Aharon Oren’s research while affiliated with Hebrew University of Jerusalem and other places

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Publications (755)


Lawrence I. (Larry) Hochstein a researcher dedicated to halophilic microorganisms of all types and environments
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November 2024

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Extremophiles

Russell H Vreeland

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Aharon Oren

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Emendation of Appendix 9 of the International Code of Nomenclature of Prokaryotes to regulate the use of connecting vowels in compound names after stems ending in the same vowel

International Journal of Systematic and Evolutionary Microbiology

Following a proposal to emend Appendix 9 of the International Code of Nomenclature of Prokaryotes with guidelines to regulate the use of connecting vowels in compound names after stems ending in the same vowel, I here report the outcome of the ballot on this proposal by the members of the International Committee on Systematics of Prokaryotes. The new guidelines to be incorporated in Appendix 9 are presented.




Proposal to add a Note to Rule 8 of the International Code of Nomenclature of Prokaryotes to clarify the meaning of the term 'stem'

International Journal of Systematic and Evolutionary Microbiology

According to the Rules of the International Code of Nomenclature of Prokaryotes (ICNP) and its appendices, names of higher taxa are formed by the addition of the appropriate suffix to the stem of the name of the type genus, and word stems derived from Latin and/or Greek are combined to compound names by means of an appropriate connecting vowel. The way the word ‘stem’ is used in the ICNP differs from the meaning of this term in textbooks of Latin and Greek grammar. We therefore propose to add a Note to Rule 8, clarifying that the term ‘stem’ when used in the ICNP corresponds with that part of the word that does not vary among the forms of the noun in the oblique cases, i.e., cases other than the nominative, and which can be obtained by deleting the ending of the genitive singular.


Selection of areas of colonized gypsum worldwide. Outcrops and similar occurrences (subaerial; 1–37; ); salars and salterns (subaquatic 38–45; ); other occurrences (sabkha 46; ); gypsum containing inclusions of fossilized microorganisms or authigenic biomarkers (47–55; 4). More information on sampling sites and their geographic locations can be found in Supplementary Data and Supplementary Table 1.
Examples of gypsum endolithic microbial colonization. (A) Gypcrete from the Atacama Desert (Cordón de Lila area), later analyzed by Raman imaging where intensity of carotenoid signal is visualized in zones rich in algal cells of the Trebouxiaceae family (B,C; adapted from Vítek et al., 2016, with permission), the red circles in C point to the regions of Raman analysis; (D) bottom gypsum specimen with distinct pigmented colonization layers from a solar saltern evaporation pond in Eilat, Israel (from Culka et al., 2014, with permission); (E) gypsum from Salar de Llamará (from Rasuk et al., 2014, with permission); (F) gypsum from Lake St. Martin impact structure in Manitoba, Canada (adapted from Rhind et al., 2014, with permission); (G,H,I): superficial outcrops of colonized Messinian selenite gypsum from Santa Nifa, Sicily (adapted from Němečková et al., 2021, with permission); the black arrow (a) in I points to black cells of presumably Gloeocapsa, whereas the yellow arrow (b) points to yellow-brown colonies, presumably Nostoc.
Examples of microscopy images obtained with different techniques applied for visualization of endolithic microbial communities within gypsum substrate from the Atacama Desert (panels A,E,I,K,L: endolithic habitats within gypsum crust from Tarapacá and panels B–D,F–H,J: endolithic habitats within gypcrete from the Cordón de Lila area respectively). SEM-BSE images (A,B) show disperse cryptoendolithic colonization of pores between gypsum grains by algae (Trebouxia cells (a) in panel B) and their associated fungal hyphae ( h in panel B). SEM-BSE image (C) shows algae in close proximity to sepiolite (s). SEM-BSE images (D,E) show cryptoendolithic cyanobacteria aggregates and in image E, cyanobacteria (c) and heterotrophic bacteria (b). SEM-BSE image (F) shows endolithic filamentous cyanobacterial cells between gypsum crystals. Note that molecular biology tools applied to this sample did not detect filamentous cyanobacteria. LT-SEM images of cryo-fractured algae cells (panel G) and cyanobacteria cells (panel H) with EPS sheaths. ESEM image of hydrated cyanobacteria aggregate (I). TEM high-resolution image (J) of ultrastructural elements of cyanobacteria cells in close proximity to sepiolite (s). FM composed image (K) of autofluorescence of viable algae cells (red signal), remains of algae cells (blue signal) and heterotrophic bacteria cells (green signal of SYBR Green II stained cells). CLSM 3D reconstruction composed image (L) of autofluorescence of viable algae cells (red signal) and heterotrophic bacteria cells (green signal of SYBR Green II stained cells). For materials and methods see Wierzchos et al. (2011) and Wierzchos et al. (2015).
Schematic representation of crypto-, chasmo-, and hypoendolithic habitats within gypsum deposits from the Atacama Desert. Modified from Wierzchos et al. (2015) under CC BY license.
Microbial colonization of gypsum: from the fossil record to the present day

