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Applied and Environmental Microbiology, January 2000, p. 425-427, Vol. 66, No. 1
0099-2240/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Phoma glomerata as a Mycoparasite of
Powdery Mildew
Raymond F.
Sullivan and
James F.
White Jr.*
Department of Plant Pathology, Cook College,
Rutgers University, New Brunswick, New Jersey 08901
Received 26 July 1999/Accepted 2 November 1999
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ABSTRACT |
Ampelomyces and Phoma species are
frequently confused with each other. Isolates previously attributed to
the genus Ampelomyces were shown to be Phoma
isolates through studies of their morphology and life cycle and
ribosomal DNA internal transcribed spacer region 1 sequence analysis.
Phoma glomerata can colonize and suppress development of
powdery mildew on oak and may have utility as a mycoparasitic agent.
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TEXT |
Powdery mildews are widespread plant
pathogens that are conspicuous by their white mycelia and powder-like
conidia (20). The fungus Ampelomyces quisqualis
Ces. is the only fungus that has been demonstrated to be generally
effective as a biocontrol agent of powdery mildew (4, 9,
16). Many morphologically similar species may be confused with
A. quisqualis (10). To evaluate this possibility,
we examined and identified Ampelomyces-like fungi isolated
from powdery mildew and compared these cultures with isolates
identified as Ampelomyces in culture collections.
Isolation and growth.
Leaves of sycamore trees (Platanus
occidentalis L.) bearing infections of powdery mildew
(Microsphaera penicillata (Wallr.:Fr.) Lèv.) were
located in South River, New Jersey, in July 1998. Microscopic
examination of the leaves revealed two types of pycnidia: stipitate
pycnidia, typical of A. quisqualis, and sessile pycnidia, typical of the genus Phoma (Fig.
1) (17). Both types of
pycnidia were removed from leaves with fine needles and placed on
potato dextrose agar (Difco, Inc., Detroit, Mich.) containing the
antibiotics gentamicin (40 mg/liter), streptomycin (40 mg/liter), and
penicillin (20 mg/liter) (PDA + 3). Two different fungi were
consistently recovered. The stipitate pycnidia developed into
slow-growing colonies whose characteristics corresponded to those
expected for A. quisqualis (5, 11). The sessile
pycnidia developed into rapidly growing colonies whose characteristics
corresponded to those of Phoma glomerata (Cda) Wollenw.
(2, 19).

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FIG. 1.
(A) Stipitate pycnidium of A. quisqualis
(arrow). (B) Section of sessile pycnidium of P. glomerata on
oak leaf (arrow). Scale bar = 20 µm.
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Agar plugs (6 mm in diameter) of mycelia cut from the margins of
rapidly growing colonies of both the South River
Ampelomyces and South River
P. glomerata isolates were transferred to
five
plates each of PDA+3 and incubated at room temperature (21 to
22°C) for 3 weeks to measure growth rates. We measured an average
growth of 8 ± 1 mm/day for the
P. glomerata isolates
and an average
growth of 0.8 ± 0.1 mm/day for the
Ampelomyces isolates. With
age, cultures of
P. glomerata produced alternarioid dictyochlamydospores
measuring
41 ± 7.5 × 12 ± 1.4 µm.
Inoculation experiments.
Koch's postulates (1, 3)
were used to establish the pathogenicity of P. glomerata to
powdery mildew. A suspension of P. glomerata conidia from
cultures grown on PDA+3 was made in sterile water (~8 × 106 conidia/ml). The conidial suspension was used to
inoculate epiphyllous mycelia of the powdery mildew Phyllactinia
guttata (Wallr.:Fr.) Lèv. on intact (left on the tree)
leaves of oak (Quercus coccinea Münch.) by moistening
an approximately 15-mm2 region on the upper surface of the
leaves. Controls were repeats of this process with sterile water. Ten
replicates of both the treatment and control were made, and the sites
of inoculation were marked by placing white tape on the reverse of the
leaves at the inoculation sites. The leaves were monitored for 30 days. During this time, control leaves developed powdery mildew cleistothecia while all leaves treated with P. glomerata conidia developed
abundant pycnidia in and around the inoculation sites but did not
produce powdery mildew cleistothecia. None of the control leaves showed development of P. glomerata pycnidia, and cleistothecia
developed normally. To fulfill Koch's postulates, pycnidia were
removed from treated leaves with fine needles and plated on PDA+3
medium to recover P. glomerata. Colonies that developed were
confirmed to be P. glomerata by observation of
dictyochlamydospores, pycnidia, and subsequent sequence analysis.
