Finally, we showed that the scallion used
by farmers in the crop rotation sequence was a
variety susceptible to M. graminicola.
Consequently, it helped maintain a significant
M. graminicola population in the soil during
the winter season before planting rice.
Scallion was previously reported as a good
host of M. graminicola. The growth and yields
of the Yellow Granex scallion variety grown
in a cropping sequence with rice in the
Philippines, was severely reduced due to M.
graminicola infection (Gergon et al., 2002).
Therefore, M. graminicola infection is not
only reducing the expected income from rice
cultivation but also from scallion. Although
crop rotation is an important practice that can
help farmers to limit nematode occurrence in
a field (Mantelin et al., 2017, Védie et al.,
2014), a wrong combination of plants can
have the opposite effect of contributing to the
proliferation of the pest followed by severe
damage to the cultivated plants. A solution for
the farmers should be using resistant rice
varieties (Dimkpa et al., 2016; Thi Phan et al.,
2017) and/or to grow non-susceptible plants
instead of scallion. If the same cropping
system persisted and no nematode control
strategies were implemented, a strongly
increasing number of M. graminicola would
be expected in the field year by year.
In order to reduce the negative impact of
this pest on rice production, it is critical to
increase the farmer’s awareness on the risk of
plant parasitic nematode infection as too many
severe nematode infections on rice are being
mis-identified. Indeed, due to limited root
development caused by the nematode
infection, parasitized plants can present the
same leaf symptoms as nutrient starvation and
water stress. The infected plants can also
present other sickness symptoms that are
originally due to M. graminicola, as this
nematode causes its host to be more
susceptible to other pathogens (Kyndt et al.,
2017). Fortunately, symptoms of infected
roots are easily identifiable and farmers can
quickly be aware of the presence of M.
graminicola when they inspect carefully the
rice root system.
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ACADEMIA JOURNAL OF BIOLOGY 2020, 42(3): 31–42
DOI: 10.15625/2615-9023/v42n3.15036
31
ROOT KNOT NEMATODE INFECTIONS PROMOTED BY AGRICULTURAL
PRACTICE MODIFICATIONS IN VIETNAM AND THE IMPACTS
ON RICE PRODUCTION
Nguyen Thi Hue1,*, Anne-Sophie Masson1,2,3, Lionel Moulin3,
Trinh Quang Phap4,5, Ha Viet Cuong6, Stéphane Bellafiore1,3
1LMI RICE2, Agriculture Genetic Institute (AGI), University of
Science and Technology of Hanoi (USTH), Ha Noi, Vietnam
2University of Montpellier, Montpellier, France
3IRD, CIRAD, University of Montpellier, IPME, Montpellier, France
4Institute of Ecology and Biology resources, VAST, Vietnam
5Graduate University of Science and Technology, VAST, Vietnam
6Faculty of Agronomy, Vietnam National University of Agriculture, Ha Noi, Vietnam
Received 5 May 2020, accepted 31 July 2020
ABSTRACT
A survey conducted on newly cultivated lowland rice fields by direct seeding method in Hai
Duong Province, Viet Nam, in March 2017 revealed high devastation of the field. In these fields,
farmers used an annual crop rotation cycle of rice-scallion-rice. Investigations on the devastated
fields revealed that the chemical and physical soil properties were appropriate for rice cultivation.
On the other hand, observations done on the root systems showed that the dead plants have
symptomatic root galls suggesting the presence of plant parasitic nematodes. Sequencing of the
internal transcribed spacer (ITS) region of the rDNA genes of the nematodes showed that the root
nematodes extracted from the infested fields belonged to Meloidogyne graminicola. The
reproductive factor of the isolated M. graminicola population on the IR64 rice variety (Oryza
sativa indica) was normal, suggesting that the impact of this plant pest was not due to the
emergence of an unusual virulent population. The combination of the three factors (wrong
cropping choice for rotation, using rice variety susceptible to M. graminicola and direct seeding)
were obviously promoting the nematode infection and its high proliferation in the surveyed
fields. Meloidogyne graminicola could parasitize and propagate in scallions of Vietnam. Since
this plant is annually cultivated on a paddy field for crop rotation, preventive measures or
alternative plant for crop rottion is necessary.
