14 research outputs found

    Main outcomes by triatomine-exposed and -unexposed area (n = 336).

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    <p>Numbers may be small than the total due to missing data. Triatomine exposed areas were surveyed in summer, triatomine unexposed in winter, which may contribute to the observed differences.</p><p>n.a. =  not applicable, since persons in the control region were not asked to collect insects.</p>*<p>Comparing exposed versus non exposed populations.</p>†<p>rashes, red or itchy spots on the body,</p>#<p>waking up at night or the morning feeling dizzy, sick, having swollen eyes or difficulties breathing.</p>§<p>Only one specimen per insect species listed per study participant.</p

    Characteristics of persons participating in a door-to-door survey in selected areas in Southern California, 2009.

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    <p>SD = standard deviation. Numbers may slightly differ from the total due to missing data. IQR = interquartile range.</p>*<p>including lizards, birds, rat, rabbits, reptiles, snake, chicken, hamster, tortoise, in addition to cats and dogs.</p

    Comparison of persons with and without self-reported symptoms matching those typical for allergies to triatomine bites in triatomine-exposed areas (n = 221).

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    <p>Tally may be slightly lower than the total due to missing data.</p>†<p>rashes, red or itchy spots on the body, waking up at night or the morning feeling dizzy, sick, having swollen eyes or difficulties breathing.</p

    Alignment of MPER sequence variants from all subjects described in this study.

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    <p>Sequences are aligned against HXB2 and a subtype C consensus sequence derived from the 2007 LANL database. Numbering is based on HXB2. MSD denotes start of the Membrane Spanning Domain. Consensus residues are color-coded by degree of conservation (red >98%, orange 90–97.9%, yellow 75–89.9%, green <75%). In panel A, IC<sub>50</sub> for mAb 4E10 is expressed as a range for all functional clones tested for each MPER variant. Positions 677, 680, 683, and 686 are color-coded for emphasis. In Panel B, Env protein sequences have been color-coded according to charge at positions 677, 680, and 683 (blue = basically charged residue, yellow = uncharged residue). All other residues (in white) are uncharged.</p

    Maximum likelihood trees of region gp160, PL samples obtained previous to BM samples.

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    <p>All trees were calculated under the GTR+G+I model, rooted with 4 subtype C reference sequences obtained from LANL sequence database. In all subjects, HIV-1 RNA sequences from the left breast (white circles) and from the right breast (gray circles) were intermixed. The scale at the bottom left of each tree corresponds to the number of substitutions per site (for example, 0.01 = 1 substitution per 100 sites).</p

    Maximum likelihood trees of region gp160, PL and BM samples obtained contemporaneously.

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    <p>All trees were calculated under the GTR+G+I model, rooted with 4 subtype C reference sequences obtained from LANL sequence database. In all subjects, HIV-1 RNA sequences from the left breast (white circles) and from the right breast (gray circles) were intermixed. The scale at the bottom left of each tree corresponds to the number of substitutions per site (for example, 0.01 = 1 substitution per 100 sites).</p

    Diversity and divergence in breast milk and plasma.

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    <p>(<b>A</b>) Comparing mean diversity of virus in breast milk and plasma HIV-1 RNA gp160 sequences of contemporaneously sampled subjects. Triangles  =  plasma, circles  =  breast milk; star  =  significant difference between plasma and breast milk diversity, p-values from Wilcoxon rank sums test. (<b>B</b>) Comparing diversity in breast milk and plasma in all contemporaneously sampled patients in aggregate, using Gilbert, Rossini, and Shankarappa's method for comparing intra-individual genetic sequence diversity between populations. Black lines are means. (<b>C</b>) Comparison of mean divergence of virus in BM and PL within contemporaneously sampled subjects. P-values from Wilcoxon rank sums test. (<b>D</b>) Comparison of viral divergence between the BM and PL of all contemporaneously sampled subjects in aggregate. P-value obtained using a GEE model. Black lines are means.</p
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