Table 1.
Summary of Marburg virus diagnostic test results for samples sent to CDC from patients A and B.
Table 2.
Summary of species, gender and age of all bats captured and tested from the August 2007 and April–May 2008 collections.
Table 3.
Summary of all Marburg virus positive bats in each collection period.
Figure 1.
Immunohistochemical localization of Marburg virus antigens in Roussetus aegypticus tissues.
In the liver, viral antigens were distributed in and around hepatocytes in a dense (A) or loose (B) perimembranous pattern. Rarely, entire hepatocytes were involved (C). These infected foci were characteristically sparse and were often associated with small collections of mononuclear inflammatory cells and hepatocyte necrosis (D and E), although infected cells could also be identified without conspicuous inflammatory infiltrates. Only rare viral antigens were seen in a few mononuclear cells of the spleen of 1 bat (F). Immunoalkaline phosphatase with napthol fast-red and hematoxylin counterstain (A–C, E, F), and hematoxylin and eosin (D); original magnifications ×100 (A, B, D, E) and ×258 (C, F).
Figure 2.
Phylogenetic analysis of full-length or partial genomes of Marburg viruses isolated from humans or bats (see Table S1 for Genbank accession numbers).
Trees shown are maximum-likelihood analyses with Bayesian posterior probabilities >50 listed at the appropriate nodes. The ebolavirus outgroup used during the Bayesian phylogenetic analyses are denoted by the small twig at the root of the tree. Marburg virus sequences from 2007 human cases in Uganda are in green, while those from bats are listed in red. (A) Analysis of full-length genomes of five Marburg virus bat isolates, 18 historical isolates, and the isolates from patients A and B (01Uga07 and 02Uga07 respectively). (B) Phylogenetic analysis of concatenated NP and VP35 sequence fragments obtained from each bat specimen compared to corresponding regions from 48 historical isolates and those from 01Uga07 and 02Uga07.