Cryptosporidium,Giardia, Cryptococcus, Pneumocystis genetic variability: cryptic biological species or clonal near-clades?

PLoS Pathog. 2014 Apr 10;10(4):e1003908. doi: 10.1371/journal.ppat.1003908. eCollection 2014 Apr.

Abstract

An abundant literature dealing with the population genetics and taxonomy of Giardia duodenalis, Cryptosporidium spp., Pneumocystis spp., and Cryptococcus spp., pathogens of high medical and veterinary relevance, has been produced in recent years. We have analyzed these data in the light of new population genetic concepts dealing with predominant clonal evolution (PCE) recently proposed by us. In spite of the considerable phylogenetic diversity that exists among these pathogens, we have found striking similarities among them. The two main PCE features described by us, namely highly significant linkage disequilibrium and near-clading (stable phylogenetic clustering clouded by occasional recombination), are clearly observed in Cryptococcus and Giardia, and more limited indication of them is also present in Cryptosporidium and Pneumocystis. Moreover, in several cases, these features still obtain when the near-clades that subdivide the species are analyzed separately ("Russian doll pattern"). Lastly, several sets of data undermine the notion that certain microbes form clonal lineages simply owing to a lack of opportunity to outcross due to low transmission rates leading to lack of multiclonal infections ("starving sex hypothesis"). We propose that the divergent taxonomic and population genetic inferences advanced by various authors about these pathogens may not correspond to true evolutionary differences and could be, rather, the reflection of idiosyncratic practices among compartmentalized scientific communities. The PCE model provides an opportunity to revise the taxonomy and applied research dealing with these pathogens and others, such as viruses, bacteria, parasitic protozoa, and fungi.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cryptosporidium / genetics*
  • Cryptosporidium / pathogenicity
  • Genetic Variation*
  • Giardia / genetics*
  • Giardia / pathogenicity
  • Linkage Disequilibrium*
  • Pneumocystis / genetics*
  • Pneumocystis / pathogenicity

Grants and funding

This study was supported by the ANR Clonix project (ANR-11-BSV7-007). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.