2014
DOI: 10.3168/jds.2014-8287
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Detection of Cronobacter species in powdered infant formula by probe-magnetic separation PCR

Abstract: Cronobacter species are opportunistic foodborne pathogens associated with serious infections in preterm neonates and infants. Based on the epidemiological research, infant formula products are considered to be the main source of infections from this organism. Therefore, accurate methods are required for detection of Cronobacter species. In this study, the specific probe and primers for detection of this organism were designed and verified. The probe-magnetic beads were prepared for sequence capture, followed b… Show more

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Cited by 18 publications
(14 citation statements)
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“…Cronobacter species have been identified as a contaminant of powdered milk formulas, with sporadic outbreaks linked to necrotizing enterocolitis, bacteremia, and meningitis. 7778 Bacteria can also colonize unlikely sources. Burkholderia cepacia and Enterobacter cloacae have the ability to hydrolyze, render inactive, and proliferate in parabens, which are esters of para-hydroxybenzoic acid that are usually antimicrobial and used as preservatives in ultrasound gel (implicated in a Burkholderia cepacia outbreak in a NICU).…”
Section: The Microbiota and Disease Risk In Extremely Preterm Infantsmentioning
confidence: 99%
“…Cronobacter species have been identified as a contaminant of powdered milk formulas, with sporadic outbreaks linked to necrotizing enterocolitis, bacteremia, and meningitis. 7778 Bacteria can also colonize unlikely sources. Burkholderia cepacia and Enterobacter cloacae have the ability to hydrolyze, render inactive, and proliferate in parabens, which are esters of para-hydroxybenzoic acid that are usually antimicrobial and used as preservatives in ultrasound gel (implicated in a Burkholderia cepacia outbreak in a NICU).…”
Section: The Microbiota and Disease Risk In Extremely Preterm Infantsmentioning
confidence: 99%
“…The sensitivity of this HRM assay in PIF without enrichment was comparable to that of PCR‐ELISA assay, which was 1.06 × 10 3 cfu/mL as previously reported (Xu et al . 2014a). The HRM assay was able to detect undesiccated Cronobacter in PIF at 0.25 cfu/25 g following a 12‐h enrichment, which is equivalent to the ESIA testing (Table ) and comparable to a multiplex real‐time PCR assay reported by Hyeon et al .…”
Section: Discussionmentioning
confidence: 99%
“…However, due to low Cronobacter numbers in contaminated PIF [113] and the inhibiting effect of food components, enrichment is still necessary in order to increase cell concentrations to the detection limit. To improve detection efficiency, methods that enrich detection targets, such as immunomagnetic separation [91] and probemagnetic separation [114] , should be developed.…”
Section: Detection Of Cronobactermentioning
confidence: 99%