2016
DOI: 10.1016/j.anaerobe.2016.10.009
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Detection of toxigenic Clostridium perfringens and Clostridium botulinum from food sold in Lagos, Nigeria

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Cited by 29 publications
(19 citation statements)
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“…SYT1 (Figure 7B) is a cell surface receptor by which the type B botulinum neurotoxin enters human neurons [Connan et al, 2017]. Selection here may be a response to pervasive foodborne bacterial contamination by Clostridium botulinum , similar to what exists in modern times [Chukwu et al, 2016]. Pierron et al [2014] named HEMGN (which Pickrell et al [2009] also identified), involved in erythrocyte differentiation, as a selection signal common to Malagasy populations derived from common ancestry with YRI.…”
Section: Discussionmentioning
confidence: 99%
“…SYT1 (Figure 7B) is a cell surface receptor by which the type B botulinum neurotoxin enters human neurons [Connan et al, 2017]. Selection here may be a response to pervasive foodborne bacterial contamination by Clostridium botulinum , similar to what exists in modern times [Chukwu et al, 2016]. Pierron et al [2014] named HEMGN (which Pickrell et al [2009] also identified), involved in erythrocyte differentiation, as a selection signal common to Malagasy populations derived from common ancestry with YRI.…”
Section: Discussionmentioning
confidence: 99%
“…SYT1 ( Figure 7B) is a cell surface receptor by which the type B botulinum neurotoxin enters human neurons (Connan et al 2017). Selection here may be a response to pervasive foodborne bacterial contamination by Clostridium botulinum, similar to what exists in modern times (Chukwu et al 2016). Pierron et al (2014) named HEMGN [which Pickrell et al (2009) also identified], involved in erythrocyte differentiation, as a selection signal common to Malagasy populations derived from common ancestry with YRI.…”
Section: Application Of G12 and G123 To Empirical Datamentioning
confidence: 98%
“…Genotyping of C. perfringens isolates, however, can overcome this problem and has become the standard for toxinotyping of C. perfringens . Polymerase chain reaction (PCR) protocols, especially multiplex PCR assay, have been established for simultaneous detection of these toxin genes ( cpa, cpb, etx, iap, cpe and cpb2 ) [ 24 , 25 , 26 , 27 ].…”
Section: Introductionmentioning
confidence: 99%