key: cord-0782979-reaw7lp6
authors: Takano, Tomomi; Wakayama, Yumeho; Doki, Tomoyoshi
title: Endocytic Pathway of Feline Coronavirus for Cell Entry: Differences in Serotype-Dependent Viral Entry Pathway
date: 2019-12-16
journal: Pathogens
DOI: 10.3390/pathogens8040300
sha: a912f654028e787673b235c9ba2eb2d161e372aa
doc_id: 782979
cord_uid: reaw7lp6

Feline coronavirus (FCoV) is a pathogen causing a lethal infectious disease in cats, feline infectious peritonitis. It has two serotypes (type I FCoV and type II FCoV). According to our previous study, type I FCoV infection is inhibited by compounds inducing intracellular cholesterol accumulation, whereas type II FCoV infection is not inhibited. Intracellular cholesterol accumulation was reported to disrupt late endosome function. Based on these findings, types I and II FCoV are considered to enter the cytosol through late and early endosomes, respectively. We investigated whether the antiviral activities of a late endosome trafficking inhibitor and cholesterol-accumulating agents are different between the FCoV serotypes. The late endosome trafficking inhibitor did not inhibit type II FCoV infection, but it inhibited type I FCoV infection. Type I FCoV infection was inhibited by cholesterol-accumulating triazoles, but not by non-cholesterol-accumulating triazoles. These phenomena were observed in both feline cell lines and feline primary macrophages. This study provides additional information on the differences in intracellular reproductive cycle between type I and type II FCoV.

Feline coronavirus (FCoV) is a positive-sense RNA virus in the species Alphacoronavirus 1 genus Alphacoronaivirus, of the subfamily Coronavirinae, in the family Coronaviridae [1] . It is divided into two serotypes (types I and II) based on the amino acid sequence of the spike (S) protein [2] . Type I FCoV is the dominant serotype (80-90%) in Europe and Asia [3] [4] [5] . FCoV can also be divided into two biotypes, feline infectious peritonitis virus (FIP virus, FIPV; virulent FCoV) and feline enteric coronavirus (FECV; avirulent FCoV), according to its pathogenesis in animals [6] . FIPV infection typically causes a lethal disease in Felidae known as FIP [7] . The hallmark pathological findings of FIP in domestic cats are serous fluid in peritoneal and pleural cavities, pyogranulomatous lesions in internal organs, and disseminated fibrinous on the serosal and organ surfaces [6] . The FIPV-infected cells in the lesion and serous effusion predominantly consist of macrophages. FIPV-infected macrophages have been suggested to exacerbate the disease condition [8] [9] [10] .

FCoVs attach to the cell surface through feline aminopeptidase N (fAPN) as the viral receptor. FCoVs enter the cell through endocytosis after attachment to the fAPN [6] . It is speculated that low endosomal pH triggers the conformation change of the spike protein of FCoV that releases the virus from the endosome to the cytosol. However, the timing of cytosol entry of each serotype was unclear.

FCoV infection is dependent on intracellular cholesterol [11] . Our previous study demonstrated that the triazole antifungal agent itraconazole blocks the intracellular trafficking of cholesterol and inhibits type I FCoV infection in a feline cell line (felis catus whole fetus-4 cells: fcwf-4 cells) [12] . Similar results were observed with U18666A, the widely studied cholesterol transport inhibitor [11] . Other researchers reported that itraconazole and U18666A blocked cholesterol egress from late endosomes [13] [14] [15] . Furthermore, cholesterol accumulation was reported to disrupt late endosome function [16, 17] . Based on this, cholesterol transport inhibitors are hypothesized to inhibit the release of type I FCoV into the cytosol by indirectly disrupting the late endosome function. However, as described above, the site of endosomal release of both FCoV serotypes has not been investigated.

In this study, we demonstrated that type I FCoV cannot replicate in cells unless it reaches late endosomes, whereas type II FCoV can even though it does not reach late endosomes. Moreover, we investigated the effects of cholesterol-accumulating triazoles (itraconazole and posaconazole) and non-cholesterol-accumulating triazoles (voriconazole and fluconazole) [18] on the infectivity of FCoV in established feline cell lines (Felis catus whole fetus-4 cells (fcwf-4 cells)) and feline primary macrophages.

Cytotoxicity assay was performed to determine the non-toxic concentration of compounds against fcwf-4 cells ( Figure 1 ). The concentrations used in this study were selected because they had low cytotoxic effects (cell viability: >83-90%) on feline cells. 