Keywords: Meloidogyne graminicola, cropping sequence, rice, scallions, virulent.
Citation: Nguyen T. H., Masson A. S., Moulin L., Trinh Q. P., Ha V. C., Bellafiore S., 2020. Root knot nematode
infections promoted by agricultural practice modifications in Vietnam and the impacts on rice production. Academia
Journal of Biology, 42(3): 31–42. https://doi.org/10.15625/2615-9023/v42n3.15036.
*Corresponding author email: huebiovfu@gmail.com
©2020 Vietnam Academy of Science and Technology (VAST)
Nguyen Thi Hue et al.
32
INTRODUCTION
Rice is the most cultivated cereal and the
most important staple food in Vietnam.
According to FAO statistics, Vietnam is ranked
at the 5th among rice producing countries in
terms of weights, after China, India, Indonesia
and Bangladesh, with 42.8 million tonnes of
paddy rice produced in 2017 (FAOSTAT,
2017). However, Vietnam ranks 26th among
rice producing countries in terms of yields, at
55,476 hg/ha in 2017. Annually, pests such as
plant parasitic nematodes (PPNs) are known to
be responsible for agricultural losses of more
than $US 80 billion (Nicol et al., 2011). they
are particularly detrimental to rice (Mantelin et
al., 2017). The most damaging PPN for rice is
Meloidogyne graminicola (M. graminicola).
This root-knot nematode (RKN) has a large
host range and geographical distribution
(Mantelin et al., 2017). RKNs are telluric
obligate plant parasites that induce gall
formation in the infected roots to facilitate
female development (Bridge and Page, 1982).
The sedentary female feeds on the plant cells in
the root galls where they hijack the plant’s
metabolism making it weaker with a small root
system and consequently severely compromise
rice yields (Bridge Page, 1982).
In Vietnam, rice is cultivated in almost all
provinces with two intensive production
regions being the Red River Delta in the North
and the Mekong Delta in the South. In the Red
River Delta, farmers routinely have two rice
crop productions a year with occasionally one
crop rotation during the offseason (e.g.
scallion, potato, sweet potato, pumpkin, corn,
sesame (Nguyen, 2009; Pham et al., 2013).
Due to the fast socio-economic changes in
Vietnam, including urban migration and
reduction of agricultural workforce (World
Bank, 2019), in some provinces, farmers have
recently stopped doing the traditional time-
consuming transplanting and shifted to direct
seedling practices. This practice saves time but
is unfortunately accompanied by unwanted side
effects like increased impacts by parasites such
as PPN (De Waele & Elsen, 2007). Previous
studies in Vietnam only noted the presence of
M. graminicola species in paddy rice
(Nguyen & Nguyen, 2000; Bellafiore et al.,
2015), but damage assessment of M.
graminicola in fields have not been conducted.
In March 2017, our survey in Hai Duong
Province revealed that several rice fields were
highly devastated. Farmers were presented
with the hypothesis that a nematode attack was
compromising their rice production.
In this study, we analyzed the reasons that
could explain the unusual proliferation of PPN
and its observed impacts on rice in Hai Duong
Province, Vietnam. Three main hypotheses
were tested: (i) A pest (nematode) highly
aggressive to rice was emerging, (ii) Farmers
used rice genotypes highly susceptible to
nematode infections, and (iii) Modification of
the farmer practices lead to the proliferation of
the pest.
MATERIALS AND METHODS
Field description, plant and soil sampling
The survey was conducted on the 11th
March, 2017 in Nam Sach district, Hai Duong
Province (21o00’51.1’’N and 106o19’33.0’’E)
(Figs. 1a, 1b). The Red River Delta of Northern
Vietnam has a tropical monsoon climate. The
three rice fields, where the survey was carried
out, are inside a ten-ha area of land with three
crops rotation per year: two rice and one
scallion crop production cycle. For a decade,
farmers have been growing scallion in the
winter before cultivating two cycles of rice in
spring and summer. Chemical fertilizers have
been mainly used (from 8 to 8.5 × 100 kg
NPK/ha/rice crop, and from 1 to 1.5 P2O5 ×
1,000 kg + 300 kg Urea + 200 KCl/ha/scallion
crop). Chemical pesticides were routinely
applied to control plant pathogens whenever
the epiphytotic of plants appeared in the field.
