7 research outputs found
Correction: A New Bacillus anthracis Found in Wild Chimpanzees and a Gorilla from West and Central Africa
A New Bacillus anthracis Found in Wild Chimpanzees and a Gorilla from West and Central Africa
Neighbour-Joining Phylogenetic Tree of the (A) <i>gyrB</i> (1,159-bp) and (B) <i>rpoB</i> (700-bp) Genes
<p>The B. anthracis strains CI and CA are marked by the box. Analyses were carried out following the procedure described by others [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.0020008#ppat-0020008-b011" target="_blank">11</a>,<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.0020008#ppat-0020008-b012" target="_blank">12</a>]. The trees were statistically evaluated with a bootstrap analysis with 1,000 bootstraps. Only relevant bootstrap values above 70% are shown for major branches.</p
Multilocus VNTR-Analysis–Based Dendrogram
<p>Eight VNTR loci were analyzed following standard protocols [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.0020008#ppat-0020008-b006" target="_blank">6</a>]. The amplification products were analyzed by DNA sequencing and compared with 89 B. anthracis reference strains [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.0020008#ppat-0020008-b004" target="_blank">4</a>] processed with Sequence Type Analysis and Recombinational Tests (START) software (K. Jolley, University of Oxford). A, B. anthracis phylogenetic group A; B, B. anthracis phylogenetic group B [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.0020008#ppat-0020008-b007" target="_blank">7</a>]; F, the newly discovered B. anthracis group from sub-Saharan rainforests including the strains B. anthracis CI and CA.</p
Hereditary Apolipoprotein AI-Associated Amyloidosis in Surgical Pathology Specimens: Identification of Three Novel Mutations in the APOA1 Gene
Apolipoprotein AI-derived (AApoAI) amyloidosis may present either as a non-hereditary form with wild-type protein deposits in atherosclerotic plaques or as a hereditary form due to germline mutations in the APOA1 gene. Currently, more than 50 apoAI variants are known, and 13 are associated with amyloidosis. We describe six patients with AApoAI amyloidosis due to APOA1 germline mutations that affect the larynx, small intestine, large intestine, heart, liver, kidney, uterus, ovary, or pelvic lymph nodes. In each patient, the amyloid showed a characteristic apple green birefringence when viewed under polarized light after Congo red staining and was immunoreactive with antibodies against apoAI. Sequence analyses revealed one known (p.Leu75Pro) and three novel APOA1 mutations that included gene variations leading to two different frameshifts (p.Asn74fs and p.Ala154fs) and one amino acid exchange (p.Leu170Pro). These three novel mutations extend our knowledge about both the location of the mutations and the organ distribution in hereditary AApoAI amyloidosis. Thirteen of the now sixteen amyloidogenic mutations are localized in two hot-spot regions that span residues 50 to 93 and 170 to 178. The organ distribution and clinical presentation of AApoAI amyloidosis seems to depend on the position of the mutation. Patients with alterations in codons 1 to 75 mostly develop hepatic and renal amyloidosis, while carriers of mutations in residues 173 to 178 mainly suffer from cardiac, laryngeal, and cutaneous amyloidosis