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离子载体类抗生素对艾美耳球虫作用阶段的研究。

Studies on the stage of action of ionophorous antibiotics against Eimeria.

作者信息

Long P L, Jeffers T K

出版信息

J Parasitol. 1982 Jun;68(3):363-71.

PMID:7097439
Abstract

Sporozoites of Eimeria tenella were treated with different anticoccidial drugs in vitro and their subsequent viability was tested by inoculating them into chicken embryos. Monensin, salinomycin, lasalocid, and arprinocid, at concentrations between 0.01 and 1.0 micrograms/ml, greatly reduced sporozoite viability as judged by mortality, hemorrhage and specific lesions in the embryo chorioallantois. Monensin was also effective in reducing the viability of sporozoites of E. mivati and E. tenella as judged by oocyst production occurring in embryos; activity of monensin was greater against E. tenella than against E. mivati. Monensin (0.1 mg) inoculated into embryos inhibited development of E. tenella. Oocysts which were produced in the presence of the drug sporulated normally and sporozoites obtained from them were fully infective. By initiating treatment of chickens with monensin at different times in relation to infection, it was shown that the drug exerts its anticoccidial effect on the primary invasive stage and on the gametogonous stage of E. tenella and E. necatrix. The effect of gametogony was tested by initiating infections with second generation merozoites of E. tenella. Significant reduction in oocyst production occurred in three of four strains of E. tenella tested. Medication with monensin initiated before merozoite inoculation was effective in inhibiting oocyst production, but medication starting 5 hr after merozoite inoculation was not. This differed from the effects of arprinocid and sulfaquinoxaline which were expressed both before and 5 hr after merozoite inoculation. The results show that the ionophorous anticoccidial drugs exert their anticoccidial action primarily against the invasive stages of Eimeria.

摘要

用不同的抗球虫药在体外处理柔嫩艾美耳球虫的子孢子,并通过将其接种到鸡胚中来检测其随后的活力。莫能菌素、盐霉素、拉沙洛西和阿普林诺昔,浓度在0.01至1.0微克/毫升之间,根据鸡胚绒毛尿囊膜的死亡率、出血和特定病变判断,大大降低了子孢子的活力。根据胚胎中卵囊的产生判断,莫能菌素在降低米氏艾美耳球虫和柔嫩艾美耳球虫子孢子的活力方面也有效;莫能菌素对柔嫩艾美耳球虫的活性比对米氏艾美耳球虫的活性更强。接种到胚胎中的莫能菌素(0.1毫克)抑制了柔嫩艾美耳球虫的发育。在药物存在下产生的卵囊正常孢子化,从它们获得的子孢子具有完全感染力。通过在与感染相关的不同时间用莫能菌素开始对鸡进行治疗,表明该药物对柔嫩艾美耳球虫和毒害艾美耳球虫的原发性侵入阶段和配子生殖阶段发挥抗球虫作用。通过用柔嫩艾美耳球虫的第二代裂殖子开始感染来测试配子生殖的效果。在测试的四株柔嫩艾美耳球虫中有三株卵囊产量显著降低。在裂殖子接种前开始用莫能菌素给药可有效抑制卵囊产生,但在裂殖子接种后5小时开始给药则无效。这与阿普林诺昔和磺胺喹恶啉的效果不同,它们在裂殖子接种前和接种后5小时均有作用。结果表明,离子载体类抗球虫药主要对艾美耳球虫的侵入阶段发挥抗球虫作用。

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