For the first rice cropping cycle in 2017, 15
days after ploughing, the farmer planted the
rice variety Bac Thom No7 (Oryza sativa
indica) by direct seeding. In the spring of
2017, due to unusual water scarcity, the fields
were exposed to a drought stress for up to 20
days. Nearly four weeks after direct seeding,
almost all seedlings died, presenting leaf
chlorosis and small root systems with swelling
galls Fig. 1c).
Root knot nematode infections promoted
33
Plants and soil sampling
Three fields, 3,000 m2 each, were
surveyed from the rice cultivated area
(Fig. 1b). Each field was subdivided in four
plots of 100 m2 each. 50 plants were randomly
collected from each plot, i.e. a total of 600
plants were analyzed. In addition, a composite
soil sample was taken per plot for physical
and chemical properties analysis Each plant or
soil sample was kept in a separate and labeled
plastic bag at 4 oC until laboratory analysis.
Plant samples were analyzed at LMI RICE2
(Ha Noi, Vietnam), and soil properties were
analyzed at the Soil Science Department,
Faculty of Land Management in the Vietnam
National University of Agriculture (VNUA,
Ha Noi, Vietnam).
Figure 1. Rice fields of Hai Duong Province in Vietnam (a), location of the surveyed fields in
Vietnam; (b) the three fields (in green) and the four plots (white) for each field where soil and
plant samples were collected; (c) infested plants (left) with small terminal root galls and
chlorosis leaves
Nematode extraction
Plants were picked up and scanned
carefully for the presence of galls characteristic
of RKN infection. The nematode extraction
was carried out using the hypochlorite
extraction method and a blender (McClure et
al., 1973) with minor modifications (Bellafiore
et al., 2015). Briefly, root galls collected in the
field were carefully washed with tap water to
remove soil then put in a 150 ml beaker
containing 0.5% hypochlorite solution for two
minutes before manually breaking the galls to
extract nematode eggs and juveniles (J2). The
mixture was then filtered through an 80 µm
sieve to remove plant root tissues. Eggs and J2
were recovered on a second 25 µm sieve,
rinsed several times with tap water in order to
remove the hypochlorite solution. Eggs and J2
were placed on a strainer covered by two damp
Kimwipe tissues on a 50 ml beaker filled with
sterile ddH2O. After being kept for two days in
the dark at room temperature, nematodes were
collected for further experiments.
Nematode identification
Firstly, rice root galls extracted from fields
were stained with acid fuchsin (Byrd et al.
1983) to confirm the presence of PPN.
Secondly, under a stereomicroscope, freshly
extracted J2 were observed and individually
collected. Nematodes were fixed in TAF (91
ml H2O; 7 ml of 40% formalin; 2 ml of
triethanolamine) and transferred to anhydrous
glycerine to make permanent slides following
Seinhorst (1959). Perineal patterns of the
swollen females were cut, cleaned, and
mounted in glycerine following Hartman &
Sasser (1985).
Twenty single J2 were picked up in 10 µl
of ddH2O and transferred individually in
twenty PCR tubes. 10 µl of 2X DNA lysis
buffer was then added to each PCR tube to
Nguyen Thi Hue et al.
34
proceed DNA extraction by a proteinase K
method as described by Bellafiore et al.
(2015). Primers rDNA2 (5’-
TTGATTACGTCCCTGCCCTTT- 3’) and
rDNA 1.58s (5’-
ACGAGCCCGAGTGATCCACCG-3’) were
used to amplify the internal transcribed spacer
(ITS) region of the rDNA gene (Vrain et al.,
1992). PCR was performed following
Bellafiore et al. (2015) with 35 PCR cycles of
95 oC for 30 seconds, 54 oC for 30 sec and
72 oC for 1 min followed by one step at 72 oC
for 10 min. Amplicons were gel-purified and
seven samples having good result after
purification were directly sent for sequencing
(Macrogen, South Korea) using primer
rDNA2. ITS sequences were blasted against
NCBI’s nucleotide-collection (nr/nt) database,
aligned with reference accession numbers M.
graminicola MgVN18 KF250488, M.
graminicola MgVN13 KF250481; M.
