Acinetobacter baumannii has become a clinical and epidemiological relevant microorganism word wide. Several studies reveal aspects important to this pathogen to cause infectious disease, such as membrane proteins apoptosisinducing, biofilm formation, resistance to oxidative stress, besides of their potential to acquire antimicrobial resistance genes. However, the mechanisms underlying the success of this pathogen remain of great interest. This study evaluated some pathogenicity factors presented by strains of Multidrug-Resistant (MDR) A. baumannii isolated from different clinical specimens of patients in Belo Horizonte city, Brazil. Genes associated to the capsule, biofilm, apoptosisinducing and quorum sensing were researched by Polymerase Chain Reaction. The hemolytic activity of the strains in six blood types from three different mammalian species (sheep, horse and human blood type A, B, O, AB, all Rh positive) and the sensitivity to oxidative stress by hydrogen peroxide occurred by disc diffusion test. In vitro apoptosis was evaluated in bone marrow macrophages obtained from BALB/c mice. Overall, patients had mean age of 60.6 years (± 17.6) and most of them (95%) were using some invasive device. All strains (29) were positive for gaiU and bap, 76% to wzc, 86% to luxI and 79% luxR, 45% to omp33 and 31% to ompA genes. In the oxidative stress test, 49% were more resistant (p<0.05) than the reference strains. In relation to in vitro tests, eight strains led to a significant reduction in the number of macrophages as compared to controls (p <0.05), among them 63% was positive to omp33 and ompA genes. The results show significant pathogenicity factors that contribute to the colonization and to the success of an infectious disease in hospitalized patients. Therefore, these data contributed to confirm the potential for aggression by these microorganisms, in addition to alerting to the need for constant improvements in nosocomial infection control protocols.