Phylogenetic analysis.
The nuclear ribosomal DNA internal
transcribed spacer region 1 (ITS1) from P. glomerata,
several Ampelomyces spp., and several Phoma spp.
were sequenced. The South River P. glomerata and A. quisqualis, as well as American Type Culture Collection (ATCC) cultures of Ampelomyces heraclei (Dejeva) Rudakov (ATCC
36804) and A. quisqualis (ATCC 200245), were grown on PDA+3.
DNA extraction, amplification, and sequencing were accomplished as
described previously (14).
Several additional ITS1 sequences identified as
Ampelomyces
spp., including
Ampelomyces humuli (Fautr.) Rudakov,
Ampelomyces quercinus (Syd.) Rudakov,
Phaeosphaeria
avenaria (Weber) Eriksson,
and
Leptosphaeria
microscopica P. Karst. were obtained from GenBank
(Fig.
2).

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FIG. 2.
Maximum likelihood phylogram based on ITS region
sequences between the 18S and 5.8S ribosomal DNA (ITS1). Bootstrap
confidence levels (percent) of branches are shown. The scale bar is
based on a total tree length of 204. Taxa included in the analysis,
GenBank numbers (if known), and their sources are as follows:
LM, L. microscopica (LMU04234); PAV,
P. avenaria (PAU77357); AQ1, A. quisqualis
(AQU82451, DSM [Deutsche Sammlung von Mikrooganismen und Zellkulturen
GmbH, Braunschweig, Germany] 2223); AQ2, A. quisqualis
(AF126818, South River); AQ3, A. quisqualis (AF126817, ATCC
200245); AQ4, A. quisqualis (AF035782); AQ5, A. quisqualis (AQU82449, CBS [Centraalbureau voor Schimmelcultures,
Baarn, The Netherlands] 130.79); AQ6, A. quisqualis
(AF035783, Ecogen AQ10); AQ7, A. quisqualis (AF035781, CBS
131.31); AQS, A. quercinus (AF035778, ATCC
36786); PG, P. glomerata (AF126816, South River);
AHE, A. heraclei (AF126819, ATCC 36804);
AHU, A. humuli (AF035779, ATCC 38616);
PAM, P. americana Morgan-Jones et White
(AF046016); PM, P. macrostoma Mont. (AF046020);
PS, P. sorghina (Sacc.) Boerema (AF046022);
DL, D. lycopersici Klebahn (AF046015); and
DB, D. bryoniae (Auersw.) Rehm (AF046014).
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The SeqLab interface for the Wisconsin Package Version 9.1 (Genetics
Computer Group, Madison, Wis.) was used to generate alignments
and make
manual adjustments. PAUP version 4.0b2 for Macintosh
(
17)
was used for phylogenetic analysis. Heuristic searches
were performed
by using maximum parsimony (
14). Bootstrapping,
using the
same criteria with 400 replicates, was performed to
determine the
confidence levels of the inferred phylogenies. Trees
found by maximum
parsimony were subjected to heuristic searches
by using maximum
likelihood criteria by the Hasegawa-Kishino-Yano
model (
6)
to find the most likely tree (See Treebase
[
http://herbaria.harvard.edu/treebase]
submission no. SN145 for
alignment and tree construction
details).
