AUTHOR=Reva Oleg , Messina Enzo , La Cono Violetta , Crisafi Francesca , Smedile Francesco , La Spada Gina , Marturano Laura , Selivanova Elena A. , Rohde Manfred , Krupovic Mart , Yakimov Michail M. 

TITLE=Functional diversity of nanohaloarchaea within xylan-degrading consortia

JOURNAL=Frontiers in Microbiology

VOLUME=Volume 14 - 2023

YEAR=2023

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2023.1182464

DOI=10.3389/fmicb.2023.1182464

ISSN=1664-302X

ABSTRACT=Extremely halophilic representatives of the phylum Candidatus Nanohaloarchaeota are obligately associated with members of other archaea; of the class Halobacteria. Using culture-independent molecular techniques, their presence in various hypersaline ecosystems around the world has been confirmed over the past decade, although, as with other members of the superphylum of nano-sized archaea known as DPANN, the vast majority of nanohaloarchaea remain uncultivated and thus, they poorly understood in terms of their metabolic capabilities and their ecophysiology. Using the (meta)genomic, transcriptomic and DNA-methylome platforms, the metabolism and functional prediction of the ecophysiology of two novel extremely halophilic symbiotic nanohaloarchaea (Ca. Nanohalococcus occultus and Ca. Nanohalovita haloferacivicina) stably cultivated in laboratory as members of a xylose-degrading binary culture with a haloarchaeal host, Haloferax lucentense, was determined. Like all known DPANN superphylum nanoorganisms, these new sugar-fermenting nanohaloarchaea lack many fundamental biosynthetic repertoires, making them exclusively dependent on their respective host for survival. In addition, given the cultivability of the new nanohaloarchaea, we managed to discover many unique features in these new organisms that have never been observed in nano-sized archaea both within the phylum Ca. Nanohaloarchaeota and the entire superphylum DPANN. This includes analysis of the expression of organism-specific non-coding regulatory (nc)RNAs (with elucidation of their 2D-secondary structures) as well as profiling of DNA methylation. While some ncRNA molecules have been predicted with high confidence as RNAs of an archaeal signal recognition particle involved in delaying protein translation, others resemble the structure of ribosome-associated ncRNAs, although none belong to any known family. Moreover, the new nanohaloarchaea have very complex cellular defense mechanisms. In addition to the defense mechanism provided by the type II restriction-modification system, consisting of Dcm-like DNA methyltransferase and Mrr restriction endonuclease, Ca. Nanohalococcus encodes active the type I-D CRISPR/Cas system, containing 77 spacers divided into two loci. Despite their diminutive genomes and as part of their host interaction mechanism, the genomes of new nanohaloarchaea do encode giant surface proteins, and one of them (9,409 amino acids-long is the largest protein of any sequenced nanohaloarchaea and the largest protein ever discovered in cultivated archaea.