Fites J Scott, Reinert Laura K, Chappell Timothy M, Rollins-Smith Louise A
Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, USA.
Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Infect Immun. 2014 Nov;82(11):4698-706. doi: 10.1128/IAI.02231-14. Epub 2014 Aug 25.
Amphibians are suffering unprecedented global declines. A leading cause is the infectious disease chytridiomycosis caused by the chytrid fungus Batrachochytrium dendrobatidis. Chytridiomycosis is a skin disease which disrupts transport of essential ions leading to death. Soluble factors produced by B. dendrobatidis impair amphibian and mammalian lymphocytes in vitro, but previous studies have not shown the effects of these inhibitory factors in vivo. To demonstrate in vivo inhibition of immunity by B. dendrobatidis, a modified delayed-type-hypersensitivity (DTH) protocol was developed to induce innate and adaptive inflammatory swelling in the feet of Xenopus laevis by injection of killed bacteria or phytohemagglutinin (PHA). Compared to previous protocols for PHA injection in amphibians, this method induced up to 20-fold greater inflammatory swelling. Using this new protocol, we measured DTH responses induced by killed bacteria or PHA in the presence of B. dendrobatidis supernatants. Swelling induced by single injection of PHA or killed bacteria was not significantly affected by B. dendrobatidis supernatants. However, swelling caused by a secondary injection of PHA, was significantly reduced by B. dendrobatidis supernatants. As previously described in vitro, factors from B. dendrobatidis appear to inhibit lymphocyte-mediated inflammatory swelling but not swelling caused by an inducer of innate leukocytes. This suggests that B. dendrobatidis is capable of inhibiting lymphocytes in a localized response to prevent adaptive immune responses in the skin. The modified protocol used to induce inflammatory swelling in the present study may be more effective than previous methods to investigate amphibian immune competence, particularly in nonmodel species.
两栖动物正遭受着前所未有的全球性数量减少。一个主要原因是由壶菌Batrachochytrium dendrobatidis引起的传染病——蛙壶菌病。蛙壶菌病是一种皮肤病,它会干扰必需离子的运输,导致死亡。B. dendrobatidis产生的可溶性因子在体外会损害两栖动物和哺乳动物的淋巴细胞,但之前的研究尚未表明这些抑制因子在体内的作用。为了证明B. dendrobatidis在体内对免疫的抑制作用,开发了一种改良的迟发型超敏反应(DTH)方案,通过注射死细菌或植物血凝素(PHA)在非洲爪蟾的足部诱导先天性和适应性炎症肿胀。与之前在两栖动物中注射PHA的方案相比,这种方法诱导的炎症肿胀高达20倍。使用这个新方案,我们测量了在存在B. dendrobatidis上清液的情况下,由死细菌或PHA诱导的DTH反应。单次注射PHA或死细菌诱导的肿胀不受B. dendrobatidis上清液的显著影响。然而,二次注射PHA引起的肿胀被B. dendrobatidis上清液显著降低。如之前在体外所描述的,来自B. dendrobatidis的因子似乎抑制淋巴细胞介导的炎症肿胀,但不抑制由先天性白细胞诱导剂引起的肿胀。这表明B. dendrobatidis能够在局部反应中抑制淋巴细胞,以防止皮肤中的适应性免疫反应。本研究中用于诱导炎症肿胀的改良方案可能比以前的方法更有效地研究两栖动物的免疫能力,特别是在非模式物种中。