Pub Date : 2025-12-15DOI: 10.1186/s12863-025-01401-7
Renshu Huang, Yafei Zhang, Muhammad Arif, Cheng Song, Lei Yang
{"title":"16S rDNA sequencing of the intestinal metagenome of Wanxi White Goose (Anser cygnoides) with different egg production abilities.","authors":"Renshu Huang, Yafei Zhang, Muhammad Arif, Cheng Song, Lei Yang","doi":"10.1186/s12863-025-01401-7","DOIUrl":"10.1186/s12863-025-01401-7","url":null,"abstract":"","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"12"},"PeriodicalIF":2.5,"publicationDate":"2025-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12822282/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145764249","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-13DOI: 10.1186/s12863-025-01398-z
Youssouf Mouliom Mfopit, Judith Sophie Engel, Rolf Nimzyk, Andrea Schaffrath, Gloria Dada Chechet, Petra Berger, Mahamat Alhadj Moussa Ibrahim, Daniel Mbunkah Achukwi, Mohammed Mamman, Emmanuel Oluwadare Balogun, Mohammed Nasir Shuaibu, Junaidu Kabir, Barbara Reinhold-Hurek, Sørge Kelm
{"title":"Complete genome sequence and genetic features of a novel Pseudomonas sp. isolate (CAM1A) from tsetse fly gut captured in Dodeo, Cameroon.","authors":"Youssouf Mouliom Mfopit, Judith Sophie Engel, Rolf Nimzyk, Andrea Schaffrath, Gloria Dada Chechet, Petra Berger, Mahamat Alhadj Moussa Ibrahim, Daniel Mbunkah Achukwi, Mohammed Mamman, Emmanuel Oluwadare Balogun, Mohammed Nasir Shuaibu, Junaidu Kabir, Barbara Reinhold-Hurek, Sørge Kelm","doi":"10.1186/s12863-025-01398-z","DOIUrl":"10.1186/s12863-025-01398-z","url":null,"abstract":"","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"11"},"PeriodicalIF":2.5,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12822146/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1186/s12863-025-01397-0
Noel Cabañas, Doga Cedden, Gregor Bucher
Objectives: Tribolium castaneum and Drosophila melanogaster are prominent insect model organisms for investigating developmental and evolutionary processes. Both have a significant kit of genetic and molecular tools and a substantial quantity of omic data at their disposal, which makes this species pair suitable for comparative genomic and gene function studies. However, for such comparisons, a rigorous assignment and compilation of the orthologs that these organisms share are essential. Here, we generated and provided a list of orthologous genes between Drosophila and Tribolium, which will be useful for future comparative genomic studies.
Data description: We made use of the reference proteomes of Tribolium castaneum and Drosophila melanogaster to infer phylogenetic orthology using the OrthoFinder platform, and employed the eggNOG 6.0 database and manual phylogenetic tree analyses to assess our results. Our analysis identified more than 9,000 orthologous genes between Drosophila and Tribolium. We posit that this comprehensive list is a valuable resource for comparative studies among these insect species, such as single-cell sequencing or large-scale gene function comparisons. The results are open-access and freely available for download or interactive exploration in iBeetleBase.
{"title":"Orthologous genes of the red flour beetle Tribolium castaneum and the vinegar fly Drosophila melanogaster.","authors":"Noel Cabañas, Doga Cedden, Gregor Bucher","doi":"10.1186/s12863-025-01397-0","DOIUrl":"10.1186/s12863-025-01397-0","url":null,"abstract":"<p><strong>Objectives: </strong>Tribolium castaneum and Drosophila melanogaster are prominent insect model organisms for investigating developmental and evolutionary processes. Both have a significant kit of genetic and molecular tools and a substantial quantity of omic data at their disposal, which makes this species pair suitable for comparative genomic and gene function studies. However, for such comparisons, a rigorous assignment and compilation of the orthologs that these organisms share are essential. Here, we generated and provided a list of orthologous genes between Drosophila and Tribolium, which will be useful for future comparative genomic studies.</p><p><strong>Data description: </strong>We made use of the reference proteomes of Tribolium castaneum and Drosophila melanogaster to infer phylogenetic orthology using the OrthoFinder platform, and employed the eggNOG 6.0 database and manual phylogenetic tree analyses to assess our results. Our analysis identified more than 9,000 orthologous genes between Drosophila and Tribolium. We posit that this comprehensive list is a valuable resource for comparative studies among these insect species, such as single-cell sequencing or large-scale gene function comparisons. The results are open-access and freely available for download or interactive exploration in iBeetleBase.</p>","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"17"},"PeriodicalIF":2.5,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12903232/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145745879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-08DOI: 10.1186/s12863-025-01388-1
Ikwhan Kim, Da-Ryung Jung, YeonGyun Jung, Ji Hoon Ha, Eun Kyung Lee, Jin Mo Kim, Jin Young Kim, Yoon Soo Cho, Jae-Ho Shin
Objectives: Heyndrickxia oleronia is a Gram-positive, rod-shaped bacterium originally isolated from termites but has gained clinical importance due to its association with Demodex mites and rosacea, a chronic inflammatory skin disease. Despite its clinical relevance, genomic resources from human-associated environments remain limited, with existing reference genomes derived from ecologically distant sources. This study aimed to provide the first complete genome sequence of H. oleronia EISK28 isolated from human facial skin to support future research on its role in skin health and disease.
