MINNESOTA
Barley Rusts in the United States in 2000
D.L. Long1, B.J. Steffenson2, K.J.
Leonard1, M.E. Hughes1, and L. A. Wanschura1
1Cereal Disease Laboratory, USDA-ARS and 2Department of
Plant Pathology, University of Minnesota
Stem
rust (Puccinia graminis f. sp. tritici). In
early April, a barley stem rust collection was made in the Uvalde, Texas
plots. This was unusual since stem rust
rarely occurs on barley in the southern U.S.
In early July, stem rust severities up to 5%
were observed on the two-rowed barley Hypana in west and south central
Minnesota plots. No stem rust was found
on barleys (e.g. Robust, etc.) carrying the resistance gene Rpg1.
Stem rust developed earlier than normal on wild
barley (Hordeum jubatum) because of
the early spring weather. In mid-July,
stem rust severities up to 10% were reported on this host growing alongside the
roadway in eastern South Dakota and west central Minnesota. Over the past two years, stem rust has been
prevalent on wild barley throughout the northern Great Plains.
In late July, severities of 70% were observed on two-rowed
barleys (e.g. Bowman) in east central South Dakota plots. Traces of stem rust also were found on two-
and six-rowed barleys growing in plots from northeastern Montana to west
central Minnesota; however, no infection was found on plants in commercial
fields. The low prevalence of stem rust
on barley this year in the northern Great Plains may be due to reduced inoculum
levels of pathotype QCC in the southern U.S. population (Table 1).
Ten races of P.
graminis f. sp. tritici were identified on barley from 33 collections in 2000
(Table 1). The most common races were
QCMJ and QCMD, comprising 51% and 12% of the isolates, respectively. Race QCCJ comprised only 2% of the isolates
compared to 83% in 1999. Race RCRS was
identified in only 2% of the total isolates compared to 46% in 1998 and 6% in
1999.
Losses to stem rust were generally light in 2000 (Table 2).
Leaf
rust (Puccinia hordei) Barley
leaf rust was first found in early April in trace amounts in plots at Uvalde,
Texas. The greatest amount of barley
leaf rust, however, occurred in North Carolina, where it caused 5% yield loss
(Table 2).
In early July, severities of 40% were reported
on the lower leaves of plants in spring barley plots in south and east central
Minnesota and east central South Dakota. In late July, traces of barley leaf
rust were found in plots in central Minnesota.
Twelve differential barley genotypes were used to identify races
of P. hordei (Table 3). These
races were designated according to a system similar to that of Roelfs and
Martens (Phytopathology 78:526-533) as shown in Table 4. Six races of barley leaf rust were
identified from nine viable collections (Table 5). The most common race identified was MCD, comprising 44% of the
collections. This race was found only
in Minnesota and North Dakota. The
other five races each comprised 11% of the collections. As in the past, virulence to Rph1, 2, 4, 8, and 11 was common, while
virulence to Rph3, 5, 6, 9, and 12
was absent. Virulence for Rph7 was observed in one race (RFD) from
Minnesota. Virulence for this gene is
rare in Midwestern populations of P. hordei, but is fairly common in the
eastern U.S.
With the exception of North Carolina, losses to P. hordei were generally light in the U.S. in 2000 (Table 2).
Stripe rust (Puccinia striiformis f. sp. hordei). In early April, stripe rust was found on winter barley cultivars and experimental lines in plots at Corvallis, Oregon. In mid-April, barley stripe rust was severe on susceptible lines and progeny in a nursery in the Sacramento Valley of California. In mid-April, stripe rust severities of 20% were reported on susceptible winter barley lines in a Skagit Valley nursery in western Washington.
By early May, stripe rust severities of 80-100% were observed on susceptible barley cultivars in nurseries in the Sacramento and San Joaquin Valleys of California. In northwestern Washington, severities of 70% were reported on susceptible winter barley cultivars at the late jointing stage.
By mid-May, barley stripe rust spread throughout
the Central Valley of California with 100% severities observed on susceptible
cultivars and breeding lines at the soft-medium dough stage.
