Mariette Truter

Mariette Truter


Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 September 2014 in Studies in Mycology
Verified
Journal Article
Open access
JWJ.H.C. Woudenberg
J.H.C. Woudenberg
MTMariette Truter
Mariette Truter
JGJ.Z. Groenewald
J.Z. Groenewald
PCP.W. Crous
P.W. Crous
The omnipresent fungal genusAlternariawas recently divided into 24 sections based on molecular and morphological data.Alternariasect.Porriis the largest section, containing almost allAlternariaspecies with medium to large conidia and long beaks, some of which are important plant pathogens (e.g.Alternaria porri, A. solaniandA. tomatophila). We constructed a multi-gene phylogeny on parts of the ITS, GAPDH, RPB2, TEF1 and Alt a 1 gene regions, which, supplemented with morphological and cultural studies, forms the basis for species recognition in sect.Porri. Our data reveal 63 species, of which 10 are newly described in sect.Porri, and 27 species names are synonymised. The three knownAlternariapathogens causing early blight on tomato all cluster in one clade, and are synonymised under the older name,A. linariae.Alternaria protenta, a species formerly only known as pathogen onHelianthus annuus, is also reported to cause early blight of potato, together withA. solaniandA. grandis. Two clades with isolates causing purple blotch of onion are confirmed asA. alliiandA. porri, but the two species cannot adequately be distinguished based on the number of beaks and branches as suggested previously. This is also found among the pathogens ofPassifloraceae, which are reduced from four to three species. In addition to the known pathogen of sweet potato,A. bataticola, three more species are delineated of which two are newly described. A newAlternariasection is also described, comprising two large-sporedAlternariaspecies with concatenate conidia.

1 May 2016 in Pedobiologia
Verified
Journal Article
Closed access
CJCharlene Janion-Scheepers
Charlene Janion-Scheepers
JMJohn Measey
John Measey
BBBrigitte Braschler
Brigitte Braschler
SCSteven L. Chown
Steven L. Chown
LCLouise Coetzee
Louise Coetzee
JWJohn R.U. Wilson
John R.U. Wilson

1 December 2015 in Plant Disease
Verified
Journal Article
Open access
NMNorman Muzhinji
Norman Muzhinji
MTMariette Truter
Mariette Truter
JWJ. W. Woodhall
J. W. Woodhall
JWJacquie Van der Waals
Jacquie Van der Waals
A survey of anastomosis groups (AG) of Rhizoctonia spp. associated with potato diseases was conducted in South Africa. In total, 112 Rhizoctonia solani and 19 binucleate Rhizoctonia (BNR) isolates were recovered from diseased potato plants, characterized for AG and pathogenicity. The AG identity of the isolates was confirmed using phylogenetic analysis of the internal transcribed spacer region of ribosomal DNA. R. solani isolates recovered belonged to AG 3-PT, AG 2-2IIIB, AG 4HG-I, AG 4HG-III, and AG 5, while BNR isolates belonged to AG A and AG R, with frequencies of 74, 6.1, 2.3, 2.3, 0.8, 12.2, and 2.3%, respectively. R. solani AG 3-PT was the most predominant AG and occurred in all the potato-growing regions sampled, whereas the other AG occurred in distinct locations. Different AG grouped into distinct clades, with high maximum parsimony and maximum-likelihood bootstrap support for both R. solani and BNR. An experiment under greenhouse conditions with representative isolates from different AG showed differences in aggressiveness between and within AG. Isolates of AG 2-2IIIB, AG 4HG-III, and AG R were the most aggressive in causing stem canker while AG 3-PT, AG 5, and AG R caused black scurf. This is the first comprehensive survey of R. solani and BNR on potato in South Africa using a molecular-based approach. This is the first report of R. solani AG 2-2IIIB and AG 4 HG-I causing stem and stolon canker and BNR AG A and AG R causing stem canker and black scurf on potato in South Africa.

24 January 2018 in European Journal of Plant Pathology
Verified
Journal Article
Closed access
PDF file
MKM. G. Kgatle
M. G. Kgatle
MTMariette Truter
Mariette Truter
TRT. M. Ramusi
T. M. Ramusi
BFB. Flett
B. Flett
TAT. A. S. Aveling
T. A. S. Aveling