Data description: H. oleronia EISK28 was isolated from human facial skin and sequenced using Oxford Nanopore long-read technology. De novo assembly resulted in a single complete circular chromosome of 5,118,808 bp with 164× coverage depth. Structural annotation identified 5,143 genes comprising 4,958 CDSs, 36 rRNAs, 144 tRNAs, 5 non-coding RNAs, and 65 pseudo genes. Functional annotation assigned the predicted CDSs to 22 of 25 COG categories and identified 93 carbohydrate-active enzymes. Secondary metabolite analysis revealed three biosynthetic gene clusters, and genome-based antibiotic resistance profiling predicted 11 resistance genes, while phenotypic testing confirmed resistance to ampicillin and penicillin. Mobile genetic element screening detected 34 insertion sequences, 2 prophages, and 16 genomic islands but no association with antibiotic resistance genes.
{"title":"Complete genome sequence of Heyndrickxia oleronia EISK28 isolated from human facial skin.","authors":"Ikwhan Kim, Da-Ryung Jung, YeonGyun Jung, Ji Hoon Ha, Eun Kyung Lee, Jin Mo Kim, Jin Young Kim, Yoon Soo Cho, Jae-Ho Shin","doi":"10.1186/s12863-025-01388-1","DOIUrl":"10.1186/s12863-025-01388-1","url":null,"abstract":"<p><strong>Objectives: </strong>Heyndrickxia oleronia is a Gram-positive, rod-shaped bacterium originally isolated from termites but has gained clinical importance due to its association with Demodex mites and rosacea, a chronic inflammatory skin disease. Despite its clinical relevance, genomic resources from human-associated environments remain limited, with existing reference genomes derived from ecologically distant sources. This study aimed to provide the first complete genome sequence of H. oleronia EISK28 isolated from human facial skin to support future research on its role in skin health and disease.</p><p><strong>Data description: </strong>H. oleronia EISK28 was isolated from human facial skin and sequenced using Oxford Nanopore long-read technology. De novo assembly resulted in a single complete circular chromosome of 5,118,808 bp with 164× coverage depth. Structural annotation identified 5,143 genes comprising 4,958 CDSs, 36 rRNAs, 144 tRNAs, 5 non-coding RNAs, and 65 pseudo genes. Functional annotation assigned the predicted CDSs to 22 of 25 COG categories and identified 93 carbohydrate-active enzymes. Secondary metabolite analysis revealed three biosynthetic gene clusters, and genome-based antibiotic resistance profiling predicted 11 resistance genes, while phenotypic testing confirmed resistance to ampicillin and penicillin. Mobile genetic element screening detected 34 insertion sequences, 2 prophages, and 16 genomic islands but no association with antibiotic resistance genes.</p>","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"9"},"PeriodicalIF":2.5,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12797905/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145710531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-08DOI: 10.1186/s12863-025-01396-1
Ummirul Mukminin Kahar, Najiha Atiqah Md Nor, Wan Nur Izrena Wan Izanni
Objectives: Marine bacteria are valuable reservoirs of novel carbohydrate-active enzymes (CAZymes) with industrial relevance. A halophilic marine bacterial strain PBL-D1, was isolated from Batu Laut beach in Selangor, Malaysia. The 16S rRNA gene sequence analysis identified strain PBL-D1 as a member of the genus Gaetbulibacter. To date, no enzymes from Gaetbulibacter spp. have been biochemically characterised. The present study reports on the annotated draft genome of Gaetbulibacter sp. PBL-D1 and comparative genome analyses of Gaetbulibacter glycoside hydrolase (GH) enzymes. These findings provide the first genomic insights into the GH repertoire of Gaetbulibacter spp., revealing unexplored enzymes with promising potential for industrial biocatalysis.
