Phage P22-mutants with increased or decreased transduction abilities

Aromatic-dependent Salmonella typhimurium are non-virulent and effective as live vaccines

Hoiseth, S. K., & Stocker, B. A. D. (1981) · Nature · doi:10.1038/291238a0 · Cited by 2,078

Gut inflammation provides a respiratory electron acceptor for Salmonella

Winter, S. E., Thiennimitr, P., Winter, M. G., Butler, B. P., Huseby, D. L., Crawford, R. W., Russell, J. M., Bevins, C. L., Adams, L. G., Tsolis, R. M., et al. (2010) · Nature · doi:10.1038/nature09415 · Cited by 1,290

The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants

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Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota

Thiennimitr, P., Winter, S. E., Winter, M. G., Xavier, M. N., Tolstikov, V., Huseby, D. L., Sterzenbach, T., Tsolis, R. M., Roth, J. R., & Bäumler, A. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107857108 · Cited by 619

Genetic analysis of Salmonella enteritidis biofilm formation: critical role of cellulose

Solano, C., García, B., Valle, J., Berasain, C., Ghigo, J., Gamazo, C., & Lasa, I. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.02802.x · Cited by 554

Multicellular and aggregative behaviour of Salmonella typhimurium strains is controlled by mutations in the agfD promoter

Römling, U., Sierralta, W. D., Eriksson, K., & Normark, S. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.00791.x · Cited by 451

Pervasive domestication of defective prophages by bacteria

Bobay, L.-M., Touchon, M., & Rocha, E. P. C. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405336111 · Cited by 384

Plasmid-associated virulence of Salmonella typhimurium

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Construction of an ASD+ Expression-Cloning Vector: Stable Maintenance and High Level Expression of Cloned Genes in a Salmonella Vaccine Strain

Nakayama, K., Kelly, S. M., & Curtiss, R. (1988) · Nature Biotechnology · doi:10.1038/nbt0688-693 · Cited by 330

Expression of Salmonella typhimurium genes required for invasion is regulated by changes in DNA supercoiling

Galán, J. E., & Curtiss, R. (1990) · Infection and Immunity · doi:10.1128/iai.58.6.1879-1885.1990 · Cited by 295

Spontaneous tandem genetic duplications in Salmonella typhimurium arise by unequal recombination between rRNA (rrn) cistrons.

Anderson, P., & Roth, J. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.5.3113 · Cited by 288

Mechanism of head assembly and DNA encapsulation in Salmonella phage P22

Botstein, D., Waddell, C. H., & King, J. (1973) · Journal of Molecular Biology · doi:10.1016/0022-2836(73)90204-0 · Cited by 284

Real-Time Evolution of New Genes by Innovation, Amplification, and Divergence

Näsvall, J., Sun, L., Roth, J. R., & Andersson, D. I. (2012) · Science · doi:10.1126/science.1226521 · Cited by 282

Variable assortment of prophages provides a transferable repertoire of pathogenic determinants in Salmonella

Figueroa‐Bossi, N., Uzzau, S., Maloriol, D., & Bossi, L. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02234.x · Cited by 276

Isolation of a temperate bacteriophage encoding the type III effector protein SopE from an epidemic Salmonella typhimurium strain

Mirold, S., Rabsch, W., Rohde, M., Stender, S., Tschäpe, H., Rüssmann, H., Igwe, E., & Hardt, W.-D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.17.9845 · Cited by 256

Salmonella typhimurium Encodes a Putative Iron Transport System within the Centisome 63 Pathogenicity Island

Zhou, D., Hardt, W.-D., & Galán, J. E. (1999) · Infection and Immunity · doi:10.1128/iai.67.4.1974-1981.1999 · Cited by 182

Salmonella enterica Serovar Typhimurium Strains with Regulated Delayed Attenuation In Vivo

Curtiss, R., Wanda, S.-Y., Gunn, B. M., Zhang, X., Tinge, S. A., Ananthnarayan, V., Mo, H., Wang, S., & Kong, W. (2009) · Infection and Immunity · doi:10.1128/iai.00693-08 · Cited by 164

Simultaneous prevention of glutamine synthesis and high-affinity transport attenuates Salmonella typhimurium virulence

Klose, K. E., & Mekalanos, J. J. (1997) · Infection and Immunity · doi:10.1128/iai.65.2.587-596.1997 · Cited by 106

Regulation of heme biosynthesis in Salmonella typhimurium: activity of glutamyl-tRNA reductase (HemA) is greatly elevated during heme limitation by a mechanism which increases abundance of the protein

Wang, L. Y., Brown, L., Elliott, M., & Elliott, T. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.9.2907-2914.1997 · Cited by 52

Iron acquisition pathways and colonization of the inflamed intestine by Salmonella enterica serovar Typhimurium

Costa, L. F., Mol, J. P. S., Silva, A. P. C., Macêdo, A. A., Silva, T. M. A., Alves, G. E. S., Winter, S., Winter, M. G., Velazquez, E. M., Byndloss, M. X., et al. (2016) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2016.10.004 · Cited by 29

Reciprocally rewiring and repositioning the Integration Host Factor (IHF) subunit genes in Salmonella enterica serovar Typhimurium: impacts on physiology and virulence

Pozdeev, G., Beckett, M. C., Mogre, A., Thomson, N. R., & Dorman, C. J. (2022) · Microbial Genomics · doi:10.1099/mgen.0.000768 · Cited by 11