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International journal of systematic and evolutionary microbiology2025; 75(3); 006679; doi: 10.1099/ijsem.0.006679

Rhodococcus parequi sp. nov., a new species isolated from equine farm soil closely related to the pathogen Rhodococcus equi.

Abstract: We present the description of the new species, , found during phylogenomic investigations of a global collection of strains identified as () . Strain PAM 2766 was isolated from horse-breeding farm soil in Normandy, France, and was indistinguishable from based on the usual identification tests. Whole-genome phylogenetic analyses located PAM 2766 in the same sublineage as , together with , , , , and . PAM 2766 is most closely related to, but sufficiently distinct from, DSM 20307 to be considered a separate species. The average nt identity (ANI) and average aa identity (AAI) values are 88.60% and 92.35, respectively, well below the species cutoff. The PAM 2766 draft genome is ~5.3 Mb in size with 68.98% G+C mol content. PAM 2766 is strictly aerobic and non-motile and produces smooth, creamy to buff-coloured colonies very similar to those of . It phenotypically differs from the latter by the ability to grow at 5 °C, a strongly positive urease test at 24 h and specificities in the carbon and nitrogen source utilization profile as determined by phenotype microarray screens. Our data indicate that PAM 2766 belongs to a novel species, for which the name sp. nov. is proposed. was avirulent in macrophage infection assays and is assumed to be non-pathogenic. The type strain is PAM 2766 (=CETC 30995=NCTC 14987).
Publication Date: 2025-03-10 PubMed ID: 40063668PubMed Central: PMC11893733DOI: 10.1099/ijsem.0.006679Google Scholar: Lookup
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Summary

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Rhocococcus parequi sp. nov. is a newly identified bacterial species isolated from soil on an equine farm in France. Although closely related to the pathogenic Rhodococcus equi, this new species can be differentiated based on genomic and phenotypic characteristics.

Overview of the Research

  • The study describes a newly discovered species, Rhodococcus parequi sp. nov., found during genomic studies of bacteria previously thought to be Rhodococcus equi.
  • A key strain, PAM 2766, was isolated from soil on a horse-breeding farm in Normandy, France.
  • This strain was very similar to Rhodococcus equi by common identification methods but differed significantly at the whole-genome level.

Isolation and Identification

  • Strain PAM 2766 was collected from equine farm soil, an environment associated with Rhodococcus equi, a known pathogen of horses.
  • Initial identification tests could not distinguish PAM 2766 from Rhodococcus equi due to similar colonial morphology and phenotypic traits.
  • However, advanced genetic analysis revealed important differences, prompting reclassification.

Genomic Analysis

  • Whole-genome phylogenetic analysis placed PAM 2766 within the Rhodococcus equi sublineage but as a distinct species.
  • PAM 2766’s genome size is around 5.3 megabases with a high G+C content (68.98%), characteristic of the genus Rhodococcus.
  • Key metrics comparing PAM 2766 to Rhodococcus equi DSM 20307 showed:
    • Average nucleotide identity (ANI) of 88.60%
    • Average amino acid identity (AAI) of 92.35%
  • These values fall well below the accepted thresholds for species identity, confirming PAM 2766 represents a new species.

Phenotypic Characteristics

  • PAM 2766 grows as smooth, creamy to buff-coloured colonies similar to Rhodococcus equi, explaining why usual tests failed to distinguish them.
  • Distinct phenotypic traits of PAM 2766 include:
    • Ability to grow at low temperature (5 °C), unlike Rhodococcus equi.
    • Strongly positive urease activity at 24 hours, differing from R. equi.
    • Unique carbon and nitrogen source utilization profiles shown by detailed phenotype microarray analysis.

Pathogenicity and Implications

  • Macrophage infection assays showed PAM 2766 is avirulent, suggesting it is non-pathogenic, unlike Rhodococcus equi which is pathogenic to horses.
  • This is important for understanding risks associated with soil microbes on equine farms.
  • The discovery improves diagnostic accuracy to distinguish pathogenic R. equi from closely related harmless species, which is critical for veterinary health management.

Conclusion and Nomenclature

  • The researchers propose classification of this strain as a novel species Rhodococcus parequi sp. nov.
  • The type strain is designated as PAM 2766 (=CETC 30995=NCTC 14987).
  • This work highlights the power of genomic tools to refine bacterial taxonomy beyond traditional methods.

