TY - JOUR
T1 - A new molecular approach to help conclude drowning as a cause of death
T2 - Simultaneous detection of eight bacterioplankton species using real-time PCR assays with TaqMan probes
AU - Uchiyama, Taketo
AU - Kakizaki, Eiji
AU - Kozawa, Shuji
AU - Nishida, Sho
AU - Imamura, Nahoko
AU - Yukawa, Nobuhiro
N1 - Funding Information:
We thank Professor Tetsuya Hayashi (Division of Bioenvironmental Science, Frontier Science Research Centre, University of Miyazaki) for valuable advice regarding bacteria, and Professor Masahiro Sakai (Department of Biochemistry and Applied Biosciences, Faculty of Agriculture, University of Miyazaki) for valuable advice regarding bacterioplankton. We also thank the staff at the Forensic Science Laboratory, Miyazaki Prefectural Police who performed the GC/MS and alcohol analysis. This study was supported by a Grant-in-Aid for Scientific Research ( No. 20590682 ) from the Ministry of Education, Culture, Sports, Science and Technology of Japan .
PY - 2012/10/10
Y1 - 2012/10/10
N2 - We developed a novel tool for concluding drowning as a cause of death. We designed nine primer pairs to detect representative freshwater or marine bacterioplankton (aquatic bacteria) and then used real-time PCR with TaqMan probes to rapidly and specifically detect them. We previously cultured the genus Aeromonas, which is a representative freshwater bacterial species, in blood samples from 94% of victims who drowned in freshwater and the genera Vibrio and/or Photobacterium that are representative marine bacteria in 88% of victims who drowned in seawater. Based on these results, we simultaneously detected eight species of bacterioplankton (Aeromonas hydrophila, A. salmonicida; Vibrio fischeri, V. harveyi, V. parahaemolyticus; Photobacterium damselae, P. leiognathi, P. phosphoreum) using three sets of triplex real-time PCR assays and TaqMan probes labelled with fluorophores (FAM, NED, Cy5). We assayed 266 specimens (109 blood, 157 tissues) from 43 victims, including 32 who had drowned in rivers, ditches, wells, sea or around estuaries. All lung samples of these 32 victims were TaqMan PCR-positive including the lung periphery into which water does not readily enter postmortem. On the other hand, findings in blood and/or closed organs (kidney or liver) were PCR-positive in 84% of the drowned victims (except for those who drowned in baths) although the conventional test detected diatoms in closed organs in only 44% of the victims. Thus, the results of the PCR assay reinforced those of diatom tests when only a few diatoms were detectable in organs due to the low density of diatoms in the water where they were found. Multiplex TaqMan PCR assays for bacterioplankton were rapid, less laborious and high-throughput as well as sensitive and specific. Therefore, these assays would be useful for routine forensic screening tests to estimate the amount and type of aspirated water.
AB - We developed a novel tool for concluding drowning as a cause of death. We designed nine primer pairs to detect representative freshwater or marine bacterioplankton (aquatic bacteria) and then used real-time PCR with TaqMan probes to rapidly and specifically detect them. We previously cultured the genus Aeromonas, which is a representative freshwater bacterial species, in blood samples from 94% of victims who drowned in freshwater and the genera Vibrio and/or Photobacterium that are representative marine bacteria in 88% of victims who drowned in seawater. Based on these results, we simultaneously detected eight species of bacterioplankton (Aeromonas hydrophila, A. salmonicida; Vibrio fischeri, V. harveyi, V. parahaemolyticus; Photobacterium damselae, P. leiognathi, P. phosphoreum) using three sets of triplex real-time PCR assays and TaqMan probes labelled with fluorophores (FAM, NED, Cy5). We assayed 266 specimens (109 blood, 157 tissues) from 43 victims, including 32 who had drowned in rivers, ditches, wells, sea or around estuaries. All lung samples of these 32 victims were TaqMan PCR-positive including the lung periphery into which water does not readily enter postmortem. On the other hand, findings in blood and/or closed organs (kidney or liver) were PCR-positive in 84% of the drowned victims (except for those who drowned in baths) although the conventional test detected diatoms in closed organs in only 44% of the victims. Thus, the results of the PCR assay reinforced those of diatom tests when only a few diatoms were detectable in organs due to the low density of diatoms in the water where they were found. Multiplex TaqMan PCR assays for bacterioplankton were rapid, less laborious and high-throughput as well as sensitive and specific. Therefore, these assays would be useful for routine forensic screening tests to estimate the amount and type of aspirated water.
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U2 - 10.1016/j.forsciint.2012.04.029
DO - 10.1016/j.forsciint.2012.04.029
M3 - Article
C2 - 22682932
AN - SCOPUS:84865614250
SN - 0379-0738
VL - 222
SP - 11
EP - 26
JO - Forensic science international
JF - Forensic science international
IS - 1-3
ER -