Opportunistic Aspergillus pathogens measured in home and hospital tap water by quantitative PCR (QPCR)

S J Vesper1, R A Haugland, M E Rogers

  • 1National Exposure Research Laboratory, US Environmental Protection Agency, Cincinnati, OH 45216, USA. vesper.stephen@epa.gov

Journal of Water and Health
|September 20, 2007
PubMed

Insights

A new, rapid DNA testing method can detect dangerous Aspergillus fungi in home tap water. This method helps protect immunocompromised patients by quickly identifying potential contamination sources.

Area of Science:

  • Environmental microbiology
  • Molecular diagnostics
  • Public health

Background:

  • Opportunistic fungal infections pose a significant risk to immunocompromised individuals.
  • Contaminated water systems can serve as a reservoir for pathogenic fungi.
  • Rapid detection methods are crucial for timely intervention and patient protection.

Purpose of the Study:

  • To evaluate a simple DNA extraction and quantitative PCR (qPCR) method for detecting Aspergillus species in water.
  • To assess the occurrence of Aspergillus fumigatus, A. flavus, A. terreus, and A. niger in domestic tap water and hospital water supplies.

Main Methods:

  • Collected water samples from kitchen taps of 60 legionellosis patients and three hospital locations.
  • Utilized a novel, simple DNA extraction technique.
  • Employed quantitative PCR (qPCR) for rapid detection and quantification of target Aspergillus DNA.

Main Results:

  • Aspergillus terreus DNA detected in 16.7% of home tap water samples.
  • Aspergillus fumigatus DNA detected in 1.7% of home tap water samples.
  • No Aspergillus species were detected in any of the hospital water samples.

Conclusions:

  • The developed DNA extraction and qPCR method is effective for rapid screening of opportunistic fungal pathogens in tap water.
  • This method provides results in approximately 3 hours, significantly faster than traditional culture methods.
  • Timely pathogen detection can facilitate prompt removal from water supplies, enhancing safety for immunocompromised patients.

Related Concept Videos

Real Time RT-PCR02:57

Real Time RT-PCR

Real-time reverse transcription-polymerase chain reaction, or Real-time RT-PCR, is an analytical tool used to determine the expression level of target genes. The method involves converting mRNA to complementary DNA with the help of an enzyme known as reverse transcriptase, followed by the PCR amplification of the cDNA. These two processes can be performed simultaneously in a single tube or separately as a two-step reaction.
The real-time quantification of the number of amplified products is...
Rapid Identification of Pathogens01:25

Rapid Identification of Pathogens

MALDI-TOF MS has transformed clinical microbiology by offering a rapid and reliable method for pathogen identification. The traditional approach to microbial identification typically involves time-consuming culture techniques and biochemical tests, which can delay the initiation of appropriate antimicrobial therapy. MALDI-TOF MS avoids these delays by using characteristic ribosomal protein mass patterns of microbial cells, enabling accurate species-level identification within minutes.Principle...
Fungal Phylum Ascomycota01:28

Fungal Phylum Ascomycota

Phylum Ascomycota, a major division within the subkingdom Dikarya, comprises a diverse range of fungal species, including both unicellular yeasts and filamentous molds such as Aspergillus and Penicillium. These fungi thrive in a variety of habitats, from aquatic ecosystems to terrestrial environments, playing crucial ecological and economic roles.Morphology and ReproductionThe defining characteristic of Ascomycetes, commonly referred to as sac fungi, is the ascus—a sac-like structure that...