Cite This Article

APA
Vazquez-Boland JA, Val-Calvo J, Duquesne F, Decorosi F, Viti C, Petry S, Scortti M. (2025). Rhodococcus parequi sp. nov., a new species isolated from equine farm soil closely related to the pathogen Rhodococcus equi. Int J Syst Evol Microbiol, 75(3), 006679. https://doi.org/10.1099/ijsem.0.006679

Publication

ISSN: 1466-5034
NlmUniqueID: 100899600
Country: England
Language: English
Volume: 75
Issue: 3
PII: 006679

Researcher Affiliations

Vazquez-Boland, José A
  • Microbial Pathogenomics Laboratory, Edinburgh Medical School (Biomedical Sciences), University of Edinburgh, Edinburgh, UK.
Val-Calvo, Jorge
  • Microbial Pathogenomics Laboratory, Edinburgh Medical School (Biomedical Sciences), University of Edinburgh, Edinburgh, UK.
Duquesne, Fabien
  • ANSES, Laboratory for Animal Health, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
Decorosi, Francesca
  • Department of Agriculture, Food, Environment and Forestry, University of Florence, Florence, Italy.
Viti, Carlo
  • Department of Agriculture, Food, Environment and Forestry, University of Florence, Florence, Italy.
Petry, Sandrine
  • ANSES, Laboratory for Animal Health, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
Scortti, Mariela
  • Microbial Pathogenomics Laboratory, Edinburgh Medical School (Biomedical Sciences), University of Edinburgh, Edinburgh, UK.

MeSH Terms

  • Rhodococcus / classification
  • Rhodococcus / genetics
  • Rhodococcus / isolation & purification
  • Animals
  • Phylogeny
  • Soil Microbiology
  • Horses / microbiology
  • DNA, Bacterial / genetics
  • Bacterial Typing Techniques
  • Rhodococcus equi / genetics
  • Rhodococcus equi / classification
  • France
  • Genome, Bacterial
  • RNA, Ribosomal, 16S / genetics
  • Base Composition
  • Farms
  • Sequence Analysis, DNA

Conflict of Interest Statement

The authors declare that there are no conflicts of interest.

