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Gonzalez-Rosales, CarolinaORCID iD iconorcid.org/0000-0003-3566-4758
Alternative names
Publications (10 of 10) Show all publications
Martinez-Hernandez, J. E., Aliaga-Tobar, V., Gonzalez-Rosales, C., Monte-Neto, R., Martin, A. J. M. & Maracaja-Coutinho, V. (2025). Comparative and systems analyses of Leishmania spp. non-coding RNAs through developmental stages. PLoS Neglected Tropical Diseases, 19(5), Article ID e0013108.
Open this publication in new window or tab >>Comparative and systems analyses of Leishmania spp. non-coding RNAs through developmental stages
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2025 (English)In: PLoS Neglected Tropical Diseases, ISSN 1935-2727, E-ISSN 1935-2735, Vol. 19, no 5, article id e0013108Article in journal (Refereed) In press
Abstract [en]

Leishmania spp. is the etiological agent of leishmaniases, neglected diseases that seek to be eradicated in the coming years. The life cycle of these parasites involves different host and stress environments. In recent years, many studies have shown that several protein-coding genes are directly involved with the development and host interactions. However, little is still known about the role of non-coding RNAs (ncRNAs) in life cycle progression. In this study, we aimed to identify the genomic structure and function of ncRNAs from Leishmania spp. and to get insights into the repertoire of ncRNAs (RNAome) of this protozoan genus. We studied 26 strains corresponding to 16 different species of Leishmania. Our RNAome analysis revealed the presence of several ncRNAs that are shared among different species, allowing us to differentiate between subgenera as well as between species that are canonically related to visceral leishmaniasis. We also studied co-expression relationships between coding genes and ncRNAs which in the amastigote developmental stage for Leishmania braziliensis and Leishmania donovani revealed the presence of miRNA-like transcripts co-expressed with several coding genes involved in starvation, survival and histone modification. This work represents the first effort to characterize the Leishmania ssp. RNAome, supporting further approaches to better understand the role of ncRNAs in gene regulation, infective process, and host-parasite interaction.

Place, publisher, year, edition, pages
Public Library of Science (PLoS), 2025
Keywords
gene-expression, functional annotation, genome, sequence, transcription, repertoire, mechanisms, alignment, plants
National Category
Microbiology Bioinformatics and Computational Biology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-139410 (URN)10.1371/journal.pntd.0013108 (DOI)001498131700001 ()40435329 (PubMedID)
Available from: 2025-06-12 Created: 2025-06-12 Last updated: 2025-06-12
Westmeijer, G., van Dam, F., Kietäväinen, R., Gonzalez-Rosales, C., Bertilsson, S., Drake, H. & Dopson, M. (2024). Candidatus Desulforudis audaxviator dominates a 975 m deep groundwater community in central Sweden. Communications Biology, 7, Article ID 1332.
Open this publication in new window or tab >>Candidatus Desulforudis audaxviator dominates a 975 m deep groundwater community in central Sweden
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2024 (English)In: Communications Biology, E-ISSN 2399-3642, Vol. 7, article id 1332Article in journal (Refereed) Published
Abstract [en]

The continental bedrock contains groundwater-bearing fractures that are home to microbial populations that are vital in mediating the Earth’s biogeochemical cycles. However, their diversity is poorly understood due to the difficulty of obtaining samples from this environment. Here, a groundwater-bearing fracture at 975 m depth was isolated by employing packers in order to characterize the microbial community via metagenomes combined with prokaryotic and eukaryotic marker genes (16S and 18S ribosomal RNA gene). Genome-resolved analyses revealed a community dominated by sulfate-reducing Bacillota, predominantly represented by Candidatus Desulforudis audaxviator and with Wood-Ljungdahl as the most prevalent pathway for inorganic carbon fixation. Moreover, the eukaryotic community had a considerable diversity and was comprised of mainly flatworms, chlorophytes, crustaceans, ochrophytes, and fungi. These findings support the important role of the Bacillota, with the sulfate reducer Candidatus Desulforudis audaxviator as its main representative, as primary producers in the often energy-limited groundwaters of the continental subsurface.

