Literature DB >> 27113012

Deciphering the virus-to-prokaryote ratio (VPR): insights into virus-host relationships in a variety of ecosystems.

Kaarle J Parikka1,2, Marc Le Romancer1, Nina Wauters3, Stéphan Jacquet4.   

Abstract

The discovery of the numerical importance of viruses in a variety of (aquatic) ecosystems has changed our perception of their importance in microbial processes. Bacteria and Archaea undoubtedly represent the most abundant cellular life forms on Earth and past estimates of viral numbers (represented mainly by viruses infecting prokaryotes) have indicated abundances at least one order of magnitude higher than that of their cellular hosts. Such dominance has been reflected most often by the virus-to-prokaryote ratio (VPR), proposed as a proxy for the relationship between viral and prokaryotic communities. VPR values have been discussed in the literature to express viral numerical dominance (or absence of it) over their cellular hosts, but the ecological meaning and interpretation of this ratio has remained somewhat nebulous or contradictory. We gathered data from 210 publications (and additional unpublished data) on viral ecology with the aim of exploring VPR. The results are presented in three parts: the first consists of an overview of the minimal, maximal and calculated average VPR values in an extensive variety of different environments. Results indicate that VPR values fluctuate over six orders of magnitude, with variations observed within each ecosystem. The second part investigates the relationship between VPR and other indices, in order to assess whether VPR can provide insights into virus-host relationships. A positive relationship was found between VPR and viral abundance (VA), frequency of visibly infected cells (FVIC), burst size (BS), frequency of lysogenic cells (FLC) and chlorophyll a (Chl a) concentration. An inverse relationship was detected between VPR and prokaryotic abundance (PA) (in sediments), prokaryotic production (PP) and virus-host contact rates (VCR) as well as salinity and temperature. No significant relationship was found between VPR and viral production (VP), fraction of mortality from viral lysis (FMVL), viral decay rate (VDR), viral turnover (VT) or depth. Finally, we summarize our results by proposing two scenarios in two contrasting environments, based on current theories on viral ecology as well as the present results. We conclude that since VPR fluctuates in every habitat for different reasons, as it is linked to a multitude of factors related to virus-host dynamics, extreme caution should be used when inferring relationships between viruses and their hosts. Furthermore, we posit that the VPR is only useful in specific, controlled conditions, e.g. for the monitoring of fluctuations in viral and host abundance over time.
© 2016 Cambridge Philosophical Society.

Entities:  

Keywords:  VBR; VPR; aquatic ecosystems; bacteria; prokaryote; relationships; virus

Mesh:

Substances:

Year:  2016        PMID: 27113012     DOI: 10.1111/brv.12271

Source DB:  PubMed          Journal:  Biol Rev Camb Philos Soc        ISSN: 0006-3231


  38 in total

1.  How adaptive immunity constrains the composition and fate of large bacterial populations.

Authors:  Madeleine Bonsma-Fisher; Dominique Soutière; Sidhartha Goyal
Journal:  Proc Natl Acad Sci U S A       Date:  2018-07-23       Impact factor: 11.205

2.  Deposition rates of viruses and bacteria above the atmospheric boundary layer.

Authors:  Isabel Reche; Gaetano D'Orta; Natalie Mladenov; Danielle M Winget; Curtis A Suttle
Journal:  ISME J       Date:  2018-01-29       Impact factor: 10.302

3.  Bee microbiomes go viral.

Authors:  Waldan K Kwong
Journal:  Proc Natl Acad Sci U S A       Date:  2020-05-12       Impact factor: 11.205

4.  Variability and host density independence in inductions-based estimates of environmental lysogeny.

Authors:  Ben Knowles; Barbara Bailey; Lance Boling; Mya Breitbart; Ana Cobián-Güemes; Javier Del Campo; Rob Edwards; Ben Felts; Juris Grasis; Andreas F Haas; Parag Katira; Linda Wegley Kelly; Antoni Luque; Jim Nulton; Lauren Paul; Gregory Peters; Nate Robinett; Stuart Sandin; Anca Segall; Cynthia Silveira; Merry Youle; Forest Rohwer
Journal:  Nat Microbiol       Date:  2017-04-28       Impact factor: 17.745

5.  Capsid Structure of Anabaena Cyanophage A-1(L).

Authors:  Ning Cui; Feng Yang; Jun-Tao Zhang; Hui Sun; Yu Chen; Rong-Cheng Yu; Zhi-Peng Chen; Yong-Liang Jiang; Shu-Jing Han; Xudong Xu; Qiong Li; Cong-Zhao Zhou
Journal:  J Virol       Date:  2021-09-22       Impact factor: 5.103

6.  Global diversity and distribution of prophages are lineage-specific within the Ralstonia solanacearum species complex.

Authors:  Samuel T E Greenrod; Martina Stoycheva; John Elphinstone; Ville-Petri Friman
Journal:  BMC Genomics       Date:  2022-10-06       Impact factor: 4.547

7.  A relationship between phages and organic carbon in wastewater treatment plant effluents.

Authors:  Oskar Modin; Nafis Fuad; Marie Abadikhah; David I'Ons; Elin Ossiansson; David J I Gustavsson; Ellen Edefell; Carolina Suarez; Frank Persson; Britt-Marie Wilén
Journal:  Water Res X       Date:  2022-06-16

Review 8.  The phages of staphylococci: critical catalysts in health and disease.

Authors:  Asma Hatoum-Aslan
Journal:  Trends Microbiol       Date:  2021-05-21       Impact factor: 17.079

9.  Messages from the dead protect bacteria from viral attack.

Authors:  Enea Maffei; Alexander Harms
Journal:  EMBO J       Date:  2021-12-27       Impact factor: 11.598

10.  Reduced bacterial mortality and enhanced viral productivity during sinking in the ocean.

Authors:  Wei Wei; Xiaowei Chen; Markus G Weinbauer; Nianzhi Jiao; Rui Zhang
Journal:  ISME J       Date:  2022-04-01       Impact factor: 11.217

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.