Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-22T14:36:01.018Z Has data issue: false hasContentIssue false

Differential Aggressiveness of Bipolaris microstegii and B. drechsleri on Japanese Stiltgrass

Published online by Cambridge University Press:  27 April 2017

William L. Bruckart III*
Affiliation:
Research Plant Pathologist, Support Scientist, Biological Science Lab Technician, and Biological Science Lab Technician, U.S. Department of Agriculture, Agricultural Research Service, Foreign Disease-Weed Science Research Unit, 1301 Ditto Avenue, Fort Detrick, MD 21702
Farivar M. Eskandari
Affiliation:
Research Plant Pathologist, Support Scientist, Biological Science Lab Technician, and Biological Science Lab Technician, U.S. Department of Agriculture, Agricultural Research Service, Foreign Disease-Weed Science Research Unit, 1301 Ditto Avenue, Fort Detrick, MD 21702
Jami L. Michael
Affiliation:
Research Plant Pathologist, Support Scientist, Biological Science Lab Technician, and Biological Science Lab Technician, U.S. Department of Agriculture, Agricultural Research Service, Foreign Disease-Weed Science Research Unit, 1301 Ditto Avenue, Fort Detrick, MD 21702
Emily L. Smallwood
Affiliation:
Research Plant Pathologist, Support Scientist, Biological Science Lab Technician, and Biological Science Lab Technician, U.S. Department of Agriculture, Agricultural Research Service, Foreign Disease-Weed Science Research Unit, 1301 Ditto Avenue, Fort Detrick, MD 21702
*
*Corresponding author’s E-mail: [email protected]

Abstract

Severe leaf blight of Japanese stiltgrass (JSG) from Bipolaris disease, causing significant decline in population density at some locations, has been reported sporadically in the field. Even so, much of the JSG in the mid-Atlantic is not diseased. Six populations of JSG from the field, one that was severely diseased by B. microstegii and the others “healthy,” were tested by artificial inoculation for susceptibility to both B. microstegii (five isolates) and B. drechsleri (three isolates). Populations of JSG in this study differed in their response to the two Bipolaris species, but within species of Bipolaris the plant responses were consistent. Plants from the diseased population of JSG from Frederick, MD, were very susceptible to B. microstegii, and plants from other populations from Maryland (three locations), Delaware, and Indiana were not. In contrast, B. drechsleri caused moderate disease on plants from all accessions but one, and it was significantly less aggressive than was B. microstegii on the susceptible accession of JSG. Results of a limited host range determination only with B. microstegii revealed hypersensitive responses, and therefore high levels of resistance, in corn (four cultivars) and sorghum (three accessions). The native, sympatric grass deertongue was not diseased in these tests. Results reveal a distinct differential response among populations of JSG to disease from B. microstegii, while in contrast, B. drechsleri is capable of causing disease on a broader range of JSG populations.

Type
Research and Education
Copyright
© Weed Science Society of America, 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Associate Editor for this paper: Rob J. Richardson, North Carolina State University.

