Bacterial Enteropathogens Faecal PCR and Culture Results
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1 Bacterial Enteropathogens Faecal PCR and Culture Results Because most diarrhoeal illness is self-limiting, microbiological investigation is usually not indicated. It should however be considered where there is severe or prolonged diarrhoea, high fevers or dysentery (blood and mucus in stools), diarrhoea in the young, the elderly and the immunosuppressed where specific treatment may be indicated, in suspected outbreak situations, and if the diarrhoea is associated with travel or is chronic in nature. The current algorithms The current processing of all faecal samples involves transportation at ambient temperature to our central laboratory at Bowen Hills. Standard processing of these faecal specimen is outlined Diagram 1. Total nucleic acid is extracted and undergoes targeted multiplex PCR for 5 parasites (Giardia, Cryptosporidium, Entamoeba histolytica, Dientamoeba fragilis and Blastocystis hominis) and five bacterial enteropathogens (Salmonella, Campylobacter, Aeromonas spp., Yersinia spp. and Shigella/Enteroinvasive E.coli [EIEC]). Diagram 1: Routine processing of faecal samples for parasitic and bacterial enteropathogens The stool sample is simultaneously inoculated into enrichment and preservation broths. Where PCR testing reveals a bacterial enteropathogen the simultaneously inoculated broth cultures are subcultured in order to make available isolates for antibiotic susceptibility testing as well as referral to public health reference laboratories. This allows for typing so as to inform potential foodborne and other outbreaks that require a public health response. Syndromic testing detects only those organisms targeted in the multiplex PCRs. Outlined in Diagram 2 are additional investigations that are performed on special request. In particular where a history of travel or seafood ingestion, refugee or immigrant status, eosinophilia, is provided, routine and additional cultures are performed regardless of PCR results.
2 Diagram 2: Syndromic testing Results are tabulated in the following figures Figure 1: % PCR and or Culture Positive for 5 Bacterial Enteropathogens / all Faecal PCR's. Figure 2: % Culture Positive for 5 Bacterial Enteropathogens / all Faecal PCR's. Figure 3: Campylobacter (PCR+Culture+ and PCR+Culture )/Total PCR+ & Percent Culture+ Figure 4: Salmonella (PCR+Culture+ and PCR+Culture )/Total PCR+ & Percent Culture+ Figure 5: Aeromonas (PCR+Culture+ and PCR+Cultureˉ)/Total PCR+ & Percent Culture+ Figure 6: Yersinia (PCR+Culture+ and PCR+Culture )/Total PCR+ & Percent Culture+ Figure 7: Shigella/EIEC (PCR+Culture+ and PCR+Culture )/Total PCR+ & Percent Culture+
3 Figure 1: % PCR and or Culture Positive for 5 Bacterial Enteropathogens Figure 2: % Culture Positive for 5 Bacterial Enteropathogens Figure 3: Campylobacter Total PCR = 21173, Total PCR+ = 1110, Total PCR+ Culture+ = 573 Total PCRˉ Culture+ = 0
4 Figure 4: Salmonella Total PCR = 21173, Total PCR+ = 404, Total PCR+ Culture+ = 346 Total PCRˉ Culture+ = 20 Figure 5: Aeromonas Total PCR = 21173, Total PCR+ = 751, Total PCR+ Culture+ = 402 Total PCRˉ Culture+ = 9 Figure 6: Yersinia Total PCR = 21173, Total PCR+ = 142, Total PCR+ Culture+ = 28 Total PCRˉ Culture+ = 0
5 Figure 7: Shigella/EIEC Total PCR = 21173, Total PCR+ = 74, Total PCR+ Culture+ = 21 Total PCRˉ Culture+ = Nicolaides Pathology (2014). If you wish to use this report or any data or graphs contained in the report you must seek the written permission of Sullivan Nicolaides Pathology. To request permission please send the following details and assurances to Marketing@snp.com.au How the work will be used? Will the work be adapted? If it will be adapted or changed in any way, give specific details of the changes. Will it be included within other content, and if so what is the overall context, and what proportion of the overall work does the copied content represent. An assurance that the work will be properly attributed and will not be falsely attributed.
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