The Pathogenic Mechanism of Enterocytozoon hepatopenaei in Litopenaeus vannamei

Enterocytozoon hepatopenaei (EHP) is a parasite in shrimp farming. EHP mainly parasitizes the hepatopancreas of shrimp, causing slow growth, which severely restricts the economic income of shrimp farmers. To explore the pathogenic mechanism of EHP, the host subcellular construction, molecular biological characteristics, and mitochondrial condition of Litopenaeus vannamei were identified using transmission electron microscopy (TEM), real-time qPCR, an enzyme assay, and flow cytometry. The results showed that EHP spores, approximately 1 μm in size, were located on the cytoplasm of the hepatopancreas. The number of mitochondria increased significantly, and mitochondria morphology showed a condensed state in the high-concentration EHP-infected shrimp by TEM observation. In addition, there were some changes in mitochondrial potential, but apoptosis was not significantly different in the infected shrimp. The qPCR results showed that the gene expression levels of hexokinase and pyruvate kinase related to energy metabolism were both upregulated in the diseased L. vannamei. Enzymatic activity showed hexokinase and lactate dehydrogenase were significantly increased in the shrimp infected with EHP, indicating EHP infection can increase the glycolysis process and decrease the oxidative phosphorylation process of L. vannamei. Previous transcriptomic data analysis results also support this conclusion.


Introduction
Aquaculture is a major source of high-quality protein for meeting human demand.Among aquaculture species, Litopenaeus vannamei is one of the most widely farmed crustacean species worldwide [1].With increasing market consumption, intensive high-density cultivation modes for L. vannamei were developed.However, high-density farming is also accompanied by frequent diseases, which lead to massive mortality of farmed shrimp and hinder the development of the shrimp industry [2].Enterocytozoon hepatopenaei (EHP) belongs to microsporidia and parasitizes the hepatopancreatic epithelial cells of L. vannamei [3,4].This parasite mainly causes growth retardation and exhibits no specific clinical symptoms, which usually results in depleted feed of diseased L. vannamei, further leading to great economic losses [5].Although there are numerous detection methods available, a thorough understanding of the disease's pathogenic mechanisms and effective prevention strategies are still lacking.This often results in a challenging situation where no direct measures can be taken when the emergence of the disease occurs [6,7].
Oxidative phosphorylation and glycolysis are the main pathways for energy production in eukaryotic organisms.However, a large set of core eukaryotic genes were jettisoned early in the evolutionary history of microsporidia.That made them lose the mitochondrial genome and the ability to generate ATP via oxidative phosphorylation [8].With the absence of oxidative phosphorylation in microsporidia, glucose is only partially metabolized via glycolysis to release 7% of its full ATP potential.And energy supply is complemented by the import of ATP molecules from the host with the help of horizontally acquired ATP/ADP translocases [8,9].Microsporidia are mainly dependent on the host cell for metabolism and energy requirements [10].In L. vannamei, energy theft by EHP causes significant growth retardation.
In order to study the energy imbalance of L. vannamei infected by EHP, L. vannamei with different EHP infection levels were collected, and energy metabolism and mitochondria characteristics of L. vannamei infected by EHP were explored.These findings can provide some basic information for pathogenic mechanisms and further target control research.

Sample Collection
L. vannamei showed retarded growth and large individual differences in the same pond in one shrimp farming factory located in Ningbo City.To explore the reasons, shrimp samples were collected from different ponds, and the length of the shrimp was recorded.Meanwhile, a PCR-amplified molecular assay was used to detect potential pathogen infection.Shrimp infected with EHP were selected and brought back to the pilot base of Ningbo University, where they were temporarily kept in 150 L aquaculture tanks with recirculating seawater at 25 • C for the subsequent experiment.

