Jordan Toby Bird

Dr. Jordan Toby Bird

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 April 2019 in mBio
Verified
Journal Article
Open access
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JBJordan Toby Bird
Jordan Toby Bird
ETEric D. Tague
Eric D. Tague
LZLaura Zinke
Laura Zinke
JSJenna M. Schmidt
Jenna M. Schmidt
ASAndrew D. Steen
Andrew D. Steen
KLKaren G. Lloyd
Karen G. Lloyd
Energy-starved microbes in deep marine sediments subsist at near-zero growth for thousands of years, yet the mechanisms for their subsistence are unknown because no model strains have been cultivated from most of these groups. We investigated Baltic Sea sediments with single-cell genomics, metabolomics, metatranscriptomics, and enzyme assays to identify possible subsistence mechanisms employed by uncultured Atribacteria, Aminicenantes, Actinobacteria group OPB41, Aerophobetes, Chloroflexi, Deltaproteobacteria, Desulfatiglans, Bathyarchaeota, and Euryarchaeota marine group II lineages. Some functions appeared to be shared by multiple lineages, such as trehalose production and NAD+-consuming deacetylation, both of which have been shown to increase cellular life spans in other organisms by stabilizing proteins and nucleic acids, respectively. Other possible subsistence mechanisms differed between lineages, possibly providing them different physiological niches. Enzyme assays and transcripts suggested that Atribacteria and Actinobacteria group OPB41 catabolized sugars, whereas Aminicenantes and Atribacteria catabolized peptides. Metabolite and transcript data suggested that Atribacteria utilized allantoin, possibly as an energetic substrate or chemical protectant, and also possessed energy-efficient sodium pumps. Atribacteria single-cell amplified genomes (SAGs) recruited transcripts for full pathways for the production of all 20 canonical amino acids, and the gene for amino acid exporter YddG was one of their most highly transcribed genes, suggesting that they may benefit from metabolic interdependence with other cells. Subsistence of uncultured phyla in deep subsurface sediments may occur through shared strategies of using chemical protectants for biomolecular stabilization, but also by differentiating into physiological niches and metabolic interdependencies. IMPORTANCE Much of life on Earth exists in a very slow-growing state, with microbes from deeply buried marine sediments representing an extreme example. These environments are like natural laboratories that have run multi-thousand-year experiments that are impossible to perform in a laboratory. We borrowed some techniques that are commonly used in laboratory experiments and applied them to these natural samples to make hypotheses about how these microbes subsist for so long at low activity. We found that some methods for stabilizing proteins and nucleic acids might be used by many members of the community. We also found evidence for niche differentiation strategies, and possibly cross-feeding, suggesting that even though they are barely growing, complex ecological interactions continue to occur over ultralong timescales.

17 March 2017 in Viruses
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Journal Article
Open access
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SWSteven Wilhelm
Steven Wilhelm
JBJordan Toby Bird
Jordan Toby Bird
KBKyle S. Bonifer
Kyle S. Bonifer
BCBenjamin C. Calfee
Benjamin C. Calfee
TCTian Chen
Tian Chen
GLGary R. LeCleir
Gary R. LeCleir
The discovery of infectious particles that challenge conventional thoughts concerning “what is a virus” has led to the evolution a new field of study in the past decade. Here, we review knowledge and information concerning “giant viruses”, with a focus not only on some of the best studied systems, but also provide an effort to illuminate systems yet to be better resolved. We conclude by demonstrating that there is an abundance of new host–virus systems that fall into this “giant” category, demonstrating that this field of inquiry presents great opportunities for future research.

