Feedback-based, system-level properties of vertebrate-microbial interactions.

Improved characterization of infectious disease dynamics is required. To that end, three-dimensional (3D) data analysis of feedback-like processes may be considered.To detect infectious disease data patterns, a systems biology (SB) and evolutionary biology (EB) approach was evaluated, which utilizes...

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Main Authors: Ariel L Rivas, Mark D Jankowski, Renata Piccinini, Gabriel Leitner, Daniel Schwarz, Kevin L Anderson, Jeanne M Fair, Almira L Hoogesteijn, Wilfried Wolter, Marcelo Chaffer, Shlomo Blum, Tom Were, Stephen N Konah, Prakash Kempaiah, John M Ong'echa, Ulrike S Diesterbeck, Rachel Pilla, Claus-Peter Czerny, James B Hittner, James M Hyman, Douglas J Perkins
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3577842?pdf=render
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spelling doaj-4533f6e439644a68a77b469af2503ee92020-11-25T01:56:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5398410.1371/journal.pone.0053984Feedback-based, system-level properties of vertebrate-microbial interactions.Ariel L RivasMark D JankowskiRenata PiccininiGabriel LeitnerDaniel SchwarzKevin L AndersonJeanne M FairAlmira L HoogesteijnWilfried WolterMarcelo ChafferShlomo BlumTom WereStephen N KonahPrakash KempaiahJohn M Ong'echaUlrike S DiesterbeckRachel PillaClaus-Peter CzernyJames B HittnerJames M HymanDouglas J PerkinsImproved characterization of infectious disease dynamics is required. To that end, three-dimensional (3D) data analysis of feedback-like processes may be considered.To detect infectious disease data patterns, a systems biology (SB) and evolutionary biology (EB) approach was evaluated, which utilizes leukocyte data structures designed to diminish data variability and enhance discrimination. Using data collected from one avian and two mammalian (human and bovine) species infected with viral, parasite, or bacterial agents (both sensitive and resistant to antimicrobials), four data structures were explored: (i) counts or percentages of a single leukocyte type, such as lymphocytes, neutrophils, or macrophages (the classic approach), and three levels of the SB/EB approach, which assessed (ii) 2D, (iii) 3D, and (iv) multi-dimensional (rotating 3D) host-microbial interactions.In all studies, no classic data structure discriminated disease-positive (D+, or observations in which a microbe was isolated) from disease-negative (D-, or microbial-negative) groups: D+ and D- data distributions overlapped. In contrast, multi-dimensional analysis of indicators designed to possess desirable features, such as a single line of observations, displayed a continuous, circular data structure, whose abrupt inflections facilitated partitioning into subsets statistically significantly different from one another. In all studies, the 3D, SB/EB approach distinguished three (steady, positive, and negative) feedback phases, in which D- data characterized the steady state phase, and D+ data were found in the positive and negative phases. In humans, spatial patterns revealed false-negative observations and three malaria-positive data classes. In both humans and bovines, methicillin-resistant Staphylococcus aureus (MRSA) infections were discriminated from non-MRSA infections.More information can be extracted, from the same data, provided that data are structured, their 3D relationships are considered, and well-conserved (feedback-like) functions are estimated. Patterns emerging from such structures may distinguish well-conserved from recently developed host-microbial interactions. Applications include diagnosis, error detection, and modeling.http://europepmc.org/articles/PMC3577842?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ariel L Rivas
Mark D Jankowski
Renata Piccinini
Gabriel Leitner
Daniel Schwarz
Kevin L Anderson
Jeanne M Fair
Almira L Hoogesteijn
Wilfried Wolter
Marcelo Chaffer
Shlomo Blum
Tom Were
Stephen N Konah
Prakash Kempaiah
John M Ong'echa
Ulrike S Diesterbeck
Rachel Pilla
Claus-Peter Czerny
James B Hittner
James M Hyman
Douglas J Perkins
spellingShingle Ariel L Rivas
Mark D Jankowski
Renata Piccinini
Gabriel Leitner
Daniel Schwarz
Kevin L Anderson
Jeanne M Fair
Almira L Hoogesteijn
Wilfried Wolter
Marcelo Chaffer
Shlomo Blum
Tom Were
Stephen N Konah
Prakash Kempaiah
John M Ong'echa
Ulrike S Diesterbeck
Rachel Pilla
Claus-Peter Czerny
James B Hittner
James M Hyman
Douglas J Perkins
Feedback-based, system-level properties of vertebrate-microbial interactions.
PLoS ONE
author_facet Ariel L Rivas
Mark D Jankowski
Renata Piccinini
Gabriel Leitner
Daniel Schwarz
Kevin L Anderson
Jeanne M Fair
Almira L Hoogesteijn
Wilfried Wolter
Marcelo Chaffer
Shlomo Blum
Tom Were
Stephen N Konah
Prakash Kempaiah
John M Ong'echa
Ulrike S Diesterbeck
Rachel Pilla
Claus-Peter Czerny
James B Hittner
James M Hyman
Douglas J Perkins
author_sort Ariel L Rivas
title Feedback-based, system-level properties of vertebrate-microbial interactions.
title_short Feedback-based, system-level properties of vertebrate-microbial interactions.
title_full Feedback-based, system-level properties of vertebrate-microbial interactions.
title_fullStr Feedback-based, system-level properties of vertebrate-microbial interactions.
title_full_unstemmed Feedback-based, system-level properties of vertebrate-microbial interactions.
title_sort feedback-based, system-level properties of vertebrate-microbial interactions.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Improved characterization of infectious disease dynamics is required. To that end, three-dimensional (3D) data analysis of feedback-like processes may be considered.To detect infectious disease data patterns, a systems biology (SB) and evolutionary biology (EB) approach was evaluated, which utilizes leukocyte data structures designed to diminish data variability and enhance discrimination. Using data collected from one avian and two mammalian (human and bovine) species infected with viral, parasite, or bacterial agents (both sensitive and resistant to antimicrobials), four data structures were explored: (i) counts or percentages of a single leukocyte type, such as lymphocytes, neutrophils, or macrophages (the classic approach), and three levels of the SB/EB approach, which assessed (ii) 2D, (iii) 3D, and (iv) multi-dimensional (rotating 3D) host-microbial interactions.In all studies, no classic data structure discriminated disease-positive (D+, or observations in which a microbe was isolated) from disease-negative (D-, or microbial-negative) groups: D+ and D- data distributions overlapped. In contrast, multi-dimensional analysis of indicators designed to possess desirable features, such as a single line of observations, displayed a continuous, circular data structure, whose abrupt inflections facilitated partitioning into subsets statistically significantly different from one another. In all studies, the 3D, SB/EB approach distinguished three (steady, positive, and negative) feedback phases, in which D- data characterized the steady state phase, and D+ data were found in the positive and negative phases. In humans, spatial patterns revealed false-negative observations and three malaria-positive data classes. In both humans and bovines, methicillin-resistant Staphylococcus aureus (MRSA) infections were discriminated from non-MRSA infections.More information can be extracted, from the same data, provided that data are structured, their 3D relationships are considered, and well-conserved (feedback-like) functions are estimated. Patterns emerging from such structures may distinguish well-conserved from recently developed host-microbial interactions. Applications include diagnosis, error detection, and modeling.
url http://europepmc.org/articles/PMC3577842?pdf=render
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