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Molecular Screening by Polymerase Chain Reaction Detects Panleukopenia Virus DNA in Formalin-Fixed Hearts from Cats with Idiopathic Cardiomyopathy and Myocarditis

Identifieur interne : 000055 ( Istex/Corpus ); précédent : 000054; suivant : 000056

Molecular Screening by Polymerase Chain Reaction Detects Panleukopenia Virus DNA in Formalin-Fixed Hearts from Cats with Idiopathic Cardiomyopathy and Myocarditis

Auteurs : Kathryn M. Meurs ; Philip R. Fox ; Alexander L. Magnon ; Si-Kwang Liu ; Jeffrey A. Towbin

Source :

RBID : ISTEX:69891B542A0AF2EC24913E6EECB25679F37BBAD2

English descriptors

Abstract

Abstract: Viral myocarditis has been suggested as an etiology for cardiomyopathy in several mammalian species. Myocarditis and idiopathic cardiomyopathy have been reported in the domestic cat, although a viral etiology has not been demonstrated. Because of the continuing interest in the potential relationship between viral myocarditis and cardiomyopathy, we evaluated hearts from cats with spontaneous, idiopathic cardiomyopathy for viral genomic material within myocytes by polymerase chain reaction, and for the presence of myocarditis by light microscopy. Thirty-one (31) formalin-fixed hearts from domestic cats who died of idiopathic cardiomyopathy were randomly selected from pathology archives. Seventeen (17) formalin-fixed hearts from healthy cats were similarly selected as normal controls. The polymerase chain reaction (PCR) was used to evaluate myocardial tissue for the presence of viral genome from feline panleukopenia virus, herpes virus, calici virus, and corona virus. Hearts were examined using light microscopy for histologic evidence of myocarditis according to the Dallas criteria. Panleukopenia virus was identified by PCR in 10 of 31 cats with cardiomyopathy but in none of the controls. Neither cardiomyopathic or control cats tested positive by PCR for herpes virus, calici virus, and corona virus. Myocarditis was detected by histologic examination in 18 of 31 cardiomyopathic cats and in none of 17 control cats. Myocarditis and or feline panleukopenia virus genome was detected in felines with idiopathic hypertrophic, dilated, and restrictive cardiomyopathy, suggesting a possible role of viral infection and inflammation in the pathogenesis of cardiomyopathy in this species.

Url:
DOI: 10.1016/S1054-8807(00)00031-4

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ISTEX:69891B542A0AF2EC24913E6EECB25679F37BBAD2

