Isolation, identification and differentiation of Campylobacter spp. using multiplex PCR assay from goats in Khartoum State, Sudan

• Published in: Tropical animal health and production 2017-03, Vol.49 (3), p.575-581
• Main Authors: Elbrissi, Atif, Sabeil, Y. A., Khalifa, Khalda A., Enan, Khalid, Khair, Osama M., El Hussein, A. M.
• Format: Article
• Language: English
• Subjects: Animals; Biomedical and Life Sciences; Campylobacter; Campylobacter - classification; Campylobacter - isolation & purification; Campylobacter coli; Campylobacter fetus; Campylobacter Infections - diagnosis; Campylobacter Infections - epidemiology; Campylobacter Infections - veterinary; Campylobacter jejuni; Campylobacter lari; Campylobacter upsaliensis; DNA, Bacterial - analysis; Feces - microbiology; Female; Food Contamination; Goat Diseases - diagnosis; Goat Diseases - epidemiology; Goats; Life Sciences; Male; Meat; Multiplex Polymerase Chain Reaction - veterinary; Public health; Regular Articles; Sensitivity and Specificity; Sudan - epidemiology; Veterinary Medicine/Veterinary Science; Zoology
• ISSN: 0049-4747; 1573-7438
• DOI: 10.1007/s11250-017-1231-x

The aim of this study was to identify and characterize thermophilic Campylobacter species in faecal samples from goats in Khartoum State, Sudan, by application of multiplex polymerase chain reaction. Campylobacteriosis is a zoonotic disease of global concern, and the organisms can be transmitted to human via food, water and through contact with farm animals and pets. There are five clinically related Campylobacter species: Campylobacter jejuni ( C. jejuni ). Campylobacter coli , Campylobacter lari , Campylobacter upsaliensis and Campylobacter fetus . Conventional cultural methods to diagnose campylobacteriosis are tedious and time consuming. Wide ranges of genes have been reported to be used for PCR-based identification of Campylobacter spp. We used a multiplex PCR assay to simultaneously detect genes from the major five clinically significant Campylobacter spp. The genes selected were hipO (hippuricase) and 23S rRNA from glyA (serine hydroxymethyl transferase) from each of C. jejuni. C. coli , C. lari , and C. upsaliensis ; and sapB2 (surface layer protein) from C. fetus subsp. fetus . The assay was used to identify Campylobacter isolates recovered from 336 cultured faecal samples from goats in three localities in Khartoum State. C. coli was the most predominant isolate (234; 69.6%), followed by C. jejuni (19; 5.7%), C. upsaliensis (13; 3.9%), C. fetus subsp . fetus (7; 2.1%) and C. lari (6; 1.8%). Twenty-nine goats showed mixed infection with Campylobacter spp., 21 of which harbored two Campylobacter spp., while eight animals were infected with three species. Ten out of twelve goats that displayed diarrhea harbored C. coli only. C. coli , C. jejuni and C. upsaliensis showed significant variation with localities. The prevalence of C. coli was significantly higher (87; 25.9%) in goats from Omdurman, whereas C. jejuni and C. upsaliensis were significantly higher (11; 3.3%, 9; 2.7%) in goats from Khartoum. The multiplex PCR assay was found to be rapid and easy to perform and had a high sensitivity and specificity for characterizing the isolates, even in mixed cultures. The study demonstrated the significance of goats as reservoirs in the dissemination of Campylobacter spp. which could be considered as potential agent of caprine enteritis and abortion as well as contamination of the wider environment posing serious public health concern in Khartoum State.