ライフサイエンスコーパス: saprophyte

1 of a pathogenic bacterium from an avirulent saprophyte.

2 or circadian timing among both pathogens and saprophytes.

3 ndary metabolite production by these sessile saprophytes.

4 Hsf1 been conserved in this obligate animal saprophyte?

5 ase and alternates between a budding haploid saprophyte and a filamentous dikaryotic pathogen.

6 hich it alternates between a budding haploid saprophyte and a filamentous dikaryotic pathogen.

7 Sinorhizobium meliloti can live as a soil saprophyte and can engage in a nitrogen-fixing symbiosis

8 It is our opinion that Bt is not primarily a saprophyte and does not require the assistance of commen

9 Alternaria brassicicola is a successful saprophyte and necrotrophic plant pathogen.

10 sus because it is a ubiquitous environmental saprophyte and normal hosts are not commonly infected.

11 Aspergillus flavus is a common saprophyte and opportunistic pathogen that produces nume

12 Burkholderia pseudomallei is a soil-dwelling saprophyte and the causative agent of melioidosis, a lif

13 N. crassa is of course a saprophyte and there is no complete sequence available f

14 ionts and pathogens, SSPs also have roles in saprophytes and function in P. ostreatus as components o

15 foraging and long-distance communication in saprophytes and mycorrhizal fungi.

16 ngi from the genus Aspergillus are important saprophytes and opportunistic human fungal pathogens tha

17 obes called oomycetes include many important saprophytes and pathogens, with the latter exhibiting ne

18 athogen, B. thailandensis is a nonpathogenic saprophyte, and B. mallei is a host-restricted pathogen.

19 es; it is found in the soil as a free-living saprophyte, and it also lives as a nitrogen-fixing intra

20 dosis is infection caused by the flagellated saprophyte Burkholderia pseudomallei.

21 n Australia caused by the gram-negative soil saprophyte Burkholderia pseudomallei.

22 ggest that Coccidioides species are not soil saprophytes, but that they have evolved to remain associ

23 erstand cellodextrin utilization in the soil saprophyte Cellvibrio japonicus found that only one of f

24 diodies, which is believed to grow as a soil saprophyte in arid deserts.

25 e bacterium that replicates as a free-living saprophyte in the environment as well as a facultative i

26 s, while the mycelial phase exists only as a saprophyte in the soil.

27 al niches and has diverse lifestyle options (saprophyte, insect pathogen and plant symbiont), that re

28 s, but it has been assumed to be an innocent saprophyte; its potential role as a cause of lung diseas

29 es to bind fibronectin when expressed in the saprophyte, Leptospira biflexa.

30 rupting O-mannosylation in the nonpathogenic saprophyte Mycobacterium smegmatis and in the human path

31 ll mycobacteria, including the nonpathogenic saprophyte Mycobacterium smegmatis.

32 lays a role in the response to stress of the saprophyte Mycobacterium smegmatis.

33 fungal pathogen Candida albicans grows as a saprophyte on mucosal surfaces.

34 pathogen that can otherwise exist as a soil saprophyte or a plant endophyte.

35 P. fluorescens (a saprophyte) or hrp mutants defective in the Hrp secretio

36 ective in type III secretion, as well as the saprophyte Pseudomonas fluorescens A506, sensed water po

37 alysis of physiological changes of the plant saprophyte Pseudomonas putida following 6 h of attachmen

38 As free-living non-motile saprophytes, Streptomyces need to adapt to a wide range

39 ted only on rich media, whereas E. coli is a saprophyte that can grow on minimal media.

40 ngus Trichoderma virens is a ubiquitous soil saprophyte that has been applied as a biological control

41 Scedosporium prolificans is a soil saprophyte that is associated with a large variety of in

42 is caused by Malassezia spp, which are human saprophytes that sometimes switch from yeast to pathogen

43 enes from P. s. syringae 61 and confers upon saprophytes the ability to secrete HopPsyA in culture an

44 a variety of lifestyles ranging from aquatic saprophytes to invasive pathogens.

45 Here we show that M. robertsii mediates the saprophyte-to-insect pathogen transition through modulat

46 Corynebacterium striatum is a ubiquitous saprophyte with the potential to cause bacteremia in imm

47 es species are generally non-pathogenic soil saprophytes, yet within their genome we can find homolog