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<note type="content">Figure 1: Agarose gel electrophoresis of the 397 base pair region of the nonstructural protein 1 of panleukopenia. Lanes 1, 2, 4, 7, 8 contain negative samples from cardiomyopathic cats. Lane 11 is a negative control, lane 12 is a positive control. The initial lane (identified by an asterisk) contains the DNA ladder</note>
<note type="content">Figure 2: Photomicrographs of representative myocardial sections from cats with cardiomyopathy and myocarditis. (Top) Section from the left ventricular free wall. Extensive mixed inflammatory infiltrate is located predominantly in the subendocardial region consisting of lymphocytes, neutrophils, and plasmacytes. Adjacent myocyte necrosis is severe. Hematoxylin and eosin stain (H&E); magnification ×200. (Bottom) Section from the right auricle. Diffuse neutrophilic infiltrate is associated with extensive myocardial necrosis which is particularly prominent in the subendocardial region. Subendocardial hemorrhage is present. Hematoxylin and eosin stain (H&E); magnification ×100</note>
<note type="content">Table 1: Polymerase Chain Reaction Conditions for Viral Amplification</note>
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<p>Abstract: Viral myocarditis has been suggested as an etiology for cardiomyopathy in several mammalian species. Myocarditis and idiopathic cardiomyopathy have been reported in the domestic cat, although a viral etiology has not been demonstrated. Because of the continuing interest in the potential relationship between viral myocarditis and cardiomyopathy, we evaluated hearts from cats with spontaneous, idiopathic cardiomyopathy for viral genomic material within myocytes by polymerase chain reaction, and for the presence of myocarditis by light microscopy. Thirty-one (31) formalin-fixed hearts from domestic cats who died of idiopathic cardiomyopathy were randomly selected from pathology archives. Seventeen (17) formalin-fixed hearts from healthy cats were similarly selected as normal controls. The polymerase chain reaction (PCR) was used to evaluate myocardial tissue for the presence of viral genome from feline panleukopenia virus, herpes virus, calici virus, and corona virus. Hearts were examined using light microscopy for histologic evidence of myocarditis according to the Dallas criteria. Panleukopenia virus was identified by PCR in 10 of 31 cats with cardiomyopathy but in none of the controls. Neither cardiomyopathic or control cats tested positive by PCR for herpes virus, calici virus, and corona virus. Myocarditis was detected by histologic examination in 18 of 31 cardiomyopathic cats and in none of 17 control cats. Myocarditis and or feline panleukopenia virus genome was detected in felines with idiopathic hypertrophic, dilated, and restrictive cardiomyopathy, suggesting a possible role of viral infection and inflammation in the pathogenesis of cardiomyopathy in this species.</p>
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<ce:given-name>Kathryn M</ce:given-name>
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<ce:text>Address for correspondence: Dr. Kathryn M. Meurs, Department of Veterinary Clinical Sciences, The Ohio State University College of Veterinary Medicine, 610 Vernon L. Tharp Street, Columbus, Ohio 43210, USA. Tel: 614-292-3551; Fax: 614-292-0895</ce:text>
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<ce:simple-para>Viral myocarditis has been suggested as an etiology for cardiomyopathy in several mammalian species. Myocarditis and idiopathic cardiomyopathy have been reported in the domestic cat, although a viral etiology has not been demonstrated. Because of the continuing interest in the potential relationship between viral myocarditis and cardiomyopathy, we evaluated hearts from cats with spontaneous, idiopathic cardiomyopathy for viral genomic material within myocytes by polymerase chain reaction, and for the presence of myocarditis by light microscopy. Thirty-one
<ce:cross-ref refid="BIB31">(31)</ce:cross-ref>
formalin-fixed hearts from domestic cats who died of idiopathic cardiomyopathy were randomly selected from pathology archives. Seventeen
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formalin-fixed hearts from healthy cats were similarly selected as normal controls. The polymerase chain reaction (PCR) was used to evaluate myocardial tissue for the presence of viral genome from feline panleukopenia virus, herpes virus, calici virus, and corona virus. Hearts were examined using light microscopy for histologic evidence of myocarditis according to the Dallas criteria. Panleukopenia virus was identified by PCR in 10 of 31 cats with cardiomyopathy but in none of the controls. Neither cardiomyopathic or control cats tested positive by PCR for herpes virus, calici virus, and corona virus. Myocarditis was detected by histologic examination in 18 of 31 cardiomyopathic cats and in none of 17 control cats. Myocarditis and or feline panleukopenia virus genome was detected in felines with idiopathic hypertrophic, dilated, and restrictive cardiomyopathy, suggesting a possible role of viral infection and inflammation in the pathogenesis of cardiomyopathy in this species.</ce:simple-para>
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<abstract lang="en">Abstract: Viral myocarditis has been suggested as an etiology for cardiomyopathy in several mammalian species. Myocarditis and idiopathic cardiomyopathy have been reported in the domestic cat, although a viral etiology has not been demonstrated. Because of the continuing interest in the potential relationship between viral myocarditis and cardiomyopathy, we evaluated hearts from cats with spontaneous, idiopathic cardiomyopathy for viral genomic material within myocytes by polymerase chain reaction, and for the presence of myocarditis by light microscopy. Thirty-one (31) formalin-fixed hearts from domestic cats who died of idiopathic cardiomyopathy were randomly selected from pathology archives. Seventeen (17) formalin-fixed hearts from healthy cats were similarly selected as normal controls. The polymerase chain reaction (PCR) was used to evaluate myocardial tissue for the presence of viral genome from feline panleukopenia virus, herpes virus, calici virus, and corona virus. Hearts were examined using light microscopy for histologic evidence of myocarditis according to the Dallas criteria. Panleukopenia virus was identified by PCR in 10 of 31 cats with cardiomyopathy but in none of the controls. Neither cardiomyopathic or control cats tested positive by PCR for herpes virus, calici virus, and corona virus. Myocarditis was detected by histologic examination in 18 of 31 cardiomyopathic cats and in none of 17 control cats. Myocarditis and or feline panleukopenia virus genome was detected in felines with idiopathic hypertrophic, dilated, and restrictive cardiomyopathy, suggesting a possible role of viral infection and inflammation in the pathogenesis of cardiomyopathy in this species.</abstract>
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<note type="content">Figure 1: Agarose gel electrophoresis of the 397 base pair region of the nonstructural protein 1 of panleukopenia. Lanes 1, 2, 4, 7, 8 contain negative samples from cardiomyopathic cats. Lane 11 is a negative control, lane 12 is a positive control. The initial lane (identified by an asterisk) contains the DNA ladder</note>
<note type="content">Figure 2: Photomicrographs of representative myocardial sections from cats with cardiomyopathy and myocarditis. (Top) Section from the left ventricular free wall. Extensive mixed inflammatory infiltrate is located predominantly in the subendocardial region consisting of lymphocytes, neutrophils, and plasmacytes. Adjacent myocyte necrosis is severe. Hematoxylin and eosin stain (H&E); magnification ×200. (Bottom) Section from the right auricle. Diffuse neutrophilic infiltrate is associated with extensive myocardial necrosis which is particularly prominent in the subendocardial region. Subendocardial hemorrhage is present. Hematoxylin and eosin stain (H&E); magnification ×100</note>
<note type="content">Table 1: Polymerase Chain Reaction Conditions for Viral Amplification</note>
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