Root Rot of Cinnamomum camphora (Linn) Presl Caused by Phytopythium vexans in China

As a famous street tree, camphor (Cinnamomum camphora) is widely planted worldwide. However, in recent years, camphor with root rot was observed in Anhui Province, China. Based on morphological characterization, thirty virulent isolates were identified as Phytopythium species. Phylogenetic analysis of combined ITS, LSU rDNA, β-tubulin, coxI, and coxII sequences assigned the isolates to Phytopythium vexans. Koch’s postulates were fulfilled in the greenhouse, and the pathogenicity of P. vexans was determined by root inoculation tests on 2-year-old camphor seedlings; the symptoms of indoor inoculation were consistent with those in the field. P. vexans can grow at 15–30 °C, with an optimal growth temperature of 25–30 °C. The results of fungicide sensitivity experiments indicated that P. vexans was the most sensitive to metalaxyl hymexazol, which may be a useful idea for the future prevention and control management of P.vexans. This study provided the first step for further research on P. vexans as a pathogen of camphor, and provided a theoretical basis for future control strategies.


Introduction
The camphor tree [Cinnamomum camphora (Linn.) Presl] is an important species of subtropical evergreen broad-leaved tree [1] that is widely distributed in Asia [2]. The tree is native to China and is often regarded as both an ornamental tree and a street tree because of its tallness and beauty [3]. Camphor is economically valuable in many ways. As one of the oldest traditional herbal medicines, it has antibacterial, antioxidant and other biological functions [4][5][6]. Camphor is usually used as a raw material for producing camphor pills [4], wood [4], essential oils [7], and perfumes [8]. Medicinal products made from camphor trees can be used to treat inflammation-related diseases such as sprains, bronchitis and rheumatism, and camphor leaves can also be made into camphor balls with different chemical components [7,9]. However, in the nursery land of the city of Xuancheng, Anhui Province, China, a large number of camphor trees were found to have root rot, which resulted in the death of camphor trees across a large area. This phenomenon has placed great pressure on the local environment and caused economic losses.
Oomycetes are a unique group of fungus-like eukaryotic microbes, many of whose genera are potential threats to the healthy growth of plants and animals [10]. As a group, they are best known as plant pathogens. Two of the more notorious genera of oomycetes are Pythium and Phytophthora, which cause economic losses to crops and plants and continue to have a devastating impact on natural ecosystems [11]. It is important to note that Phytophthora cinnamomum is an important root pathogen with a wide host range of more than 900 species of host plants worldwide [12]. Pythium also contains destructive species which cause root rot, seedling wilt, and stem rot in agronomic and vegetable crops [13]. Economic losses caused by oomycetes are estimated to exceed billions of dollars worldwide. In cases in which an oomycete becomes established in nursery soil, it can influence the roots of the plant and spread through various routes [14].
In the past, the use of protective fungicides has not been sufficient to control the development of soilborne oomycetes [15]. At the end of the last century, metalaxyl, dexon and etridizole began to be applied to control Pythium in the field; these fungicides can sterilize seeds and also be sprayed directly in the soil to play a preventive role [16]. Currently, there are several different chemical groups that control oomycetes, such as phenylamides (PAs), dithiocarbamates (e.g., mancozeb), and chlorothalonil [17]. Oxathiapiprolin and fluopicolide have recently been considered to be resistant to some genera of oomycetes, such as Pythium and Phytophthora; they have been shown to have a significant inhibitory effect on the release and activity of zoospores, mycelial growth and the sporulation ability of oomycetes [18,19].
Phytopythium is a recently established genus between Phytophthora and Pythium in terms of age, with similar characteristics. The sporangia of Phytopythium are more similar to those of Phytophthora, and the mode of discharge of zoospores, zoospores being created in the vesicle, is similar to that of Pythium [20][21][22]. The classification of taxa in the genus Pythium was revised on the basis of morphological differences in sporangia and the phylogenetic analysis of the LSU rDNA and coxI mDNA regions, from which four new genera were established: Ovatisporangium, Globisporangium, Elongisporangium, and Pilasporangium [23]. Ovatisporangium is treated with the same name as Phytopythium [24]. Phytopythium vexans has caused crown and root rot in Prunus serrulata Lindl. in Tennessee [25] and widespread leaf blight and root rot of Manihot esculenta in Brazil [26].
This study presents the features of oomycetes associated with root rot of camphor trees in Anhui Province, China, which caused serious damage and placed pressure on the local ecological environment. The objectives of this study were as follows. First, we aimed to identify oomycete pathogens that cause root rot in camphor trees by Koch's postulates. Second, molecular biology and morphological identification were used to identify the pathogen. Third, fungicides with obvious inhibitory effects on the mycelial growth of the pathogen were screened by a media plate phenotyping experiment.

