Insects as alternative hosts for phytopathogenic bacteria

Phytopathogens have evolved specialized pathogenicity determinants that enable them to colonize their specific plant hosts and cause disease, but their intimate associations with plants also predispose them to frequent encounters with herbivorous insects, providing these phytopathogens with ample opportunity to colonize and eventually evolve alternative associations with insects. Decades of research have revealed that these associations have resulted in the formation of bacterial-vector relationships, in which the insect mediates dissemination of the plant pathogen. Emerging research, however, has highlighted the ability of plant pathogenic bacteria to use insects as alternative hosts, exploiting them as they would their primary plant host. The identification of specific bacterial genetic determinants that mediate the interaction between bacterium and insect suggests that these interactions are not incidental, but have likely arisen following the repeated association of microorganisms with particular insects over evolutionary time. This review will address the biology and ecology of phytopathogenic bacteria that interact with insects, including the traditional role of insects as vectors, as well as the newly emerging paradigm of insects serving as alternative primary hosts. Also discussed is one case where an insect serves as both host and vector, which may represent a transitionary stage in the evolution of insect-phytopathogen associations.     

Regulation of the type III secretion system in phytopathogenic bacteria

The type III secretion system (TTSS) is a specialized protein secretion machinery used by numerous gram-negative bacterial pathogens of animals and plants to deliver effector proteins directly into the host cells. In plant-pathogenic bacteria, genes encoding the TTSS were discovered as hypersensitive response and pathogenicity (hrp) genes, because mutation of these genes typically disrupts the bacterial ability to cause diseases on host plants and to elicit hypersensitive response on nonhost plants. The hrp genes and the type III effector genes (collectively called TTSS genes hereafter) are repressed in nutrient-rich media but induced when bacteria are infiltrated into plants or incubated in nutrient-deficient inducing media. Multiple regulatory components have been identified in the plant-pathogenic bacteria regulating TTSS genes under various conditions. In Ralstonia solanacearum, several signal transduction components essential for the induction of TTSS genes in plants are dispensable for the induction in inducing medium. In addition to the inducing signals, recent studies indicated the presence of negative signals in the plant regulating the Pseudomonas syringae TTSS genes. Thus, the levels of TTSS gene expression in plants likely are determined by the interactions of multiple signal transduction pathways. Studies of the hrp regulons indicated that TTSS genes are coordinately regulated with a number of non-TTSS genes.     

Helper bacteria and pathogenicity assessments

In the field, pathogens exist in a diverse and dynamic ecological environment with other organisms (Blakeman, 1993; Preece & Dickinson, 1971). We tend to assume that these other organisms are 'benign' or perhaps in competition with the pathogen to occupy a particular niche. However, bacteria are often observed to be in close association with pathogens, as witnessed by the difficulty of eliminating them during isolation of pathogens involved in plant diseases. We now have clear evidence (Dewey et al ., pp. 489–497 in this issue) that they are sometimes neither benign, nor in competition, but actually helping the pathogen successfully infect its host even when the bacteria themselves are not pathogens of that host.     

Influence of subculturing some phytopathogenic bacteria on their carbohydrate utilizing profile

The capability of carbohydrate utilization shown by some freshly-isolated phytopathogenic bacteria (i.e. Pseudomonas syringae pv. syringae, Ps.s. pv. actinidiae, Ps.s. pv. lachrymans Ps. cichorii, Xanthomonas campestris pv. campestris ) was assessed by means of the API system and compared with that shown by the same isolates when they were subsequently subcultured for I week and for 1 month on nutrient agar and on the medium B of King et al. All isolates showed a differential capability of utilization during the subcultures of the laboratory culture media. In some cases, the utilization of some carbohydrates was not shown during the in vitro growth. On the other hand, the life on bacterial culture media induced the capability to utilize other carbohydrates. The need for standardization of recent techniques for the assessment of organic compound utilization is stressed.     

Visualization of pathogenicity regions in bacteria

We show here how pathogenicity islands can be analysed using GenomeAtlases, which is a method for visualising repeats, DNA structural characteristics, and base composition of chromosomes and plasmids. We have applied this method to the E. coliplasmid pO157, and the Y. pestisplasmid pPCP1. In both cases pathogenic genes were shown to differ in A+Tcontent and structural properties. Furthermore, examination of an antibiotic resistance gene cluster from S. typhimuriumshowed that the same was true for genes encoding antibiotic resistance.