Traditionally, the Microsporidia were primarily studied in insects and fish. There were only a few human cases of microsporidiosis reported until the advent of AIDS, when the number of human microsporidian infections dramatically increased and the importance of these new pathogens to medicine became evident. Over a dozen different kinds of microsporidia infecting humans have been reported. While some of these infections were identified in new genera (Enterocytozoon, Vittaforma), there were also infections identified from established genera such as Pleistophora and Encephalitozoon. The genus Pleistophora, originally erected for a species described from fish muscle, and the genus Encephalitozoon, originally described from disseminated infection in rabbits, suggested a link between human infections and animals. In the 1980's, three Pleistophora sp. infections were described from human skeletal muscle without life cycles presented. Subsequently, the genus Trachipleistophora was established for a human-infecting microsporidium with developmental differences from species of the genus Pleistophora. Thus, the existence of a true Pleistophora sp. or spp. in humans was put into question. We have demonstrated the life-cycle stages of the original Pleistophora sp. (Ledford et al. 1985) infection from human muscle, confirming the existence of a true Pleistophora species in humans, P. ronneafiei Cali et Takvorian, 2003, the first demonstrated in a mammalian host. Another human infection, caused by a parasite from invertebrates, was Brachiola algerae (Vavra et Undeen, 1970) Lowman, Takvorian et Cali, 2000. The developmental stages of this human muscle-infecting microsporidium demonstrate morphologically what we have also confirmed by molecular means, that B. algerae, the mosquito parasite, is the causative agent of this human skeletal muscle infection. B. algerae had previously been demonstrated in humans but only in surface infections, skin and eye. The diagnostic features of B. algerae and P. ronneafiei infections in human skeletal muscle are presented. While Encephalitozoon cuniculi has been known as both an animal (mammal) and human parasite, the idea of human microsporidial infections derived from cold-blooded vertebrates and invertebrates has only been suggested by microsporidian phylogeny based on small subunit ribosomal DNA sequences but has not been appreciated. The morphological data presented here demonstrate these relationships. Additionally, water, as a link that connects microsporidial spores in the environment to potential host organisms, is diagrammatically presented.
The effect of CO2 increase on gas exchange and water-use effíciency (WUE) in three temperate deciduous species (Fagus crenata, Ginkgo biloba and Alnus firma) under gradually-developing drought-stress was assessed. Seedlings were grown within transparent open-top cabinets and maintained for 4 monťhs at mean CO2 concentrations of either 350 (ambient; C350) or 700 pmol moT’ (elevated; C700) and combined with five water regimes [leaf water potential, higher than -0.3 (well- watered), -0.5 and -0.8 (moderate drought), -1.0 and lower than -1.2 MPa (serious drought-stress)]. Increase in CO2 concentration induced a 60 % average increase in net photosynthetic rate (P^) under well-watered conditions. The effect of C700 became more pronounced with drought stress established, with an 80 % average increase in at as low as -0.8 MPa; leaf conductance to water vapour transfer (gs) and transpiration rate (£), however, were significantly decreased. Consequently, WUE increased under drought, through drought stress affected potential E sooner than potential P^. The interaction of CO2 x drought stress on WUE was significant in that Pn was stimulated while E in C700 enriched plants resembled that of C350 plants under drought. Hence if a doubling of atmospheric CO2 concentration occurs by the mid 2U* century, then greater P^ in F. crenata, G. biloba and^. firma may be expected and the drought susceptibility of these species will be substantially enhanced.
Relatively few effective compounds are available for treating microsporidiosis in humans. In this study, several compounds were assayed for activity against Encephalitozoon intestinalis (Cali, Kotier et Orenstein, 1993) and Vittaforina corneae Shadduck, Meccoli, Davis ct Font, 1990 in vitro. Of the benzimidazoles tested, albendazole was most effective and the MIC50 values were 8.0 ng/ml and 55.0 ng/ml for E. intestinalis and V. corneae, respectively. Fumagillin and its analogue, TNP-470 were nearly equally effective against both E. intestinalis and V. comeae. The MIC50 values of fumagillin were 0.52 ng/ml and 0.81 ng/ml, and the MIC5() values of TNP-470 were 0.35 ng/ml and 0.38 ng/ml for E. intestinalis and V. comeae, respectively. In addition, 12 of 44 purines and pteridines with putative tubulin binding activity that were synthesized at Southern Research Institute (SRI), inhibited microsporidia) replication by more than 50% at concentrations that were not toxic to the host cells. Several chitin synthesis/assembly inhibitors inhibited growth of the microsporidia in vitro but were toxic for the host cells making it difficult to interpret the results. One exception was Iufcnuron, which caused no significant toxicity to the host cells and expressed approximate MICS0 values of 2.95 pg/ml and 6.3 pg/ml against E. intestinalis and V. comeae, respectively. These results warrant further studies on albendazole, fumagillin, TNP-470, lufenuron, and the selected SRI purines and pteridines for developing therapeutic strategies for microsporidiosis.