graminicola HM623442.1; M. naasi,
JN157863; M. arenaria, AF387092; M.
incognita, KC464469; M. javanica
AY438555; M. hapla LC030362.1 and
LC030359; Hirschmanniella oryzae,
EU722286 and Globodera rostochiensis
GQ294519.1 using MUSCLE v3.8.31 (Edgar,
2004) and cleaned with GBLOCKS
(Castresana, 2000). The phylogenetic tree
using the ITS sequence of Meloidogyne
isolated at Hai Duong and other nematode
species was constructed using Maximum
Likelihood (ML) analysis in MEGA 6
software with 1000 bootstrap replications.
Reproduction factor and virulence test
The scallion cultivar and IR64 cultivar
(Oryza sativa) were grown to assess their
susceptibility to M. graminicola under
controlled conditions (28 oC, 16 hours light-8
hours dark). Before transplanting, the scallion
bulbs were treated for 10 min in 1% aqueous
sodium hypochlorite solution before being
rinsed several times with tap water. Scallion
were grown in 20 × 20 cm pots previously
filled with autoclaved sandy soil made of 50%
sand and 50% potting soil and watered every
three days in order to conserve a non-
saturated soil. Two weeks after planting, each
plant was inoculated with 200 J2 (initial
population “Pi”). Concurrently, 10 days old
IR64 seedlings cultivated in small columns
containing autoclaved sand were inoculated
with 200 freshly hatched J2s. At 27 days,
post-inoculation (dpi) roots were collected,
one gram of root was stained with acid
fuchsin (Byrd et al., 1983).
Nematode in rice and scallion roots were
extracted according to the method described
above. Under stereomicroscope, for each root
system, eggs and nematodes were counted and
the sum of eggs and J2 gave the final
population density “Pf”. The reproductive
factor (Rf) was calculated according to the
ratio: Rf = Pf/Pi. This experiment was
repeated twice. Five plants for scallion and 10
plants for rice genotype were used for each
repeat. Plants with Rf < 1 were considered
resistant, and Rf > 1 as susceptible (Soriano et
al., 1999). The Rf of first repeat was present
in the result.
Statistical analyses for the reproductive
factor and soil properties
All statistical analyses were performed
using R software (R core Team, 2015). Two
sample Student’s t-tests were used to compare
the different means in Rf of rice and scallion
with 95 percent confidence interval. Variance
analysis was used to compare the three fields
for the different parameters of soil properties
using the Kruskal Wallis test.
RESULTS
Soil characteristics
Measured pH (pH H2O and pH KCl) as
well as chemical contents, including organic
carbon (OC), organic matter (OM), nitrogen
(N), sulfur (S) and cation exchange capacity
(CEC), were in a range suitable for rice
growing (McCall 1980; Dwevedi et al.,
2017; Mccauley et al., 2017). No significant
differences were observed for each
parameter in the four repeats of each field
and among the three fields (p > 0.05). The
average of the four repeats in each field for
each property is summarized in table 1.
Only phosphorous (P), measured by P2O5
Root knot nematode infections promoted
35
(%), were present in a relatively high level
in the three prospected fields. With a pH
below 6.5, phosphorus uptake by the plant is
optimum and therefore the field did not
need any more chemical P input (Pagliari et
al., 2017).
Table 1. Physical and chemical properties of soil in Nam Sach, Hai Duong
Field
pH
H2O
pH
KCl
Total content
Avail.
SO42-
(mg/100
g)
CEC
(meq/100
g)
< 0.002
mm
0.002–
0.02 mm
0.02–2
mm
OC
(%)
OM
(%)
N
(%)
P2O5
(%)
S
(%)
%
1 6.33a 5.68a 1.63a 2.81a 0.15a 0.29a 0.02a 30.36a 13.15a 20.9a 43.2a 35.9a
2 6.23a 5.75a 1.47a 2.53a 0.15a 0.26a 0.02a 39.64a 12.65a 20.4a 42.6a 37.0a
3 6.18a 5.70a 1.54a 2.65a 0.15a 0.27a 0.02a 43.21a 13.28a 22.7a 42.4a 35.0a
Note: Column numbers followed by the same letter (a) are not significantly different at P = 0.05 as
determined by Kruskal-Wallis test.