References

This article includes 57 references
  1. Arahal DR, Bull CT, Christensen H, Chuvochina M, Dunlap C. Judicial opinion 130. Int J Syst Evol Microbiol 2024;74:006414.
    doi: 10.1099/ijsem.0.006414pmc: PMC11261725pubmed: 38841989google scholar: lookup
  2. Zopf W. Ueber ausscheidung von fettfarbstoffen (Lipochromen) seitens gewisser spaltpilze. Berichte der Deutschen Botanischen Gesellschaft 1891;9:22–28.
  3. Parte AC, Sardà Carbasse J, Meier-Kolthoff JP, Reimer LC, Göker M. List of prokaryotic names with standing in nomenclature (LPSN) moves to the DSMZ. Int J Syst Evol Microbiol 2020;70:5607–5612.
    doi: 10.1099/ijsem.0.004332pmc: PMC7723251pubmed: 32701423google scholar: lookup
  4. Kämpfer P, Dott W, Martin K, Glaeser SP. Rhodococcus defluvii sp. nov., isolated from wastewater of a bioreactor and formal proposal to reclassify [Corynebacterium hoagii] and Rhodococcus equi as Rhodococcus hoagii comb. nov.. Int J Syst Evol Microbiol 2014;64:755–761.
    doi: 10.1099/ijs.0.053322-0pubmed: 24198057google scholar: lookup
  5. Alvarez HM. Biology of Rhodococcus, 2nd ed.. .
    doi: 10.1007/978-3-030-11461-9google scholar: lookup
  6. Lee SD, Kim Y-J, Kim IS. Rhodococcus subtropicus sp. nov., a new actinobacterium isolated from a cave. Int J Syst Evol Microbiol 2019;69:3128–3134.
    doi: 10.1099/ijsem.0.003601pubmed: 31364963google scholar: lookup
  7. Prescott JF. Rhodococcus equi: an animal and human pathogen. Clin Microbiol Rev 1991;4:20–34.
    doi: 10.1128/CMR.4.1.20pmc: PMC358176pubmed: 2004346google scholar: lookup
  8. Vázquez-Boland JA, Meijer WG. The pathogenic actinobacterium Rhodococcus equi: what’s in a name. Mol Microbiol 2019;112:1–15.
    doi: 10.1111/mmi.14267pmc: PMC6852188pubmed: 31099908google scholar: lookup
  9. Sangal V, Goodfellow M, Jones AL, Sutcliffe IC. A stable home for an equine pathogen: valid publication of the binomial prescottella equi gen.. Int J Syst Evol Microbiol 2022;72:005551.
    doi: 10.1099/ijsem.0.005551pubmed: 36107761google scholar: lookup
  10. Oren A, Göker M. Notification of changes in taxonomic opinion previously published outside the IJSEM. List of changes in taxonomic opinion no. 40. Int J Syst Evol Microbiol 2024;74:006482.
    doi: 10.1099/ijsem.0.006482pubmed: 38299467google scholar: lookup
  11. Val-Calvo J, Vázquez-Boland JA. Mycobacteriales taxonomy using network analysis-aided, context-uniform phylogenomic approach for non-subjective genus demarcation. mBio 2023;14:e0220723.
    doi: 10.1128/mbio.02207-23pmc: PMC10653829pubmed: 37796005google scholar: lookup
  12. Navas J, González-Zorn B, Ladrón N, Garrido P, Vázquez-Boland JA. Identification and mutagenesis by allelic exchange of choE, encoding a cholesterol oxidase from the intracellular pathogen Rhodococcus equi. J Bacteriol 2001;183:4796–4805.
  13. González-Zorn B, Domínguez-Bernal G, Suárez M, Ripio MT, Vega Y. The smcL gene of Listeria ivanovii encodes a sphingomyelinase C that mediates bacterial escape from the phagocytic vacuole. Mol Microbiol 1999;33:510–523.
  14. Ladrón N, Fernández M, Agüero J, González Zörn B, Vázquez-Boland JA. Rapid identification of Rhodococcus equi by a PCR assay targeting the choE gene. J Clin Microbiol 2003;41:3241–3245.
  15. Rodríguez-Lázaro D, Lewis DA, Ocampo-Sosa AA, Fogarty U, Makrai L. Internally controlled real-time PCR method for quantitative species-specific detection and vapA genotyping of. Appl Environ Microbiol 2006;72:4256–4263.
    doi: 10.1128/AEM.02706-05pmc: PMC1489618pubmed: 16751540google scholar: lookup
  16. Ocampo-Sosa AA, Lewis DA, Navas J, Quigley F, Callejo R. Molecular epidemiology of Rhodococcus equi based on traA, vapA, and vapB virulence plasmid markers.. J Infect Dis 2007;196:763–769.
    doi: 10.1086/519688pubmed: 17674320google scholar: lookup
