ライフサイエンスコーパス: S. hyodysenteriae

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1 However, if both motile bacteria and S. hyodysenteriae migrated in the cut, the motile bacter

2 al to those of digested chromosomal DNA from S. hyodysenteriae.

3 The LPS and endotoxin extracts from S. hyodysenteriae induced a dose-dependent expression of

4 d agar, thereby saving time and media; (iii) S. hyodysenteriae could sometimes be isolated free of ot

5 Treatment of intact S. hyodysenteriae with different concentrations of digit

6 tivated flagellar genes were introduced into S. hyodysenteriae, and allelic exchange at the targeted

7 sliced agar was more effective in isolating S. hyodysenteriae from swine with chronic diarrhea and n

8 fied bacteriophages induced from cultures of S. hyodysenteriae A203 (deltaflaA1 593-762::cat) were ad

9 te that induced VSH-1 virions package DNA of S. hyodysenteriae and are capable of transferring host g

10 otein purified from the membrane fraction of S. hyodysenteriae.

11 Migration of S. hyodysenteriae from the central streak was apparent b

12 ence of cecal lesions and the persistence of S. hyodysenteriae in the gut.

13 etic carriers of SD in which the shedding of S. hyodysenteriae was low.

14 lonization, we constructed a novel strain of S. hyodysenteriae which is deficient in both FlaA1 and F

15 has been designated VSH-1 (VSH for virus of S. hyodysenteriae).

16 If only S. hyodysenteriae migrated in the cut, they migrated to

17 f the cut where they formed colonies and the S. hyodysenteriae located along the edges of the cut bet

18 traction for the serpentine movement of the S. hyodysenteriae and for the flagellar movement of the

19 ents hybridized with probes complementary to S. hyodysenteriae chromosomal genes nox and flaA1.

20 Although motile bacteria were present where S. hyodysenteriae located, the growth of the motile bact

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