Increase of stripe
rust on winter barley in eastern Washington was slowed by dry weather in early
and mid-May, but in late May, the disease resumed its increase. By late June, stripe rust was starting to
increase also on spring barley in eastern Washington with severities ranging
from 20-50% on susceptible cultivars.
In California and Pacific Northwest, losses to stripe rust ranged from 2-6%. Losses to stripe rust would have been much greater, but many fields planted to susceptible cultivars were sprayed with fungicides.
Barley
crown rust (Puccinia coronata var. hordei). In
mid-June, traces of crown rust were observed on barley near the buckthorn
nurseries at Fargo, North Dakota and St. Paul, Minnesota.
In late June, traces of crown rust were found in
plots and fields in eastern South Dakota and in south central and east central
Minnesota plots.
No losses were reported for barley due to crown
rust infection.
Table 1. Races of Puccinia graminis f. sp. tritici
identified from barley in 2000 |
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No. of a |
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State |
Source |
Coll |
Isol |
QCCJ |
QCMD |
QCMJ |
QCMS |
QCRS |
QKMS |
RCMJ |
RCMS |
RCRS |
RMRS |
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MN |
Nursery |
11 |
14 |
|
7 |
71 |
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|
7 |
7 |
|
7 |
|
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MT |
Nursery |
3 |
2 |
|
|
|
|
|
|
|
100 |
|
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|
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ND |
H. jubatum
|
2 |
2 |
|
|
100 |
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|
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SD |
Nursery |
4 |
3 |
|
33 |
33 |
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|
33 |
|
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|
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H. jubatum
|
8 |
9 |
|
22 |
56 |
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|
22 |
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TX |
Field |
4 |
12 |
8 |
8 |
33 |
33 |
8 |
8 |
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Nursery |
1 |
1 |
|
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|
|
|
|
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|
100 |
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U.S. |
Field |
4 |
12 |
8 |
8 |
33 |
33 |
8 |
8 |
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Nursery |
19 |
20 |
|
10 |
55 |
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10 |
15 |
5 |
5 |
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H. jubatum
|
10 |
11 |
|
18 |
64 |
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18 |
|
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Total |
33 |
43 |
2 |
12 |
51 |
9 |
2 |
2 |
9 |
7 |
2 |
2 |
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a Coll = collections; Isol = isolates. |
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Table 2. Estimated losses in barley due to rust in
2000 |
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Losses due to: |
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1000 |
Yield in |
Production |
Stem rust |
Leaf rust |
Stripe rust |
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acres |
bushels |
in 1000 |
|
1000 |
|
1000 |
|
1000 |
State |
harvested |
per acre |
bushels |
% |
bushels |
% |
bushels |
% |
bushels |
AZ |
36 |
114.0 |
4,104 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
CA |
85 |
68.0 |
5,780 |
T* |
T |
1.0 |
62.2 |
6.0 |
372.9 |
CO |
105 |
115.0 |
12,075 |
0.0 |
0.0 |
T |
T |
0.0 |
0.0 |
ID |
730 |
76.0 |
55,480 |
0.0 |
0.0 |
0.0 |
0.0 |
T |
T |
KS |
7 |
35.0 |
245 |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
KY |
8 |
75.0 |
600 |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
MI |
19 |
60.0 |
1,140 |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
MN |
240 |
64.0 |
15,360 |
T |
T |
T |
T |
0.0 |
0.0 |
MT |
950 |
40.0 |
38,000 |
0.0 |
0.0 |
0.0 |
0.0 |
T |
T |
NE |
6 |
27.0 |
162 |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
NC |
18 |
80.0 |
1,440 |
0.0 |
0.0 |
5.0 |
75.8 |
|
|
ND |
1,780 |
56.0 |
99,680 |
T |
T |
T |
T |
|
|
OK |
NA** |
NA |
NA |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
OR |
140 |
60.0 |
8,400 |
0.0 |
0.0 |
0.0 |
0.0 |
5.0 |
442.1 |
PA |
75 |
71.0 |
5,325 |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
SC |
NA |
NA |
NA |
0.0 |
0.0 |
0.0 |
0.0 |
|
|
SD |
105 |
55.0 |
5,775 |