Microorganisms inhabiting gypsum have been observed in environments that differ greatly in water availability. Gypsum colonized by microorganisms, including cyanobacteria, eukaryotic algae, and diverse heterotrophic communities, occurs in hot, arid or even hyperarid environments, in cold environments of the Antarctic and Arctic zones, and in saline and hypersaline lakes and ponds where gypsum precipitates. Fossilized microbial remnants preserved in gypsum were also reported. Gypsum protects the endolithic microbial communities against excessive insolation and ultraviolet radiation, while allowing photosynthetically active radiation to penetrate through the mineral substrate. We here review the worldwide occurrences of microbially colonized gypsum and the specific properties of gypsum related to its function as a substrate and habitat for microbial life on Earth and possibly beyond. Methods for detecting and characterizing endolithic communities and their biomarkers in gypsum are discussed, including microscopic, spectroscopic, chemical, and molecular biological techniques. The modes of adaptation of different microorganisms to life within gypsum crystals under different environmental conditions are described. Finally, we discuss gypsum deposits as possible targets for the search for microbial life or its remnants beyond Earth, especially on Mars, where sulfate-rich deposits occur, and propose strategies to detect them during space exploration missions.


Citations (49)


... This study reports the isolation of a novel Rhodococcus species that is closely related to R. equi, with potential implications in the identification of this pathogen and in studies on its ecology, epidemiology and environmental distribution. Here we use the name R. equi instead of the synonym Prescottella equi (Magnusson 1923) Sangal et al. 2022 [9], and the circumscription of the genus Rhodococcus Zopf 1891 as emended by Val-Calvo and Vázquez-Boland 2023 [10]. This emendation was based on a recent study that examined the Mycobacteriales taxonomy using a network analysis-aided, context-uniform phylogenomic approach for non-subjective genus demarcation [11]. ...

Reference:

Rhodococcus parequi sp. nov., a new species isolated from equine farm soil closely related to the pathogen Rhodococcus equi
Notification of changes in taxonomic opinion previously published outside the IJSEM. List of changes in taxonomic opinion no. 40

International Journal of Systematic and Evolutionary Microbiology

... The highest relative abundance of Salinibacter was observed in the Italian and Vietnamese freshly harvested halite STP and VS8 brine (69.2% and 91.3%, respectively). It is well-know that Salinibacter uses the "salt-in" strategy known from the archaeal Halobacteriota and is a major component of hypersaline aquatic ecosystems worldwide ( [77] for further references). In contrast, to the ubiquitous Salinibacter, the gammaproteobacterium Halovibrio was exclusive to brine and predominated in the Hai Lý samples, comprising 45.8% and 38.75% of the community, respectively. ...

Novel insights into the diversity of halophilic microorganisms and their functioning in hypersaline ecosystems

npj Biodiversity

... enshiensis' [4], but the name was still not validly published under the ICNP since Sinirhodobacter was validly published later (in 2018) and has no priority over Paenirhodobacter (in 2014). Meanwhile, the genus Sedimentimonas was proposed with one species in 2022, neighboured with the genus Sinirhodobacter in phylogenomic trees, and validly published very recently [22]. ...

