Evidence map›Paper›PMID 27338471›Full record

ReviewToxins2016

Is qPCR a Reliable Indicator of Cyanotoxin Risk in Freshwater?

Ana Beatriz F Pacheco, Iame A Guedes, Sandra M F O Azevedo

Abstract readReview
In one paragraph

Review in Toxins, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. CladoceranToxins · 2025
    Article
  6. Review
  7. Intraspecific divergence withinProceedings. Biological sciences · 2025
    Article
  8. Article
  9. Article
  10. Early Detection Methods for Toxic Cyanobacteria Blooms.Pathogens (Basel, Switzerland) · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Science advances · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ana Beatriz F PachecoCarlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro 21949-902, Brazil. biafp@biof.ufrj.br.
Iame A GuedesCarlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro 21949-902, Brazil. iameguedes@gmail.com.
Sandra M F O AzevedoCarlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro 21949-902, Brazil. sazevedo@biof.ufrj.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The wide distribution of cyanobacteria in aquatic environments leads to the risk of water contamination by cyanotoxins, which generate environmental and public health issues. Measurements of cell densities or pigment contents allow both the early detection of cellular growth and bloom monitoring, but these methods are not sufficiently accurate to predict actual cyanobacterial risk. To quantify cyanotoxins, analytical methods are considered the gold standards, but they are laborious, expensive, time-consuming and available in a limited number of laboratories. In cyanobacterial species with toxic potential, cyanotoxin production is restricted to some strains, and blooms can contain varying proportions of both toxic and non-toxic cells, which are morphologically indistinguishable. The sequencing of cyanobacterial genomes led to the description of gene clusters responsible for cyanotoxin production, which paved the way for the use of these genes as targets for PCR and then quantitative PCR (qPCR). Thus, the quantification of cyanotoxin genes appeared as a new method for estimating the potential toxicity of blooms. This raises a question concerning whether qPCR-based methods would be a reliable indicator of toxin concentration in the environment. Here, we review studies that report the parallel detection of microcystin genes and microcystin concentrations in natural populations and also a smaller number of studies dedicated to cylindrospermopsin and saxitoxin. We discuss the possible issues associated with the contradictory findings reported to date, present methodological limitations and consider the use of qPCR as an indicator of cyanotoxin risk.

Indexed as

Real-Time Polymerase Chain ReactionAlkaloidsBacterial ToxinsCyanobacteriaCyanobacteria ToxinsEnvironmental MonitoringFresh WaterHarmful Algal BloomMicrocystinsRNA, Ribosomal, 16SSaxitoxinUracilAlkaloidsBacterial ToxinsCyanobacteria ToxinscylindrospermopsinmicrocystinMicrocystinsRNA, Ribosomal, 16SSaxitoxinUracilbloomcyanobacteriacylindrospermopsinmicrocystinsaxitoxin

Identifiers

PMID27338471
PMCPMC4926139

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.