Histopathological Analysis
After fluorescence quantification of EHP pathogens, L. vannamei naturally infected with different levels of EHP (Figure 1) were selected for transmission electron microscopy observation.
metabolized via glycolysis to release 7% of its full ATP potential.And energy s complemented by the import of ATP molecules from the host with the help of hori acquired ATP/ADP translocases [8,9].Microsporidia are mainly dependent on the for metabolism and energy requirements [10].In L. vannamei, energy theft by EH significant growth retardation.
In order to study the energy imbalance of L. vannamei infected by EHP, L. v with different EHP infection levels were collected, and energy metabolism and m dria characteristics of L. vannamei infected by EHP were explored.These findings vide some basic information for pathogenic mechanisms and further target co search.

Sample Collection
L. vannamei showed retarded growth and large individual differences in t pond in one shrimp farming factory located in Ningbo City.To explore the shrimp samples were collected from different ponds, and the length of the shr recorded.Meanwhile, a PCR-amplified molecular assay was used to detect potent ogen infection.Shrimp infected with EHP were selected and brought back to the p of Ningbo University, where they were temporarily kept in 150 L aquaculture ta recirculating seawater at 25℃ for the subsequent experiment.

Histopathological Analysis
After fluorescence quantification of EHP pathogens, L. vannamei naturally with different levels of EHP (Figure 1) were selected for transmission electron mic observation.The specific steps were as follows: EHP-infected shrimp hepatopancreas quickly peeled off and fixed in 3% glutaraldehyde at 4 °C for 24 h.After wash buffer, samples were fixed in 1% osmic acid at 4 °C for 2 h.After rinsing with PBS, were dehydrated with a graded ethanol series (30%, 50%, 70%, and 90%) follow graded acetone series (90% and 100%).After that, the samples were immersed in a of epoxy resin and acetone.After drying, samples were cut with an ultra-thin mi The specific steps were as follows: EHP-infected shrimp hepatopancreases were quickly peeled off and fixed in 3% glutaraldehyde at 4 • C for 24 h.After washing with buffer, samples were fixed in 1% osmic acid at 4 • C for 2 h.After rinsing with PBS, samples were dehydrated with a graded ethanol series (30%, 50%, 70%, and 90%) followed by a graded acetone series (90% and 100%).After that, the samples were immersed in a mixture of epoxy resin and acetone.After drying, samples were cut with an ultra-thin microtome, and sections were stained with uranyl acetate and double-stained with lead citrate.Section observations were carried out using an H-7650 transmission electron microscope (Hitachi, Tokyo Japan).

EHP Artificial Infection Experiment
A batch of healthy and well-growing shrimp was purchased from another shrimp farm.The healthy shrimp group and the infected shrimp group were set.Each group with 100 shrimp was raised in separate 120 L aquariums.The infected group was fed with the hepatopancreas of the strong positive EHP-detected L. vannamei, while the control group was fed with healthy shrimp hepatopancreas.Both groups were fed twice a day continuously for 3 days.Samples were collected on the 7th and 14th day after infection for subsequent analyses.The relative quantification result of EHP in the sample was calculated using fluorogenic quantitative PCR with a previously reported primer [11].

Gene Expression Changes Related to Glucose Metabolism
In this study, the expression levels of hexokinase (HK) and pyruvate kinase (PK), the key genes in glycolysis, were detected in the diseased L. vannamei samples.More specifically, RNA extraction of the samples collected on the 7th and 14th days after infection was performed.After the reverse transcription, quantitative real-time PCR was used to detect the expression of HK and PK.The primer sequences are listed in Table 1.RT-PCR was performed using the SYBR qPCR Master Mix fluorescent quantitation kit.Each gene was repeated three times, and the specificity of each primer pair was checked using melting curve analysis.β-actin was used as the reference gene [12].The relative gene expression levels were analyzed using the 2 −∆∆Ct method [13].

Determination of Enzymatic Activities Related to Energy Metabolism
Enzymes related to energy metabolism, including cytochrome c oxidase (CCO), hexokinase (HK), succinate dehydrogenase (SDH), lactate dehydrogenase (LDH), and pyruvate kinase (PK), were detected in this study (Figure 2).The CCO activity assay was slightly modified based on the method of Liu et al. [14], and the oxidation of reduced cytochrome c was measured at a wavelength of 550 nm.The HK assay method was carried out based on the previous method reported by Eleazar [15].SDH, LDH, and PK were determined using test kits purchased from Nanjing Jiancheng Bioengineering Institute.

