Proposal for reclassifying Tellurirhabdus species within the genus Larkinella

Review Article

Proposal for reclassifying Tellurirhabdus species within the genus Larkinella

Syed Raziuddin Quadri1,2*, Wesam Nofal1,2, Muhannad Alruwaili1,2
Adv. life sci., vol. 12, no. 2, pp. 413-417, May 2025
*Corresponding Author: 
Syed Raziuddin Quadri (Email: syed.quadri@nbu.edu.sa)
Authors' Affiliations
 1. Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, Northern Border University, P. O. Box 1321, Arar-91431, Northern Borders – Kingdom of Saudi Arabia
2. Centre for Health Research, Northern Border University, Arar-91431, Northern Borders – Kingdom of Saudi Arabia 
 

[Date Received: 20/10/2024; Date Revised: 05/01/2025Date Available Online31/08/2025]


Abstractaa download_button
Introduction
Methods 
Results

Discussion
References


Abstract

Background: Members of the genera Larkinella and Tellurirhabdus are Gram-negative, aerobic, and consist of menaquinone (MK)-7 as their main isoprenoid quinone. Recent analysis suggests that both genera share similar characteristics. The taxonomic position of the genera Larkinella and Tellurirhabdus has been evaluated using genomic analysis.

Methods: The quality of the genomic sequences of Larkinella and Tellurirhabdus was assessed after they were downloaded from NCBI (https://www.ncbi.nlm.nih.gov/). Average nucleotide identity (ANI) and average amino acid identity (AAI) data was used for evaluating their genomic relatedness.

Results: The AAI values between Larkinella and Tellurirhabdus were above the threshold value of genus delineation (>60–65 %) indicating that they are members of the same genus. The ANI values among Larkinella and Tellurirhabdus species were below 95-96% indicating they were different species.

Conclusion: We propose transferring Tellurirhabdus bombi to the genus Larkinella as Larkinella bombi comb. nov. and Tellurirhabdus rosea to the genus Larkinella as Larkinella roseola nom. nov. based on our research findings.

KeywordsLarkinella; Tellurirhabdus; Reclassification; Average amino acid identity; Average nucleotide identity  

Introduction6th button-01


The genera Larkinella and Tellurirhabdus were proposed by Vancanneyt et al., [1] and Choi et al., [2] respectively. The genus Larkinella consists of 11 species with validly published names (https://lpsn.dsmz.de/genus/larkinella; accessed on 1/11/2024) [3], while the genus Tellurirhabdus consists of two species with validly published names (https://lpsn.dsmz.de/genus/tellurirhabdus; accessed on 1/11/2024) [3]. Members of the genera Larkinella and Tellurirhabdus exhibit similar characteristics, including being Gram-negative, aerobic, and having MK-7 as their main isoprenoid quinone [1, 2]. Larkinella species were reported from various ecological niches like water of a steam generator [1], soil [4, 5], manganese mine soil [6], fermented bovine products [7], decomposing wood [8], beach sand [9], etc. Tellurirhabdus species were reported from soil [2] and bumblebee [10]. Recently, during the description of one Tellurirhabdus novel species (Tellurirhabdus bombi) it was observed that Tellurirhabdus species shared similar features as that of Larkinella species [10] and hence the present study was carried out to evaluate the taxonomic position of Tellurirhabdus species. 

6th button-01Methods


Molecular Evolutionary Genetics Analysis (MEGA) software (version 7.0) [11] was used to construct phylogenetic trees based on aligned 16S rRNA gene sequences (aligned using Clustal W [12]). The analyses utilized maximum-likelihood (ML) [13], neighbour-joining (NJ) [14], and maximum-parsimony (MP) [15] methods, each performed with 1000 bootstrap replications [16]. The evolutionary distances for the NJ and ML algorithms were calculated using Kimura’s two-parameter model [17]. Uniform rates across sites were assumed, and alignment gaps or missing data at all sites were treated with complete deletion before tree reconstruction. For the ML tree, the initial trees for the heuristic search were generated automatically using the neighbour-joining and BioNJ algorithms, based on a pairwise distance matrix computed with the maximum composite likelihood method [18]. The genome sequence of Tellurirhabdus and Larkinella species namely Tellurirhabdus bombi IE-0392T (CP090557), Tellurirhabdus rosea U15T (CP111085), Larkinella soli MIMbqt9T (QTJY00000000), Larkinella insperata LMG 22510T (CP110973), Larkinella arboricola DSM 21851T (QLMC00000000), Larkinella terrae KCTC 52001T (WJXZ00000000), Larkinella rosea KCTC 52004T (RQJO00000000), Larkinella punicea ZZJ9T (QOWE00000000), and Larkinella knui KCTC 42998T (RQJP00000000) were downloaded from NCBI (https://www.ncbi.nlm.nih.gov/). Dyadobacter fermentans DSM 18053T (CP001619) used as an outgroup was also downloaded from NCBI (https://www.ncbi.nlm.nih.gov/). The genome size and G+C content were calculated using an in-house Perl script, while genome completeness and contamination were assessed with CheckM [19]. The presence of tRNA was detected using tRNAscan-SE [20]. Type Strain Genome Server (TYGS) was used to construct the phylogenomic tree [21] and the result was visualized using Interactive Tree of Life (iTOL) version 6  [22]. The average amino acid identity value (AAI) was calculated using CompareM (https://github.com/dparks1134/CompareM [23, 24]). The average nucleotide identity (ANI) value was calculated using the Pyani software package, which included the ANIb parameter [25, 26].