Field Survey, Oomycete Isolation and Purification
Early in the second half of 2021, sixty camphor trees began to die, with symptoms first appearing in September and developing more rapidly in autumn. By the end of 2021, the incidence of disease in the field was about 88.3% (265 symptomatic trees), and about 27% of the 300 camphor trees surveyed died (81 dead trees). The pathogen can infest seedlings at different times of the year and cause tree death within a relatively short period of time, placing considerable strain on the ecological environment. Under normal growth, camphor is an evergreen tree year-round; however, after infection with the pathogen, the leaves gradually fade to green and yellow ( Figure 1A). At a later stage, the leaves crumpled and easily fell off until the whole tree died ( Figure 1B,C). The branches and stems become black and necrotic, and eventually, the whole tree dies. The xylem appears brown in longitudinal sections, and the root epidermis rots and falls off ( Figure 1D,E).
In this study, one oomycete was consistently isolated from all tissue masses in the 30 root samples investigated.

Molecular Identification and Phylogenetic Analysis
All sequences obtained in this study were compared with Phytopythium isolates available in GenBank, and the homology of all isolates was verified by BLAST calculation of nucleotide identity. All sequences of 30 isolates were deposited in GenBank, and the accession numbers for the sequences of the 31 reference Phytopythium sp. isolates in the GenBank database are presented in Table 3. To produce the phylogenetic tree, we used a total of 294 sequences from 62 isolates. Phylogenetic analysis was based on sequences from 5 genomic regions: ITS, LSU rDNA, β-tubulin, coxI and coxII. For these loci, fragments of 951 bp, 683 bp, 715 bp, 670 bp and 534 bp were obtained by PCR amplification and bidirectional sequencing. In this study, one oomycete was consistently isolated from all tissue masses in the 30 root samples investigated.

Molecular Identification and Phylogenetic Analysis
All sequences obtained in this study were compared with Phytopythium isolates available in GenBank, and the homology of all isolates was verified by BLAST calculation of nucleotide identity. All sequences of 30 isolates were deposited in GenBank, and the accession numbers for the sequences of the 31 reference Phytopythium sp. isolates in the Gen-Bank database are presented in Table 3. To produce the phylogenetic tree, we used a total of 294 sequences from 62 isolates. Phylogenetic analysis was based on sequences from 5 genomic regions: ITS, LSU rDNA, β-tubulin, coxI and coxII. For these loci, fragments of 951 bp, 683 bp, 715 bp, 670 bp and 534 bp were obtained by PCR amplification and bidirectional sequencing.
Two separate tree-building methods were used to sequence and analyze individual gene sequences before building a phylogenetic tree with five sets of gene chains. By comparison, no apparent conflicting contradictions were found in the individual gene phylogenies, so the ITS, coxI, coxII, LSU rDNA and β-tubulin datasets could be combined and concatenated. Cluster analysis was performed using sequences downloaded from the NCBI database. The concatenated matrix contained 3553 bp nucleotides. The tree topology obtained by Bayesian analysis and ML analysis was basically the same, which indicated that the evolutionary relationship of the isolates was statistically supported (Figure 2). Clustering of isolates obtained from camphor samples with the reference strain P. vexans was statistically supported by phylogenetic analysis, with 99% bootstrap proportions and a 1 BPP, resulting in a separate clade within the Phytopythium fraction ( Figure 2). The isolates obtained from camphor samples were closely related to P. vexans and clustered with P. vexans isolate 2D111, with statistical support of 100% BP and 1 BPP. Phylogenetic analysis showed that all the isolates obtained in this study were highly similar to the previously reported isolates of P. vexans. Therefore, the pathogen was confirmed to be P. vexans. Two separate tree-building methods were used to sequence and analyze individual gene sequences before building a phylogenetic tree with five sets of gene chains. By comparison, no apparent conflicting contradictions were found in the individual gene phylogenies, so the ITS, coxI, coxII, LSU rDNA and β-tubulin datasets could be combined and concatenated. Cluster analysis was performed using sequences downloaded from the NCBI database. The concatenated matrix contained 3553 bp nucleotides. The tree topology obtained by Bayesian analysis and ML analysis was basically the same, which indicated that the evolutionary relationship of the isolates was statistically supported (Figure 2). Clustering of isolates obtained from camphor samples with the reference strain P. vexans was statistically supported by phylogenetic analysis, with 99% bootstrap proportions and a 1 BPP, resulting in a separate clade within the Phytopythium fraction ( Figure 2). The isolates obtained from camphor samples were closely related to P. vexans and clustered with P. vexans isolate 2D111, with statistical support of 100% BP and 1 BPP. Phylogenetic analysis showed that all the isolates obtained in this study were highly similar to the previously reported isolates of P. vexans. Therefore, the pathogen was confirmed to be P. vexans.

