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Dive into the research topics where Alejandro P. Rooney is active.

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Featured researches published by Alejandro P. Rooney.


Proceedings of the National Academy of Sciences of the United States of America | 2002

Evolution of moth sex pheromones via ancestral genes

Wendell L. Roelofs; Weitian Liu; Guixia Hao; Hongmei Jiao; Alejandro P. Rooney; Charles E. Linn

Mate finding in most moth species involves long-distance signaling via female-emitted sex pheromones. There is a great diversity of pheromone structures used throughout the Lepidoptera, even among closely related species. The conundrum is how signal divergence has occurred. With strong normalizing selection pressure on blend composition and response preferences, it is improbable that shifts to pheromones of diverse structures occur through adaptive changes in small steps. Here, we present data supporting the hypothesis that a major shift in the pheromone of an Ostrinia species occurred by activation of a nonfunctional desaturase gene transcript present in the pheromone gland. We also demonstrate the existence of rare males that respond to the new pheromone blend. Their presence would allow for asymmetric tracking of male response to the new blend and, thus, evolution of an Ostrinia species with structurally different sex pheromone components.


Proceedings of the National Academy of Sciences of the United States of America | 2008

Identifying the fundamental units of bacterial diversity: A paradigm shift to incorporate ecology into bacterial systematics

Alexander F. Koeppel; Elizabeth B. Perry; Johannes Sikorski; Danny Krizanc; Andrew Warner; David M. Ward; Alejandro P. Rooney; Evelyne Brambilla; Nora Connor; Rodney M. Ratcliff; Eviatar Nevo; Frederick M. Cohan

The central questions of bacterial ecology and evolution require a method to consistently demarcate, from the vast and diverse set of bacterial cells within a natural community, the groups playing ecologically distinct roles (ecotypes). Because of a lack of theory-based guidelines, current methods in bacterial systematics fail to divide the bacterial domain of life into meaningful units of ecology and evolution. We introduce a sequence-based approach (“ecotype simulation”) to model the evolutionary dynamics of bacterial populations and to identify ecotypes within a natural community, focusing here on two Bacillus clades surveyed from the “Evolution Canyons” of Israel. This approach has identified multiple ecotypes within traditional species, with each predicted to be an ecologically distinct lineage; many such ecotypes were confirmed to be ecologically distinct, with specialization to different canyon slopes with different solar exposures. Ecotype simulation provides a long-needed natural foundation for microbial ecology and systematics.


Proceedings of the National Academy of Sciences of the United States of America | 2003

Molecular genetics and evolution of pheromone biosynthesis in Lepidoptera

Wendell L. Roelofs; Alejandro P. Rooney

A great diversity of pheromone structures are used by moth species (Insecta: Lepidoptera) for long-distance mating signals. The signal/response channel seems to be narrow for each species, and a major conundrum is how signal divergence has occurred in the face of strong selection pressures against small changes in the signal. Observations of various closely related and morphologically similar species that use pheromone components biosynthesized by different enzymes and biosynthetic routes underscore the question as to how major jumps in the biosynthetic routes could have evolved with a mate recognition system that is based on responses to a specific blend of chemicals. Research on the desaturases used in the pheromone biosynthetic pathway for various moth species has revealed that one way to make a major shift in the pheromone blend is by activation of a different desaturase from mRNA that already exists in the pheromone gland. Data will be presented to support the hypothesis that this process was used in the evolution of the Asian corn borer, Ostrinia furnacalis species. In that context, moth sex-pheromone desaturase genes seem to be evolving under a birth-and-death process. According to this model of multigene family evolution, some genes are maintained in the genome for long periods of time, whereas others become deleted or lose their functionality, and new genes are created through gene duplication. This mode of evolution seems to play a role in moth speciation, as exemplified by the case of the Asian corn borer and European corn borer, Ostrinia nubilalis species.


Phytopathology | 2013

One fungus, one name

David M. Geiser; Takayuki Aoki; Charles W. Bacon; Scott E. Baker; Madan K. Bhattacharyya; Mary E. Brandt; Daren W. Brown; L. W. Burgess; S. Chulze; Jeffrey J. Coleman; J. C. Correll; Sarah F. Covert; Pedro W. Crous; Christina A. Cuomo; G. Sybren de Hoog; Antonio Di Pietro; Wade H. Elmer; Lynn Epstein; Rasmus John Normand Frandsen; Stanley Freeman; Tatiana Gagkaeva; Anthony E. Glenn; Thomas R. Gordon; Nancy F. Gregory; Kim E. Hammond-Kosack; Linda E. Hanson; María del Mar Jiménez-Gasco; Seogchan Kang; H. Corby Kistler; Gretchen A. Kuldau