Comparison of the soil texture with the 12
major textural classes and particle size scale
(Malla, 2017) revealed that the three fields in
Hai Duong Province were characterized by a
loamy soil which is appropriate for growing
most plant varieties including rice and scallion
(Brown, 2007).
Morphology characters and molecular
identification
Morphological characters of M.
gramminicola Golden & Birchfield fit
descriptions by Hirschmann (1985), Nguyen
& Nguyen (2000) and Perry at al. (2009).
Females with pearly white body, small neck,
body length (L = 570.09 ± 54.11 μm)
(Fig. 2A). Lip region smooth, anteriorly
flattened, not distinctly set off from neck
(Fig. 2B). Rounded stylet knobs with
posteriorly sloping anterior margins, 11.03 ±
1.1 μm long (Fig. 2B). Excretory-secretory
pore very distinct, generally located about one
and one-half-stylet lengths or more from base
of unprotruded stylet (Fig. 2B). Perineal
pattern prominent with distinct and
characteristic striations (Fig. 2C). The J2
character by body cylindrical vermiform,
tapering markedly toward posterior end (L =
464.57 ± 42 μm). Stylet slender; knobs small,
oval-shaped and backwardly sloping, stylet
length (11.07 ± 0.69 µm). Lip region flat
anteriorly, continuous with body, and weakly
sclerotized (Fig. 2D); 0Tail shape and tail
terminus rounded, often slightly clavate with
tail length (68.84 ± 5.77 µm), hyaline tail
length (20.20 ± 2.87 µm) (Fig. 2E).
Figure 2. Morphological character of M. graminicola females from Hai Duong. A: Entire body,
B: Head region, C: Perineal pattern, D: Anterior end of juvenile stage 2, E: Juvenile tail tip
Nguyen Thi Hue et al.
36
500 base pair (bp.) in the ITS region of
Hai Duong PPN was amplified by PCR and
sequenced. Comparison of the amplified
sequences with other available sequences
using Nucleotide Basic Local Alignment
Search Tool (BLASTN)
( revealed that
among the seven PPN sequenced, all were
M. graminicola with a high level of
similarity from 99.67% to 100%. Sequence
alignment against reference M. graminicola
populations (MgVN18 KF250488) did not
present intraspecific variation. The
sequenced rDNA region was identical to that
of M. graminicola VN13 (accession number
KF250481) a population previously isolated
from the same region (Bellafiore et al.,
2015). The phylogenetic trees showed that
the seven Hai Duong Meloidogyne isolates
were in the same clade as the three reference
M. graminicola (KF250488, KF250481 and
HM623442). In this tree, the closest but
significantly distant RKN species is M.
naasi (JN157863) and the RKN isolated
from Hai Duong are more distant from
Meloidogyne hapla LC030362.1
LC030359.1; Meloidogyne javanica
(AY438555), Meloidogyne incognita
(KC464469) and Meloidogyne arenaria
(AF387092) (Fig. 3).
Figure 3. Evolutionary relationships of ITS sequences are estimated using maximum-likelihood.
Branches with bootstrap support > 70% are indicated (1000 replications). The scale bar denotes
0.02 substitutions per nucleotide position. All positions containing gaps and missing data were
eliminated. (1 HD, 6 HD, 11 HD, 14 HD, 15 HD, 16 HD, 19 HD: the sequence of Meloidogyne
collected in Hai Duong rice field)
Reproduction and pathogenicity of M.
graminicola
At the time of the survey, only rice was
cultivated and some unplanted scallion bulbs
remained on the edges of the fields.
Therefore, the susceptibility to M.
graminicola of the scallion used during the
crop rotation in winter was tested under
controlled conditions in a grow chamber.
Root knot nematode infections promoted
37
After 27 dpi, small galls were easily
identified in the root system (Fig. 4B). Acid
fuchsin staining confirmed the susceptibility
of scallion and rice varieties cultivated by
farmers in this field (Figs. 4A, 4B). M.
graminicola eggs and females were present
in abundance in the roots of the scallion
plants (Fig. 4C).