Morphological Identification and Biological Characteristics
The colonies of four representative isolates grew rapidly and the colonies covered the surface of 90 mm V8-agar medium in 3 days at 25 • C. Morphological features were recorded based on visual observation. The isolates showed white colonies on CMA medium with no obvious radiolucent pattern ( Figure 3A,F), and grew better on PDA medium, with colonies showing a fluffier and richer mycelium with a radial morphology ( Figure 3B,G). Those cultured on V8-agar medium had a velvety blooming colony morphology with no visible sporangium formation on the surface ( Figure 3C,H). However, the abundance of aerial hyphae varied among the types of medium. The hyphae on the PDA medium presented a petal-like and radial shape, and the isolates had the densest and most abundant mycelia on the V8-agar and PDA media. After 3 days of culture, the colonies on the PDA medium radiated in the form of rose petals, and the hyphae gradually became dense and velvet-like from the center to the edge; the hyphae were irregularly dispersed on the PCA medium ( Figure 3D,I). The growth of the colonies on GPYA medium was weak, but the hyphae were also abundant ( Figure 3E,J).

Morphological Identification and Biological Characteristics
The colonies of four representative isolates grew rapidly and the colonies covered the surface of 90 mm V8-agar medium in 3 days at 25 °C. Morphological features were recorded based on visual observation. The isolates showed white colonies on CMA medium with no obvious radiolucent pattern ( Figure 3A,F), and grew better on PDA medium, with colonies showing a fluffier and richer mycelium with a radial morphology ( Figure 3B,G). Those cultured on V8-agar medium had a velvety blooming colony morphology with no visible sporangium formation on the surface ( Figure 3C,H). However, the abundance of aerial hyphae varied among the types of medium. The hyphae on the PDA medium presented a petal-like and radial shape, and the isolates had the densest and most abundant mycelia on the V8-agar and PDA media. After 3 days of culture, the colonies on the PDA medium radiated in the form of rose petals, and the hyphae gradually became dense and velvet-like from the center to the edge; the hyphae were irregularly dispersed on the PCA medium ( Figure 3D,I). The growth of the colonies on GPYA medium was weak, but the hyphae were also abundant ( Figure 3E,J). The isolates have distinct papillae (or protrusions) and proliferating free sporangia inside. After 3 days of water incubation, these traits were observed under a microscope. The shape of the sporangia was round to ovoid, with a smooth surface, and a rich matrix could be seen inside the sporangia ( Figure 4B,C). It was also possible to observe empty sporangia ( Figure 4A). Some of the oospores were surrounded by oogonia or showed The isolates have distinct papillae (or protrusions) and proliferating free sporangia inside. After 3 days of water incubation, these traits were observed under a microscope. The shape of the sporangia was round to ovoid, with a smooth surface, and a rich matrix could be seen inside the sporangia ( Figure 4B,C). It was also possible to observe empty sporangia ( Figure 4A). Some of the oospores were surrounded by oogonia or showed short protuberances ( Figure 4D-F). The average size of the sporangia was 13.19 × 12.41 µm, and the size of the sporangia ranged from 12.62-16.36 × 8.57-16.45 µm (n = 100). Based on colony morphology, color and sporangia, the isolates were identified as P. vexans. The isolates have distinct papillae (or protrusions) and proliferating free sporangia inside. After 3 days of water incubation, these traits were observed under a microscope. The shape of the sporangia was round to ovoid, with a smooth surface, and a rich matrix could be seen inside the sporangia ( Figure 4B,C). It was also possible to observe empty sporangia ( Figure 4A). Some of the oospores were surrounded by oogonia or showed short protuberances ( Figure 4D-F). The average size of the sporangia was 13.19 × 12.41 μm, and the size of the sporangia ranged from 12.62-16.36 × 8.57-16.45 μm (n = 100). Based on colony morphology, color and sporangia, the isolates were identified as P. vexans. The isolates grew in the range of 15-30 °C, and 25-30 °C was the optimal temperature for growth ( Figure 5). The colony hyphae were most dense and fluffy when the temperature range was 25-30 °C, and the colony did not grow when the temperature reached 35 °C ( Figure 6). The isolates grew in the range of 15-30 • C, and 25-30 • C was the optimal temperature for growth ( Figure 5). The colony hyphae were most dense and fluffy when the temperature range was 25-30 • C, and the colony did not grow when the temperature reached 35 • C ( Figure 6).