Transcriptome Analysis
Energy-metabolism-related pathway and differentially expressed gene (DEG) anal yses were performed using transcriptome data previously obtained by our lab [16].I particular, the changes in the oxidative phosphorylation pathway in EHP-infected shrimp were considered.

Mitochondrial Membrane Potential and Apoptosis
To investigate the effects of EHP on the L. vannamei mitochondrial function in relatio to glucose metabolism, analyses of mitochondrial membrane potential and cell apoptosi were conducted in both healthy and infected groups.The hepatopancreas of L. vanname was taken, and 2.5 g tissue was homogenized with 20 mL isolation buffer (320 mM su crose, 10 mM Tris, 10 mM EGTA, 0.5% BSA, pH 7.3) at the lowest speed for 30 s.Then, th homogenate was centrifuged at 800 g for 10 min, and the supernatant was collected a 12,000 g for 15 min to precipitate the mitochondria.The obtained mitochondrial pellet wa suspended in 0.25 mL of isolation buffer for subsequent mitochondrial characterizatio analysis.All the above operations were carried out on ice except for centrifugation at 4℃ The protein concentration of the mitochondria was determined using the BCA reagen Then, the purified mitochondria were used, and the mitochondrial membrane potentia was detected using the JC-1 enhanced mitochondrial membrane potential detection ki (Beyotime).When the mitochondrial membrane potential is low, JC-1 exists as a mono mer, whereas when the mitochondrial membrane potential is high, JC-1 will reaggregat in the mitochondrial matrix to form a polymer.Then, the relative ratio of monomers t polymers is often used to measure changes in mitochondrial membrane potential.
At the same time, single-cell suspensions were prepared using the hepatopancreas o L. vannamei.After being filtered with a 100 µm mesh and resuspended in complete cultur medium, a single-cell suspension was used to explore the cell apoptosis rate with the An nexin V-FITC apoptosis detection kit (Beyotime).Specifically, the hepatopancreatic cell were stained with FITC and PI and incubated in the dark for 15 min at room temperature and then the cell apoptosis of L. vannamei in the healthy and infected groups was detected using a flow cytometer.

Statistical Analysis
The experimental data were collated by Microsoft Excel, 2021 and the experimenta results were statistically analyzed by SPSS Statistics 25.0 (one-way ANOVA), and the Dun can method was used for multiple comparisons between groups.When p < 0.05, the dif ference was statistically significant.

Transcriptome Analysis
Energy-metabolism-related pathway and differentially expressed gene (DEG) analyses were performed using transcriptome data previously obtained by our lab [16].In particular, the changes in the oxidative phosphorylation pathway in EHP-infected shrimp were considered.

Mitochondrial Membrane Potential and Apoptosis
To investigate the effects of EHP on the L. vannamei mitochondrial function in relation to glucose metabolism, analyses of mitochondrial membrane potential and cell apoptosis were conducted in both healthy and infected groups.The hepatopancreas of L. vannamei was taken, and 2.5 g tissue was homogenized with 20 mL isolation buffer (320 mM sucrose, 10 mM Tris, 10 mM EGTA, 0.5% BSA, pH 7.3) at the lowest speed for 30 s.Then, the homogenate was centrifuged at 800 g for 10 min, and the supernatant was collected at 12,000 g for 15 min to precipitate the mitochondria.The obtained mitochondrial pellet was suspended in 0.25 mL of isolation buffer for subsequent mitochondrial characterization analysis.All the above operations were carried out on ice except for centrifugation at 4 • C. The protein concentration of the mitochondria was determined using the BCA reagent.Then, the purified mitochondria were used, and the mitochondrial membrane potential was detected using the JC-1 enhanced mitochondrial membrane potential detection kit (Beyotime).When the mitochondrial membrane potential is low, JC-1 exists as a monomer, whereas when the mitochondrial membrane potential is high, JC-1 will reaggregate in the mitochondrial matrix to form a polymer.Then, the relative ratio of monomers to polymers is often used to measure changes in mitochondrial membrane potential.
At the same time, single-cell suspensions were prepared using the hepatopancreas of L. vannamei.After being filtered with a 100 µm mesh and resuspended in complete culture medium, a single-cell suspension was used to explore the cell apoptosis rate with the Annexin V-FITC apoptosis detection kit (Beyotime).Specifically, the hepatopancreatic cells were stained with FITC and PI and incubated in the dark for 15 min at room temperature, and then the cell apoptosis of L. vannamei in the healthy and infected groups was detected using a flow cytometer.