To confirm whether FCoV accesses late endosomes for cell entry, we investigated the effects of 25-hydroxycholesterol (25-HC), a non-specific late endosome trafficking inhibitor [19] , on FCoV. We assessed whether 25-HC inhibits late endosome function using intracellular cholesterol accumulation as an index. The 25-HC affected cholesterol accumulation in a dose-dependent manner (Figure 2A Figure 2C ), suggesting that type I FCoV enters via late endosomes. To confirm this hypothesis, we examined the effects of viral infection after 4-bromobenzaldehyde N-(2,6-dimethylphenyl) semicarbazone (EGA) treatment, which specifically inhibits transport from early to late endosomes [20] . EGA significantly suppressed FCoV-I KU2 infection, but not FCoV-II 79-1146 infection ( Figure 3 ). 

Based on the above results and our previous study [11, 12] , different FCoV serotypes may enter feline cells through different endocytic routes: FCoV-I KU2 is released from late endosomes into the cytosol, whereas FCoV-II 79-1146 is released from early endosomes into the cytosol. Cholesterol accumulation was previously reported to disrupt late endosome function [16, 17] . Therefore, we investigated the effects of cholesterol-accumulating triazoles (itraconazole and posaconazole) and non-cholesterol-accumulating triazoles (voriconazole and fluconazole) on the infectivity of FCoV. 

We next investigated whether findings similar to those observed in fcwf-4 cells are observed in macrophages, the target of virulent FCoV (FIPV). The concentration of triazole antifungals disrupting late endosome function in feline primary macrophages was confirmed, i.e., the concentration at which triazole antifungals accumulate intracellular cholesterol was measured. Both itraconazole and posaconazole clearly induced cholesterol accumulation at 20 µM (Figure 7 ). In contrast, voriconazole and posaconazole did not induce cholesterol accumulation even at the concentration limit not exhibiting cytotoxicity (Figure 7) . We then examined whether FCoV can replicate in primary macrophages with disrupted late endosome function. In this experiment, only type I FCoV was used in consideration of the limited number of cats. In addition, no cytopathic effects are observed, and no virus is produced in the culture supernatant in type I FCoV-infected primary macrophages. Taking these conditions into consideration, viral infection of macrophages was judged based on the detection of FCoV N protein. As a result, N protein levels of FCoV-I KU2 were reduced by itraconazole and posaconazole, but not by voriconazole or fluconazole, in primary macrophages, similar to in fcwf-4 cells (Figure 8 ). 

Viruses employ several entry strategies. After endocytosis, virus entry occurs at early or late endosomes [21] [22] [23] [24] [25] . According to previous studies, there are two cell entry types in coronavirus infection: Cytosol entry through early endosomes (e.g., MERS-CoV, infectious bronchitis virus, and human coronavirus NL-63) and late endosomes (e.g., SARS-CoV) [26, 27] . Burkard et al. reported that FCoV (serotype is unclear) enters the cytosol through late endosomes [26] . We demonstrated that types I and II FCoV enter the cytosol through late and early endosomes, respectively ( Figure 9 ). To our knowledge, viruses that enter the cytosol at different times among serotypes have not been reported other than FCoV observed in this study. The FCoV serotypes are distinguished based on the amino acid sequence of S protein [2] , i.e., timing of the serotypes to transit to the cytosol is dependent on S protein. Indeed, cleavage of coronavirus S protein in endosomes plays an important role in cytosol entry [28] [29] [30] . Cathepsin L is an endosomal protease involved in S protein cleavage of coronaviruses [31] [32] [33] . Cholesterol accumulation in late endosomes is observed in cells with inhibited cathepsin L activity [34] . Of note, the inhibition of cathepsin L activity does not influence the multiplication of FCoV-II 79-1146 [35] . Further investigation is necessary to clarify whether S protein cleavage by cathepsin L or cholesterol transport influences cytosol entry by FCoV.

The 25-hydroxycholesterol is oxysterol produced by cholesterol-25-hydroxylase induced by interferon [36] . Although 25-hydroxycholesterol inhibits several viral infections [36] [37] [38] [39] [40] [41] , many points remain unclear with regard to its antiviral activity. Civra et al. reported that 25-hydroxycholesterol accumulates cholesterol in late endosomes and inhibits rotavirus infection [19] . Based on their report, 25-hydroxycholesterol exhibits its antiviral activity through disrupting late endosome function. We confirmed that 25-hydroxycholesterol inhibits type I FCoV infection at the cholesterol-accumulating concentration, i.e., type I FCoV infection was blocked by 25-hydroxycholesterol through the same mechanism as that of rotavirus infection inhibition. Based on this finding, 25-hydroxycholesterol can be applied as a potent antiviral agent for FCoV. However, oxysterols, such as 25-hydroxycholesterol, induce arteriosclerosis [42, 43] . Therefore, further investigation is necessary to use 25-hydroxycholesterol as an antiviral agent for FIP. High-concentration (100 µM) 25-hydroxycholesterol inhibited type II FCoV infection by 60%. The reason for this is unclear, but a large amount of 25-hydroxycholesterol incorporated by endocytosis may have physically blocked type II FCoV release from early endosomes.