Pathogenicity Tests
Phytopythium vexans (representive isolates ZS01, ZS02, ZS03 and ZS04) caused symptoms of camphor wilt at 14 days after inoculation. Nevertheless, no symptoms occurred in the control group. Fourteen days after inoculation, the plants in the control group grew vigorously, with emerald-green leaves spreading outward ( Figure 7A). The inoculated plant leaves began to droop with symptoms of wilting ( Figure 7B). Then, 21 days after inoculation, the symptoms gradually worsened, the degree of blight increased each day, and death occurred on day 38 ( Figure 7C-E). Compared with that of the control seedlings, the growth vigor of the inoculated camphor seedlings became weaker, while the uninoculated camphor seedlings grew healthy, and the root vigor of the inoculated seedlings was weakened and degraded. No symptoms were found on uninoculated plants ( Figure  7F), and the root tissue was robust ( Figure 7F). The longitudinal section of the stem of the

Pathogenicity Tests
Phytopythium vexans (representive isolates ZS01, ZS02, ZS03 and ZS04) caused symptoms of camphor wilt at 14 days after inoculation. Nevertheless, no symptoms occurred in the control group. Fourteen days after inoculation, the plants in the control group grew vigorously, with emerald-green leaves spreading outward ( Figure 7A). The inoculated plant leaves began to droop with symptoms of wilting ( Figure 7B). Then, 21 days after inoculation, the symptoms gradually worsened, the degree of blight increased each day, and death occurred on day 38 ( Figure 7C-E). Compared with that of the control seedlings, the growth vigor of the inoculated camphor seedlings became weaker, while the uninoculated camphor seedlings grew healthy, and the root vigor of the inoculated seedlings was weakened and degraded. No symptoms were found on uninoculated plants ( Figure 7F), and the root tissue was robust ( Figure 7F). The longitudinal section of the stem of the camphor inoculated with isolates was dark and dull in color ( Figure 7H), and the xylem stripes in the longitudinal section of the stem were clear and healthy ( Figure 7G). The leaves of camphor seedlings inoculated with isolates turned yellow and withered, and the roots decayed and were fibrous and easily detached. The longitudinal section of the roots was rough and accompanied by darkening symptoms (Figure 7J), and the surface of the longitudinal section of the root of the control group was clear and bright ( Figure 7I). The reisolations were recovered from symptomatic root tissue, and the cultures were similar in character and morphology to the isolates. DNA sequences extracted from reisolation obtained from inoculated roots matched the DNA sequences of the isolates used for inoculation, and the symptoms on artificially inoculated seedlings were similar to those in the field, thus satisfying Koch's postulates.

Susceptibility of Phytopythium Isolates to Fungicides
The four representative strains showed similar biological responses to the five fungicides ( Figure 8). All five fungicides showed significant growth inhibition on the representative isolates on V8-agar media; metalaxyl hymexazol had lower EC 50 on mycelial growth than the other four fungicides, and difenoconazole had the highest EC 50 on mycelial growth of the representative isolates, and the weakest inhibition effect (Table 1). These results indicated that metalaxyl hymexazol was the most effective fungicide against Phytopythium sp. in this study. was rough and accompanied by darkening symptoms (Figure 7J), and the surface of the longitudinal section of the root of the control group was clear and bright ( Figure 7I). The reisolations were recovered from symptomatic root tissue, and the cultures were similar in character and morphology to the isolates. DNA sequences extracted from reisolation obtained from inoculated roots matched the DNA sequences of the isolates used for inoculation, and the symptoms on artificially inoculated seedlings were similar to those in the field, thus satisfying Koch's postulates.