Maximum parsimony analysis resulted in ten trees. Maximum likelihood
analysis of these trees resulted in one tree (

ln L =
1200, tree
length = 204, consistency index = 0.78, homoplasy index
= 0.22, retention index = 0.79). The South River
P. glomerata is identical to
A. heraclei and
A. humuli, and they group together
with
A. quercinus in
the
Didymella/Phoma clade (Fig.
2). Our South
River
A. quisqualis isolate grouped in the
Ampelomyces clade
with
Ecogen's
A. quisqualis AQ10. There was strong
bootstrap support
for the
Ampelomyces (90%) and
Phoma (100%)
clades.
Distinguishing Phoma from Ampelomyces.
Stipitate pycnidia developing into slow-growing colonies characterize
A. quisqualis (5, 11). Sessile pycnidia
developing into rapidly growing colonies characterize P. glomerata (2, 19). The cultures identified as A. heraclei, A. humuli, and A. quercinus are
typical representatives of their species.
The process of pycnidium formation in association with the powdery
mildew is also different between the two genera.
Ampelomyces spp. infect conidiogenous cells of powdery mildew, internally
colonizing and forming pycnidia within the conidiophore; the pycnidia
appear stipitate (Fig.
1).
Phoma sp. does not appear to
internally
infect conidiogenous cells, and pycnidia are formed directly
on
the leaf surface; they are sessile (Fig.
1). While many species
of
Phoma are plant pathogens (
17),
P. glomerata is not. However,
Phoma can grow
saprophytically in tissues of plants and is known
to be a secondary
invader of diseased tissues, perhaps feeding
on fungal saprophytes or
pathogens of diseased tissues (
12,
17,
19).
P. glomerata has been isolated from species of the
powdery mildew
genus
Microsphaera in the United States (this study)
and
Russia (as
A. quercinus) and from species of the genus
Sphaerotheca (as
A. humuli) in Russia
(
15). It also has been isolated from
the downy mildew of
grapes (
Plasmopara viticola (Berk. et Curt.)
Berl. et De
Toni) in Russia (as
A. heraclei) (
15). It is
apparent
that
P. glomerata has a widespread
distribution.
Potential new mycoparasitic agent.
Currently a single strain
of fungus, A. quisqualis AQ10 Biofungicide, is in commercial
use for biocontrol of powdery mildew on grapes and other crops
(7). This strain grouped within the divergent
Ampelomyces clade and appears to correctly represent a
species of that genus. A few reports have identified Phoma
species that are antagonistic to fungal plant pathogens. A
Phoma sp. (P66A) significantly reduced conidial germination
of an apple scab (Venturia inaequalis (Cooke) Wint.)
(13), and Phoma etheridgei Hutch. & Hirat.
produced antifungal compounds inhibitory to the tree pathogen
Phellinus tremulae (Bond) Bond et Borisov (8).
Our results suggest that
P. glomerata is frequently
misidentified as
A. quisqualis or other species of
Ampelomyces. Additionally,
P. glomerata often may
inhabit powdery mildew infections and may
be an important component of
a hyperparasitic guild of fungi that
naturally infect powdery mildews.
Further study is warranted to
evaluate the effectiveness of
P. glomerata in the hyperparasitic
control of fungal plant
pathogens.
Nucleotide sequence accession numbers.
The following sequences
were deposited in GenBank: A. quisqualis ATCC 200245 and
South River, P. glomerata South River, A. heraclei ATCC 36804. Their accession numbers are listed in the legend for Fig. 2.
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FOOTNOTES |
*
Corresponding author. Mailing address: Department of
Plant Pathology, 386 Foran Hall, Cook College, Rutgers University, New Brunswick, NJ 08901. Phone: (732) 932-9375, ext. 357. Fax: (732) 932-9377. E-mail: jwhite{at}aesop.rutgers.edu.
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Applied and Environmental Microbiology, January 2000, p. 425-427, Vol. 66, No. 1
0099-2240/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.