Gulbahar M Y, Davis W C, Guvenc T, Yarim M, Parlak U, Kabak Y B
University of Ondokuz Mayis, Faculty of Veterinary Medicine, Department of Pathology, Kurupelit, 55139 Samsun, Turkey.
Vet Pathol. 2007 Sep;44(5):589-99. doi: 10.1354/vp.44-5-589.
The present study describes the pathogenetic mechanisms of myocarditis in 9 lambs that died in a foot-and-mouth disease outbreak in Samsun, Turkey. In all the heart samples tested, ELISA and sequencing for phylogenetic analyses showed that the virus, namely O/TUR/Samsun/05, was associated with the PanAsia pandemic strain of foot-and-mouth disease virus (FMDV) type O. The lambs had myocardial lesions but no typical vesicular lesions. In situ reverse transcription showed that many cardiomyocytes and some interstitial cells were positive for FMDV type O. Inflammatory infiltration, hyaline degeneration, and necrosis of sheets of myocytes were observed. The cellular infiltrates were mononuclear cells, including many lymphocytes, macrophages, a few plasma cells, and neutrophils. Major histocompatibility complex Class II+ dendritic and mononuclear cells, gammadelta T cells, CD172A+ and CD14+ macrophages and monocytes, and IgM+ B cells were detected mainly in the infected hearts. Inducible nitric oxide synthetase (iNOS) was seen mostly in areas of inflammation infiltrated by large numbers of cells. Of the 2 alpha-subunits of integrin known to be used as receptors by FMDV in epithelial tissues, CD49e (integrin alpha5) was detected in the membranes of cardiac myocytes with intercalated discs, but CD51 (integrin alphaV) was not detected in cardiac myocytes from infected or normal lambs. Interstitial and inflammatory cells were positive for both integrin subunits. The terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL)-positive signal was detected in the nuclei of both cardiac myocytes and interstitial cells from infected lambs. These findings suggest that the iNOS expressed by inflammatory cells in lesions may have a deleterious effect on cardiac myocytes in these lesions.
本研究描述了在土耳其萨姆松口蹄疫疫情中死亡的9只羔羊心肌炎的发病机制。在所有检测的心脏样本中,酶联免疫吸附测定(ELISA)和用于系统发育分析的测序表明,该病毒,即O/TUR/Samsun/05,与口蹄疫病毒O型的泛亚大流行毒株有关。这些羔羊有心肌损伤,但无典型水疱性损伤。原位逆转录显示,许多心肌细胞和一些间质细胞对口蹄疫病毒O型呈阳性。观察到炎症浸润、透明变性和成片心肌细胞坏死。细胞浸润为单核细胞,包括许多淋巴细胞、巨噬细胞、少数浆细胞和中性粒细胞。主要组织相容性复合体II类+树突状细胞和单核细胞、γδT细胞、CD172A+和CD14+巨噬细胞和单核细胞以及IgM+B细胞主要在受感染的心脏中检测到。诱导型一氧化氮合酶(iNOS)主要见于大量细胞浸润的炎症区域。已知在上皮组织中被口蹄疫病毒用作受体的2种整合素α亚基中,CD49e(整合素α5)在有闰盘的心肌细胞膜中被检测到,但在受感染或正常羔羊的心肌细胞中未检测到CD51(整合素αV)。间质细胞和炎症细胞对两种整合素亚基均呈阳性。在受感染羔羊的心肌细胞和间质细胞核中均检测到末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)阳性信号。这些发现表明,病变中炎症细胞表达的iNOS可能对这些病变中的心肌细胞产生有害影响。