Rodríguez-Tovar Luis E, Villarreal-Marroquín Alejandra, Nevárez-Garza Alicia M, Castillo-Velázquez Uziel, Rodríguez-Ramírez Heidi G, Navarro-Soto Magda C, Zárate-Ramos Juán J, Hernández-Vidal Gustavo, Trejo-Chávez Armando
Cuerpo Académico de Zoonosis y Enfermedades Emergentes (Rodríguez, Villarreal, Nevárez, Castillo, Rodríguez, Navarro, Trejo), Department of Immunology, FMVZ-UANL, Campus de Ciencias Agropecuarias, General Escobedo, Nuevo León, Mexico.
Cuerpo Académico de Epidemiología Veterinaria (Zarate), Department of Immunology, FMVZ-UANL, Campus de Ciencias Agropecuarias, General Escobedo, Nuevo León, Mexico.
J Vet Diagn Invest. 2017 May;29(3):269-277. doi: 10.1177/1040638716668559. Epub 2017 Feb 16.
Encephalitozoon cuniculi is an important microsporidian pathogen that is considered an emergent, zoonotic, and opportunistic. It infects both domestic and laboratory rabbits, generating severe chronic interstitial and granulomatous nephritis with fibrosis and granulomatous encephalitis. Encephalitozoonosis is diagnosed in paraffin-embedded sections by examining the spores in the host tissues. The spores are difficult to observe when the samples are stained with hematoxylin and eosin (H&E), particularly when there is an inflammatory reaction and tissue damage. The spores are easily mistaken for other microorganisms, such as fungi (yeasts), protozoa, and bacteria. In our study, we used kidney samples from E. cuniculi-positive rabbits and employed 14 recommended histologic stains for detecting microsporidia spores: alcian blue, calcofluor white, Giemsa, Gram, Grocott, H&E, Luna, Luxol fast blue, Masson trichrome, modified trichrome stain (MTS), periodic acid-Schiff reaction (PAS), Van Gieson, Warthin-Starry (WS), and Ziehl-Neelsen (ZN).We concluded that MTS and Gram stain, detected by light microscopy, and calcofluor white stain, detected by ultraviolet light microscopy, are the best stains for detecting spores of E. cuniculi in paraffin-embedded tissues from infected rabbits. These stains were superior to WS, ZN, Giemsa, and PAS for identifying spores without background "noise" or monochromatic interference. Also, they allow individual spores to be discerned in paraffin-embedded tissues. MTS allows observation of the polar tube, polaroplast, and posterior vacuole, the most distinctive parts of the spore.
兔脑炎微孢子虫是一种重要的微孢子虫病原体,被认为是一种新出现的、人畜共患的机会性致病原。它感染家兔和实验兔,引发严重的慢性间质性和肉芽肿性肾炎并伴有纤维化以及肉芽肿性脑炎。通过检查宿主组织中的孢子,可在石蜡包埋切片中诊断兔脑炎微孢子虫病。当样本用苏木精和伊红(H&E)染色时,孢子很难观察到,尤其是在存在炎症反应和组织损伤的情况下。这些孢子很容易被误认为是其他微生物,如真菌(酵母)、原生动物和细菌。在我们的研究中,我们使用了来自兔脑炎微孢子虫阳性兔子的肾脏样本,并采用了14种推荐的组织学染色方法来检测微孢子虫孢子:阿尔辛蓝、钙荧光白、吉姆萨、革兰氏、格罗科特、H&E、卢娜、卢索尔坚牢蓝、马森三色染色法、改良三色染色法(MTS)、过碘酸-希夫反应(PAS)、范吉森、沃辛-斯塔里(WS)和齐尔-尼尔森(ZN)。我们得出结论,通过光学显微镜检测的MTS和革兰氏染色,以及通过紫外光显微镜检测的钙荧光白染色,是检测感染兔子石蜡包埋组织中兔脑炎微孢子虫孢子的最佳染色方法。这些染色方法在识别孢子时优于WS、ZN、吉姆萨和PAS,不会产生背景“噪声”或单色干扰。此外,它们能够在石蜡包埋组织中辨别单个孢子。MTS能够观察到极丝、极质体和后液泡,这些是孢子最具特征的部分。