6th button-01Results


The genome sizes of the Tellurirhabdus and Larkinella species ranged from 4941522 to 8175905 bp, with G+C content ranging from 48.8 to 57.6%. The number of tRNAs ranged from 39 to 50. The genome was >90% complete, with <5% contamination. Detailed genome traits of Tellurirhabdus and Larkinella species are mentioned in Table 1. In the present study, the ANI values (Table 2) among Larkinella, Tellurirhabdus, and Dyadobacter species were below 95-96%. In the phylogenomic tree, Larkinella and Tellurirhabdus species showed a distinct clade (Figure. 1). A similar clade was noticed when the trees were constructed using NJ, ML, and MP methods (Figure S1, S2, and S3). In the present study, the AAI values among Larkinella and Tellurirhabdus were evaluated. Based on the data in Table 3, the AAI value between Tellurirhabdus rosea U15T and the analyzed Larkinella species ranged from 68.7% to 70.1%, while the value between Tellurirhabdus bombi IE-0392T and the Larkinella species ranged from 70.8% to 71.3%.

6th button-01Discussion


The genera Larkinella and Tellurirhabdus are the members of the family Spirosomataceae [3]. Both genera are Gram-negative and aerobic [1, 2]. Recently Zhang et al., reported that Tellurirhabdus species share phenotypic and chemotaxonomic characteristics similar to Larkinella species [10]. The present study reviewed the taxonomic status of the taxa Larkinella and Tellurirhabdus. The genomes were downloaded and their quality assessed using CheckM, as it offers methods for assessing genome quality and providing reliable estimates of completeness and contamination by utilizing ubiquitous, single-copy genes within a phylogenetic lineage [19]. Good-quality genomes exhibit completeness levels more than 90% and contamination levels less than 5% [19]. The Larkinella and Tellurirhabdus genomes downloaded from NCBI have high completeness and low contamination levels (>90 and <5%, respectively), indicating high quality genomes [19]. 

The ANI value was introduced for species-level delineation and a cut-off value of 95-96% was proposed [27]. In the present study, the ANI values among Larkinella, Tellurirhabdus, and Dyadobacter species were below 95-96% indicating they were different species [27]. Similarly, AAI was introduced to delineate strains at the genus level by measuring the average amino acid identity of all shared genes between two strains, allowing for an assessment of their genetic relatedness [28] and the threshold value of >60–65 % was also proposed [28, 29]. The AAI values between Larkinella and Tellurirhabdus were above the threshold value of genus delineation (>60–65 %) indicating that they were members of the same genus. Since the genus Larkinella was published earlier than Tellurirhabdus [1, 2] hence Tellurirhabdus species should be transferred to the genus Larkinella. We propose transferring Tellurirhabdus bombi as Larkinella bombi comb. nov. Since Tellurirhabdus rosea would be a later homonym of Larkinella rosea, a name already assigned to a species in the genus Larkinella, the name Larkinella roseola nom. nov. is proposed. In addition, the culture deposition certificates of Tellurirhabdus species are depicted in Figure S4.

The taxonomic position of the genera Larkinella and Tellurirhabdus was evaluated using genome analysis. The genome size of Larkinella and Tellurirhabdus species ranged from 4941522-8175905 bp and their G+C content ranged from 48.8-57.6%. The number of tRNAs ranged from 39-50. CheckM analysis revealed that Larkinella and Tellurirhabdus species genome completeness and contamination were >90 and <5%, respectively indicating good-quality genomes. The ANI values among Larkinella and Tellurirhabdus species were below the cut-off for species delineation indicating they were different species. However, the AAI values were above the cut-off value (>60–65 %) for genus delineation indicating they belong to the same genus. Based on the above results, we propose to transfer Tellurirhabdus rosea to the genus Larkinella as Larkinella roseola nom. nov., and Tellurirhabdus bombi as Larkinella bombi comb. nov.

Larkinella roseola (ro.se'o.la. N.L. fem. adj. roseola, rose-colored, pink).

Basonym: Tellurirhabdus rosea Choi et al.

The description of this species is the same as provided by Choi et al., [2] for Tellurirhabdus rosea. The type strain is U15T (= KCTC 62116T = JCM 32361T). Larkinella bombi (bom’bi. L. n. bombus a boom, a deep hollow noise, buzzing, also the zoological genus name of the bumblebee; N.L. gen. n. bombi of Bombus, of a bumblebee).

Basonym: Tellurirhabdus bombi Zhang et al.

The description of this species is the same as provided by Zhang et al., [10] for Tellurirhabdus bombi. The type strain is IE-0392T (= GDMCC 1.2794T = JCM 35040T).

Tables and Figures

Acknowledgement 


All the authors  would like to thank Deanship of Scientific Research, Department of Medical Laboratory Technology and Centre for Health Research at Northern Border University, Arar.

Funding


The author Syed Raziuddin Quadri extends his appreciation to the Deanship of Scientific Research at Northern Border University, Arar, KSA for funding this research work through the project number NBU-FFR-2024-2046-06.

Data Availability


All datasets generated or analysed during this study are included in the manuscript.

Ethics Statement


This article does not contain any studies on human participants or animals performed by the authors.

Author Contributions


Syed Raziuddin Quadri conceptualized, supervised, and edited the article. Wesam Nofal and Muhannad Alruwaili performed the literature search and conducted the genome analysis.

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