  17. Halbert ND, Reitzel RA, Martens RJ, Cohen ND. Evaluation of a multiplex polymerase chain reaction assay for simultaneous detection of Rhodococcus equi and the vapA gene.. Am J Vet Res 2005;66:1380–1385.
    doi: 10.2460/ajvr.2005.66.1380pubmed: 16173481google scholar: lookup
  18. Valero-Rello A, Hapeshi A, Anastasi E, Alvarez S, Scortti M. An invertron-like linear plasmid mediates intracellular survival and virulence in bovine isolates of Rhodococcus equi.. Infect Immun 2015;83:2725–2737.
    doi: 10.1128/IAI.00376-15pmc: PMC4468562pubmed: 25895973google scholar: lookup
  19. Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data.. Bioinformatics 2014;30:2114–2120.
  20. Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.. J Comput Biol 2012;19:455–477.
    doi: 10.1089/cmb.2012.0021pmc: PMC3342519pubmed: 22506599google scholar: lookup
  21. Gurevich A, Saveliev V, Vyahhi N, Tesler G. QUAST: quality assessment tool for genome assemblies.. Bioinformatics 2013;29:1072–1075.
  22. Riesco R, Trujillo ME. Update on the proposed minimal standards for the use of genome data for the taxonomy of prokaryotes.. Int J Syst Evol Microbiol 2024;74:006300.
    doi: 10.1099/ijsem.0.006300pmc: PMC10963913pubmed: 38512750google scholar: lookup
  23. Letek M, González P, Macarthur I, Rodríguez H, Freeman TC. The genome of a pathogenic Rhodococcus: cooptive virulence underpinned by key gene acquisitions.. PLoS Genet 2010;6:e1001145.
  24. Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P. DNA–DNA hybridization values and their relationship to whole-genome sequence similarities.. Int J Syst Evol Microbiol 2007;57:81–91.
    doi: 10.1099/ijs.0.64483-0pubmed: 17220447google scholar: lookup
  25. Jain C, Rodriguez-R LM, Phillippy AM, Konstantinidis KT, Aluru S. High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries.. Nat Commun 2018;9:5114.
    doi: 10.1038/s41467-018-07641-9pmc: PMC6269478pubmed: 30504855google scholar: lookup
  26. Konstantinidis KT, Rosselló-Móra R, Amann R. Uncultivated microbes in need of their own taxonomy.. ISME J 2017;11:2399–2406.
    doi: 10.1038/ismej.2017.113pmc: PMC5649169pubmed: 28731467google scholar: lookup
  27. Meier-Kolthoff JP, Carbasse JS, Peinado-Olarte RL, Göker M. TYGS and LPSN: a database tandem for fast and reliable genome-based classification and nomenclature of prokaryotes.. Nucleic Acids Res 2022;50:D801–D807.
    doi: 10.1093/nar/gkab902pmc: PMC8728197pubmed: 34634793google scholar: lookup
  28. Lane DJ. 16S/23S rRNA Sequencing.. .
  29. Anastasi E, MacArthur I, Scortti M, Alvarez S, Giguère S. Pangenome and phylogenomic analysis of the pathogenic actinobacterium Rhodococcus equi.. Genome Biol Evol 2016;8:3140–3148.
    doi: 10.1093/gbe/evw222pmc: PMC5174736pubmed: 27638249google scholar: lookup
  30. Rainey FA, Burghardt J, Kroppenstedt RM, Klatte S, Stackebrandt E. Phylogenetic analysis of the genera Rhodococcus and Nocardia and evidence for the evolutionary origin of the genus Nocardia from within the radiation of Rhodococcus species.. Microbiol 1995;141:523–528.
  31. Kim M, Oh H-S, Park S-C, Chun J. Towards a taxonomic coherence between average nucleotide identity and 16S rRNA gene sequence similarity for species demarcation of prokaryotes. Int J Syst Evol Microbiol. 2014;64:346–351. doi: 10.1099/ijs.0.059774-0.
    doi: 10.1099/ijs.0.059774-0pubmed: 24505072google scholar: lookup
  32. Zhang D, Su Z, Li L, Tang WZ. Rhodococcus spongiicola sp. nov. and Rhodococcus xishaensis sp. nov., from marine sponges. Int J Syst Evol Microbiol. 2021;71:004863. doi: 10.1099/ijsem.0.004863.
    doi: 10.1099/ijsem.0.004863pubmed: 34296990google scholar: lookup
  33. Kämpfer P, Glaeser SP, Blom J, Wolf J, Benning S, et al. Rhodococcus pseudokoreensis sp. nov. isolated from the rhizosphere of young M26 apple rootstocks. Arch Microbiol. 2022;204:505. doi: 10.1007/s00203-022-03079-2.
    doi: 10.1007/s00203-022-03079-2pmc: PMC9300504pubmed: 35857201google scholar: lookup