Susceptibility of Phytopythium Isolates to Fungicides
The four representative strains showed similar biological responses to the five fungicides ( Figure 8). All five fungicides showed significant growth inhibition on the representative isolates on V8-agar media; metalaxyl hymexazol had lower EC50 on mycelial growth than the other four fungicides, and difenoconazole had the highest EC50 on mycelial growth of the representative isolates, and the weakest inhibition effect (Table 1). These results indicated that metalaxyl hymexazol was the most effective fungicide against Phytopythium sp. in this study.

Discussion
The pathogen that causes root rot can not only infect camphor, but can also infect

Discussion
The pathogen that causes root rot can not only infect camphor, but can also infect other potential host plants in the nursery. It is very necessary to identify the pathogen that causes root rot of camphor in a timely manner. Based on morphological identification and molecular and phylogenetic analysis, Phytopythium vexans was identified as the causal agent of root rot on camphor in China. According to previous studies, there have been no reports about P. vexans causing root rot on camphor in the world.
Pythium is usually classified based on morphological characteristics, such as the shape and size of sporangia and oogonia, and the number and position of antheridia [27,28]. However, these characteristics are very similar among the members of Pythium, and it is difficult to classify and identify Pythium by morphological characteristics alone. Based on previous studies, to date, phylogenetic analysis of Pythium is mainly based on the rDNA large subunit (LSU rDNA), ITS, β-tubulin, and cytochrome oxidase II (coxII) gene sequences [29][30][31][32][33][34]. In this study, phylogenetic analysis of a combination of ITS, LSU rDNA, coxI, coxII, and β-tubulin sequence data indicated that isolates from all collected samples were single species. The phylogenetic tree showed that the P. vexans obtained from the roots of camphor in this study were similar to those reported in other studies ( Figure 2).
Phytopythium vexans (formerly known as Pythium vexans) is distributed worldwide and can cause root rot, stem rot, crown rot and leaf ulcers in many woody ornamentals [35]. According to previous academic research in South Africa, the pathogen mainly causes diseases in woody plants and economic crops, such as apples [36] and kiwifruit [37]. The incidence of brown root rot of ramie caused by P. vexans has caused over 40% of production losses in China [38]. In addition to seriously affecting cash crops such as fruit, it can also harm woody ornamentals such as ginkgo and red maples [35]; it has also been isolated from infected Anthurium andraeanum in Korea [39]. To summarize, the ecological loss caused by P. vexans worldwide is huge, so the ecological threat of P. vexans to the environment cannot be underestimated.
Temperature is environmental factor that is generally considered to be the main factor affecting the prevalence of plant diseases [40]. In this study, the optimum growth temperature of the representative isolates ranged from 25 • C to 30 • C; this is consistent with the results of previous studies on the optimum growth temperature for P. vexans [41,42]. Therefore, timely intervention of pathogens should be conducted before the appropriate growth temperature is reached. There were abundant water sources around the nursery site, and the environment was relatively humid, which may explain the prevalence of pathogens in the nursery site. Such pathogens will proliferate in a high-humidity environments, produce sporangia, release highly infectious zoospores when the conditions are suitable, and begin to infect suitable host plants. This finding indicates that future field management measures should include appropriate irrigation methods according to the growth characteristics and needs of crops. At the same time, the health of water sources is also one of the important factors preventing infection by this pathogen. It is well known that water is the main substrate for P. vexans, and a drop of water can spread zoospores within a radius of one meter because the pathogen is prone to encounter suitable environmental conditions in water, thereby releasing infectious zoospores [43]. From the perspective of controlling the development of disease, determining the biological characteristics of pathogens is very important for the prevention and control of plant disease epidemics, which can provide a scientific basis for disease prevention and control. The temperature experiment in this study proved that the time of application of fungicide should be determined before the optimal growth temperature of the pathogen is reached.
Phytopythium vexans is a soil-borne pathogen that has a wide range of transmission pathways in nurseries and spreads rapidly. The presence of the pathogen should be detected as soon as possible to help prevent the occurrence of the disease [44]. Soil-borne diseases can affect the health and appearance of a plant and even its economic value, so timely intervention is essential. There are various management measures for soil-borne diseases, such as improving the environmental conditions of nursery land, introducing relevant laws and regulations, breeding highly resistant varieties, and implementing biological and chemical control [45]. When the pathogen begins to infect plants in the soil of the field, it is very necessary to inhibit the growth of mycelial and sporangium production in a timely manner. In 2020, soybeans grown in Huang-Huai area of China have been infected by Pythium and Phytopythium. In the control of the dominant strains of the isolates, the researchers selected the fungicides containing metalaxyl, and the EC 50 values obtained were all less than 1 µg/mL. Based on the experiments of this study, metalaxyl hymexazol had the best growth inhibition effect on P. vexans, and the EC 50 value was less than 0.01 µg/mL. In 2022, soybean growing areas in the United States were also affected by some species of Phytophthora, Pythium, and Phytopythium, and researchers used a fungicide mixed with oxathiapiprolin and metalaxyl to control oomycetes more effectively than oxathiapiprolin alone. [46,47]. This indicates that in future field control, appropriate use of fungicides containing metalaxyl can effectively prevent the spread of oomycete pathogens. The next step is to quickly determine the concentration of effective fungicides to maximize the protection of plants from these pathogens, and then test it on the host plant to obtain the optimal application concentration.
As an important roadside and ornamental tree, camphor is widely planted in China. The isolation and identification of the pathogenic species described herein provide new ideas and references for the cultivation and management of camphor trees in China. Regarding camphor root rot, there are many issues that need to be further studied and solved. P. vexans may pose a great threat to the environment in the future, as the pathogen can infect a wider range of hosts. Testing of the soil in and around the sites wherein camphor root rot occurs and rational use of fungicides and fertilizers are both recommended in order to actively maintain appropriate environmental conditions and prevent the occurrence of the disease.