In this letter, we advocate recognizing the genus Fusarium as the sole name for a group that includes virtually all Fusarium species of importance in plant pathology, mycotoxicology, medicine, and basic research. This phylogenetically guided circumscription will free scientists from any obligation to use other genus names, including teleomorphs, for species nested within this clade, and preserve the application of the name Fusarium in the way it has been used for almost a century. Due to recent changes in the International Code of Nomenclature for algae, fungi, and plants, this is an urgent matter that requires community attention. The alternative is to break the longstanding concept of Fusarium into nine or more genera, and remove important taxa such as those in the F. solani species complex from the genus, a move we believe is unnecessary. Here we present taxonomic and nomenclatural proposals that will preserve established research connections and facilitate communication within and between research communities, and at the same time support strong scientific principles and good taxonomic practice.


Phytopathology | 2013

One fungus, one name: defining the genus Fusarium in a scientifically robust way that preserves longstanding use.

David M. Geiser; Takayuki Aoki; Charles W. Bacon; Scott E. Baker; Madan K. Bhattacharyya; Mary E. Brandt; Daren W. Brown; L. W. Burgess; S. Chulze; Jeffrey J. Coleman; J. C. Correll; Sarah F. Covert; Pedro W. Crous; Christina A. Cuomo; G. Sybren de Hoog; Antonio Di Pietro; Wade H. Elmer; Lynn Epstein; Rasmus John Normand Frandsen; Stanley Freeman; Tatiana Gagkaeva; Anthony E. Glenn; Thomas R. Gordon; Nancy F. Gregory; Kim E. Hammond-Kosack; Linda E. Hanson; María del Mar Jiménez-Gasco; Seogchan Kang; H. Corby Kistler; Gretchen A. Kuldau

In this letter, we advocate recognizing the genus Fusarium as the sole name for a group that includes virtually all Fusarium species of importance in plant pathology, mycotoxicology, medicine, and basic research. This phylogenetically guided circumscription will free scientists from any obligation to use other genus names, including teleomorphs, for species nested within this clade, and preserve the application of the name Fusarium in the way it has been used for almost a century. Due to recent changes in the International Code of Nomenclature for algae, fungi, and plants, this is an urgent matter that requires community attention. The alternative is to break the longstanding concept of Fusarium into nine or more genera, and remove important taxa such as those in the F. solani species complex from the genus, a move we believe is unnecessary. Here we present taxonomic and nomenclatural proposals that will preserve established research connections and facilitate communication within and between research communities, and at the same time support strong scientific principles and good taxonomic practice.


International Journal of Systematic and Evolutionary Microbiology | 2009

Phylogeny and molecular taxonomy of the Bacillus subtilis species complex and description of Bacillus subtilis subsp. inaquosorum subsp. nov.

Alejandro P. Rooney; Neil P. J. Price; Christopher J. Ehrhardt; James L. Swezey; Jason D. Bannan

The Bacillus subtilis species complex is a tight assemblage of closely related species. For many years, it has been recognized that these species cannot be differentiated on the basis of phenotypic characteristics. Recently, it has been shown that phylogenetic analysis of the 16S rRNA gene also fails to differentiate species within the complex due to the highly conserved nature of the gene, yet DNA-DNA hybridization values fall well below 70 % for the same species comparisons. As a complementary approach, we propose that phylogenetic analysis of multiple protein-coding loci can be used as a means to detect and differentiate novel Bacillus taxa. Indeed, our phylogenetic analyses revealed the existence of a previously unknown group of strains closely related to, but distinct from, Bacillus subtilis subsp. spizizenii. Results of matrix-assisted laser desorption ionization-time of flight mass spectrometry analyses revealed that the group produces a novel surfactin-like lipopeptide with mass m/z 1120.8 that is not produced by the other currently recognized subspecies. In addition, the group displayed differences in the total cellular content of the fatty acids C(16 : 0) and iso-C(17 : 1)omega10c that distinguish it from the closely related B. subtilis subsp. spizizenii. Consequently, the correlation of these novel phenotypic traits with the phylogenetic distinctiveness of this previously unknown subspecies group showed that phylogenetic analysis of multiple protein-coding loci can be used as a means to detect and differentiate novel Bacillus taxa. Therefore, we propose that this new group should be recognized as representing a novel taxon, Bacillus subtilis subsp. inaquosorum subsp. nov., with the type strain NRRL B-23052(T) (=KCTC 13429(T)=BGSC 3A28(T)).


International Journal of Systematic and Evolutionary Microbiology | 2018

Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes

Jongsik Chun; Aharon Oren; Antonio Ventosa; Henrik Christensen; David R. Arahal; Milton S. da Costa; Alejandro P. Rooney; Hana Yi; Xue Wei Xu; Sofie E. De Meyer; Martha E. Trujillo

Advancement of DNA sequencing technology allows the routine use of genome sequences in the various fields of microbiology. The information held in genome sequences proved to provide objective and reliable means in the taxonomy of prokaryotes. Here, we describe the minimal standards for the quality of genome sequences and how they can be applied for taxonomic purposes.