Statistical Analysis
The experimental data were collated by Microsoft Excel, 2021 and the experimental results were statistically analyzed by SPSS Statistics 25.0 (one-way ANOVA), and the Duncan method was used for multiple comparisons between groups.When p < 0.05, the difference was statistically significant.

Ultrastructural Pathology
To observe ultrastructural pathological characteristics in tissues, transmission electron microscopy (TEM) analysis of hepatopancreas in shrimp naturally infected with EHP was performed.EHP spores, approximately 1 µm in size, were present in the cytoplasm of the hepatopancreas (Figure 3).In the high-concentration EHP infection group, the number of mitochondria increased significantly and showed obvious aggregation (Figure 3C,D).In the low-concentration EHP infection group, mitochondrial staining was lighter and more extended (Figure 3B).

Ultrastructural Pathology
To observe ultrastructural pathological characteristics in tissues, transmission electron microscopy (TEM) analysis of hepatopancreas in shrimp naturally infected with EHP was performed.EHP spores, approximately 1 µm in size, were present in the cytoplasm of the hepatopancreas (Figure 3).In the high-concentration EHP infection group, the number of mitochondria increased significantly and showed obvious aggregation (Figure 3C,D).In the low-concentration EHP infection group, mitochondrial staining was lighter and more extended (Figure 3B).

Gene Expression Analysis
In the EHP artificial infection experiment, quantitative results showed EHP content in the second week was 185-fold higher than that in the first week, which indicated the EHP content increased significantly with the increase in infection time.Fluorescence quantitative results of gene expression show that the key gene hexokinase was significantly upregulated in the diseased shrimp (Figure 4).The relative expression level of hexokinase in the first week was higher than that in the second week (p <= 0.001).

Gene Expression Analysis
In the EHP artificial infection experiment, quantitative results showed EHP content in the second week was 185-fold higher than that in the first week, which indicated the EHP content increased significantly with the increase in infection time.Fluorescence quantitative results of gene expression show that the key gene hexokinase was significantly upregulated in the diseased shrimp (Figure 4).The relative expression level of hexokinase in the first week was higher than that in the second week (p ≤ 0.001).

Energy-Metabolism-Related Enzyme Detection
After a week of infection, the hexokinase and lactate dehydrogenase activities of the hepatopancreas were significantly increased in the EHP-infected group.Meanwhile, the activity of the pyruvate dehydrogenase was slightly increased, but the difference was not significant.There was no significant change in the activities of cytochrome C oxidase and succinate dehydrogenase (Figure 5).

Energy-Metabolism-Related Enzyme Detection
After a week of infection, the hexokinase and lactate dehydrogenase activities o hepatopancreas were significantly increased in the EHP-infected group.Meanwhil activity of the pyruvate dehydrogenase was slightly increased, but the difference wa significant.There was no significant change in the activities of cytochrome C oxidas succinate dehydrogenase (Figure 5).After two weeks of EHP infection, compared with the healthy group, the activit hexokinase, pyruvate kinase, and lactate dehydrogenase in the hepatopancreas of sh were significantly increased in the EHP infection group, while the activities of succ dehydrogenase and cytochrome C oxidase were significantly decreased (Figure 6).