Place, publisher, year, edition, pages
Nature Publishing Group, 2024
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-133065 (URN)10.1038/s42003-024-07027-2 (DOI)001338949000004 ()39406897 (PubMedID)2-s2.0-85206437301 (Scopus ID)
Funder
Swedish Research Council, 2018-04311
Available from: 2024-10-18 Created: 2024-10-18 Last updated: 2025-05-30Bibliographically approved
Sepúlveda-Rebolledo, P., Gonzalez-Rosales, C., Dopson, M., Pérez-Rueda, E., Holmes, D. S. & Valdés, J. H. (2024). Comparative genomics sheds light on transcription factor-mediated regulation in the extreme acidophilic Acidithiobacillia representatives. Research in Microbiology, 175(1-2), Article ID 104135.
Open this publication in new window or tab >>Comparative genomics sheds light on transcription factor-mediated regulation in the extreme acidophilic Acidithiobacillia representatives
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2024 (English)In: Research in Microbiology, ISSN 0923-2508, E-ISSN 1769-7123, Vol. 175, no 1-2, article id 104135Article in journal (Refereed) Published
Abstract [en]

Extreme acidophiles thrive in acidic environments, confront a multitude of challenges, and demonstrate remarkable adaptability in their metabolism to cope with the ever-changing environmental fluctuations, which encompass variations in temperature, pH levels, and the availability of electron acceptors and donors. The survival and proliferation of members within the Acidithiobacillia class rely on the deployment of transcriptional regulatory systems linked to essential physiological traits. The study of these transcriptional regulatory systems provides valuable insights into critical processes, such as energy metabolism and nutrient assimilation, and how they integrate into major genetic-metabolic circuits. In this study, we examined the transcriptional regulatory repertoires and potential interactions of forty-three Acidithiobacillia complete and draft genomes, encompassing nine species. To investigate the function and diversity of Transcription Factors (TFs) and their DNA Binding Sites (DBSs), we conducted a genome-wide comparative analysis, which allowed us to identify these regulatory elements in representatives of Acidithiobacillia. We classified TFs into gene families and compared their occurrence among all representatives, revealing conservation patterns across the class. The results identified conserved regulators for several pathways, including iron and sulfur oxidation, the main pathways for energy acquisition, providing new evidence for viable regulatory interactions and branch-specific conservation in Acidithiobacillia. The identification of TFs and DBSs not only corroborates existing experimental information for selected species, but also introduces novel candidates for experimental validation. Moreover, these promising candidates have the potential for further extension to new representatives within the class.

Place, publisher, year, edition, pages
Elsevier, 2024
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-126362 (URN)10.1016/j.resmic.2023.104135 (DOI)001162386800001 ()37678513 (PubMedID)2-s2.0-85173175249 (Scopus ID)
Available from: 2024-01-11 Created: 2024-01-11 Last updated: 2025-06-02Bibliographically approved
Dopson, M., Rezaei Somee, M., Gonzalez-Rosales, C., Lui, L. M., Turner, S., Buck, M., . . . Bertilsson, S. (2024). Novel candidate taxa contribute to key metabolic processes in Fennoscandian Shield deep groundwaters. ISME Communications, 4(1), Article ID ycae113.
Open this publication in new window or tab >>Novel candidate taxa contribute to key metabolic processes in Fennoscandian Shield deep groundwaters
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2024 (English)In: ISME Communications, E-ISSN 2730-6151, Vol. 4, no 1, article id ycae113Article in journal (Refereed) Published
Abstract [en]