1 April 2014 in Plant Disease
Verified
Journal Article
Open access
NMNorman Muzhinji
Norman Muzhinji
JWJ. W. Woodhall
J. W. Woodhall
MTMariette Truter
Mariette Truter
JWJacquie Van der Waals
Jacquie Van der Waals
Rhizoctonia solani consists of 13 anastomosis groups (AGs) designated AG1 to 13. AG3-PT is considered the predominant AG in potatoes (4) and is associated with quantitative and qualitative yield losses. Qualitative losses are typically associated with the tuber blemish disease, black scurf. However, atypical tuber blemishes such as elephant hide consisting of corky lesions on the tuber surface (2) have also been attributed to Rhizoctonia. Such atypical blemishes are not considered specific to Rhizoctonia, making direct-cause effect estimates difficult (1). Koch's postulates for the elephant hide symptom and R. solani AG3-PT have not been completed. Recently, growth cracking and scab lesions were observed on potato tubers in South Africa and attributed to a new Streptomyces species (3). These lesions and cracks were similar to elephant hide symptoms attributed to R. solani AG3-PT. Therefore, the cause of the elephant hide symptom in South Africa was investigated further. Symptoms of elephant hide and cracking have been observed on tubers from the Eastern Free State, KwaZulu-Natal, Limpopo, Mpumalanga, North-Eastern Cape, Northern Cape, North West, Sandveld, and Western Free State growing regions. In 2012, three samples of potato tubers (cv. BP1) with elephant hide and cracking were selected for analysis. These samples were collected from Clanwilliam in the Sandveld potato growing region. Tubers were surface sterilized with 1% NaOCl; sections of affected tissue were excised and plated onto potato dextrose agar (PDA). Rhizoctonia-like colonies were identified and after further sub-culturing on PDA, three representative isolates (Rh3, Rh4, and Rh6) of R. solani from each sample were obtained. For each isolate, genomic DNA was extracted and the rDNA ITS region sequenced using ITS1-F and ITS4 (2). The resulting sequences (KF234142, KF234143, and KF234144) were at least 98% identical to other AG3-PT sequences on GenBank (JX27814 and KC157664). To confirm Koch's postulates, pathogenicity tests were conducted with the three isolates. PDA plugs of each isolate were added to 10 g of barley grains which were incubated for 14 days until fully colonized. The barley grains were then used to inoculate disease-free mini-tubers (cv. BP1) in 5l pots containing a sand-clay-pine bark mixture (1:1:1 ratio). Potato plants inoculated with sterile barley grains served as controls. Plants were held for 120 days in a greenhouse at 22°C with light for 12 h a day. Incidence of the elephant hide symptom for isolates Rh3, Rh4, and Rh6 was 58%, 33%, and 37.5%, respectively. Growth cracking and black scurf were also observed with each isolate. R. solani AG3-PT was successfully re-isolated from symptomatic tubers, confirming Koch's postulates. This is the first report of R. solani AG3-PT causing elephant hide in potato tubers in South Africa. Elephant hide caused by R. solani AG3-PT has been reported in tubers from France (2) and the United Kingdom (3), but Koch's postulates were not proven. In this study, Koch's postulates were proven for R. solani AG3-PT causing scab or elephant hide symptom and cracking in potato tubers. R. solani AG3-PT should thus be considered in addition to Streptomyces as a cause of this symptom and control strategies should also consider R. solani AG3-PT. References: (1) G. J. Banville et al. Pages 321-330 in: Rhizoctonia Species: Taxonomy, Molecular Biology, Ecology, Pathology and Disease Control, B. Sneh et al., eds. Kluwer Academic Publishers, Dordrecht, The Netherlands, 1996. (2) M. Fiers et al. Eur. J. Plant. Pathol. 128:353, 2010. (3) R. Gouws and A. McLeod. Plant Dis. 96:1223, 2012. (4) J. W. Woodhall et al. Eur. J. Plant. Pathol. 136:273, 2013.

3 October 2023 in Crop Science
Verified
Journal Article
Open access
SLSunette M Laurie
Sunette M Laurie
MMMapula Julia Mulabisana
Mapula Julia Mulabisana
RSRene Sutherland
Rene Sutherland
DSDharini Sivakumar
Dharini Sivakumar
KPKgabo Pofu
Kgabo Pofu
MBMichael W. Bairu
Michael W. Bairu
The 2030 Agenda for Sustainable Development Goals of the United Nations puts forward a transformational vision to cope with food security, nutrition, and health challenges, in which sweet potato can play an important role. Globally, sweet potato production is valued at $53.83 billion. The Agricultural Research Council of South Africa (ARC) sweet potato research and development (R&D) program over the past seven decades delivered 31 genetically improved cultivars via demand‐led breeding, managed the collection and maintenance of 375 accessions, contributed toward the optimization of cultivation practices, developed crop protection and diagnostic services, and provided streamlined seed systems and technology transfer in processing and enterprise development. The ARC's work is part of a large number of interdependent global programs committed to improving livelihoods and nutrition through sweet potato. This review shares and analyses major achievements, highlights unique research contributions achieved through partnerships, and discusses bottlenecks on funding and uptake of technologies. New research imperatives will involve root phenotyping, employing marker‐based technologies, and genome‐wide association studies through new funding received recently. Exploration of the commercialization potential of processed products made from orange‐fleshed sweet potato will be a major focus of the R&D program. Expansion of partnerships, marketing, and financing will be important for future contribution of sweet potato to the economy.