A Theorem on Matroid Homomorphism

This note generalizes a result contained in a previous paper [ J. Sanders, Circuit preserving edge maps II, J. Combin. Theory Ser. B 42 (1987), 146-155].Comment: 5 pages, 0 figure

Supplementary tables from Type X strains of <i>Toxoplasma gondii</i> are virulent for southern sea otters (<i>Enhydra lutris nereis)</i> and present in felids from nearby watersheds

Table S1. Selected loci used for genotyping Toxoplasma gondii isolates obtained from brains of infected sea otters (n=135) in California between 1998-2015.; Table S2. Univariable analysis for risk factors associated with sea otter (n=116) deaths due to Toxoplasma gondii infection as a primary cause.; Table S3. Univariable analysis for risk factors associated with presence of Type X RFLP Toxoplasma gondii genotype in sea otters (n=135)

LC-MS/MS spectral counts of functionally interesting proteins identified in sporocyst/sporozoite fractions of <i>Toxoplasma gondii</i> oocysts – SRS family proteins.

<p>LC-MS/MS spectral counts of functionally interesting proteins identified in sporocyst/sporozoite fractions of <i>Toxoplasma gondii</i> oocysts – SRS family proteins.</p

LC-MS/MS spectral counts of functionally interesting proteins identified in sporocyst/sporozoite fractions of <i>Toxoplasma gondii</i> oocysts – other proteins of interest.

<p>LC-MS/MS spectral counts of functionally interesting proteins identified in sporocyst/sporozoite fractions of <i>Toxoplasma gondii</i> oocysts – other proteins of interest.</p

Data S1 from Type X strains of <i>Toxoplasma gondii</i> are virulent for southern sea otters (<i>Enhydra lutris nereis)</i> and present in felids from nearby watersheds

Molecular characterization results for assessing genetic diversity of Toxoplasma gondii isolates (N=29

Supplementary data 2 from Type X strains of <i>Toxoplasma gondii</i> are virulent for southern sea otters (<i>Enhydra lutris nereis)</i> and present in felids from nearby watersheds

Detailed genotyping results categorized by RFLP and MLST for Toxoplasma gondii isolates obtained from southern sea otter (N=135

LC-MS/MS spectral counts of most abundantly detected proteins in <i>Toxoplasma gondii</i> oocyst wall fractions showing spectral counts (% of all spectral counts) in each experimental group.

<p>LC-MS/MS spectral counts of most abundantly detected proteins in <i>Toxoplasma gondii</i> oocyst wall fractions showing spectral counts (% of all spectral counts) in each experimental group.</p

Summary of LC-MS/MS spectral counts and protein identification in sporocyst/sporozoite and oocyst wall fractions of <i>Toxoplasma gondii</i> oocysts.

<p>Summary of LC-MS/MS spectral counts and protein identification in sporocyst/sporozoite and oocyst wall fractions of <i>Toxoplasma gondii</i> oocysts.</p

LC-MS/MS spectral counts of abundantly detected proteins in <i>Toxoplasma gondii</i> sporocyst/sporozoite fractions.

<p>LC-MS/MS spectral counts of abundantly detected proteins in <i>Toxoplasma gondii</i> sporocyst/sporozoite fractions.</p

The <i>Toxoplasma gondii</i> oocyst and sporocyst walls are autofluorescent under UV excitation.

<p>A. Epifluorescent and bright field images of intact, mature oocysts 10 days after exposure to maturing conditions showing intact oocysts (“oocyst”), isolated sporocysts (“sporocyst”), and isolated oocyst walls (“wall”), the latter two fractions being derived from mature oocysts by glass bead disruption and gradient centrifugation as detailed in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0029955#s4" target="_blank">materials and methods</a>. B. A detailed schematic of the oocyst components illustrating the absence of the outer layer of the oocyst wall (ow) following treatment with bleach. The inner layer of the wall (iw) and sporocyst walls (Spw) remain intact following bleach treatment. The mature oocyst contains two sporocysts, each with 4 sporozoites (spz).</p