Objective – To perform a qualitative evaluation of procalcitonin gene (CALCA) expression in a tissue-specific manner in dogs with signs of the systemic inflammatory response syndrome (SIRS). Design – Observational study. Setting – University Veterinary Teaching Hospital. Animals – Nine clinical cases and 5 research dogs. Interventions – None. Measurements and Main Results – Fresh tissue samples (thyroid, lung, liver, spleen) from 9 dogs that died with a diagnosis of parvoviral infection or SIRS were collected and immediately stored at –801C. Diagnosis of parvoviral infection was based on clinical signs, positive fecal antigen test, and confirmed by polymerase chain reaction (PCR). Clinical diagnosis of SIRS was based on the clinical criteria reported in veterinary literature. Necropsy was performed on all subjects in the study. Furthermore, thyroid, lung, liver, spleen were collected from 5 normal research dogs immediately postmortem for testing. The 9 dogs with a clinical diagnosis of SIRS died from either parvovirus (n55), bacterial sepsis (n53), or neoplasia (n51). CALCAwas amplified by PCR in the following samples: thyroid (9/9), spleen (6/9), lung (4/9), liver (3/9). Only thyroid expressed CALCA in the 5 normal dogs. Conclusions – In SIRS, extrathyroidal transcription of CALCA was documented. Quantitative analysis (realtime polymerase chain reaction) in a wider population of SIRS and normal dogs will provide essential information about the extent and source of extrathyroidal expression of canine CALCA induced by septic and nonseptic systemic inflammation.

Evaluation of CALC-I gene (CALCA) expression in tissues of dogs with signs of the systemic inflammatory response syndrome / M. Giunti; A. Peli; M. Battilani; S. Zacchini; G. Militerno; C.M. Otto. - In: JOURNAL OF VETERINARY EMERGENCY AND CRITICAL CARE. - ISSN 1479-3261. - ELETTRONICO. - 20 (5):(2010), pp. 523-527. [10.1111/j.1476-4431.2010.00575.x]

Evaluation of CALC-I gene (CALCA) expression in tissues of dogs with signs of the systemic inflammatory response syndrome

GIUNTI, MASSIMO;PELI, ANGELO;BATTILANI, MARA;MILITERNO, GIANFRANCO;
2010

Abstract

Objective – To perform a qualitative evaluation of procalcitonin gene (CALCA) expression in a tissue-specific manner in dogs with signs of the systemic inflammatory response syndrome (SIRS). Design – Observational study. Setting – University Veterinary Teaching Hospital. Animals – Nine clinical cases and 5 research dogs. Interventions – None. Measurements and Main Results – Fresh tissue samples (thyroid, lung, liver, spleen) from 9 dogs that died with a diagnosis of parvoviral infection or SIRS were collected and immediately stored at –801C. Diagnosis of parvoviral infection was based on clinical signs, positive fecal antigen test, and confirmed by polymerase chain reaction (PCR). Clinical diagnosis of SIRS was based on the clinical criteria reported in veterinary literature. Necropsy was performed on all subjects in the study. Furthermore, thyroid, lung, liver, spleen were collected from 5 normal research dogs immediately postmortem for testing. The 9 dogs with a clinical diagnosis of SIRS died from either parvovirus (n55), bacterial sepsis (n53), or neoplasia (n51). CALCAwas amplified by PCR in the following samples: thyroid (9/9), spleen (6/9), lung (4/9), liver (3/9). Only thyroid expressed CALCA in the 5 normal dogs. Conclusions – In SIRS, extrathyroidal transcription of CALCA was documented. Quantitative analysis (realtime polymerase chain reaction) in a wider population of SIRS and normal dogs will provide essential information about the extent and source of extrathyroidal expression of canine CALCA induced by septic and nonseptic systemic inflammation.
2010
Evaluation of CALC-I gene (CALCA) expression in tissues of dogs with signs of the systemic inflammatory response syndrome / M. Giunti; A. Peli; M. Battilani; S. Zacchini; G. Militerno; C.M. Otto. - In: JOURNAL OF VETERINARY EMERGENCY AND CRITICAL CARE. - ISSN 1479-3261. - ELETTRONICO. - 20 (5):(2010), pp. 523-527. [10.1111/j.1476-4431.2010.00575.x]
M. Giunti; A. Peli; M. Battilani; S. Zacchini; G. Militerno; C.M. Otto
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/92158
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