The continental deep biosphere contains a vast reservoir of microorganisms, although a large proportion of its diversity remains both uncultured and undescribed. In this study, the metabolic potential (metagenomes) and activity (metatranscriptomes) of the microbial communities in Fennoscandian Shield deep subsurface groundwaters were characterized with a focus on novel taxa. DNA sequencing generated 1270 de-replicated metagenome-assembled genomes and single-amplified genomes, containing 7 novel classes, 34 orders, and 72 families. The majority of novel taxa were affiliated with Patescibacteria, whereas among novel archaea taxa, Thermoproteota and Nanoarchaeota representatives dominated. Metatranscriptomes revealed that 30 of the 112 novel taxa at the class, order, and family levels were active in at least one investigated groundwater sample, implying that novel taxa represent a partially active but hitherto uncharacterized deep biosphere component. The novel taxa genomes coded for carbon fixation predominantly via the Wood-Ljungdahl pathway, nitrogen fixation, sulfur plus hydrogen oxidation, and fermentative pathways, including acetogenesis. These metabolic processes contributed significantly to the total community's capacity, with up to 9.9% of fermentation, 6.4% of the Wood-Ljungdahl pathway, 6.8% of sulfur plus 8.6% of hydrogen oxidation, and energy conservation via nitrate (4.4%) and sulfate (6.0%) reduction. Key novel taxa included the UBA9089 phylum, with representatives having a prominent role in carbon fixation, nitrate and sulfate reduction, and organic and inorganic electron donor oxidation. These data provided insights into deep biosphere microbial diversity and their contribution to nutrient and energy cycling in this ecosystem.

Place, publisher, year, edition, pages
Oxford University Press, 2024
Keywords
deep biosphere, metagenomics, metatranscriptomics, Candidatus
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-133143 (URN)10.1093/ismeco/ycae113 (DOI)001333231200001 ()39421601 (PubMedID)
Available from: 2024-10-28 Created: 2024-10-28 Last updated: 2025-04-10Bibliographically approved
Dopson, M., Gonzalez-Rosales, C., Holmes, D. S. S. & Mykytczuk, N. (2023). Eurypsychrophilic acidophiles: From (meta)genomes to low-temperature biotechnologies. Frontiers in Microbiology, 14, Article ID 1149903.
Open this publication in new window or tab >>Eurypsychrophilic acidophiles: From (meta)genomes to low-temperature biotechnologies
2023 (English)In: Frontiers in Microbiology, E-ISSN 1664-302X, Vol. 14, article id 1149903Article, review/survey (Refereed) Published
Abstract [en]

Low temperature and acidic environments encompass natural milieus such as acid rock drainage in Antarctica and anthropogenic sites including drained sulfidic sediments in Scandinavia. The microorganisms inhabiting these environments include polyextremophiles that are both extreme acidophiles (defined as having an optimum growth pH < 3), and eurypsychrophiles that grow at low temperatures down to approximately 4 degrees C but have an optimum temperature for growth above 15 degrees C. Eurypsychrophilic acidophiles have important roles in natural biogeochemical cycling on earth and potentially on other planetary bodies and moons along with biotechnological applications in, for instance, low-temperature metal dissolution from metal sulfides. Five low-temperature acidophiles are characterized, namely, Acidithiobacillus ferriphilus, Acidithiobacillus ferrivorans, Acidithiobacillus ferrooxidans, "Ferrovum myxofaciens," and Alicyclobacillus disulfidooxidans, and their characteristics are reviewed. Our understanding of characterized and environmental eurypsychrophilic acidophiles has been accelerated by the application of "omics" techniques that have aided in revealing adaptations to low pH and temperature that can be synergistic, while other adaptations are potentially antagonistic. The lack of known acidophiles that exclusively grow below 15 degrees C may be due to the antagonistic nature of adaptations in this polyextremophile. In conclusion, this review summarizes the knowledge of eurypsychrophilic acidophiles and places the information in evolutionary, environmental, biotechnological, and exobiology perspectives.

Place, publisher, year, edition, pages
Frontiers Media S.A., 2023
Keywords
acidic (microbial) environments, astrobiology, bio-applications, polyextremophile, snowball earth, stenopsychrophile
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-120762 (URN)10.3389/fmicb.2023.1149903 (DOI)000957934100001 ()37007468 (PubMedID)2-s2.0-85151262011 (Scopus ID)
Available from: 2023-05-17 Created: 2023-05-17 Last updated: 2025-02-05Bibliographically approved
Gonzalez-Rosales, C., Vergara, E., Dopson, M., Valdes, J. H. & Holmes, D. S. (2022). Integrative Genomics Sheds Light on Evolutionary Forces Shaping the Acidithiobacillia Class Acidophilic Lifestyle. Frontiers in Microbiology, 12, Article ID 822229.
Open this publication in new window or tab >>Integrative Genomics Sheds Light on Evolutionary Forces Shaping the Acidithiobacillia Class Acidophilic Lifestyle
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2022 (English)In: Frontiers in Microbiology, E-ISSN 1664-302X, Vol. 12, article id 822229Article in journal (Refereed) Published
Abstract [en]

