Pseudomonas are a topic that attracts researchers from all over the life sciences. These bacteria are nutritionally extraordinarily versatile and are colonizing a wide range of animated and inanimate niches which range from aquatic habitats, soil, and plants to animals and humans. Some species are major plant pathogens or significant causes of nosocomial infections in humans whereas others promote plant growth or degrade pollutants. Thus, the Pseudomonas conferences have become a venue for researchers from many disciplines who usually will not meet each other during their academic career.

The Pseudomonas conferences belong to the few regular events that are solely organized by individuals and not by any institution. Initially held as an EMBO workshop in 1986, the Pseudomonas conferences have become a regular biennial event that is hosted by a dedicated Pseudomonas researcher and his local team (Table 1). Many, but not all, conferences were supported by learned societies. Conference proceedings have been published as monographs or – more often – topics emerging at the conferences were presented as primary research papers in Special Issues of, e.g., FEMS Microbiology Letters or Environmental Microbiology.

During the first decade almost, equal shares of contributions were allocated to Pseudomonas aeruginosa , Pseudomonas fluorescens , Pseudomonas putida , Pseudomonas syringae , and ‘other pseudomonads,’ after that, the type species P. aeruginosa was becoming more and more dominant. First, the rare pseudomonads were getting exotic followed by the P. syringae pathovars with only a minority of P. putida and P. fluorescens research finally persisting in the mainstream centered around topics on P. aeruginosa . In parallel, the meetings were going more and more medical driven by P. aeruginosa being a model organism to study chronic biofilm infections. The focus shifted to pathogenicity, virulence, antimicrobial resistance and infectious disease in man.

Although the P. aeruginosa infections in cystic fibrosis airways are the author’s hobby horse, I miss the multidisciplinary character of the early conferences. The first meeting in Geneva has been and still is my favorite. Within the nutshell of Pseudomonas , I became confronted with fascinating stuff from all white, green and red biology ranging from Pseudomonas plant pathogens in the mountains of Hawaii, the monitoring of released recombinant bacteria in some remote river in Saskatchewan, amazing metabolizers of halogenated hydrocarbons in polluted soils to the structure-function analysis of exotoxin A.

Genome biology has also been a long-running topic. Initial chromosome maps were generated by genetic mapping of markers exploiting the natural mechanisms of gene exchange of bacteria, i.e., transduction, transformation and conjugation, followed by the construction of low-resolution physical maps in the early 1990s and finally by whole genome sequencing. A highlight at the Maui meeting in 1999 was the presentation of the P. aeruginosa PAO1 genome sequence. Thereafter, the genome sequences of reference strains of other relevant Pseudomonas taxa and the diversity of the accessory genome regarding mobile genomic islands were investigated. With the advent of second-generation sequencing technologies about ten years ago, genomics could speed up. Pangenomes were constructed, and population genomics scanned genome diversity – globally or in specific niches with antimicrobial resistance and the microevolution of P. aeruginosa in cystic fibrosis airways being significant topics of interest.

Signaling and social microbiology emerged in the mid-1990s. Starting with homoserine and quinolone signaling, more and more complex signaling networks were elucidated over the years. Highlights of the 2000 – 2010 conferences were the discoveries of regulatory non-coding RNAs and c-di-GMP and GacS/GacA/rsmZ signal transduction pathways. For example, genome-wide transcriptional profiling resolved a signaling network that reciprocally regulates genes associated with acute infection and chronic persistence in P. aeruginosa . I would like to conclude my overview of the history of the Pseudomonas conference with a tribute to a plasmid (and thus to Ken Timmis, Juan Ramos, and Victor de Lorenzo and colleagues who organized the first conference in Geneva): the TOL plasmid. TOL allows mineralization of toluene and m-xylene. During biodegradation, an intermediate is synthesized and converted into a toxic dead-end product. The Pseudomonas researchers have resolved the transcriptional control circuit how the cells protect themselves from generating this harmful compound.