Validation List no. 217. Valid publication of new names and new combinations effectively published outside the IJSEM

International Journal of Systematic and Evolutionary Microbiology

... One of the most important resources in culture collections is type strains. The taxonomy of prokaryotes has evolved from phenotype-based classification to polyphasic methods, ultimately leading to genome-based taxonomic approaches [3] . Since 2018, genome sequence data have been required by the International Journal of Systematic and Evolutionary Microbiology (IJSEM) when publishing a new species. ...

Advancements in prokaryotic systematics and the role of Bergey's International Society for Microbial Systematics (BISMiS) in addressing challenges in the meta-data era

National Science Review

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Rashidin Abdugheni

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... To determine the phylogenetic position and relationships of PAM 2766 T , we generated a core-genome phylogeny using all available genome assemblies for the type strains of each species of the genus Rhodococcus (as emended by Val-Calvo and Vázquez-Boland 2023 [11,39]) with status name "correct" in the LPSN repository (https://lpsn.dsmz.de/genus/rhodococcus, accessed January 2024) ( Table S1). ...

Validation List no. 216. Valid publication of new names and new combinations effectively published outside the IJSEM

International Journal of Systematic and Evolutionary Microbiology

... Specifically, we found that the variation in several key species known to be affected by epilepsy or other CNS disease states were particularly modified in a time x treatment group interaction effect, including Akkermansiaceae, Lachnospiraceae, Lactobacillaceae, and Erysipelotrichaceae ( Figure 5A and Table S1). Further, proportional distribution of all species in each treatment group exhibited marked shifts over time ( Figure 5B); the gut microbiome of SAL pre-treated animals was predominantly made up of Bacillota (Firmicutes) 19 and Bacteroidota, across all . CC-BY-NC-ND 4.0 International license available under a (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. ...

On validly published names, correct names, and changes in the nomenclature of phyla and genera of prokaryotes: a guide for the perplexed

npj Biofilms and Microbiomes

... 5) [20]. The phylogenomic analysis was performed based on the Genome Taxonomy Database (GTDB) as described previously [21], and Halorutilus salinus F3-133 T was selected as the outgroup. ...

Proposed minimal standards for description of new taxa of the class Halobacteria

International Journal of Systematic and Evolutionary Microbiology

... However, this proposal overlooked the fact that, according to the International Code of Nomenclature of Prokaryotes [7], Flagellimonas should have been used. Subsequently, a new publication was issued to resolve the matter [8]. Currently, Flagellimonas contains 42 validly published species with Flagellimonas eckloniae as the type species (https://lpsn.dsmz.de/genus/flagellimonas). ...

Reclassification of Allomuricauda and Muricauda species as members of the genus Flagellimonas Bae et al. 2007 and emended description of the genus Flagellimonas

International Journal of Systematic and Evolutionary Microbiology

... Originally, the order was affiliated with the phylum Euryarchaeota [2]. However, an updated phylogenetic reconstruction from Genome Taxonomy Database (GTDB) firmly placed these organisms as a separate phylum, namely Thermoplasmatota [8,9]. According to this classification, the phylum Thermoplasmatota comprises classes 'Ca. ...

Validation List no. 215. Valid publication of new names and new combinations effectively published outside the IJSEM

International Journal of Systematic and Evolutionary Microbiology

... For the case presented here, although Proteus Müller, 1786 was replaced and is no longer available nowadays in zoological nomenclature [11], it should be noted that Rule 51b(4) of the ICNP [5,6] makes no reference to the status of protozoan names under the zoological code and, therefore, the current wording does not require that only valid or available names be taken into consideration with regards establishing whether names are homonyms [19,20]. In this way, due to the homonymy between the prokaryotic generic name Proteus Hauser 1885 (Approved Lists 1980) and the protozoan genus name Proteus Müller, 1786, the name Proteus Hauser 1885 (Approved Lists 1980), which was validly published before 31 December 2000 and has standing today, should be considered illegitimate and in need of replacement according to Rules 51b(4) and 54 of the ICNP [5,6]. ...

Is the bacterial genus name Rhodococcus Zopf 1891 illegitimate? Request for an Opinion
  • Citing Article
  • January 2024

International Journal of Systematic and Evolutionary Microbiology