  34. Beak JH, Baek W, Jeong SE, Lee SC, Jin HM, et al. Rhodococcus oxybenzonivorans sp. nov., a benzophenone-3-degrading bacterium, isolated from stream sediment. Int J Syst Evol Microbiol. 2022;72:005433.
    pubmed: 35704462
  35. Kusuma AB, Fenylestari G, Ammar F, Nououi I, Goodfellow M. Rhodococcus indonesiensis sp. nov. a new member of the Rhodococcus ruber lineage isolated from sediment of a neutral hot spring and reclassification of Rhodococcus electrodiphilus (ramaprasad et al. 2018) as a later heterotypic synonym of Rhodococcus ruber (Kruse 1896) goodfellow and alderson 1977 (approved lists 1980) Int J Syst Evol Microbiol. 2018;74:006236.
    pubmed: 38214280
  36. Hassler HB, Probert B, Moore C, Lawson E, Jackson RW, et al. Phylogenies of the 16S rRNA gene and its hypervariable regions lack concordance with core genome phylogenies. Microbiome. 2022;10:104. doi: 10.1186/s40168-022-01295-y.
    doi: 10.1186/s40168-022-01295-ypmc: PMC9264627pubmed: 35799218google scholar: lookup
  37. Bartoš O, Chmel M, Swierczková I. The overlooked evolutionary dynamics of 16S rRNA revises its role as the “gold standard” for bacterial species identification. Sci Rep. 2024;14:9067. doi: 10.1038/s41598-024-59667-3.
    doi: 10.1038/s41598-024-59667-3pmc: PMC11032355pubmed: 38643216google scholar: lookup
  38. Chalita M, Kim YO, Park S, Oh HS, Cho JH, et al. EzBioCloud: a genome-driven database and platform for microbiome identification and discovery. Int J Syst Evol Microbiol. 2024;74:006421. doi: 10.1099/ijsem.0.006421.
    doi: 10.1099/ijsem.0.006421pmc: PMC11261700pubmed: 38888585google scholar: lookup
  39. Oren A, Göker M. Validation List no. 216. Valid publication of new names and new combinations effectively published outside the IJSEM. Int J Syst Evol Microbiol. 2024;74:006229. doi: 10.1099/ijsem.0.006229.
    doi: 10.1099/ijsem.0.006229pmc: PMC10995726pubmed: 38546332google scholar: lookup
  40. Contreras-Moreira B, Vinuesa P. GET_HOMOLOGUES, a versatile software package for scalable and robust microbial pangenome analysis. Appl Environ Microbiol. 2013;79:7696–7701. doi: 10.1128/AEM.02411-13.
    doi: 10.1128/AEM.02411-13pmc: PMC3837814pubmed: 24096415google scholar: lookup
  41. Vinuesa P, Ochoa-Sánchez LE, Contreras-Moreira B. Get_phyloMarkers, a software package to select optimal orthologous clusters for phylogenomics and inferring pan-genome phylogenies, used for a critical geno-taxonomic revision of the genus Stenotrophomonas. Front Microbiol. 2018;9:771. doi: 10.3389/fmicb.2018.00771.
    doi: 10.3389/fmicb.2018.00771pmc: PMC5938378pubmed: 29765358google scholar: lookup
  42. Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32:268–274. doi: 10.1093/molbev/msu300.
    doi: 10.1093/molbev/msu300pmc: PMC4271533pubmed: 25371430google scholar: lookup
  43. Orro A, Cappelletti M, D’Ursi P, Milanesi L, Di Canito A, et al. Genome and phenotype microarray analyses of Rhodococcus sp. BCP1 and Rhodococcus opacus R7: Genetic determinants and metabolic abilities with environmental relevance. PLoS One. 2015;10:e0139467. doi: 10.1371/journal.pone.0139467.
  44. Round J, Roccor R, Li SN, Eltis LD. A fatty acyl coenzyme A reductase promotes wax ester accumulation in Rhodococcus jostii RHA1. Appl Environ Microbiol. 2017;83:e00902-17. doi: 10.1128/AEM.00902-17.
    doi: 10.1128/AEM.00902-17pmc: PMC5626984pubmed: 28778885google scholar: lookup
  45. MacArthur I, Anastasi E, Alvarez S, Scortti M, Vázquez-Boland JA. Comparative genomics of Rhodococcus equi virulence plasmids indicates host-driven evolution of the vap pathogenicity island. Genome Biol Evol. 2017;9:1241–1247. doi: 10.1093/gbe/evx057.
    doi: 10.1093/gbe/evx057pmc: PMC5434932pubmed: 28369330google scholar: lookup
  46. von Bargen K, Haas A. Molecular and infection biology of the horse pathogen Rhodococcus equi. FEMS Microbiol Rev. 2009;33:870–891. doi: 10.1111/j.1574-6976.2009.00181.x.