Energy-Metabolism-Related Enzyme Detection
After a week of infection, the hexokinase and lactate dehydrogenase activities of hepatopancreas were significantly increased in the EHP-infected group.Meanwhile, activity of the pyruvate dehydrogenase was slightly increased, but the difference was significant.There was no significant change in the activities of cytochrome C oxidase a succinate dehydrogenase (Figure 5).After two weeks of EHP infection, compared with the healthy group, the activities hexokinase, pyruvate kinase, and lactate dehydrogenase in the hepatopancreas of shri were significantly increased in the EHP infection group, while the activities of succin dehydrogenase and cytochrome C oxidase were significantly decreased (Figure 6).After two weeks of EHP infection, compared with the healthy group, the activities of hexokinase, pyruvate kinase, and lactate dehydrogenase in the hepatopancreas of shrimp were significantly increased in the EHP infection group, while the activities of succinate dehydrogenase and cytochrome C oxidase were significantly decreased (Figure 6).

EHP Effects on Energy Metabolism of L. vannamei Based on Transcriptome
The Illumina sequencing and quality assessment, analysis of DEGs, and validation analysis of transcriptomics can be found in previously published literature [16].Based on the transcriptome data, this article focuses on analyzing the energy-metabolism-related genes and signaling pathways of low-concentration and high-concentration EHP-infected groups.The KEGG analyses of differentially expressed genes (DEGs) between the lowconcentration EHP-infected group (group C) and the high-concentration EHP-infected group (group A) were classified into five branches: metabolism, cellular processes, environmental information processing, genetic information processing, and organismal systems.Among these five branches, metabolism was the most enriched information pathway for the DEGs, including amino acid metabolism, carbohydrate metabolism, lipid metabolism, energy metabolism, and metabolism of other amino acids.The DEGs related to energy metabolism are shown in Table 2.Among them, Cox5b was the most significantly downregulated in high-concentration EHP infection, while Inorganic pyrophosphatase was the most significantly upregulated gene (Figure 7).These findings indicate that highconcentration EHP infection suppresses the oxidative phosphorylation pathway by Cox5b.

EHP Effects on Energy Metabolism of L. vannamei Based on Transcriptome
The Illumina sequencing and quality assessment, analysis of DEGs, and validation analysis of transcriptomics can be found in previously published literature [16].Based on the transcriptome data, this article focuses on analyzing the energy-metabolism-related genes and signaling pathways of low-concentration and high-concentration EHP-infected groups.The KEGG analyses of differentially expressed genes (DEGs) between the lowconcentration EHP-infected group (group C) and the high-concentration EHP-infected group (group A) were classified into five branches: metabolism, cellular processes, environmental information processing, genetic information processing, and organismal systems.Among these five branches, metabolism was the most enriched information pathway for the DEGs, including amino acid metabolism, carbohydrate metabolism, lipid metabolism, energy metabolism, and metabolism of other amino acids.The DEGs related to energy metabolism are shown in Table 2.Among them, Cox5b was the most significantly downregulated in high-concentration EHP infection, while Inorganic pyrophosphatase was the most significantly upregulated gene (Figure 7).These findings indicate that high-concentration EHP infection suppresses the oxidative phosphorylation pathway by Cox5b.

Mitochondrial Membrane Potential Changes
Mitochondrial membrane potential changes were estimated using JC-1 staining methods.In the first week, the ratio of monomers to polymers in the mitochondria of EHPinfected L. vannamei was significantly higher than that in the healthy group, indicating a significant decrease in mitochondrial membrane potential in the infected group.However, in the second week, the mitochondrial membrane potential still decreased to a certain extent but had no significant difference (Table 3).

Hepatopancreas Cell Apoptosis
During the first and second weeks of infection, primary hepatopancreas cells were isolated from both infected and healthy groups of shrimp to detect the level of cell apoptosis.The results showed no significant difference in cell apoptosis in the shrimp infected with EHP during the first and second weeks (Figure 8).

Mitochondrial Membrane Potential Changes
Mitochondrial membrane potential changes were estimated using JC-1 staining methods.In the first week, the ratio of monomers to polymers in the mitochondria of EHPinfected L. vannamei was significantly higher than that in the healthy group, indicating a significant decrease in mitochondrial membrane potential in the infected group.However, in the second week, the mitochondrial membrane potential still decreased to a certain extent but had no significant difference (Table 3).
Table 3. Mitochondrial membrane potential detection based on JC-1.

