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抗囊壁抗体和麦胚凝集素对蓝氏贾第鞭毛虫脱囊的抑制作用。

Inhibition of Giardia lamblia excystation by antibodies against cyst walls and by wheat germ agglutinin.

作者信息

Meng T C, Hetsko M L, Gillin F D

机构信息

Division of Infectious Diseases, Department of Medicine, University of California at San Diego Medical Center, 92103-8416, USA.

出版信息

Infect Immun. 1996 Jun;64(6):2151-7. doi: 10.1128/iai.64.6.2151-2157.1996.

Abstract

Although excystation is crucial to the initiation of infection by Giardia lamblia, little is known about the regulation of this important process. We have been able to reliably induce excystation in vitro by mimicking cyst passage through the stomach and upper small intestine by the exposure of in vitro-derived cysts to an acidic, reducing environment (stage I) followed by protease treatment at a slightly alkaline pH (stage II). Preexposure of cysts to polyclonal rabbit antiserum against purified cyst walls (PCWs) or to wheat germ agglutinin (WGA) inhibited excystation by > 90%. Adsorption of either ligand with PCWs eliminated inhibition, demonstrating specificity for cyst wall epitopes. Inhibition by WGA was reversed by either chitotriose or sialic acid, while inhibition by polyclonal antibodies against PCWs (anti-PCW) was reversed only by sialic acid, which also inhibited binding of both ligands to intact cysts and to cyst wall antigens in immunoblots. Binding of anti-PCW did not affect acidification of cyst cytoplasm during stage I. Exposure of cysts to anti-PCW and WGA prior to, but not after, stage II was sufficient to inhibit excystation, and inhibition could be partially reversed by increasing the protease concentration during stage II. A 7- to 10-fold higher proportion of WGA- and anti-PCW-treated cysts than control cysts remained intact after stage II. Our results suggest that these ligands, which bind cyst wall epitopes, inhibit excystation, most likely by interfering with proteolysis of cyst wall glycoproteins during stage II.

摘要

尽管脱囊对于蓝氏贾第鞭毛虫感染的起始至关重要,但对于这一重要过程的调控却知之甚少。我们已经能够通过模拟囊肿在胃和小肠上段的通过过程,可靠地在体外诱导脱囊,即让体外培养的囊肿先暴露于酸性、还原性环境(阶段I),随后在略碱性pH下进行蛋白酶处理(阶段II)。将囊肿预先暴露于针对纯化囊壁(PCW)的多克隆兔抗血清或麦胚凝集素(WGA)可使脱囊抑制率>90%。用PCW吸附任一配体均可消除抑制作用,证明对囊壁表位具有特异性。WGA的抑制作用可被壳三糖或唾液酸逆转,而针对PCW的多克隆抗体(抗PCW)的抑制作用仅被唾液酸逆转,唾液酸在免疫印迹中也抑制了两种配体与完整囊肿及囊壁抗原的结合。抗PCW的结合在阶段I期间不影响囊肿细胞质的酸化。在阶段II之前而非之后将囊肿暴露于抗PCW和WGA足以抑制脱囊,并且通过在阶段II期间增加蛋白酶浓度可部分逆转抑制作用。在阶段II之后,经WGA和抗PCW处理的囊肿比对照囊肿保持完整的比例高7至10倍。我们的结果表明,这些结合囊壁表位的配体抑制脱囊,很可能是通过在阶段II期间干扰囊壁糖蛋白的蛋白水解作用。

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