ライフサイエンスコーパス: S. enteritidis

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1 S. enteritidis was found to attach specifically to fibro

2 S. enteritidis was isolated from 8 of 226 ice cream prod

3 chi3985 induced excellent protection against S. enteritidis in chickens.

4 comprises a positive selection step against S. enteritidis and a negative selection step against a m

5 capable of detecting DNA polymorphisms among S. enteritidis isolates.

6 vidence that SEF14 fimbriae are expressed by S. enteritidis in vivo, previous studies showed that SEF

7 arried nonpasteurized liquid eggs containing S. enteritidis.

8 highly selective and can successfully detect S. enteritidis down to 600 CFU mL(-1) (equivalent to 18

9 as Salmonella enterica serotype Enteritidis (S. enteritidis) and Escherichia coli O157:H7, has genera

10 Salmonella enterica serotype Enteritidis (S. enteritidis) is a major food-borne pathogen, and its

11 in Salmonella enterica serovar Enteritidis (S. enteritidis) and closely related serovars, suggesting

12 lation for S. enteritidis LPS as well as for S. enteritidis LPS purchased from Sigma Chemical Co., th

13 nts the published level of glucosylation for S. enteritidis LPS as well as for S. enteritidis LPS pur

14 le, rapid, and powerful subtyping method for S. enteritidis.

15 with a 14-kDa fimbrial protein isolated from S. enteritidis (68% reduction in attachment).

16 other Salmonella enterica serovars including S. enteritidis and S. dublin can also kill C. elegans.

17 it from other Salmonella species, including S. enteritidis and S. choleraesuis.

18 aptamers, twelve rounds of selection to live S. enteritidis and S. typhimurium were performed, altern

19 We defined an outbreak-associated case of S. enteritidis infection as one in which S. enteritidis

20 acture of ice cream associated with cases of S. enteritidis infection were compared with those of pro

21 amers have the capacity to inhibit growth of S. enteritidis and S. typhimurium in bacterial cultures;

22 play significant roles in the interaction of S. enteritidis with granulosa cells.

23 rvations indicated that clinical isolates of S. enteritidis are highly heterogeneous in their ability

24 Eight isolates of S. enteritidis phage type 8 that failed to be discrimina

25 as used to examine a panel of 29 isolates of S. enteritidis which had been previously characterized b

26 n extensive analysis of clinical isolates of S. enteritidis, demonstrate the complex nature of Salmon

27 ence characteristics of clinical isolates of S. enteritidis, we determined the 50% lethal doses (LD(5

28 ght and transmission electron micrographs of S. enteritidis invasion of granulosa cells showed organi

29 f the chicken ovaries by invasive strains of S. enteritidis.

30 ssential for efficient uptake or survival of S. enteritidis in macrophages.

31 ng methods for the epidemiological typing of S. enteritidis.

32 against challenge with S. typhimurium F98 or S. enteritidis 27A PT 8 in birds from vaccinated hens an

33 Results of this study demonstrated that S. enteritidis interacts with granulosa cells in a speci

34 We estimate that S. enteritidis gastroenteritis developed in 224,000 pers

35 pool showing the highest binding affinity to S. enteritidis, a DNA sequence of high affinity to the b

36 This RAPD approach to S. enteritidis subtyping provided more discriminatory po

37 selection of highly specific DNA aptamers to S. enteritidis and S. typhimurium.

38 of S. enteritidis infection as one in which S. enteritidis was cultured from a person who became ill

39 not confer protection against challenge with S. enteritidis, presumably because lpf phase-off variant

40 IFN-gamma +/+ mice following injection with S. enteritidis LPS, despite sustaining 11-fold reduction

41 l of 65 arbitrary primers were screened with S. enteritidis isolates of different phage types.

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