T |
T |
0.0 |
0.0 |
|
|
TX |
NA |
NA |
NA |
T |
T |
T |
T |
0.0 |
0.0 |
UT |
78 |
70.0 |
5,460 |
0.0 |
0.0 |
0.0 |
0.0 |
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VA |
65 |
89.0 |
5,785 |
0.0 |
0.0 |
0.0 |
0.0 |
|
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WA |
490 |
70.0 |
34,300 |
0.0 |
0.0 |
0.1 |
35.0 |
2.0 |
700.7 |
WI |
50 |
64.0 |
3,200 |
0.0 |
0.0 |
T |
T |
|
|
WY |
95 |
83.0 |
7,885 |
0.0 |
0.0 |
0.0 |
0.0 |
|
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Total of above |
5,082 |
61.0 |
310,196 |
|
T |
|
173.0 |
|
1515.7 |
U.S. % loss |
|
|
T |
|
0.06 |
|
0.49 |
|
|
U.S. Total |
5,211 |
61.4 |
320,195 |
|
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*T = Trace **NA = Not Available,
therefore not included in loss totals. |
Table 3. Barley genotypes used to differentiate
isolates of Puccinia hordei |
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Genotype |
|
Resistance gene(s) |
Sudan |
|
Rph1 |
Peruvian |
|
Rph2 |
Estate |
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Rph3 |
Gold |
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Rph4 |
Magnif |
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Rph5 |
Bowman/Bolivia selection |
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Rph6 |
Cebada Capa |
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Rph7 |
Egypt 4 |
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Rph8 |
Hor 2596 |
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Rph9 |
Clip BC8 |
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Rph10 |
Clip BC67 |
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Rph11 |
Triumph |
|
Rph12 |
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Table 4. A proposed North American system of
pathotype nomenclature for Puccinia
hordei based on 12 differential
barley hostsa |
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Infection phenotype of pathogen
and barley Rph genes |
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Set 1 |
Rph1 |
Rph2 |
Rph3 |
Rph4 |
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Set 2 |
Rph5 |
Rph6 |
Rph7 |
Rph8 |
|
Ph-code |
Set 3 |
Rph9 |
Rph10 |
Rph11 |
Rph12 |
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B |
Low |
Low |
Low |
Low |
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C |
Low |
Low |
Low |
High |
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D |
Low |
Low |
High |
Low |
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F |
Low |
Low |
High |
High |
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G |
Low |
High |
Low |
Low |
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H |
Low |
High |
Low |
High |
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J |
Low |
High |
High |
Low |
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K |
Low |
High |
High |
High |
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L |
High |
Low |
Low |
Low |
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M |
High |
Low |
Low |
High |
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N |
High |
Low |
High |
Low |
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P |
High |
Low |
High |
High |
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Q |
High |
High |
Low |
Low |
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R |
High |
High |
Low |
High |
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S |
High |
High |
High |
Low |
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|
T |
High |
High |
High |
High |
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a Pathotype designations are
based on the infection phenotypes of the pathogen isolate on the 12
differential barley hosts. Low =
incompatibility (infection phenotypes 0, 0;, 1, or 2) and High =
compatibility (infection phenotypes 3 or 4).
The infection phenotypes from set 1 determine the first letter of the
code, those from set 2 the second, etc. |
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Table 5. Races of Puccinia hordei identified from the United States in 2000 |
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Number of |
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State |
collections |
Source |
Pathotypes and (no. of
collections) |
Minnesota |
4 |
Nursery |
MCD (2), RCD (1), RFD (1) |
Minnesota |
1 |
Field |
MCD (1) |
North Dakota |
2 |
Nursery
|
MCD (1), MCJ (1) |
South Dakota |
1 |
Nursery |
RBD (1) |
Virginia |
1 |
Nursery |
MCB (1) |
TOTAL |
9 |
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