Hepatopancreas Cell Apoptosis
During the first and second weeks of infection, primary hepatopancreas cells were isolated from both infected and healthy groups of shrimp to detect the level of cell apoptosis.The results showed no significant difference in cell apoptosis in the shrimp infected with EHP during the first and second weeks (Figure 8).

Discussions
EHP is a very serious pathogen in shrimp culture.However, due to the unique intra cellular parasitic features, the complex pathogenicity, and unclear invasion mechanisms there is still a lack of effective treatment and prevention measures for EHP.In this study the pathogenic mechanism of EHP infection in hosts based on energy flow has been ex plored.
Ultrastructural pathological characteristics in the hepatopancreas of shrimp showed the number of mitochondria increased significantly and showed obvious aggregation in the high-concentration EHP infection group.However, in the low-concentration EHP in fection group, mitochondrial staining was lighter and more extended.In L. vannamei, mi tochondria are responsible for synthesizing ATP molecules required for cell function providing sufficient energy to support life activities [17].The increase in mitochondria in the EHP-infected shrimp means that the body needs more energy for the EHP pathogen and host.
In addition to their function in energy metabolism, mitochondria also participate in functions such as free radical production, aging, and cell apoptosis [18].The changes in mitochondrial morphology under electron microscopy also indicated that EHP may affec not only host energy metabolism but also other functions of the host.Moreover, mitochon drial membrane potential plays a key role in maintaining normal cellular metabolism.The potential difference between the inner and outer mitochondrial membranes is an im portant driving force for ATP synthesis and affects cell metabolism and energy status.A decrease in the mitochondrial membrane potential can lead to an imbalance in cellula energy metabolism [19].In this study, the mitochondrial membrane potential of the in fected group was significantly lower than that of the healthy group in the first week o EHP infection, and there was no significant difference in the second week of EHP infec tion, implying that early EHP infection leads to mitochondrial damage and that the mito chondria were partially restored in the late stage.It is speculated that during the acute infection period of EHP, invasion and proliferation of EHP within cells may lead to dam