Field Survey, Oomycete Isolation and Purification
In 2021, planted camphor plots in the city of Xuancheng (118 • 75 , 30 • 94 ), Anhui Province, China, were surveyed for the occurrence of root rot. The 9-10 year old camphor trees in the planting area (300 trees) were investigated, and the external symptoms of tree diseases were recorded. Disease incidence was calculated by counting the number of symptomatic trees, asymptomatic trees, and dead trees. The local area is more loosely managed, with a high level of human activity and low-lying terrain that is prone to waterlogging, which is not conducive to the growth of camphor trees. Thirty symptomatic tissues obtained from the roots of diseased plants were washed first in tap water and then in sterile distilled water and cut into small pieces of 0.5-1 cm 2 . These small pieces were soaked in 75% ethanol for 45 s for surface disinfection and then drained with sterile filter paper. Pieces were transferred to V8 (vegetable juice)-PARP-agar medium [48] in 90 mm-diameter Petri dishes and incubated at 28 • C in the dark for 4 days. The PARP contained pimaricin (20 mg/L), ampicillin (125 mg/L), rifampin (10 mg/L), and pentachloronitrobenzene (20 mg/L) [49]. Pure cultures were obtained by transferring the mycelial of the margins of the colonies to V8-agar medium [48].

Molecular Identification and Phylogenetic Tree of Phytopythium sp.
The genomic DNA of isolates' strains was obtained from mycelial colonies using the cetyltrimethylammonium bromide method (CTAB) [50]. In short, a small amount of mycelium was cut into a 2 mL sterile centrifuge tube, the bottom of the tube was filled with 500 mL 2% CTAB and 500 mL chloroform, and the tube was placed in a shaker at 200 r/min at 25 • C for 1.5 h and centrifuged at 13,000 r/min for 15 min after removal. After centrifugation, 300 µL of the supernatant was transferred to another 1.5 mL sterile centrifuge tube containing 600 µL absolute ethanol, and then centrifuged at 13,000 r/min for 5 min. The supernatant was discarded, and 1 mL 75% ethanol was added for elution twice, followed by centrifugation at 13,000 r/min for 5 min. Then, the solution was placed in an oven (at 65 • C) to wait for the ethanol to evaporate, and 30 µL sterile deionized water was added for precipitation to obtain a crude DNA suspension.
The primer pairs used for sequence amplification of the rDNA internal transcribed spacer (ITS), large subunit (LSU rDNA), β-tubulin and cytochrome c oxidase I and II (coxI and coxII) genes are listed in Table 2. Each 50 µL reaction mixture contained 25 µL of Green PCR Master Mix, 17 µL of sterile deionized water, 4 µL of DNA, and 2 µL each of the upstream and downstream primers. The PCR products were electrophoresed (150 V for 25 min) on 2% agarose gels and sequenced at the Shanghai Sangon Biological Technology Company. All sequences obtained in this study were uploaded in GenBank (Table 3). Table 2. Primer sequences used for molecular identification of isolates.