Data description: The draft genome of Gaetbulibacter sp. PBL-D1 is 3,433,971 bp in size, has a G+C content of 33.0%, and encodes 3,068 protein-coding genes. The CAZymes analysis revealed that Gaetbulibacter genomes harboured at least nine putative GH-encoding genes, grouped into starch-degrading and β-glucan-degrading enzymes. These enzymes are of industrial importance, particularly in food processing and biofuel production. Collectively, PBL-D1 and other available Gaetbulibacter genomes serve as attractive sources of GH candidates that may be useful in polysaccharide degradation.
{"title":"Genome sequence of Gaetbulibacter sp. PBL-D1 isolated from a Malaysian beach: insights into glycoside hydrolase repertoires.","authors":"Ummirul Mukminin Kahar, Najiha Atiqah Md Nor, Wan Nur Izrena Wan Izanni","doi":"10.1186/s12863-025-01396-1","DOIUrl":"10.1186/s12863-025-01396-1","url":null,"abstract":"<p><strong>Objectives: </strong>Marine bacteria are valuable reservoirs of novel carbohydrate-active enzymes (CAZymes) with industrial relevance. A halophilic marine bacterial strain PBL-D1, was isolated from Batu Laut beach in Selangor, Malaysia. The 16S rRNA gene sequence analysis identified strain PBL-D1 as a member of the genus Gaetbulibacter. To date, no enzymes from Gaetbulibacter spp. have been biochemically characterised. The present study reports on the annotated draft genome of Gaetbulibacter sp. PBL-D1 and comparative genome analyses of Gaetbulibacter glycoside hydrolase (GH) enzymes. These findings provide the first genomic insights into the GH repertoire of Gaetbulibacter spp., revealing unexplored enzymes with promising potential for industrial biocatalysis.</p><p><strong>Data description: </strong>The draft genome of Gaetbulibacter sp. PBL-D1 is 3,433,971 bp in size, has a G+C content of 33.0%, and encodes 3,068 protein-coding genes. The CAZymes analysis revealed that Gaetbulibacter genomes harboured at least nine putative GH-encoding genes, grouped into starch-degrading and β-glucan-degrading enzymes. These enzymes are of industrial importance, particularly in food processing and biofuel production. Collectively, PBL-D1 and other available Gaetbulibacter genomes serve as attractive sources of GH candidates that may be useful in polysaccharide degradation.</p>","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"8"},"PeriodicalIF":2.5,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12798019/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145710549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-08DOI: 10.1186/s12863-025-01381-8
Tae Seon Cha, Soojin Lim, Keeman Lee, Seunghui Lee, Seojeong Choi, Yejin Seo, Kyunglee Lee, Seon Young Park, Ji Hyung Kim
Objectives: Pseudolactococcus raffinolactis-a lactic acid-producing bacterium recently reclassified from Lactococcus-demonstrates emerging potential for probiotics and food applications. We report the complete genome of strain GCULR isolated from a stranded spotted seal (Phoca largha) in Korea, to provide genomic data for understanding beneficial bacteria in marine mammals.
Data description: P. raffinolactis strain GCULR was isolated from a stranded spotted seal in Korea, and its whole genome was sequenced using PacBio and Illumina X-10 platforms. Its complete genome comprises a single circular chromosome of 2,270,555 bp with 39.9% GC content and no plasmids. Annotation revealed 2,260 genes, including 2,145 protein-coding sequences, 56 transfer RNAs, 13 ribosomal RNAs, 3 non-coding RNAs, and 43 pseudogenes. Comparative analysis showed an average nucleotide identity of 99.3% with strain WiKim0068, confirming its close relationship with a food-derived isolate. Genome-based screening revealed the presence of several potential virulence- and antimicrobial resistance-associated genes and two intact prophage regions. AntiSMASH analysis predicted a conserved bacteriocin biosynthetic cluster, indicating its functional potential. These findings offer novel insights into the beneficial bacteria in endangered marine mammals and expand our understanding of the ecological and functional diversity of P. raffinolactis.