Figure 4. A: The typical root galls of Bac Thom rice variety in M. graminicola infested field. B:
The terminal root galls of scallion bulbs after inoculated with M. graminicola. C: The eggs of
M. graminicola (arrow) are released by the female directly in the root of scallion bulbs
After 27 dpi, the measurement of Rf
revealed significant differences between IR64
and scallion plants (p-value < 0.001) with the
Rf value in IR64 (19.25) being five times
higher than that in scallions (3.96) (Fig. 4).
Therefore, the varieties of rice and scallion
used by farmers are susceptible to infection
with M. graminicola.
Figure 5. Reproduction factors of M. graminicola on O. sativa cv. IR64 and local scallion cv.
The graph shows the average values of reproductive factor of scallion and IR64 in two repeat.
The number of replicated plants is n = 5 for scallion and n = 10 for rice
DISCUSSION
Based on morphological observations and
DNA barcoding, we showed that the 10 ha of
the farm inspected in Hai Duong Province
were severely infected with PPN, M.
graminicola. This globally distributed species
has become a serious pest in several tropical
countries in Asia and notably in Vietnam in
deep water and irrigated systems (Cuc & Prot,
1992; Cuc & Prot, 1995, Bridge et al., 2005;
Bellafiore et al., 2015; Jain et al., 2012;
Davide, 1988; Mantelin et al., 2017).
However, to our knowledge, this is the first
time that this species causes a massive
Nguyen Thi Hue et al.
38
infection in the country leading to almost
100% plant damage in a 10 ha field. Usually,
M. graminicola infection in a field is limited
to several small areas and the infection can be
revealed by patch formation in the field where
the plants are chlorotic and show a delay in
their development (Mantelin et al., 2017). We
therefore investigated the reasons that could
explain this preliminary observation where M.
graminicola could potentially devastate rice
agriculture and farmer economy.
In the field, we systematically noticed that
all plants with abnormal development were
infected by PPN, which suggested that the
selected varieties were highly susceptible to M.
graminicola under natural growing conditions.
In order to assess the aggressiveness of this
specific Hai Duong M. graminicola population,
we tested the infectivity of this population
against IR64, an Oryza sativa indica species
known to be a good host for M. graminicola
(Soriano et al., 1999) and routinely used to
study rice-nematode interactions. The
aggressiveness of the Hai Duong M.
graminicola on IR64 was similar to the results
observed with other populations collected in
Vietnam and in other countries. For instance, in
Vietnam, 20 M. graminicola populations have
been collected in 10 sites from different rice
growing regions. After two life cycles, all
Vietnamese M. graminicola populations were
highly reproductive on rice cv. IR64 with a Rf
value ranging from 11 to 19 (Bellafiore et al.,
2015), similar to the isolate collected in Hai
Duong (Rf of 19.25). This suggests that the
high level of M. graminicola infection as
observed in prospected Hai Duong fields is not
due to the emergence/selection of a more
aggressive host pathogen with a superior
fitness but rather the plants becoming more
susceptible to the infection due to exceptional
agro-ecosystem conditions.
Physical changes in the soil are known to
affect nematode behaviors (Oka Y., 2010). We
analyzed the soil physical and chemical
properties of the infested fields but only the
content of P was relatively high and all the
other parameters were in an optimum range
for rice production. The high P value could be
due to massive use of phosphorus fertilizers
by farmers for intensive rice and scallion
production. There are three main form of
phosphorous in the soil: active P, fixed P and
soluble P. Plants will firstly uptake soluble P
which contains a mix of inorganic P and
organic P with inorganic P being the major
type, followed by active and fixed P (Pagliari
et al., 2017; Nishigaki et al., 2019).
Continuous addition of more P in the soil
could increase more fertility in the soil but P
could also be fixed and become unavailable
(Pagliari et al., 2017), resulting in
environmental pollution (Choudhury et al.,
2007). However, high levels of phosphate will
not negatively impact the crops and no
correlation between P abundance and
nematode infection has been previously
reported. Therefore, the physical and chemical
properties did not reflect any major
characteristic that could explain the
abundance of M. graminicola.
We, therefore, investigated if farmers
applied a specific agricultural practice that
could explain the high infection level. In Asia,
farmers mainly use wet direct seeding method
to cultivate rice by broadcasting or drilling
into drained, well-puddled seedbeds or into
shallow standing water (Balasubramanian et
al., 2002) in which the two first seedbed types
might be convenient conditions for M.
graminicola infectivity. Indeed, this nematode
can quickly invade the young rice roots when
infested soils are drained (Manser, 1968).
