ライフサイエンスコーパス: Neospora

1 cally Plasmodium, Toxoplasma, Leishmania and Neospora.

2 ful in determining the zoonotic potential of Neospora.

3 Neospora 2001 was held, 13-15 September 2001, at the Mor

4 stainable control measures were discussed at Neospora 2001.

5 m Neospora-infected mice proliferate to both Neospora and Toxoplasma antigens in vitro and secrete su

6 picomplexan parasites, including Plasmodium, Neospora, and Eimeria, no genetic evidence of its contri

7 SA format and was not inhibited by sera from Neospora antibody-negative cows.

8 rm of SECIS element in Toxoplasma gondii and Neospora canine, single-celled apicomplexan parasites of

9 The routine diagnosis of Neospora caninum abortion is based upon histopathologic

10 y expressed by coccidian parasites including Neospora caninum and Eimeria tenella.

11 Neospora caninum and Hammondia heydorni are two coccidia

12 osure to canine parvovirus, Ehrlichia canis, Neospora caninum and perhaps rabies virus, but not with

13 Holstein cattle experimentally infected with Neospora caninum develop parasite-specific CD4+ cytotoxi

14 tion in dogs in 1984, the protozoan parasite Neospora caninum has been found to infect a wide range o

15 rom researching the vertical transmission of Neospora caninum in cattle that the terms 'vertical', 'c

16 Bovine abortions due to Neospora caninum infection are a major cattle-production

17 Neospora caninum is a coccidial protozoan parasite that

18 The protozoan Neospora caninum is a primary infectious cause of aborti

19 Neospora caninum is an apicomplexan parasite responsible

20 Neospora caninum is an apicomplexan parasite that is clo

21 Neospora caninum is an obligate intracellular protozoan

22 Infection with the protozoan parasite Neospora caninum is emerging as a major cause of reprodu

23 Cattle infected with Neospora caninum readily experience transplacental paras

24 e would decrease the frequency of congenital Neospora caninum transmission.

25 es that are thought to be protective against Neospora caninum would be detrimental to the pregnancy.

26 e (Eimeria tenella, Sarcocystis neurona, and Neospora caninum).

27 Neospora caninum, a causative agent of bovine abortions,

28 pulations for detection of serum antibody to Neospora caninum, a major cause of bovine abortion.

29 Neospora caninum, a protozoan parasite closely related t

30 tablished a system specifically designed for Neospora caninum, and used this system as a heterologous

31 hin pathways/networks for Toxoplasma gondii, Neospora caninum, Cryptosporidium and Theileria species,

32 xiella burnetii, Francisella tularensis, and Neospora caninum, estimate concentrations of persistent

33 used by the intracellular protozoan parasite Neospora caninum, is fatal when there is a complete lack

34 PCR test did not amplify Toxoplasma gondii, Neospora caninum, Leishmania infantum, Cryptosporidium p

35 erinary interest, including Eimeria tenella, Neospora caninum, Plasmodium falciparum, Sarcocystis neu

36 In contrast, a closely related apicomplexan, Neospora caninum, was unable to inhibit IFN-gamma-induce

37 lly diverse Toxoplasma strains but also with Neospora caninum, which is closely related to Toxoplasma

38 th the closely related apicomplexan parasite Neospora caninum.

39 oplasma gondii is also true for its relative Neospora caninum.

40 of protection against congenital transfer of Neospora caninum.

41 he emerging or re-emerging parasites such as Neospora, Cryptosporidium and Cyclospora.

42 outhern blots of amplification products from Neospora DNA but not to Southern blots with amplified DN

43 In addition, Neospora DNA was amplified from the brain, heart, and lu

44 Vaccine-induced protection was Neospora dose dependent.

45 antigens with sera from cows with confirmed Neospora-induced abortion revealed at minimum 14 major a

46 ominant antigens recognized by antisera from Neospora-infected animals.

47 recognized consistently and specifically by Neospora-infected cattle.

48 igen was consistently inhibited by sera from Neospora-infected cows in a CI-ELISA format and was not

49 The CD8+ T cells from Neospora-infected mice proliferate to both Neospora and

50 ide an effective method for the detection of Neospora infection in fetuses and dams from nonhuman pri

51 nd immunohistochemistry for the diagnosis of Neospora infections in bovine or primate fetuses.

52 This article discusses how Neospora invades cells, how it infects and causes diseas

53 Neospora is a newly recognized genus of pathogenic cocci

54 Neospora is a newly recognized Toxoplasma-like cyst-form

55 with culture-derived tachyzoites of a bovine Neospora isolate, and tissue samples from various major

56 AAL also binds to Hammondia and Neospora nuclei but not to more distantly related apicom

57 n the pathogenesis seen among Toxoplasma and Neospora parasite strains.

58 of whole blood or amniotic fluid spiked with Neospora parasites.

59 In addition, Neospora PCR products were successfully amplified from w

60 genera Cryptosporidium, Giardia, Leishmania, Neospora, Plasmodium, Toxoplasma, Trichomonas and Trypan

61 ular techniques, we show that Toxoplasma and Neospora possess both canonical and noncanonical SECIS e

62 A Neospora-specific chemiluminescent probe hybridized to S

63 ducts were confirmed by hybridization with a Neospora-specific DNA probe.

64 Protected mice had significantly decreased Neospora-specific IgG1 compared with nonmodulated mice.

65 of the small-subunit rRNA gene sequences of Neospora spp. and other apicomplexa coccidia, oligonucle

66 sequence differed from that of the probe for Neospora spp. by a single base pair was used to distingu

67 The PCR system detected as few as one Neospora tachyzoite in the culture medium or five tachyz

68 their different host ranges, Toxoplasma and Neospora use a conserved mechanism to co-opt these host