{"title":"Complete genome sequence of Pseudolactococcus raffinolactis strain GCULR from a spotted seal (Phoca largha) in Korea.","authors":"Tae Seon Cha, Soojin Lim, Keeman Lee, Seunghui Lee, Seojeong Choi, Yejin Seo, Kyunglee Lee, Seon Young Park, Ji Hyung Kim","doi":"10.1186/s12863-025-01381-8","DOIUrl":"10.1186/s12863-025-01381-8","url":null,"abstract":"<p><strong>Objectives: </strong>Pseudolactococcus raffinolactis-a lactic acid-producing bacterium recently reclassified from Lactococcus-demonstrates emerging potential for probiotics and food applications. We report the complete genome of strain GCULR isolated from a stranded spotted seal (Phoca largha) in Korea, to provide genomic data for understanding beneficial bacteria in marine mammals.</p><p><strong>Data description: </strong>P. raffinolactis strain GCULR was isolated from a stranded spotted seal in Korea, and its whole genome was sequenced using PacBio and Illumina X-10 platforms. Its complete genome comprises a single circular chromosome of 2,270,555 bp with 39.9% GC content and no plasmids. Annotation revealed 2,260 genes, including 2,145 protein-coding sequences, 56 transfer RNAs, 13 ribosomal RNAs, 3 non-coding RNAs, and 43 pseudogenes. Comparative analysis showed an average nucleotide identity of 99.3% with strain WiKim0068, confirming its close relationship with a food-derived isolate. Genome-based screening revealed the presence of several potential virulence- and antimicrobial resistance-associated genes and two intact prophage regions. AntiSMASH analysis predicted a conserved bacteriocin biosynthetic cluster, indicating its functional potential. These findings offer novel insights into the beneficial bacteria in endangered marine mammals and expand our understanding of the ecological and functional diversity of P. raffinolactis.</p>","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":"26 1","pages":"93"},"PeriodicalIF":2.5,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12683817/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145710529","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-06DOI: 10.1186/s12863-025-01389-0
Kgaugelo Edward Lekota, Lydia Cecilia Sizana, Ntelekwane George Khasapane
Objectives: This study presents the whole-genome sequence of Streptococcus agalactiae 40LHNT and 10RH2NT, isolated from bovine milk with subclinical mastitis in the North-West Province of South Africa. The objective was to characterize the genomes to understand the antibiotic resistance and virulent potential of the isolates.
Data description: Genomic DNA of S. agalactiae strains was extracted and sequenced using the Oxford Nanopore MiniON platform. De novo assembly was carried out using Flye v. v2.9, resulting in an average draft genome size of 2.25 Mb for both strains, assembled into 4 contigs for strain 40LHNT and 91 contigs for strain 10RH2NT with an average GC content of 35.5% for both strains. Genome quality assessment revealed an average completeness of 92.64% and a contamination level of 1.6%. For both strains, the closest reference type strain was S. agalactiae NCTC8181 (accession GCA_900458965.1), showing an average nucleotide identity of 97%, thereby confirming species-level identity and close genetic relatedness. Annotation using the NCBI Prokaryotic Genome Annotation Pipeline identified 2,067 and 1977 protein-coding genes for strains 40LHNT and 10RH2NT, respectively..