Direct seeding methods have many benefits
such as reduction of labor work but also have
side effects, such as promoting weed
development and in some conditions, disease
and pest infections (Farooq et al., 2011).
According to Farooq et al. (2011), grain yields
in direct seeding field were lower than this in
transplanting field, whereas others reported
that the rice yields of direct seeding under
good management control was equal to, or
even higher than those of transplanted rice
(Huang et al., 2011; Liu et al., 2015). Because
M. graminicola has a wide range of hosts
which include many common weeds in the
rice field, direct seeding methods could create
Root knot nematode infections promoted
39
favorable conditions for M. graminicola
proliferation on the weeds which continue to
infect rice in the next season (De Waele &
Elsen, 2007; MacGowan & Landon, 1989). In
the prospected area of the Hai Duong
Province, several farmers modified their
agricultural practices from traditional
transplanting to direct seeding method. We
observed that the farmers that had shifted to
the direct seeding method suffered severe
damage due to a massive M. graminicola
infection.
Finally, we showed that the scallion used
by farmers in the crop rotation sequence was a
variety susceptible to M. graminicola.
Consequently, it helped maintain a significant
M. graminicola population in the soil during
the winter season before planting rice.
Scallion was previously reported as a good
host of M. graminicola. The growth and yields
of the Yellow Granex scallion variety grown
in a cropping sequence with rice in the
Philippines, was severely reduced due to M.
graminicola infection (Gergon et al., 2002).
Therefore, M. graminicola infection is not
only reducing the expected income from rice
cultivation but also from scallion. Although
crop rotation is an important practice that can
help farmers to limit nematode occurrence in
a field (Mantelin et al., 2017, Védie et al.,
2014), a wrong combination of plants can
have the opposite effect of contributing to the
proliferation of the pest followed by severe
damage to the cultivated plants. A solution for
the farmers should be using resistant rice
varieties (Dimkpa et al., 2016; Thi Phan et al.,
2017) and/or to grow non-susceptible plants
instead of scallion. If the same cropping
system persisted and no nematode control
strategies were implemented, a strongly
increasing number of M. graminicola would
be expected in the field year by year.
In order to reduce the negative impact of
this pest on rice production, it is critical to
increase the farmer’s awareness on the risk of
plant parasitic nematode infection as too many
severe nematode infections on rice are being
mis-identified. Indeed, due to limited root
development caused by the nematode
infection, parasitized plants can present the
same leaf symptoms as nutrient starvation and
water stress. The infected plants can also
present other sickness symptoms that are
originally due to M. graminicola, as this
nematode causes its host to be more
susceptible to other pathogens (Kyndt et al.,
2017). Fortunately, symptoms of infected
roots are easily identifiable and farmers can
quickly be aware of the presence of M.
graminicola when they inspect carefully the
rice root system.
CONCLUSION
The RKN found in Hai Duong fields were
morphologically and molecularly identified as
M. graminicola-a serious pathogenic species
in rice. For the first time in Vietnam, our
experiment showed that M. graminicola could
parasitize and propagate in scallions of
Vietnam although this plant is annually
cultivated on a paddy field for crop rotation. A
combination of three factors (wrong crop
choice for rotation, rice variety susceptible to
M. graminicola and direct seeding) obviously
favored the nematode infection and its high
proliferation in the surveyed fields. The
results of this study suggested some
recommendations: 1. Using a crop rotation
system with at least one plant not susceptible
to M. graminicola. If planting two susceptible
crops (e.g. scallion and rice) is vital for the
farmers, then a precise water management
system is required to flood the field to limit
the nematode infection. 2. Using rice varieties
less or not susceptible to nematode infection.
If no specific nematode control is planned
(soil solarization, use of resistant cultivars),
avoid direct seeding and irrigation delay as
both are favorable to M. graminicola
infection. We recommend transplanting young
rice plants from a non-infected nursery in a
flooded field. Under flooding conditions,
RKN like M. graminicola are unable to
penetrate the root system and cause significant
rice yield loss.
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