Both FCoV serotypes use the endosomal pathway for cell entry [11, 44] . However, the timing of cytosol entry of each serotype was unclear. EGA prevents transport from early endosomes to late endosomes [20] . Type II FCoV infection was not inhibited by EGA, demonstrating that type II FCoV enters the cytosol before it reaches late endosomes. In contrast, EGA inhibited type I FCoV infection. Thus, type I FCoV requires late endosomes to enter the cytosol. We tried to directly demonstrate that type I FCoV reaches late endosomes, i.e., we investigated colocalization of a late endosome marker, Rab7, and the virion, but we were unable to find a commercial anti-Rab7 antibody that reacts with feline Rab7. It is necessary to produce an antibody reacting with feline Rab7 and confirm the hypothesis described above.

Based on previous reports, triazole antifungals are classified into two types: cholesterolaccumulating triazoles (itraconazole and posaconazole) and non-cholesterol-accumulating triazoles (voriconazole and fluconazole) [18] . To our knowledge, the reason for these differences has not been clarified. These differences may be due to the structure of each drug. The structure of itraconazole is similar to that of posaconazole but different from those of voriconazole and fluconazole. Trinh et al. reported that itraconazole and posaconazole bind the sterol-sensing domain (SDD) of Niemann-Pick disease type C1 (NPC1) [45] . U18666A and 25-hydroxycholesterol, which induce cholesterol accumulation similarly to itraconazole, bind SDD [46, 47] . Unlike these drugs, voriconazole and fluconazole may be unable to bind SDD. On the other hand, it was suggested that itraconazole, posaconazole, U18666A, and 25-hydroxycholesterol interfere with the binding of type I FCoV to NPC1, in addition to inducing cholesterol accumulation, by binding SDD [48] . However, in cells treated with SDD-binding cholesterol, type I FCoV infection increased. Thus, inhibition of type I FCoV infection by the above drugs is not related to binding of the virus to the SDD of NPC1.

FCoV-infected macrophages play an important role in the development of FIP [8] [9] [10] . We previously analyzed the mechanism of FCoV infection in feline primary macrophages [44] . Type I and type II FCoV are incorporated by endocytosis when they attach to the cell surface of macrophages, but it is unclear why FCoV that entered macrophages was not degraded. Considering these results, FCoV incorporated by macrophages may escape degradation by macrophage lysosomes by escaping into the cytosol from early/late endosomes.

In general, the infectivity of type I FCoV in feline cells is lower than that of type II FCoV. Recently, O'Brien et al. established fcwf-4 cells (fcwf-4 CU) that permit type I FCoV replication [49] . They noted lower interferon sensitivity as a factor enabling type I FCoV infection of this cell line [49, 50] . As described above, 25-hydroxycholesterol inhibiting type I FCoV infection is induced in cells by interferon, suggesting that 25-hydroxycholesterol is not induced in fcwf-4 CU even though interferon is produced after infection. If this hypothesis is correct, the reason for increased infection by type I FCoV of fcwf-4 CU may be reduced 25-hydroxycholesterol production.

In this study, we indirectly demonstrated that type I FCoV cannot enter the cytosol unless it reaches late endosomes, whereas type II FCoV can even though it does not reach late endosomes. Our findings warrant further studies to elucidate the mechanism of cell entry by FCoV.

