scholarly journals Determination of Salmonella enterica Leaf Internalization Varies Substantially According to the Method and Conditions Used to Assess Bacterial Localization

2021 ◽  
Vol 12 ◽  
Author(s):  
Madhvi Chahar ◽  
Yulia Kroupitski ◽  
Rachel Gollop ◽  
Eduard Belausov ◽  
Maeli Melotto ◽  
...  

In a previous study, comparing the internalization of S. enterica serovar Typhimurium in various leaves by confocal microscopy, we have demonstrated that the pathogen failed to internalize tomato leaves. Numerous reasons may account for these findings, yet one such factor might be the methodology employed to quantify leaf internalization. To this end, we have systematically studied leaf localization of a Green-fluorescent protein-labeled Salmonella strain in tomato, lettuce, and Arabidopsis leaves by surface sterilization and enumeration of the surviving bacteria, side by side, with confocal microscopy observations. Leaf sterilization was performed using either sodium hypochlorite, silver nitrate, or ethanol for 1 to 7min. The level of internalization varied according to the type of disinfectant used for surface sterilization and the treatment time. Treatment of tomato leaves with 70% ethanol for up to 7min suggested possible internalization of Salmonella, while confocal microscopy showed no internalization. In the case of in lettuce and Arabidopsis leaves, both the plate-count technique and confocal microscopy demonstrated considerable Salmonella internalization thought different sterilization conditions resulted in variations in the internalization levels. Our findings highlighted the dependency of the internalization results on the specific disinfection protocol used to determine bacterial localization. The results underscore the importance of confocal microscopy in validating a particular surface sterilization protocol whenever a new pair of bacterial strain and plant cultivar is studied.

2008 ◽  
Vol 71 (2) ◽  
pp. 397-401 ◽  
Author(s):  
MICHELLE D. DANYLUK ◽  
MARIA T. BRANDL ◽  
LINDA J. HARRIS

The ability of Salmonella to migrate from an external aqueous environment through the almond hull and shell, and to colonize the kernel, was evaluated in two ways. First, the outer surface of shell halves from five varieties of almonds that differed in shell hardness were placed in contact with a suspension of Salmonella enterica serovar Enteritidis phage type 30 for 24hat24°C. Salmonella Enteritidis was isolated from the inside of these almond shells in 46 and 100% of the samples, by direct swabbing of the inner surface of the shell and by enrichment from the swab, respectively. These findings suggested that hardness of the shell is not a significant factor in the migration of the pathogen through that tissue. In addition, both motile and nonmotile strains of S. enterica serovar Typhimurium migrated through the almond shells to the same extent under the conditions of this assay, indicating that bacterial migration through the wet shell may be a passive process. Second, whole almonds (intact hull, shell, and kernel) were soaked for 24 to 72 h at 24°C in a suspension of Salmonella Enteritidis phage type 30 labeled with the green fluorescent protein. Green fluorescent protein–labeled Salmonella cells were observed on the outer and inner surfaces of both the almond hull and shell, and on the kernel, by confocal laser scanning microscopy. Our data provide direct evidence that wet conditions allow for Salmonella migration through the hull and shell and onto the almond kernel, thus providing a means by which almond kernels may become contaminated in the field.


2005 ◽  
Vol 127 (32) ◽  
pp. 11214-11215 ◽  
Author(s):  
Anwar Usman ◽  
Omar F. Mohammed ◽  
Erik T. J. Nibbering ◽  
Jian Dong ◽  
Kyril M. Solntsev ◽  
...  

2015 ◽  
Vol 7 (9) ◽  
pp. 3728-3734 ◽  
Author(s):  
Min Chen ◽  
Shuangyang Ding ◽  
Kai Wen ◽  
Sanlei Xie ◽  
Qi Wang ◽  
...  

A schematic diagram of the FLISA based on a fluobody for the determination of AVMs. Note: FLISA, fluorescence-linked immunosorbent assay; GFP, green fluorescent protein; fluobody, fluorescent single-domain antibody; ABM, abamectin; OVA, ovalbumin; and AVMs, avermectins.


Author(s):  
T. Murakami ◽  
O.G. Doerre ◽  
L.D. Peachey ◽  
E.S. Weinberg

Fluorescent dyes have been extremely useful in determining cell lineages in the developing zebrafish embryo. For example, injection of FITC-dextran into blastomeres has allowed the determination of a tissue fate map at late blastula and a description of cell movements during gastrulation. Here we describe the use of green fluorescent protein (GFP) as a tracer dye for cell movements in developing early zebrafish (Danio rerio) embryos. Since GFP was purified and cloned from the jellyfish Aequorea victoria, it has attracted great attention from biologists as an in vivo tracer and a reporter gene. The protein requires no cofactors or substrates for its fluorescence. This property allows one to inject GFP DNA constructs or in vitro synthesized GFP mRNA into individual cells which can then be expected to continuously synthesize the protein, thus obviating the dilution and bleaching effects often observed when fixed amounts of fluorescent tracer dyes are injected into dividing cells.


Bioimaging ◽  
1998 ◽  
Vol 6 (1) ◽  
pp. 54-61 ◽  
Author(s):  
G Jung ◽  
J Wiehler ◽  
W G�hde ◽  
J Tittel ◽  
Th Basch� ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document