scholarly journals Molecular detection of Mycoplasma pneumoniae among patients with severe respiratory and influenza-like illness in South Africa, 2012-2013

2014 ◽  
Vol 21 ◽  
pp. 345 ◽  
Author(s):  
M. Carrim ◽  
N. Wolter ◽  
M. du Plessis ◽  
L. de Gouveia ◽  
S. Walaza ◽  
...  
PLoS ONE ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. e94681 ◽  
Author(s):  
Genevie M. Ntshoe ◽  
Johanna M. McAnerney ◽  
Stefano Tempia ◽  
Lucille Blumberg ◽  
Jocelyn Moyes ◽  
...  

2001 ◽  
Vol 39 (3) ◽  
pp. 1184-1186 ◽  
Author(s):  
J. W. Dorigo-Zetsma ◽  
R. P. Verkooyen ◽  
H. P. van Helden ◽  
H. van der Nat ◽  
J. M. van den Bosch

2018 ◽  
Vol 11 (1) ◽  
pp. 96-100 ◽  
Author(s):  
Oikwathaile Onosi ◽  
Nicole S. Upfold ◽  
Michael D. Jukes ◽  
Garry A. Luke ◽  
Caroline Knox

2021 ◽  
Author(s):  
Chun Yat Chu ◽  
Gert Marais ◽  
Christoffel Opperman ◽  
Deelan Doolabh ◽  
Arash Iranzadeh ◽  
...  

Assessment of the unknown performance of saliva for the detection of the novel SARS-CoV-2 variant of concern (VOC) B.1.351 (501Y.V2) lineage is essential as saliva has been shown to be an equivalent, less invasive and a less costly alternative to nasopharyngeal swabs for the molecular detection of SARS-CoV-2 infection in pre-variant studies. Between 1st August 2020 and 16th January 2021, we enrolled 410 eligible ambulatory participants who presented to Groote Schuur Hospital (GSH) in Cape Town, South Africa for SARS-CoV-2 testing. Of these, 300 were enrolled prior to, and 110 after, the initial detection and replacement of wild-type by the B.1.351 variant. All participants provided a supervised self-collected mid-turbinate (MT) and saliva (SA) swab, in addition to the standard HCW collected NP swab which were all tested by RT-PCR in an accredited diagnostic laboratory. Positive percent agreement to NP swab for SA swabs pre- and post-variant were 51.5% and 72.5% respectively while these values for MT swabs were 75.8% and 77.5%. The negative percent agreement for all swab types during all periods was >98%. The basis for this marked improvement of SA swabs as a diagnostic sample for B.1.351 virus is still being investigated.


2008 ◽  
Vol 157 (1-2) ◽  
pp. 123-127 ◽  
Author(s):  
Paul Tshepo Matjila ◽  
Andrew L. Leisewitz ◽  
Frans Jongejan ◽  
Henk J. Bertschinger ◽  
Barend L. Penzhorn

Plant Disease ◽  
2020 ◽  
Vol 104 (3) ◽  
pp. 841-846 ◽  
Author(s):  
Alana Den Breeyen ◽  
Jessica Rochefort ◽  
Andre Russouw ◽  
Julia Meitz-Hopkins ◽  
Cheryl L. Lennox

Phlyctema vagabunda is responsible for significant postharvest losses in ‘Cripps Pink’ apples in South Africa. The first objective of this study was to determine the presence and incidence of P. vagabunda on stored commercial ‘Cripps Pink’ apple in five major pome fruit growing regions in the Western Cape. As the fungus remains latent until postharvest, the second objective was to develop a rapid molecular detection tool to determine the presence of P. vagabunda on asymptomatic ‘Cripps Pink’ apples from two commercial orchards. Postharvest disease incidence in ‘Cripps Pink’ apples in the Western Cape ranged from 0 to 73% in the 2010/2011, 0 to 6% in 2011/2012, and 0 to 30% in 2012/2013 seasons. P. vagabunda spores were also detected on ‘Cripps Pink’ fruit from December to February and from March to April. In December and January, P. vagabunda spores were detected on the ‘Hillieri’ crab apple pollinator. The knowledge that P. vagabunda conidia are present on the surface of ‘Cripps Pink’ apples and ‘Hillieri’ crab apples during the growing season could be applied to improving current management practices in the orchards.


Author(s):  
Tsepo A. Ramatla ◽  
Nthabiseng Mphuthi ◽  
Taole Ramaili ◽  
Moeti O. Taioe ◽  
Oriel M.M. Thekisoe ◽  
...  

2020 ◽  
Vol 110 (6) ◽  
pp. 1174-1179 ◽  
Author(s):  
Michael J. Stulberg ◽  
Gem Santillana ◽  
David J. Studholme ◽  
Beth Kasiborski ◽  
Mary Ortiz-Castro ◽  
...  

Xanthomonas vasicola pv. vasculorum (syn. X. campestris pv. vasculorum) was initially identified as the causal agent of bacterial leaf streak of corn in South Africa. The pathovar vasculorum causes disease on sugarcane and corn, but a subset of these strains was noted for its increased disease severity in corn. This subset was reclassified as X. campestris pv. zeae in the early 1990s and was found to have slightly different biochemical and genetic properties than isolates from sugarcane. There has been an emergence of X. campestris pv. zeae-like strains of X. vasicola pv. vasculorum in both the United States and Argentina since 2010. We performed whole genome sequencing on U.S. isolates to confirm their identity. Informed by comparative genomics, we then developed specific TaqMan qPCR and loop-mediated isothermal amplification (LAMP) assays for the detection of this specific subset of X. vasicola pv. vasculorum strains. The qPCR 4909 assay was tested against 27 xanthomonads (diverse representation), 32 DNA extractions from corn leaves confirmed as positive or negative for the bacterium, 41 X. vasicola pv. vasculorum isolates from corn in the United States and Argentina, and 31 additional bacteria associated with corn, sugarcane, or sorghum. In all cases the assay was shown to be specific for the X. vasicola pv. vasculorum isolates that cause more severe disease on corn. We then tested the LAMP 166 assay against the 27 xanthomonads and 32 corn leaf DNA samples, and we found this assay was also specific for this subset of X. vasicola pv. vasculorum isolates. We also developed a live/dead cells distinction protocol using propidium monoazide prior to DNA extraction for analyzing seed washes using these assays. These two detection assays can be useful for both diagnosticians and researchers to specifically identify the X. vasicola pv. vasculorum isolates that cause more severe symptoms on corn.


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