Discussions
EHP is a very serious pathogen in shrimp culture.However, due to the unique intracellular parasitic features, the complex pathogenicity, and unclear invasion mechanisms, there is still a lack of effective treatment and prevention measures for EHP.In this study, the pathogenic mechanism of EHP infection in hosts based on energy flow has been explored.
Ultrastructural pathological characteristics in the hepatopancreas of shrimp showed the number of mitochondria increased significantly and showed obvious aggregation in the high-concentration EHP infection group.However, in the low-concentration EHP infection group, mitochondrial staining was lighter and more extended.In L. vannamei, mitochondria are responsible for synthesizing ATP molecules required for cell function, providing sufficient energy to support life activities [17].The increase in mitochondria in the EHP-infected shrimp means that the body needs more energy for the EHP pathogen and host.
In addition to their function in energy metabolism, mitochondria also participate in functions such as free radical production, aging, and cell apoptosis [18].The changes in mitochondrial morphology under electron microscopy also indicated that EHP may affect not only host energy metabolism but also other functions of the host.Moreover, mitochondrial membrane potential plays a key role in maintaining normal cellular metabolism.The potential difference between the inner and outer mitochondrial membranes is an important driving force for ATP synthesis and affects cell metabolism and energy status.A decrease in the mitochondrial membrane potential can lead to an imbalance in cellular energy metabolism [19].In this study, the mitochondrial membrane potential of the infected group was significantly lower than that of the healthy group in the first week of EHP infection, and there was no significant difference in the second week of EHP infection, implying that early EHP infection leads to mitochondrial damage and that the mitochondria were partially restored in the late stage.It is speculated that during the acute infection period of EHP, invasion and proliferation of EHP within cells may lead to damage in mitochondrial function in the hepatopancreas, while in the second week, although the mitochondrial membrane potential partially recovered, it still showed a certain degree of difference compared to the healthy group.The results of cell apoptosis showed that EHP infection had no significant effect on the apoptosis of hepatopancreas cells, indicating that EHP infection does not cause significant cell apoptosis, consistent with the conclusion that EHP does not directly cause death in L. vannamei.
In transcriptomic data analysis, energy-metabolism-related pathways revealed 13 DEGs associated with energy metabolism pathways.Cox5b encodes the peripheral nuclearencoded subunit of mitochondrial cytochrome c oxidase subunit 5B, which is part of a multi-subunit, dual-genome-encoded protein complex catalyzing the final step of the mitochondrial electron transport chain.Previous studies have shown that Cox5b deficiency leads to a reduction in cytochrome c oxidase activity, indicating that has a regulatory role [20].Mitochondrial proteins play a critical role in the respiratory chain, and the downregulation of protein genes can induce mitochondrial dysfunction [21].This gene is significantly downregulated in the high infection group of EHP, indicating that high concentrations of EHP infection can inhibit Cox5b gene expression and, therefore, suppress mitochondrial cytochrome c oxidase activity.Inorganic pyrophosphatase can catalyze chemical reactions to produce some important phosphate substances, such as ATP, NADH, FADH, and other compounds, which are extremely important biological energy sources.It can be seen that inorganic pyrophosphatase plays a huge role in maintaining normal metabolism and operation of organisms [22,23].In addition, the tpi1b gene (Triosephosphate isomerase B) encodes a metabolic enzyme involved in the glycolytic pathway.In the infection group of EHP, inorganic pyrophosphatase and tpi1b were significantly upregulated, suggesting that EHP may enhance the host's glycolytic pathway, accelerate glucose metabolism, and generate ATP.
In the enzyme activity and gene expression analysis, the glycolysis pathway and anaerobic respiration-related enzyme activities were higher than those of the healthy group in the first week of EHP infection, indicating that the glycolysis pathway and anaerobic respiration were activated.In the second week of EHP infection, the glycolysis pathway and anaerobic respiration were still activated, while the tricarboxylic acid cycle and oxidative phosphorylation levels decreased.The quantitative gene expression results in this study were consistent with the enzyme activity detection results.When subjected to environmental stress and other unfavorable conditions, L. vannamei switches to anaerobic energy metabolism and activates its enzymatic pathways, which promotes the generation of ATP [24].In response to EHP infection, L. vannamei exhibits an activated state of glycolysis in the first and second weeks, and it is speculated that L. vannamei may enhance its tolerance to EHP by increasing the rate of glycolysis, thereby leading to a reduction in energy consumption for growth; this is possibly the key reason for its growth retardation.Lactate dehydrogenase (LDH) catalyzes the bidirectional conversion of lactate to pyruvate and is a glycolytic enzyme that provides additional energy supply when the organism is under stress [25].In this study, the LDH activity was significantly increased during the first and second weeks of EHP infection, resulting in an increase in the conversion of pyruvate to lactate and enhancing anaerobic metabolism in tissues.Many cancer cells exhibit a preference for glycolysis, even in the presence of oxygen, which manifests as high levels of glucose uptake and lactate production [26].The Warburg effect is an abnormal glycolysis response that is associated with cancer cells.This preference is due to changes and abnormal activation in gene expression and signaling pathways.Some scholars have proposed metabolic changes resembling the Warburg effect are induced by a nonmammalian virus [27,28].In this paper, we propose that EHP also induces this effect for the first time, which is beneficial for EHP self-growth.After EHP infection, the energy metabolism pattern of L. vannamei is similar to that of cancer cells, with an increase in glycolysis and anaerobic respiration and a suppression of oxidative phosphorylation and aerobic respiration.This metabolic shift may be due to EHP's energy theft in the host leading to abnormal gene expression and signaling pathways in L. vannamei.

Figure 1 .
Figure 1.Shrimp with different concentrations of EHP infection.Note: A is the shrimp sam a high concentration of EHP infection; B is the shrimp sample with a low concentratio infection.

