunni Lal ; Bhandari, Mahendra. / 1H-nuclear magnetic resonance spectroscopy for identifying and quantifying common uropathogens : A metabolic approach to the urinary tract infection. In: BJU International. 2009 ; Vol. 104, No. 2. pp. 236-244.
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AB - OBJECTIVE To address the shortcomings of urine culture for the diagnosis of urinary tract infection (UTI), we used 1H-nuclear magnetic resonance (NMR) spectroscopy for identifying and quantifying Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia and Proteus mirabilis. PATIENTS, SUBJECTS AND METHODS Urine samples from patients with suspected UTI (617), healthy volunteers (50) and commercially available standard strains of E. coli, K. pneumonia, P. aeruginosa, Enterobacter, Acinobacter, Pr. mirabilis, Citrobacter frundii, Streptococcus saprophyticus and Enterococcus faecalis were assessed between 2003 and 2006. 1H-NMR spectra were recorded on a 400 MHz spectrophotometer; to quantify the bacteria we estimated the areas under the spectral peaks of the specific metabolic product compared with the known concentration of trimethyl silyl propionic acid. All urine specimens were cultured in addition to an assessment by NMR spectroscopy. RESULTS Preliminary urinary spectroscopy of the unprocessed samples showed peaks of nonspecific metabolites such as succinate, acetate, lactate and ethanol, indicating infected samples. Based on the results from processed samples, 93% (240/256) of E. coli, 92% (101/110) of K. pneumoniae, 93% (56/60) of P. aeruginosa and eight of 10 Pr. mirabilis could be diagnosed with NMR (numerator) and urine culture (denominator). The remaining samples were sterile and/or had a bacterial population of 3 colony-forming units (CFU)/mL. The NMR method diagnosed bacterial densities of >103 CFU. CONCLUSIONS The identification of the common uropathogens E. coli, K. pneumoniae, P. aeruginosa and Pr. mirabilis by NMR spectroscopy has a shorter reporting time and can be used to differentiate between infected, contaminated and sterile specimens.

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