Extreme acidophiles thrive in environments rich in protons (pH values <3) and often high levels of dissolved heavy metals. They are distributed across the three domains of the Tree of Life including members of the Proteobacteria. The Acidithiobacillia class is formed by the neutrophilic genus Thermithiobacillus along with the extremely acidophilic genera Fervidacidithiobacillus, Igneacidithiobacillus, Ambacidithiobacillus, and Acidithiobacillus. Phylogenomic reconstruction revealed a division in the Acidithiobacillia class correlating with the different pH optima that suggested that the acidophilic genera evolved from an ancestral neutrophile within the Acidithiobacillia. Genes and mechanisms denominated as "first line of defense" were key to explaining the Acidithiobacillia acidophilic lifestyle including preventing proton influx that allows the cell to maintain a near-neutral cytoplasmic pH and differ from the neutrophilic Acidithiobacillia ancestors that lacked these systems. Additional differences between the neutrophilic and acidophilic Acidithiobacillia included the higher number of gene copies in the acidophilic genera coding for "second line of defense" systems that neutralize and/or expel protons from cell. Gain of genes such as hopanoid biosynthesis involved in membrane stabilization at low pH and the functional redundancy for generating an internal positive membrane potential revealed the transition from neutrophilic properties to a new acidophilic lifestyle by shaping the Acidithiobacillaceae genomic structure. The presence of a pool of accessory genes with functional redundancy provides the opportunity to "hedge bet" in rapidly changing acidic environments. Although a core of mechanisms for acid resistance was inherited vertically from an inferred neutrophilic ancestor, the majority of mechanisms, especially those potentially involved in resistance to extremely low pH, were obtained from other extreme acidophiles by horizontal gene transfer (HGT) events.

Place, publisher, year, edition, pages
Frontiers Media S.A., 2022
Keywords
acidophiles, pH homeostasis, extremophiles, acid mine drainage (AMD), evolution, comparative genomics
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-110873 (URN)10.3389/fmicb.2021.822229 (DOI)000763657200001 ()35242113 (PubMedID)2-s2.0-85125666346 (Scopus ID)2022 (Local ID)2022 (Archive number)2022 (OAI)
Available from: 2022-03-18 Created: 2022-03-18 Last updated: 2024-01-17Bibliographically approved
Vergara, E., Neira, G., González, C., Cortez, D., Dopson, M. & Holmes, D. S. (2020). Evolution of Predicted Acid Resistance Mechanisms in the Extremely Acidophilic Leptospirillum Genus. Genes, 11(4), Article ID 389.
Open this publication in new window or tab >>Evolution of Predicted Acid Resistance Mechanisms in the Extremely Acidophilic Leptospirillum Genus
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2020 (English)In: Genes, E-ISSN 2073-4425, Vol. 11, no 4, article id 389Article in journal (Refereed) Published
Abstract [en]

Organisms that thrive in extremely acidic environments (≤pH 3.5) are of widespread importance in industrial applications, environmental issues, and evolutionary studies. Leptospirillum spp. constitute the only extremely acidophilic microbes in the phylogenetically deep-rooted bacterial phylum Nitrospirae. Leptospirilli are Gram-negative, obligatory chemolithoautotrophic, aerobic, ferrous iron oxidizers. This paper predicts genes that Leptospirilli use to survive at low pH and infers their evolutionary trajectory. Phylogenetic and other bioinformatic approaches suggest that these genes can be classified into (i) “first line of defense”, involved in the prevention of the entry of protons into the cell, and (ii) neutralization or expulsion of protons that enter the cell. The first line of defense includes potassium transporters, predicted to form an inside positive membrane potential, spermidines, hopanoids, and Slps (starvation-inducible outer membrane proteins). The “second line of defense“ includes proton pumps and enzymes that consume protons. Maximum parsimony, clustering methods, and gene alignments are used to infer the evolutionary trajectory that potentially enabled the ancestral Leptospirillum to transition from a postulated circum-neutral pH environment to an extremely acidic one. The hypothesized trajectory includes gene gains/loss events driven extensively by horizontal gene transfer, gene duplications, gene mutations, and genomic rearrangements