  47. Hondalus MK, Mosser DM. Survival and replication of Rhodococcus equi in macrophages. Infect Immun. 1994;62:4167–4175. doi: 10.1128/iai.62.10.4167-4175.1994.
  48. González-Iglesias P, Scortti M, MacArthur I, Hapeshi A, Rodriguez H, et al. Mouse lung infection model to assess Rhodococcus equi virulence and vaccine protection. Vet Microbiol. 2014;172:256–264. doi: 10.1016/j.vetmic.2014.03.026.
    doi: 10.1016/j.vetmic.2014.03.026pubmed: 24852140google scholar: lookup
  49. Giguère S, Hondalus MK, Yager JA, Darrah P, Mosser DM, et al. Role of the 85-kilobase plasmid and plasmid-encoded virulence-associated protein a in Iitracellular survival and virulence of Rhodococcus equi. Infect Immun. 1999;67:3548–3557. doi: 10.1128/IAI.67.7.3548-3557.1999.
  50. Coulson GB, Agarwal S, Hondalus MK.Characterization of the role of the pathogenicity island and vapG in the virulence of the intracellular actinomycete pathogen Infect Immun 2010783323–3334. 10.1128/IAI.00081-10
    doi: 10.1128/IAI.00081-10pmc: PMC2916281pubmed: 20439471google scholar: lookup
  51. Oren A, Arahal DR, Göker M, Moore ERB, Rossello-Mora R, et al. International Code of Nomenclature of Prokaryotes. Prokaryotic Code (2022 Revision) Int J Syst Evol Microbiol. 2023;73:005585. doi: 10.1099/ijsem.0.005585.
    doi: 10.1099/ijsem.0.005585pubmed: 37219928google scholar: lookup
  52. Ripio MT, Geoffroy C, Domínguez G, Alouf JE, Vázquez-Boland JA. The sulphydryl-activated cytolysin and a sphingomyelinase C are the major membrane-damaging factors involved in cooperative (CAMP-like) haemolysis of Listeria spp. Res Microbiol. 1995;146:303–313. doi: 10.1016/0923-2508(96)81053-9.
    doi: 10.1016/0923-2508(96)81053-9pubmed: 7569324google scholar: lookup
  53. Sun M, Zhu B, Liu J, Qin K, Peng F. Rhodococcus antarcticus sp. nov., isolated from a till sample of Collins glacier front, Antarctica. Int J Syst Evol Microbiol. 2023;73:005940. doi: 10.1099/ijsem.0.005940.
    doi: 10.1099/ijsem.0.005940pubmed: 37417252google scholar: lookup
  54. Yoon S-H, Ha S-M, Kwon S, Lim J, Kim Y, et al. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol. 2017;67:1613–1617. doi: 10.1099/ijsem.0.001755.
    doi: 10.1099/ijsem.0.001755pmc: PMC5563544pubmed: 28005526google scholar: lookup
  55. Rodriguez-R LM, Konstantinidis KT. The enveomics collection: a toolbox for specialized analyses of microbial genomes and metagenomes. PeerJ Preprints. 2016;4:e1900v1901. doi: 10.7287/peerj.preprints.1900.
  56. Goodfellow M, Beckham AR, Barton MD. Numerical classification of Rhodococcus equi and related actinomycetes. J App Bacteriol. 1982;53:199–207. doi: 10.1111/j.1365-2672.1982.tb04677.x.
  57. Kelly BG, Wall DM, Boland CA, Meijer WG. Isocitrate lyase of the facultative intracellular pathogen Rhodococcus equi. Microbiol. 2002;148:793–798. doi: 10.1099/00221287-148-3-793.
    doi: 10.1099/00221287-148-3-793pubmed: 11882714google scholar: lookup

Citations

This article has been cited 3 times.
  1. Yerlikaya Z, Karagülle B, Otlu B, Muz A. From Paddock to Foal: Prevalence and Genotypic Diversity of Rhodococcus equi on Stud Farms in Türkiye.. Vet Sci 2026 Jan 10;13(1).
    doi: 10.3390/vetsci13010072pubmed: 41600728google scholar: lookup
  2. Göker M, Christensen H, Fingerle V, Kostovski M, Margos G, Moore ERB, Oren A, Patrick S, Reischl U, Vázquez-Boland JA. List of Recommended Names for bacteria of medical importance: report of the Ad Hoc Committee on Mitigating Changes in Prokaryotic Nomenclature.. Int J Syst Evol Microbiol 2025 Oct;75(10).
    doi: 10.1099/ijsem.0.006943pubmed: 41129200google scholar: lookup
  3. Val-Calvo J, Scortti M, Göker M, Vázquez-Boland JA. Leveraging the subgenus category to address monophyletic genus over-splitting: illustration with recently proposed Mycobacteriales genera.. Int J Syst Evol Microbiol 2025 Sep;75(9).
    doi: 10.1099/ijsem.0.006917pubmed: 40981605google scholar: lookup