Figure 1 .
Figure 1.Shrimp with different concentrations of EHP infection.Note: A is the shrimp sample with a high concentration of EHP infection; B is the shrimp sample with a low concentration of EHP infection.

Figure 2 .
Figure 2. Flow chart of glucose metabolism.Note: The text marked in red indicates the enzym activity detected in this study.

Figure 2 .
Figure 2. Flow chart of glucose metabolism.Note: The text marked in red indicates the enzyme activity detected in this study.

Figure 3 .
Figure 3. Histopathological analysis of hepatopancreatic tissues at different concentrations of EHP infection by transmission electron microscopy.Notes: (A,B) represent low-concentration EHP infection groups; (C,D) represent high-concentration EHP infection groups; NC means cell nucleus; red arrows represent EHP; white arrows represent mitochondria.

Figure 3 .
Figure 3. Histopathological analysis of hepatopancreatic tissues at different concentrations of EHP infection by transmission electron microscopy.Notes: (A,B) represent low-concentration EHP infection groups; (C,D) represent high-concentration EHP infection groups; NC means cell nucleus; red arrows represent EHP; white arrows represent mitochondria.

Figure 4 .
Figure 4. HK and PK gene expression in the hepatopancreas of L. vannamei.Notes: HK repr the hexokinase gene; PK represents the pyruvate kinase gene; *** means p <= 0.001.

Figure 5 .
Figure 5. Enzyme activity analysis in the infected shrimp in the first week.Notes: The control represents the healthy group (orange ) and the experiment group represents the artificial inf group (blue); ** means p <= 0.01, *** means p <= 0.001; HK is hexokinase, PK is pyruvate kinase is succinate dehydrogenase, CCO is cytochrome c oxidase, and LDH is lactate dehydrogenase

Figure 4 .
Figure 4. HK and PK gene expression in the hepatopancreas of L. vannamei.Notes: HK represents the hexokinase gene; PK represents the pyruvate kinase gene; *** means p ≤ 0.001.

Figure 5 .
Figure 5. Enzyme activity analysis in the infected shrimp in the first week.Notes: The control gro represents the healthy group (orange ) and the experiment group represents the artificial infect group (blue); ** means p <= 0.01, *** means p <= 0.001; HK is hexokinase, PK is pyruvate kinase, S is succinate dehydrogenase, CCO is cytochrome c oxidase, and LDH is lactate dehydrogenase.

Figure 5 .
Figure 5. Enzyme activity analysis in the infected shrimp in the first week.Notes: The control group represents the healthy group (orange ) and the experiment group represents the artificial infection group (blue); ** means p ≤ 0.01, *** means p ≤ 0.001; HK is hexokinase, PK is pyruvate kinase, SDH is succinate dehydrogenase, CCO is cytochrome c oxidase, and LDH is lactate dehydrogenase.

Figure 6 .
Figure 6.Enzyme activity analysis in the infected shrimp in the second week.Notes: The relevant annotations are consistent with those in Figure 5; ** means p <= 0.01, *** means p <= 0.001.

Figure 6 .
Figure 6.Enzyme activity analysis in the infected shrimp in the second week.Notes: The relevant annotations are consistent with those in Figure 5; ** means p ≤ 0.01, *** means p ≤ 0.001.

Figure 7 .
Figure 7. DEGs involved in oxidative phosphorylation pathway in group C vs. group A. Notes: Red indicates upregulated DEGs; dark green represents downregulated DEGs.

Figure 7 .
Figure 7. DEGs involved in oxidative phosphorylation pathway in group C vs. group A. Notes: Red indicates upregulated DEGs; dark green represents downregulated DEGs.

Figure 8 .
Figure 8.The analysis of cell apoptosis using flow cytometry.

Table 2 .
DEGs enriched in energy metabolism pathway in group C vs. group A.

Table 2 .
DEGs enriched in energy metabolism pathway in group C vs. group A.

Table 3 .
Mitochondrial membrane potential detection based on JC-1.