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Related Experiment Video

Updated: May 26, 2026

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses
11:29

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses

Published on: December 3, 2011

Cost-effective method for microbial source tracking using specific human and animal viruses.

Silvia Bofill-Mas1, Ayalkibet Hundesa, Byron Calgua

  • 1Laboratory of Water and Food Viral Pollution, Department of Microbiology, Faculty of Biology, University of Barcelona.

Journal of Visualized Experiments : Jove
|December 14, 2011
PubMed
Summary

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This study introduces a streamlined, cost-effective method for concentrating viruses from water samples. The new one-step protocol enables accurate identification of human and animal fecal contamination sources using quantitative PCR.

Area of Science:

  • Environmental microbiology and virology
  • Water quality assessment
  • Microbial Source Tracking (MST)

Background:

  • Microbial contamination poses significant health risks, with traditional bacterial indicators showing limitations.
  • Viruses are more resistant to inactivation and offer better source tracking capabilities than bacterial indicators.
  • Human adenoviruses (HAdV) and JC polyomaviruses (JCPyV) are established markers for human fecal contamination.

Purpose of the Study:

  • To present a simplified, cost-effective one-step protocol for concentrating viruses from large water volumes.
  • To enable the use of specific viral markers, including porcine adenoviruses (PAdV) and bovine polyomaviruses (BPyV), for microbial source tracking.
  • To facilitate high-throughput analysis of viral contamination in various water matrices.

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Last Updated: May 26, 2026

Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses
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Cost-effective Method for Microbial Source Tracking Using Specific Human and Animal Viruses

Published on: December 3, 2011

Viral Tracing of Genetically Defined Neural Circuitry
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High-throughput Detection of Respiratory Pathogens in Animal Specimens by Nanoscale PCR
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Main Methods:

  • A one-step viral concentration protocol involving acidification, skimmed milk flocculation, sedimentation, and centrifugation.
  • Concentrated viral nucleic acid extraction followed by quantitative PCR (qPCR) for specific adenovirus and polyomavirus detection.
  • Application of the method to diverse water types, including groundwater, bathing water, seawater, and river water.

Main Results:

  • The one-step protocol significantly reduces processing time and complexity compared to traditional two-step methods.
  • The method demonstrates high throughput, reliability, and cost-effectiveness for analyzing multiple water samples simultaneously.
  • Successful application in identifying viral contamination sources in groundwater samples, demonstrating its practical utility.

Conclusions:

  • The developed one-step viral concentration and qPCR method is a reliable and efficient tool for microbial source tracking.
  • This approach overcomes previous bottlenecks, enabling broader application of viruses as indicators of fecal contamination.
  • The protocol's cost-effectiveness and high-throughput nature make it suitable for routine water quality monitoring.