Sponge-Cell Culture? A Molecular Identification Method for Sponge Cells

2003 ◽  
Vol 5 (5) ◽  
pp. 443-449 ◽  
Author(s):  
Detmer Sipkema ◽  
Hans G.H.J. Heilig ◽  
Antoon D.L. Akkermans ◽  
Ronald Osinga ◽  
Johannes Onji ◽  
...  
2019 ◽  
Vol 55 (3) ◽  
pp. 149-158 ◽  
Author(s):  
Stephanie Munroe ◽  
Kenneth Sandoval ◽  
Dirk E. Martens ◽  
Detmer Sipkema ◽  
Shirley A. Pomponi

2018 ◽  
Vol 2018 ◽  
pp. 1-9
Author(s):  
Ji Hye Park ◽  
Sang Eon Shin ◽  
Kwang Soo Ko ◽  
Seong Hwan Park

Estimation of postmortem interval (PMI) is paramount in modern forensic investigation. After the disappearance of the early postmortem phenomena conventionally used to estimate PMI, entomologic evidence provides important indicators for PMI estimation. The age of the oldest fly larvae or pupae can be estimated to pinpoint the time of oviposition, which is considered the minimum PMI (PMImin). The development rate of insects is usually temperature dependent and species specific. Therefore, species identification is mandatory for PMImin estimation using entomological evidence. The classical morphological identification method cannot be applied when specimens are damaged or have not yet matured. To overcome this limitation, some investigators employ molecular identification using mitochondrial cytochrome c oxidase subunit I (COI) nucleotide sequences. The molecular identification method commonly uses Sanger’s nucleotide sequencing and molecular phylogeny, which are complex and time consuming and constitute another obstacle for forensic investigators. In this study, instead of using conventional Sanger’s nucleotide sequencing, single-nucleotide polymorphisms (SNPs) in the COI gene region, which are unique between fly species, were selected and targeted for single-base extension (SBE) technology. These SNPs were genotyped using a SNaPshot® kit. Eleven Calliphoridae and seven Sarcophagidae species were covered. To validate this genotyping, fly DNA samples (103 adults, 84 larvae, and 4 pupae) previously confirmed by DNA barcoding were used. This method worked quickly with minimal DNA, providing a potential alternative to conventional DNA barcoding. Consisting of only a few simple electropherogram peaks, the results were more straightforward compared with those of the conventional DNA barcoding produced by Sanger’s nucleotide sequencing.


2008 ◽  
Vol 20 (1) ◽  
pp. 151-155 ◽  
Author(s):  
Xiaoying Zhang ◽  
Gaël Le Pennec ◽  
Renate Steffen ◽  
Wener E. G. Müller ◽  
Wei Zhang

2004 ◽  
Vol 70 (11) ◽  
pp. 6695-6705 ◽  
Author(s):  
Cheonghoon Lee ◽  
Seung-Hoon Lee ◽  
Euiri Han ◽  
Sang-Jong Kim

ABSTRACT Viral contamination in environmental samples can be underestimated because a single cell line might reproduce only some enteric viruses and some enteric viruses do not exhibit apparent cytopathic effects in cell culture. To overcome this problem, we evaluated a cell culture-PCR assay based on a combination of A549 and Buffalo green monkey kidney (BGMK) cell lines as a tool to monitor infectious adenoviruses and enteroviruses in river water. Water samples were collected 10 times at each of four rivers located in Gyeonggi Province, South Korea, and then cultured on group 1 cells (BGMK cells alone) and group 2 cells (BGMK and A549 cells). Reverse transcription and multiplex PCR were performed, followed by phylogenetic analysis of the amplicons. Thirty (75.0%) of the 40 samples were positive for viruses based on cell culture, and the frequency of positive samples grown on group 2 cells (65.0%) was higher than the frequency of positive samples grown on group 1 cells (50.0%). The number of samples positive for adenoviruses was higher with A549 cells (13 samples) than with BGMK cells (one sample); the numbers of samples positive for enteroviruses were similar with both types of cells. By using phylogenetic analysis, adenoviral amplicons were grouped into subgenera A, C, D, and F, and enteroviral amplicons were grouped into coxsackieviruses B3 and B4 and echoviruses 6, 7, and 30, indicating that A549 and BGMK cells were suitable for recovering a wide range of adenoviral and enteroviral types. The cell culture-PCR assay with a combination of A549 and BGMK cells and molecular identification could be a useful tool for monitoring infectious adenoviruses and enteroviruses in aquatic environments.


Insects ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 401
Author(s):  
Yoamel Milián-García ◽  
Lauren A. A. Janke ◽  
Robert G. Young ◽  
Aruna Ambagala ◽  
Robert H. Hanner

eDNA metabarcoding is an effective molecular-based identification method for the biosurveillance of flighted insects. An eDNA surveillance approach maintains specimens for secondary morphological identification useful for regulatory applications. This study identified Culicoides species using eDNA metabarcoding and compared these results to morphological identifications of trapped specimens. Insects were collected using ultraviolet (UV) lighted fan traps containing a saturated salt (NaCl) solution from two locations in Guelph, Ontario, Canada. There were forty-two Culicoides specimens collected in total. Molecular identification detected four species, C. biguttatus, C. stellifer, C. obsoletus, and C. mulrennani. Using morphological identification, two out of these four taxonomic ranks were confirmed at the species level (C. biguttatus and C. stellifer) and one was confirmed at the subgenus level (Avaritia [C. obsoletus]). No molecular detection of Culicoides species occurred in traps with an abundance of less than three individuals per taxon. The inconsistency in identifying Culicoides specimens to the species level punctuates the need for curated DNA reference libraries for Culicoides. In conclusion, the saturated salt (NaCl) solution preserved the Culicoides’ morphological characteristics and the eDNA.


Author(s):  
Shirley A. Pomponi ◽  
Robin Willoughby ◽  
Michelle Kelly-Borges
Keyword(s):  

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