References

Literature Cited

Averill, KM, Mortensen, DA, Smithwick, EAH, Post, E (2016) Deer feeding selectivity for invasive plants. Biol Invasions 18:12471263 Google Scholar
Bauer, JT, Flory, SL (2011) Suppression of the woodland herb Senna hebecarpa by the invasive grass Microstegium vimineum . Am Midl Nat 165:105115 Google Scholar
Bruckart, WL III, Eskandari, FM, Lane, WA (2014) First report of leaf necrosis on Microstegium vimineum caused by Bipolaris microstegii in Maryland. Plant Dis 98:852 CrossRefGoogle ScholarPubMed
Crous, PW, et al. (2012). Fungal Planet description sheets: 128–153. Persoonia 29:146–201. (No. 129: Bipolaris microstegii Minnis, Rossman, Kleczewski & S. L. Flory, sp. nov. pages 150–151)CrossRefGoogle Scholar
Crous, PW, et al. (2013). Fungal Planet description sheets: 154–213. Persoonia 31:188–296. (No. 213: Bipolaris drechsleri Manamgoda & Minnis, sp. nov. pages 291–292)Google Scholar
Culley, EM, Huebner, CD, Novy, A (2016) Regional and local genetic variation in Japanese stiltgrass (Microstegium vimineum). Invasive Plant Sci Manag 9:96111 CrossRefGoogle Scholar
de Lima Nechet, K, Barreto, RW, Mizubuti, ESG (2006) Bipolaris euphorbiae as a biological control agent for wild poinsettia (Euphorbia heterophylla): host-specificity and variability in pathogen and host populations. Biocontrol (Dordrecht) 51:259275 CrossRefGoogle Scholar
Ehrenfeld, JG (2003) Effects of exotic plant invasions on soil nutrient cycling processes. Ecosystems 6:503523 CrossRefGoogle Scholar
Farr, DF, Rossman, AY (2016). Fungal Databases, Systematic Mycology and Microbiology Laboratory, ARS, USDA. http://nt.ars-grin.gov/fungaldatabases. Accessed: August 18, 2016Google Scholar
Flory, SL, Clay, K (2010a). Non-native grass invasion alters native plant composition in experimental communities. Biol Invasions 12:12851294 Google Scholar
Flory, SL, Clay, K (2010b). Non-native grass invasion suppresses forest succession. Oecologia 164:10291038 Google Scholar
Flory, SL, Kleczewski, N, Clay, K (2011) Ecological consequences of pathogen accumulation on an invasive grass. Ecosphere 2(10): Article 120. doi: 10.1890/ES11-00191.1 Google Scholar
Kleczewski, NM, Flory, SL (2010) Leaf blight disease on the invasive grass Microstegium vimineum caused by a Bipolaris sp. Plant Dis 94:807811 CrossRefGoogle ScholarPubMed
Kleczewski, NM, Flory, SL, Clay, K (2012) Variation in pathogenicity and host range of Bipolaris sp. causing leaf blight disease on the invasive grass Microstegium vimineum . Weed Sci 60:486493 Google Scholar
Knight, TM, Dunn, JL, Smith, LA, Davis, J, Kalisz, S (2009) Deer facilitate invasive plant success in a Pennsylvania forest understory. Nat Areas J 29:110116 Google Scholar
Lakshmanan, P, Jeyarajan, R, Vidhyasekaran, P (1990) Leaf and stem blight of Euphorbia geniculata incited by Bipolaris zeicola . Phytoparasitica 18:353355 Google Scholar
Lee, M, Flory, SL, Phillips, R (2012) Positive feedbacks to growth of an invasive grass through alteration of nitrogen cycling. Oecologia 170:457465 CrossRefGoogle ScholarPubMed
Manamgoda, DS, Rossman, AY, Castlebury, LA, Crous, PW, Madrid, H, Chukeatirote, E, Hyde, KD (2014) The genus Bipolaris . Stud Mycol 79:221288 Google Scholar
Mortensen, DA, Rauschert, ESJ, Nord, AN, Jones, BP (2009) Forest roads facilitate the spread of invasive plants. Invasive Plant Sci Manag 2:191199 CrossRefGoogle Scholar
Simao, MC, Flory, SL, Rudgers, JA (2010) Experimental plant invasion reduces arthropod abundance and richness across multiple trophic levels. Oikos 119:15531562 Google Scholar
Stricker, KB, Harmon, PF, Goss, EM, Clay, K, Flory, SL (2016) Emergence and accumulation of novel pathogens suppress an invasive species. Ecol Lett 19:469477 Google Scholar
Swearingen, J, Slattery, B, Reshetiloff, K, Zwicker, S (2010). Plant Invaders of Mid-Atlantic Natural Areas. 4th edn. Washington, DC: National Park Service and U.S. Fish and Wildlife Service. 168 ppGoogle Scholar
[USDA-NRCS] U.S. Department of Agriculture, Natural Resources Conservation Service (2013) The PLANTS Database. Greensboro, NC: National Plant Data Team. http://plants.usda.gov. Accessed: June 27, 2013Google Scholar
Winder, RS, Van Dyke, CG (1990) The pathogenicity, virulence, and biocontrol potential of two Bipolaris species on johnsongrass (Sorghum halepense). Weed Sci 38:8994 CrossRefGoogle Scholar
Yandoc, CB, Charudattan, R (2004) Suppression of cogongrass (Imperata cylindrica) by a bioherbicidal fungus and plant competition. Weed Sci 52:649653 CrossRefGoogle Scholar