Isolamento de Staphylococcus de queijo minas frescal e detecção de genes de enterotoxinas
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Palavras-chave

PCR
Staphylococcus
queijo

Como Citar

1.
Costa J de CB da, Freitas EI de, Lemos AA de, Rosas C de O, Medeiros V de M, Warnken MB, Miyazaki NHT, Marin VA. Isolamento de Staphylococcus de queijo minas frescal e detecção de genes de enterotoxinas. Rev Inst Adolfo Lutz [Internet]. 1º de fevereiro de 2012 [citado 19º de abril de 2024];71(2):250-8. Disponível em: https://periodicos.saude.sp.gov.br/RIAL/article/view/32422

Resumo

Neste trabalho foi realizado o isolamento de Staphylococcus spp. de queijo minas frescal, e para esta finalidade foi padronizado um protocolo multiplex PCR (M-PCR) para efetuar a detecção de genes de enterotoxinas clássicas (sea, seb, sec, sed e see) de Staphylococcus aureus, usando-se o gene femA como controle positivo para cepas de S. aureus. Foi testada a detecção direta de bactérias de amostras de queijo minas frescal e do alimento artificialmente contaminado. Cento e onze colônias (104 coagulase-positivas e sete coagulase-negativas) foram selecionadas e analisadas por M-PCR e, dentre essas, 34 colônias (30.62%) foram positivas para pelo menos um dos cinco genes de enterotoxinas analisados. Os genes que codificam as enterotoxinas sea e seb foram os mais frequentemente detectados. O estudo de isolamento de estafilococos coagulase-positivos revelaram que 40% das amostras demonstraram contagens bacterianas acima do limite considerado como aceitável pela legislação brasileira.
https://doi.org/10.53393/rial.2012.v71.32422
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Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.

Copyright (c) 2012 Juliana de Castro Beltrão da Costa, Elaine Ibrahim de Freitas, Anderson Almeida de Lemos, Carla de Oliveira Rosas, Valéria de Mello Medeiros, Márcia Barbosa Warnken, Neide Hiromi Tokumaru Miyazaki, Victor Augustus Marin

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