The fcwf-4 cells (kindly supplied by Dr. M. C. Horzinek of Utrecht University) were grown in Eagle's minimum essential medium (MEM) containing 50% L-15 medium, 5% fetal calf serum (FCS), 100 U/mL of penicillin, and 100 µg /mL of streptomycin. For the primary macrophages, feline primary macrophages were selected. Feline alveolar macrophages were obtained from four specific-pathogen-free (SPF) cats aged 3-5 years by bronchoalveolar lavage with Hank's balanced salt solution. Feline primary macrophages were maintained in D-MEM supplemented with 10% FCS, 100 U/mL of penicillin, and 100 µg/mL of streptomycin. SPF cats were maintained in a temperature-controlled isolated facility. The experiment using animals was approved by the President of Kitasato University through the judgment of the Institutional Animal Care and Use Committee of Kitasato University and performed in accordance with the Guidelines for Animal Experiments of Kitasato University. Sample sizes were determined based on our previous study, and the minimum number of cats was used. The FCoV-I KU-2 was isolated in our laboratory. The FCoV-II 79-1146 was kindly provided by Dr. M. C. Horzinek of Utrecht University. These viruses were grown in fcwf-4 cells at 37 • C.

The 25-HC (cholesterol transport inhibitor), EGA (late endosome trafficking inhibitor), posaconazole, voriconazole, and fluconazole were purchased from Sigma Aldrich Japan (Tokyo, Japan). Itraconazole was purchased from Janssen Pharma-central K. K. (Tokyo, Japan). The 25-HC was dissolved in methanol. EGA, Posaconazole, voriconazole, and fluconazole were dissolved in dimethyl sulfoxide (DMSO). Itraconazole was dissolved in 40% (w/v) hydroxypropyl-beta-cyclodextrin (HbCD) solution. All compounds were adjusted to 10 mM with solvent, aliquoted, and stored at-30 • C until use. On the day of the experiments, these compounds were diluted to the desired concentrations in maintenance medium.

The fcwf-4 cells were seeded on 96-well plates. The compounds were added to the wells in triplicate. After incubation for defined periods, the culture supernatants were removed, WST-8 solution (Kishida Chemical, Osaka, Japan) was added, and the cells were returned to the incubator for 1 h. The absorbance of formazan produced was measured at 450 nm using a 96-well spectrophotometric plate reader, as described by the manufacturer. Percentage viability was calculated using the following formula: Cytotoxicity (%) = [(OD of compound-untreated cells−compound-treated cells)/(OD of compound-untreated cells)] × 100.

Confluent fcwf-4 cell monolayers were cultured in medium containing compounds at the indicated concentrations in 24-well multi-plates at 37 • C for 24 h. Cells were washed and the virus (MOI 0.01) was adsorbed into the cells at 37 • C for 1 h. After washing, cells were cultured in carboxymethyl cellulose (CMC)-MEM. The cell monolayers were incubated at 37 • C for 48 h, fixed and stained with 1% crystal violet solution containing 10% buffered formalin, and the resulting plaques were then counted. The plaque reduction percentage was calculated using the following formula: Plaque reduction percentage (%) = [(plaque number of compound-treated cells)/(plaque number of compound-untreated cells)] × 100.

Feline cells (fcwf-4 cells or feline primary macrophages) were cultured in each well of an 8-well Lab-Tek Chamber Slide (Thermo Fisher Scientific, Waltham, MA, USA). Semi-confluent cell monolayers were cultured in medium containing each compound at 37 • C for 24 h. Cells were washed and the virus (MOI 0.01) was adsorbed into the cells at 37 • C for 1 h (3 h in the case of macrophages). After washing, cells were cultured in MEM. The cell monolayers were incubated at 37 • C. After 24 h, N protein levels were measured by immunofluorescence assay (IFA), as described previously [51] . To recognize FCoV N protein, mAb E22-2 (mouse IgG1) prepared by our laboratory was used [51] . Nuclei were stained with 4 ,6-diamidino-2-phenylindole (DAPI; Dojindo Laboratories, Kumamoto, Japan).

The cellular cholesterol content of fcwf-4 cells was evaluated by the Cholesterol Cell-Based Detection Assay Kit (Cayman chemical, USA) according to the manufacturer's instructions. Briefly, fcwf-4 cells were grown on an 8-well Lab-Tek Chamber Slide (Thermo Fisher Scientific, Waltham, MA, USA). Semi-confluent fcwf-4 cell monolayers were cultured in medium containing compounds at 37 • C for 24 h. After fixing and staining, filipin III-binding cells were analyzed using a Leica DM4B microscope and LAS X integrated imaging system (Leica Microsystems, Wetzlar, Germany).

Data from only two groups were analyzed by the Student's t-test (Welch's t-test or Bartlett's test), and data from multiple groups were analyzed by one-way ANOVA followed by Tukey's test. 

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25-Hydroxycholesterol and 27-hydroxycholesterol inhibit human rotavirus infection by sequestering viral particles into late endosomes

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This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license

We thank Kumi Satoh for supporting the experiments.

The authors declare no conflict of interest.