Detection of virulence and specific genes of Salmonella sp. indigenous from Jember, Indonesia

Ria Yulian (Program of Biology Education, Faculty of Teacher Trainning and Education, Universitas Jember. Jl. Kalimantan X, Jember 68121, East Java, Indonesia)
Erlia Narulita (Program of Biology Education, Faculty of Teacher Trainning and Education, Universitas Jember. Jl. Kalimantan X, Jember 68121, East Java, Indonesia)
MOCHAMMAD IQBAL (Program of Biology Education, Faculty of Teacher Trainning and Education, Universitas Jember. Jl. Kalimantan X, Jember 68121, East Java, Indonesia)
DESY ROCHMIYAH SARI (Program of Biology Education, Faculty of Teacher Trainning and Education, Universitas Jember. Jl. Kalimantan X, Jember 68121, East Java, Indonesia)
IRMA SURYANINGSIH (Program of Biology Education, Faculty of Teacher Trainning and Education, Universitas Jember. Jl. Kalimantan X, Jember 68121, East Java, Indonesia)
DIAN EKA APRILIA FITRIA NINGRUM (Department of Islamic Primary School Teacher Education, Faculty of Tarbiyah and Teacher Training, Universitas Islam Negeri Maulana Malik Ibrahim Malang. Jl. Tarbiyah, Malang 65144, East Java, Indonesia)

Biodiversitas Journal of Biological Diversity
Vol. 21 No. 7 (2020)

Abstract. Yulian R, Narulita E, Iqbal M, Rochmiyah D, Suryaningsih I, Ningrum DEAF. 2020. Detection of virulence and specific genes of Salmonella sp. indigenous from Jember, Indonesia. Biodiversitas 21: 2889-2892. The bacterium Salmonella sp. is the most common cause of foodborne infection in humans. It has the ability to invAde the host, Salmonellosis is highly influenced by the combination of chromosome and plasmid in which Salmonella Pathogenisitas Islands (SPIs) are the biggest gene in the chromosome that are responsible to build specific interaction between Salmonella and the host. This research performed detection on virulence and specific genes in the SPIs area using PCR method for two Salmonella spp. bacterial isolates originated from Jember which were KP2 and P21D. Seven pairs of primers including stn, fimA, spvR (virulence genes), invA, ivaB, spvC, and fliC-d (specific genes) were used. The result revealed that P21D bacteria containing 3 virulence genes i.e. stn, fimA, and spvR. Meanwhile, only two virulent genes stn, and spvR were present in KP2 bacteria. For the detection of specific genes, three genes invA, ivaB, and spvC were present while fliC-d genes were not detected. Only two, invA, and ivaB genes were detected in P21D bacteria, while spvC, and fliC-d were not detected.