Literature DB >> 28560277

Theoretical assessment data for the binding of sepsis causing pathogens to ApoH beads.

Manjula Ramya Vutukuru1, Nivedita Mitra1.   

Abstract

The data presented in this paper supports the research article "A rapid, highly sensitive and culture-free detection of pathogens from blood by positive enrichment" ( Vutukuru et al., 2016) [1]. We compared a list of sepsis causing pathogens to the ApoH binding data given to us by ApoH technologies. The data highlights the binding of ApoH beads to sepsis causing pathogens.

Entities:  

Year:  2017        PMID: 28560277      PMCID: PMC5440752          DOI: 10.1016/j.dib.2017.04.052

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table

Value of the data

The data demonstrates the value of using ApoH beads for pathogen enrichment in the original paper [1]. The data presented here will allow other researches to replicate these experiments and allow them to use the tools we used here in other similar contexts.

Data

The data presented in Table 2 supports the research article “A rapid, highly sensitive and culture-free detection of pathogens from blood by positive enrichment” [1].
Table 2

Suspected primary microbiologic pathogens in septic shock [5] and their binding to ApoH beads from the ApoH-CaptoBAC kit.

Table 1 shows a list of primers and probes used in the study [2], [3], [4]. These primers and probes have been used in qPCR experiments to quantify the pathogens from whole blood, after ApoH bead binding.
Table 1

Primers and probes used in the study. Numbers in square brackets indicate the references from where the sequence was taken.

Primer/Probe nameSequence
E. coli 16S rDNA – Forward [2]5′ – CCAGACTCCTACGGGAGGCAG – 3′
E. coli 16S rDNA – Reverse [2]5′ – CGTATTACCGCGGCTGCTG – 3′
E. gallinarum 16S rDNA – Forward [2]5′ – CCAGACTCCTACGGGAGGCAG – 3′
E. gallinarum 16S rDNA – Reverse [2]5′ – CGTATTACCGCGGCTGCTG – 3′
C.tropicalis 18S rDNA – Forward [3]5′ – CATTGCGCCCTTTGGTATTC – 3′
C.tropicalis 18S rDNA – Reverse [3]5′ – GTTGAGCAATACGCTAGGTTTG – 3′
E. coli tna rRNA – Forward [4], 126 bp amplicon5′ – GGGGCGGTGACGCAG– 3′
E. coli tna rRNA – Forward [4], 372 bp amplicon5′ – CATTACCATTCGTGTTATTG– 3′
E. coli tna rRNA – Reverse [4], 126 bp and 372 bp amplicon5′ –CCTGGTGAGTCGGAATGGTG– 3′
E. coli V3 Taqman Probe [2]VIC – 5′ – TTGACGTTACCCGCAGAAGAAGCA – 3′–BHQ
E. gallinarum V3 Taqman Probe [2]FAM – 5′ – TGGACGAAAGTCTGACCGAGCAAC– 3′–BHQ
C.tropicalis Taqman Probe [3]JOE– 5′ – TGAGCGTCATTTCTCCCTCAAACCC– 3′–BHQ
E. coli tna Taqman Probe [4]CY5– 5′ – CGATGATGCGCGGCG– 3′–BHQ
Primers and probes used in the study. Numbers in square brackets indicate the references from where the sequence was taken. Table 2 shows a list of sepsis causing pathogen [5] and their respective prevalence. The pathogens highlighted in yellow have been shown to bind with ApoH beads as listed in the ApoH technologies website (http://www.apohtech.com/index.php?id=2). Suspected primary microbiologic pathogens in septic shock [5] and their binding to ApoH beads from the ApoH-CaptoBAC kit.
Subject areaBiology
More specific subject areaMolecular Diagnostics
Type of dataTable
How data was acquiredTheoretical assessment
Data formatAnalyzed
Experimental factorsList of sepsis causing pathogens is obtained from the literature and the list of ApoH binding to pathogens is obtained from ApoH technologies web site. This information is based on experimental studies conducted by ApoH technologies.
Experimental featuresAn assessment was done to look at the % of sepsis causing pathogens that bind to ApoH beads, to determine the universality of the ApoH enrichment technology.
Data source locationThe data sources are listed in the References.
Data accessibilityWithin the data in brief article
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