Indexing & Abstracting Of Trends in Microbiology YEAR 2015 Published by LIBRARY & INFORMATION CENTRE INDIAN PHARMACOPOEIA COMMISSION Ministry of Health & Family Welfare Government of India

Until recently, the origin of the HIV-1 group M pandemic largely remained a scientific mystery. The use of comprehensive evolutionary analyses has revealed a unique story regarding viral migration, starting in the 1920s in Kinshasa, and the social and infrastructural changes associated with the early spread of this deadly virus. Cell-size maintenance: universal strategy revealed Suckjoon Jun, Sattar Taheri-Araghi Abstract How cells maintain a stable size has fascinated scientists since the beginning of modern biology, but has remained largely mysterious. Recently, however, the ability to analyze single bacteria in real time has provided new, important quantitative insights into this long-standing question in cell biology. Bridging the gap between viable but non-culturable and antibiotic persistent bacteria Mesrop Ayrapetyan, Tiffany C. Williams, James D. Oliver Abstract Microbial dormancy is a widespread phenomenon employed by bacteria to evade environmental threats including antibiotics. This intrinsic mechanism of antibiotic tolerance has drawn special attention to the role of dormancy in human disease, particularly in regards to recurrent infections. Two dormancy states, the viable but non-culturable state and bacterial persistence, both produce antibiotic-tolerant populations capable of withstanding prolonged lethal treatment. Currently described as two distinct forms of dormancy, they are rarely discussed in the same context. We argue here that these two dormant states are closely related phenomena which are part of a shared ‘dormancy continuum’. This discussion is intended to stimulate discourse about these seemingly different but very similar dormant states. Diversity and disease pathogenesis in Mycobacterium tuberculosis Digby F. Warner, Anastasia Koch, Valerie Mizrahi Abstract The increasing availability of whole-genome sequence (WGS) data for Mycobacterium tuberculosis, the bacterium that causes tuberculosis (TB), suggests that circulating genotypes have been molded by three dominant evolutionary forces: long-term persistence within the human population, which requires a core programme of infection, disease, and transmission; selective pressure on specific genomic loci, which provides evidence of lineage-specific adaptation to host populations; and drug exposure, which has driven the rapid emergence of resistant isolates following the global implementation of anti-TB chemotherapy. Here, we provide an overview of these factors in considering the implications of genotypic diversity for disease pathogenesis, vaccine efficacy, and drug treatment.