Place, publisher, year, edition, pages
MDPI, 2020
Keywords
Nitrospira, acid mine drainage (AMD), acid resistance, bioleaching, comparative genomics, evolution, extreme acidophile, horizontal gene transfer (HGT), phylogenetics
National Category
Evolutionary Biology
Research subject
Ecology, Evolutionary Biology
Identifiers
urn:nbn:se:lnu:diva-102713 (URN)10.3390/genes11040389 (DOI)000537224600013 ()32260256 (PubMedID)2-s2.0-85083023320 (Scopus ID)2020 (Local ID)2020 (Archive number)2020 (OAI)
Available from: 2021-05-05 Created: 2021-05-05 Last updated: 2024-07-04Bibliographically approved
Esparza, M., Jedlicki, E., González, C., Dopson, M. & Holmes, D. (2019). Effect of CO2 Concentration on Uptake and Assimilation of Inorganic Carbon in the Extreme Acidophile Acidithiobacillus ferrooxidans. Frontiers in Microbiology, 10, 1-15, Article ID 603.
Open this publication in new window or tab >>Effect of CO2 Concentration on Uptake and Assimilation of Inorganic Carbon in the Extreme Acidophile Acidithiobacillus ferrooxidans
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2019 (English)In: Frontiers in Microbiology, E-ISSN 1664-302X, Vol. 10, p. 1-15, article id 603Article in journal (Refereed) Published
Abstract [en]

This study was motivated by surprising gaps in the current knowledge of microbial inorganic carbon (Ci) uptake and assimilation at acidic pH values (pH < 3). Particularly striking is the limited understanding of the differences between Ci uptake mechanisms in acidic versus circumneutral environments where the Ci predominantly occurs either as a dissolved gas (CO2) or as bicarbonate (HCO3-), respectively. In order to gain initial traction on the problem, the relative abundance of transcripts encoding proteins involved in Ci uptake and assimilation was studied in the autotrophic, polyextreme acidophile Acidithiobacillus ferrooxidans whose optimum pH for growth is 2.5 using ferrous iron as an energy source, although they are able to grow at pH 5 when using sulfur as an energy source. The relative abundance of transcripts of five operons (cbb1 -5) and one gene cluster (can-sulP) was monitored by RT-qPCR and, in selected cases, at the protein level by Western blotting, when cells were grown under different regimens of CO2 concentration in elemental sulfur. Of particular note was the absence of a classical bicarbonate uptake system in A. ferrooxidans. However, bioinformatic approaches predict that sulP, previously annotated as a sulfate transporter, is a novel type of bicarbonate transporter. A conceptual model of CO2 fixation was constructed from combined bioinformatic and experimental approaches that suggests strategies for providing ecological flexibility under changing concentrations of CO2 and provides a portal to elucidating Ci uptake and regulation in acidic conditions. The results could advance the understanding of industrial bioleaching processes to recover metals such as copper at acidic pH. In addition, they may also shed light on how chemolithoautotrophic acidophiles influence the nutrient and energy balance in naturally occurring low pH environments.

Place, publisher, year, edition, pages
Frontiers Media S.A., 2019
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-81537 (URN)10.3389/fmicb.2019.00603 (DOI)000463397000001 ()2-s2.0-85068205987 (Scopus ID)
Available from: 2019-04-01 Created: 2019-04-01 Last updated: 2024-01-17Bibliographically approved
Liljeqvist, M., Ossandon, F. J., González, C., Rajan, S., Stell, A., Valdes, J., . . . Dopson, M. (2015). Metagenomic analysis reveals adaptations to a cold-adapted lifestyle in a low-temperature acid mine drainage stream. FEMS Microbiology Ecology, 91(4), Article ID fiv011.
Open this publication in new window or tab >>Metagenomic analysis reveals adaptations to a cold-adapted lifestyle in a low-temperature acid mine drainage stream
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2015 (English)In: FEMS Microbiology Ecology, ISSN 0168-6496, E-ISSN 1574-6941, Vol. 91, no 4, article id fiv011Article in journal (Refereed) Published
Abstract [en]

