Monitoring of ochratoxin A and ochratoxin-producing fungi in traditional salami manufactured in Northern Italy

被引:30
作者
Merla, C. [1 ,2 ,3 ]
Andreoli, G. [1 ]
Garino, C. [2 ,3 ]
Vicari, N. [1 ]
Tosi, G. [4 ]
Guglielminetti, M. L. [5 ]
Moretti, A. [6 ]
Biancardi, A. [6 ]
Arlorio, M. [2 ,3 ]
Fabbi, M. [1 ]
机构
[1] Ist Zooprofilatt Sperimentale Lombardia & Emilia, Sez Diagnost Pavia, Str Campeggi 59-61, I-27100 Pavia, Italy
[2] Univ Piemonte Orientale, Dipartimento Sci Farmaco, Largo Donegani 2, I-28100 Novara, Italy
[3] Univ Piemonte Orientale, Drug & Food Biotechnol DFB Ctr, Largo Donegani 2, I-28100 Novara, Italy
[4] Ist Zooprofilatt Sperimentale Lombardia & Emilia, Sez Diagnost Forli, Via don Eugenio Servadei 3-E-3-F, I-47122 Forli, Italy
[5] Univ Pavia, Dipartimento Sci Terra & Ambiente, Lab Micol, Via S Epifanio 14, I-27100 Pavia, Italy
[6] Ist Zooprofilatt Sperimentale Lombardia & Emilia, Lab Micotossine & Tossicol, Via Bianchi 9, I-25124 Brescia, Italy
关键词
Salami; Aspergillus; Penicillium; Ochratoxin A; otanpsPN gene; Mycotoxin; DRY-CURED HAM; PENICILLIUM-NORDICUM; ASPERGILLUS-WESTERDIJKIAE; LIQUID-CHROMATOGRAPHY; FOOD-PRODUCTS; MOLDS; OTA; BIOSYNTHESIS; STRAINS; GROWTH;
D O I
10.1007/s12550-017-0305-y
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Fungi have a crucial role in the correct maturation of salami, but special attention should be addressed to the production of the nephrotoxic, immunotoxic, and carcinogenic mycotoxin ochratoxin A (OTA). In a monitoring study conducted in Northern Italy, OTA was detected by liquid chromatography coupled with mass spectrometry in 13 out 133 samples of traditional salami (9.8% of the total count). Mycological analysis of these samples yielded 247 fungal isolates which were identified to species level. The most frequent species were Penicillium nalgiovense, P. solitum, and P. chrysogenum. P. nordicum, an OTA-producing species commonly found in proteinaceous food, was not found in these samples. Three isolates were found to be Aspergillus westerdijkiae, an OTA-producing species. In order to check the results of the microbiological identification, 19 different strains of Aspergillus and 94 of Penicillium were tested for the presence of a sequence common to OTA-producing fungi by real-time PCR. None of the studied isolates, including the three A. westerdijkiae, possessed the otanpsPN target which is common to OTA-producing strains. Two out of three isolates of the A. westerdijkiae were also PCR-negative for the otanpsPN gene and did not produce OTA in culture. Conversely, this target sequence was amplified from the DNA purified from 14 salami casings including three casings harboring A. westerdijkiae. The amplification of sequences specific for OTA-producing strains performed on total genomic DNA extracted directly from salami casings provided a more suitable approach than PCR analysis of isolates from salami for the OTA-related otanpsPN gene to evaluate the risk of OTA contamination.
引用
收藏
页码:107 / 116
页数:10
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