Evolution | 2001

HISTORICAL POPULATION SIZE CHANGE OF BOWHEAD WHALES INFERRED FROM DNA SEQUENCE POLYMORPHISM DATA

Alejandro P. Rooney; Rodney L. Honeycutt; James N. Derr

Abstract.— Nucleotide sequence data from the mitochondrial control region were used from a phylogenetic context to investigate the long‐term history of a population of bowhead whales (Balaena mysticetus). In addition, the coalescence time of these sequences was used to estimate the age of the inferred patterns of population size change. The results indicate that mitochondrial genetic polymorphism was not affected by a recent bottleneck that occurred near the turn of the 20th century, thereby preserving the signature of historical population size change in the mitochondrial genome. Further analysis showed that this population underwent an expansion initiated in the Middle to Late Pleistocene. As such, early Holocene changes in Arctic sea ice distribution appear to have had little influence on patterns of genetic variability in this population.


Applied and Environmental Microbiology | 2010

Ecology of Speciation in the Genus Bacillus

Nora Connor; Johannes Sikorski; Alejandro P. Rooney; Sarah M Kopac; Alexander F. Koeppel; Andrew Burger; Scott G. Cole; Elizabeth B. Perry; Danny Krizanc; Nicholas C. Field; Michele Slaton; Frederick M. Cohan

ABSTRACT Microbial ecologists and systematists are challenged to discover the early ecological changes that drive the splitting of one bacterial population into two ecologically distinct populations. We have aimed to identify newly divergent lineages (“ecotypes”) bearing the dynamic properties attributed to species, with the rationale that discovering their ecological differences would reveal the ecological dimensions of speciation. To this end, we have sampled bacteria from the Bacillus subtilis-Bacillus licheniformis clade from sites differing in solar exposure and soil texture within a Death Valley canyon. Within this clade, we hypothesized ecotype demarcations based on DNA sequence diversity, through analysis of the clades evolutionary history by Ecotype Simulation (ES) and AdaptML. Ecotypes so demarcated were found to be significantly different in their associations with solar exposure and soil texture, suggesting that these and covarying environmental parameters are among the dimensions of ecological divergence for newly divergent Bacillus ecotypes. Fatty acid composition appeared to contribute to ecotype differences in temperature adaptation, since those ecotypes with more warm-adapting fatty acids were isolated more frequently from sites with greater solar exposure. The recognized species and subspecies of the B. subtilis-B. licheniformis clade were found to be nearly identical to the ecotypes demarcated by ES, with a few exceptions where a recognized taxon is split at most into three putative ecotypes. Nevertheless, the taxa recognized do not appear to encompass the full ecological diversity of the B. subtilis-B. licheniformis clade: ES and AdaptML identified several newly discovered clades as ecotypes that are distinct from any recognized taxon.


Fems Microbiology Letters | 2009

Isolation and characterization of rhamnolipid‐producing bacterial strains from a biodiesel facility

Alejandro P. Rooney; Neil P. J. Price; Karen Ray; Tsung-Min Kuo

Novel strains of rhamnolipid-producing bacteria were isolated from soils at a biodiesel facility on the basis of their ability to grow on glycerol as a sole carbon source. Strains were identified as Acinetobacter calcoaceticus, Enterobacter asburiae, Enterobacter hormaechei, Pantoea stewartii, and Pseudomonas aeruginosa. The strains of the former five species were found to produce rhamnolipids in quantities the same as, or similar to, coisolated strains of P. aeruginosa. Measurements of surface tension revealed that that emulsifying properties of these strains were similar to levels displayed by rhamnolipids produced by P. aeruginosa. Results of matrix-assisted laser desorption/ionization time-of-flight MS analyses revealed that the predominant compounds made by all strains were C10-C10 mono- and dirhamnolipids. Notably, E. hormaechei and one strain of A. calcoaceticus produced rhamnolipids in amounts similar to the pseudomonads. As all strains examined were from the same taxonomic class of Proteobacteria, further examination of this group may reveal many additional species not previously known to produce rhamnolipids in addition to novel strains of species currently known to produce rhamnolipids.

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Christopher A. Dunlap

National Center for Agricultural Utilization Research

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David M. Geiser

Pennsylvania State University

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David A. Schisler

National Center for Agricultural Utilization Research

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Ephantus J. Muturi

United States Department of Agriculture

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Kerry O’Donnell

National Center for Agricultural Utilization Research

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Stacy Sink

National Center for Agricultural Utilization Research

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