An acid mine drainage (pH 2.5-2.7) stream biofilm situated 250 m below ground in the low-temperature (6-10 degrees C) Kristineberg mine, northern Sweden, contained a microbial community equipped for growth at low temperature and acidic pH. Metagenomic sequencing of the biofilm and planktonic fractions identified the most abundant microorganism to be similar to the psychrotolerant acidophile, Acidithiobacillus ferrivorans. In addition, metagenome contigs were most similar to other Acidithiobacillus species, an Acidobacteria-like species, and a Gallionellaceae-like species. Analyses of the metagenomes indicated functional characteristics previously characterized as related to growth at low temperature including cold-shock proteins, several pathways for the production of compatible solutes and an anti-freeze protein. In addition, genes were predicted to encode functions related to pH homeostasis and metal resistance related to growth in the acidic metal-containing mine water. Metagenome analyses identified microorganisms capable of nitrogen fixation and exhibiting a primarily autotrophic lifestyle driven by the oxidation of the ferrous iron and inorganic sulfur compounds contained in the sulfidic mine waters. The study identified a low diversity of abundant microorganisms adapted to a low-temperature acidic environment as well as identifying some of the strategies the microorganisms employ to grow in this extreme environment.

Keywords
metagenome, acid mine drainage, psychrotolerant, Acidithiobacillus ferrivorans, low temperature
National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-46289 (URN)10.1093/femsec/fiv011 (DOI)000355327300002 ()2-s2.0-84942673444 (Scopus ID)
Available from: 2015-09-14 Created: 2015-09-14 Last updated: 2023-05-17Bibliographically approved
González, C., Yanquepe, M., Cardenas, J. P., Valdes, J., Quatrini, R., Holmes, D. S. & Dopson, M. (2014). Genetic variability of psychrotolerant Acidithiobacillus ferrivorans revealed by (meta)genomic analysis.. Research in Microbiology, 165(9), 726-734
Open this publication in new window or tab >>Genetic variability of psychrotolerant Acidithiobacillus ferrivorans revealed by (meta)genomic analysis.
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2014 (English)In: Research in Microbiology, ISSN 0923-2508, E-ISSN 1769-7123, Vol. 165, no 9, p. 726-734Article in journal (Refereed) Published
Abstract [en]

Acidophilic microorganisms inhabit low pH environments such as acid mine drainage that is generated when sulfide minerals are exposed to air. The genome sequence of the psychrotolerant Acidithiobacillus ferrivorans SS3 was compared to a metagenome from a low temperature acidic stream dominated by an A. ferrivorans-like strain. Stretches of genomic DNA characterized by few matches to the metagenome, termed 'metagenomic islands', encoded genes associated with metal efflux and pH homeostasis. The metagenomic islands were enriched in mobile elements such as phage proteins, transposases, integrases and in one case, predicted to be flanked by truncated tRNAs. Cus gene clusters predicted to be involved in copper efflux and further Cus-like RND systems were predicted to be located in metagenomic islands and therefore, constitute part of the flexible gene complement of the species. Phylogenetic analysis of Cus clusters showed both lineage specificity within the Acidithiobacillus genus as well as niche specificity associated with an acidic environment. The metagenomic islands also contained a predicted copper efflux P-type ATPase system and a polyphosphate kinase potentially involved in polyphosphate mediated copper resistance. This study identifies genetic variability of low temperature acidophiles that likely reflects metal resistance selective pressures in the copper rich environment.

National Category
Microbiology
Research subject
Ecology, Microbiology
Identifiers
urn:nbn:se:lnu:diva-37349 (URN)10.1016/j.resmic.2014.08.005 (DOI)000347660400004 ()25172573 (PubMedID)2-s2.0-84922212527 (Scopus ID)
Available from: 2014-09-29 Created: 2014-09-29 Last updated: 2023-05-17Bibliographically approved
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ORCID iD: ORCID iD iconorcid.org/0000-0003-3566-4758

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