Cronobacter spp. is an emerging pathogen that causes meningitis, sepsis, bacteremia, and necrotizing enterocolitis in neonates and children. The present study developed an assay integrating real-time PCR and high resolution melting (HRM) analysis targeting the OmpA gene for the specific detection and rapid identification of Cronobacter spp. (formerly Enterobacter sakazakii) in powdered infant formula. Eleven Cronobacter field isolates and 25 reference strains were examined using one pair of primers, having the accuracy of 100% in reference to conventional methods. The assay was proved to be highly sensitive with a detection limit of 102 CFU/ml without pre-enrichment, and highly concordant (100%) when compared with ISO-IDF 22964 in 89 actual samples. The method performed for Cronobacter spp. detection was less than 24 h, drastically shortened, compared to several days using standard culturing method, it is probe-free and reduces a risk of PCR carryover. Moreover, all Cronobacter strains examined in this study were genotyped into two species according to their HRM profiles. The established method should provide a molecular tool for direct detection and simultaneous genotyping of Cronobacter spp. in powdered infant formula.

Cryptocaryon irritans is a ciliated obligate parasite of marine fish, causing white spot disease in tropical and sub-tropical regions. Recent studies have shown that fish can mount immune responses against C. irritans and acquire protection. The present study compared the protective immunity in grouper (Epinephelus coioides) against C. irritans induced by theronts, trophonts and tomonts via intraperitoneal (i.p.) injection and tentatively identified an immobilization antigen. Specific antibody titres of immunized fish serum were determined by enzyme-linked immunosorbent assay and immobilization assays at weeks 0, 1, 2, 4, 6 and 8 post-immunization, and immunized grouper were challenged with theronts to detect the survival percentage of fish. Fish immunized with theronts produced higher levels of serum antibody against C. irritans than fish immunized with trophonts or tomonts. A significantly higher level of immune protection was achieved in fish immunized with theronts but not in fish immunized with tomonts or trophonts. Western blot analysis using polyclonal immobilization antibodies of rabbit immunized with theront revealed an immunoreactive band of the protective (immobilization) antigens of C. irritans, the size of which is approximately 34 kDa. The sera of mice immunized with the protein could immobilize theronts of C. irritans. These results demonstrated that the theront stage of C. irritans elicited stronger protective immunity than the trophont and tomont stages in grouper. The tentative identification of protective antigen provides the solid foundation for the development of a defined vaccine against C. irritans.

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Cryptocaryon irritans is one of the most important protozoan pathogens of marine fish, causing the "white spot" disease and posing a significant problem to marine aquaculture. In the present study, a C. irritans-specific reverse primer (S15) was designed based on the published sequence of the second internal transcribed spacer (ITS-2) of ribosomal DNA (rDNA) of C. irritans and used together with the conserved forward primer P1 to develop a specific polymerase chain reaction (PCR) assay for direct, rapid, and specific detection of C. irritans. The specificity of these primers was tested with both closely and distantly related ciliates (Pseudokeroronpsis rubra, Pseudokeroronpsis carnae, Euplotes sp. 1, Ichthyophthirius multifiliis, Pseudourostyla cristata, and Paramecium caudaium), and only C. irritans was detected and no product was amplified from any other ciliates examined in this study using the specific primer set P1-S15. The specific PCR assay was able to detect as low as 45 pg of C. irritans DNA and a nested PCR assay using two primer sets (P1/NC2, P1/S15) increased the sensitivity, allowing the detection of a single C. irritans. The species-specific PCR assays should provide useful tools for the diagnosis, prevention, and molecular epidemiological investigations of C. irritans infection in marine fish.

Clonorchis sinensis and Opisthorchis viverrini are both important fish-borne pathogens, causing serious public health problem in Asia. The present study developed an assay integrating real-time PCR and high resolution melting (HRM) analysis for the specific detection and rapid identification of C. sinensis and O. viverrini. Primers targeting COX1 gene were highly specific for these liver flukes, as evidenced by the negative amplification of closely related trematodes. Assays using genomic DNA extracted from the two flukes yielded specific amplification and their identity was confirmed by sequencing, having the accuracy of 100% in reference to conventional methods. The assay was proved to be highly sensitive with a detection limit below 1 pg of purified genomic DNA, 5 EPG, or 1 metacercaria of C. sinensis. Moreover, C. sinensis and O. viverrini were able to be differentiated by their HRM profiles. The method can reduce labor of microscopic examination and the contamination of agarose electrophoresis. Moreover, it can differentiate these two flukes which are difficult to be distinguished using other methods. The established method provides an alternative tool for rapid, simple, and duplex detection of C. sinensis and O. viverrini.

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Cryptocaryon irritans is a ciliated obligate parasite of marine fish, causing white spot disease in tropical and subtropical regions. Recent studies have shown that fish can mount immune response against C. irritans and acquire protection. The present study compared the protective immunity in grouper (Epinephelus coioides) against C. irritans induced by theronts, trophonts and tomonts via intraperitoneal (i.p.) injection, and tentatively identified an immobilization antigen. Fish immunized with theronts produced higher levels of serum antibody against C. irritans than fish immunized with trophonts or tomonts. Significantly higher level of immune protection was achieved in fish immunized with theronts, but not in fish immunized with tomonts or trophonts. Western blot analysis using polyclonal immobilization antibodies of rabbit immunized with theront revealed an immunoreactive band of the protective (immobilization) antigens of C. irritans, the size of which is approximately 34 kDa. The sera of mice immunized with the protein could immobilize theronts of C. irritans. These results demonstrated that the theront stage of C. irritans elicited stronger protective immunity than the trophont and tomont stages in grouper. The tentative identification of protective antigen provides the solid foundation for the development of a defined vaccine against C. irritans.