Survival of a bacterioferritin deletion mutant of Brucella melitensis 16M in human monocyte-derived macrophages.
AUTOR(ES)
Denoel, P A
RESUMO
A bacterioferritin (BFR) deletion mutant of Brucella melitensis 16M was generated by gene replacement. The deletion was complemented with a broad-host-range vector carrying the wild-type bfr gene, pBBR-bfr. The survival and growth of the mutant, B. melitensis PAD 2-78, were similar to those of its parental strain in human monocyte-derived macrophages (MDM). These results suggest that BFR is not essential for the intracellular survival of B. melitensis in human MDM.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=175622Documentos Relacionados
- Deletion of purE attenuates Brucella melitensis 16M for growth in human monocyte-derived macrophages.
- Lipoprotein lipase secretion by human monocyte-derived macrophages.
- Growth kinetics of human cytomegalovirus are altered in monocyte-derived macrophages.
- Fate of Chlamydia trachomatis in human monocytes and monocyte-derived macrophages.
- Beta interferon inhibits Toxoplasma gondii growth in human monocyte-derived macrophages.