目的:本研究报道了从南非西北省亚临床乳腺炎牛乳中分离的无乳链球菌40LHNT和10RH2NT的全基因组序列。目的是表征基因组,以了解分离物的抗生素耐药性和毒力潜力。数据描述:利用Oxford Nanopore MiniON平台提取无乳链球菌的基因组DNA并进行测序。使用Flye v. v2.9进行从头组装,两株菌株的平均基因组草图大小为2.25 Mb,菌株40LHNT和菌株10RH2NT分别组装为4个和91个片段,两株菌株的平均GC含量为35.5%。基因组质量评估结果显示,平均完整性为92.64%,污染水平为1.6%。两株菌株中,最接近的参考型菌株为S. agalactiae NCTC8181 (accession GCA_900458965.1),平均核苷酸同源性为97%,从而确定了种水平的同源性和密切的遗传亲缘关系。利用NCBI原核基因组注释管道分别鉴定出40LHNT和10RH2NT菌株的2067个和1977个蛋白质编码基因。
{"title":"Draft genomes of two Streptococcus agalactiae from bovine mastitis in the North-West Province, South Africa.","authors":"Kgaugelo Edward Lekota, Lydia Cecilia Sizana, Ntelekwane George Khasapane","doi":"10.1186/s12863-025-01389-0","DOIUrl":"10.1186/s12863-025-01389-0","url":null,"abstract":"<p><strong>Objectives: </strong>This study presents the whole-genome sequence of Streptococcus agalactiae 40LHNT and 10RH2NT, isolated from bovine milk with subclinical mastitis in the North-West Province of South Africa. The objective was to characterize the genomes to understand the antibiotic resistance and virulent potential of the isolates.</p><p><strong>Data description: </strong>Genomic DNA of S. agalactiae strains was extracted and sequenced using the Oxford Nanopore MiniON platform. De novo assembly was carried out using Flye v. v2.9, resulting in an average draft genome size of 2.25 Mb for both strains, assembled into 4 contigs for strain 40LHNT and 91 contigs for strain 10RH2NT with an average GC content of 35.5% for both strains. Genome quality assessment revealed an average completeness of 92.64% and a contamination level of 1.6%. For both strains, the closest reference type strain was S. agalactiae NCTC8181 (accession GCA_900458965.1), showing an average nucleotide identity of 97%, thereby confirming species-level identity and close genetic relatedness. Annotation using the NCBI Prokaryotic Genome Annotation Pipeline identified 2,067 and 1977 protein-coding genes for strains 40LHNT and 10RH2NT, respectively..</p>","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"7"},"PeriodicalIF":2.5,"publicationDate":"2025-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12797599/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145696445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-05DOI: 10.1186/s12863-025-01393-4
Juan José Morales-Aguilar, Erika Camacho-Beltrán, Melina López-Meyer, Gabriel Rincón-Enríquez, Evangelina Esmeralda Quiñones-Aguilar
Objectives: The bacterial genus Exiguobacterium includes many versatile species isolated from diverse environments. This draft genome can serve as a fundamental tool for subsequent studies, including the design of specific primers for strain identification, and as a basis for comparative genomics.
Data description: Herein, we report the draft genome sequence of Exiguobacterium acetylicum GM-14, which was isolated from a conventionally grown bean (Phaseolus vulgaris) field located in Culiacán, Sinaloa, Mexico. The nucleotide sequence of this genome was deposited into NCBI GenBank under accession number PRJNA 1,175,395. In this report, we introduce the entire genomic sequence of Exiguobacterium acetylicum GM-14, which is 3,139,301 bp long, with a 47.3% G + C content and 3,178 coding sequences (CDSs). The use of the Exiguobacterium acetylicum GM-14 genome to help analyse possible virulence genes will contribute to the development of control strategies.
{"title":"Draft genome sequence of Exiguobacterium acetylicum GM-14 isolated from beans.","authors":"Juan José Morales-Aguilar, Erika Camacho-Beltrán, Melina López-Meyer, Gabriel Rincón-Enríquez, Evangelina Esmeralda Quiñones-Aguilar","doi":"10.1186/s12863-025-01393-4","DOIUrl":"10.1186/s12863-025-01393-4","url":null,"abstract":"<p><strong>Objectives: </strong>The bacterial genus Exiguobacterium includes many versatile species isolated from diverse environments. This draft genome can serve as a fundamental tool for subsequent studies, including the design of specific primers for strain identification, and as a basis for comparative genomics.</p><p><strong>Data description: </strong>Herein, we report the draft genome sequence of Exiguobacterium acetylicum GM-14, which was isolated from a conventionally grown bean (Phaseolus vulgaris) field located in Culiacán, Sinaloa, Mexico. The nucleotide sequence of this genome was deposited into NCBI GenBank under accession number PRJNA 1,175,395. In this report, we introduce the entire genomic sequence of Exiguobacterium acetylicum GM-14, which is 3,139,301 bp long, with a 47.3% G + C content and 3,178 coding sequences (CDSs). The use of the Exiguobacterium acetylicum GM-14 genome to help analyse possible virulence genes will contribute to the development of control strategies.</p>","PeriodicalId":72427,"journal":{"name":"BMC genomic data","volume":" ","pages":"6"},"PeriodicalIF":2.5,"publicationDate":"2025-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12797445/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145688754","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}