12 August 2020 in The ISME Journal
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Journal Article
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RFRyan K. Fritts
Ryan K. Fritts
JBJordan Toby Bird
Jordan Toby Bird
MBMegan G. Behringer
Megan G. Behringer
ALAnna Lipzen
Anna Lipzen
JMJoel Martin
Joel Martin
JMJames B. McKinlay
James B. McKinlay
Interactive microbial communities are ubiquitous, influencing biogeochemical cycles and host health. One widespread interaction is nutrient exchange, or cross-feeding, wherein metabolites are transferred between microbes. Some cross-fed metabolites, such as vitamins, amino acids, and ammonium (NH4+), are communally valuable and impose a cost on the producer. The mechanisms that enforce cross-feeding of communally valuable metabolites are not fully understood. Previously we engineered a cross-feeding coculture between N2-fixing Rhodopseudomonas palustris and fermentative Escherichia coli. Engineered R. palustris excretes essential nitrogen as NH4+ to E. coli, while E. coli excretes essential carbon as fermentation products to R. palustris. Here, we sought to determine whether a reciprocal cross-feeding relationship would evolve spontaneously in cocultures with wild-type R. palustris, which is not known to excrete NH4+. Indeed, we observed the emergence of NH4+ cross-feeding, but driven by adaptation of E. coli alone. A missense mutation in E. coli NtrC, a regulator of nitrogen scavenging, resulted in constitutive activation of an NH4+ transporter. This activity likely allowed E. coli to subsist on the small amount of leaked NH4+ and better reciprocate through elevated excretion of fermentation products from a larger E. coli population. Our results indicate that enhanced nutrient uptake by recipients, rather than increased excretion by producers, is an underappreciated yet possibly prevalent mechanism by which cross-feeding can emerge.

5 July 2022 in PLOS Neglected Tropical Diseases
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Journal Article
Open access
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GVGopinath Venugopal
Gopinath Venugopal
JBJordan Toby Bird
Jordan Toby Bird
CWCharity L Washam
Charity L Washam
HRHayden Roys
Hayden Roys
ABAnne Bowlin
Anne Bowlin
TWTiffany Weinkopff
Tiffany Weinkopff
Leishmaniaparasites cause cutaneous leishmaniasis (CL), a disease characterized by disfiguring, ulcerative skin lesions. Both parasite and host gene expression following infection with variousLeishmaniaspecies has been investigated in vitro, but global transcriptional analysis followingL.majorinfection in vivo is lacking. Thus, we conducted a comprehensive transcriptomic profiling study combining bulk RNA sequencing (RNA-Seq) and single-cell RNA sequencing (scRNA-Seq) to identify global changes in gene expression in vivo followingL.majorinfection. Bulk RNA-Seq analysis revealed that host immune response pathways like the antigen processing and presentation pathway were significantly enriched amongst differentially expressed genes (DEGs) upon infection, while ribosomal pathways were significantly downregulated in infected mice compared to naive controls. scRNA-Seq analyses revealed cellular heterogeneity including distinct resident and recruited cell types in the skin following murineL.majorinfection. Within the individual immune cell types, several DEGs indicative of many interferon induced GTPases and antigen presentation molecules were significantly enhanced in the infected ears including macrophages, resident macrophages, and inflammatory monocytes. Ingenuity Pathway Analysis of scRNA-Seq data indicated the antigen presentation pathway was increased with infection, while EIF2 signaling is the top downregulated pathway followed by eIF4/p70S6k and mTOR signaling in multiple cell types including macrophages, blood and lymphatic endothelial cells. Altogether, this transcriptomic profile highlights known recruitment of myeloid cells to lesions and recognizes a potential role for EIF2 signaling in murineL.majorinfection in vivo.

19 September 2017 in Environmental Microbiology Reports
Verified
Journal Article
Closed access
LZLaura A. Zinke
Laura A. Zinke
MMMegan M. Mullis
Megan M. Mullis
JBJordan Toby Bird
Jordan Toby Bird
IMIan P.G. Marshall
Ian P.G. Marshall
BJBo Barker Jørgensen
Bo Barker Jørgensen
BRBrandi Kiel Reese
Brandi Kiel Reese

15 February 2019 in Applied and Environmental Microbiology
Verified
Journal Article
Open access
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LZLaura A. Zinke
Laura A. Zinke
CGClemens Glombitza
Clemens Glombitza
JBJordan Toby Bird
Jordan Toby Bird
HRHans Røy
Hans Røy
BJBo Barker Jørgensen
Bo Barker Jørgensen
BRBrandi Kiel Reese
Brandi Kiel Reese
Sediments sequester organic matter over geologic time scales and impact global climate regulation. Microbial communities in marine sediments drive organic matter degradation, but the factors controlling their assemblages and activities, which in turn impact their role in organic matter degradation, are not well understood. Hence, determining the role of microbial communities in carbon cycling in various sediment types is necessary for predicting future sediment carbon cycling. We examined microbial communities in Baltic Sea sediments, which were deposited across various climatic and geographical regimes to determine the relationship between microbial potential for breakdown of organic matter and abiotic factors, including geochemistry and sediment lithology. The findings from this study will contribute to our understanding of carbon cycling in the deep biosphere and how microbial communities live in deeply buried environments.