Primer
Sequence ( NA = Information is not available. Species and isolates obtained in this study are shown in bold. The sequences derived from the isolates in this study and the sequences related to the Phytopythium sp. in Genbank were used to construct the phylogenetic tree; Phytophthora nicotianae was used as the outgroup. (Table 3). BioEdit version 7.0.9.0 software was used to align the nucleotide sequences, and the missing bases in these sequences were manually corrected [51]. Phylogenetic trees of combined genes were constructed using two independent optimality search criteria: Bayesian inference (BI) and maximum likelihood (ML) criteria. The ML analysis was performed using IQ-TREE [52], and the GTR+G+I model was chosen to estimate branch stability by 1000 bootstrap replicates. The BI analysis was performed using PhyloSuite version 1

Morphological Observations and Biological Characteristics
Four isolates (ZS01, ZS02, ZS03 and ZS04 based on preliminary phylogenetic analyses) were selected for morphological observation and biological characterization.
Isolates were cultured on potato dextrose agar medium (PDA), corn meal agar medium (CMA), potato carrot agar (PCA) medium, V8-agar medium and peptone yeast glucose agar medium (GPYA) in the dark at 25 • C for 3 days, and the morphology and color of the colonies were recorded. The identification of oomycete pathogens was initially based on the observation of morphological characteristics, as well as the characteristics of sporangia. To induce the production of sporangia, five plugs (2 mm × 2 mm) of isolates were transferred to 10% V8 liquid medium and cultivated for 3 days until the mycelial plugs became mycelial mats. Then, the V8 liquid was replaced with sterile water. To stimulate sporangial production, five drops of soil extract solution were added to each medium [48]. This operation was repeated for approximately 3 days, and the hyphae produced many sporangia. The oomycete structures of four isolates (ZS01, ZS02, ZS03 and ZS04) were examined and recorded. To observe more subtle features, the sterile water carrying the sporangia hyphae was fixed on a glass slide, and a Zeiss Axio imager A2m microscope was used to observe and measure the size of the sporangia at a magnification of 40×. Over 50 sporangia were randomly observed per isolate, and the experiment was repeated twice.
To determine the optimal growth temperature of the isolates, mycelial plugs (6 mm diameter) were placed on fresh V8-agar medium (90 mm diameter) and incubated from 15 to 35 • C at 5 • C intervals. Experiments were carried out at five temperatures, with five replicates per isolate. The colony growth diameter was measured and recorded daily. These experiments were conducted twice.

Pathogenicity Test
Four isolates selected for morphological and biological identification were used in pathogenicity tests. Pathogenicity testing of isolates was carried out on healthy 2-year-old camphor trees. The isolates were incubated on V8-agar medium for 3 days, and some of the mycelial plugs were transferred to 10% V8 liquid for 3-5 days until abundant mycelial mats were produced. To stimulate sporangia production, the V8 liquid was decanted, and then appropriate amounts of sterile water and soil extract solution were added. The operation was repeated three times at 24 h intervals until sporangia were observed under the microscope. The sporangia suspension was inoculated onto the roots of the camphor, and plants treated with sterile V8 liquid disks were used as controls. The inoculated plants were placed in high humidity and a constant temperature of 28 • C for observation. There were five replicates per treatment and control group. The experiments were conducted three times simultaneously.
To fulfil Koch's postulates, symptomatic tissue sections were excised from the root margins and transferred to a V8-PARP-agar medium for reisolation, and the isolation was confirmed by morphological identification and molecular identification. The primers used for molecular identification were ITS, LSU rDNA, β-tubulin, coxI and coxII (Table 2).

Institutional Review Board Statement:
Not applicable for studies not involving humans or animals.

Informed Consent Statement: Not applicable.
Data Availability Statement: All data generated or analyzed during this study are included in this article.