key: cord-0004921-7e4yu2do authors: Homberger, F. R. title: Maternally-derived passive immunity to enterotropic mouse hepatitis virus date: 1992 journal: Arch Virol DOI: 10.1007/bf01321123 sha: 3043a0ee5238a31b8b7bdb8fee2576034872aa74 doc_id: 4921 cord_uid: 7e4yu2do Maternally-derived antibody to enterotropic mouse hepatitis virus (MHV) strain Y was transferred to pups by both intrauterine (IgG) and lactogenic (IgA and IgG) routes. Antibody present in the gastric whey of pups suckling immune dams dropped to undetectable levels by weaning age (21 days post partum). MHV-specific IgG was found in the serum of passively immune pups up to 10 weeks of age. Immune dams transferred equal levels of antibody to 3 consecutive litters of pups, without evidence of decline. Immunoblots showed that IgA and IgG in whey and serum were directed against nucleoprotein N and glycoprotein S. MHV-specific IgM was not detected in any sample. Coronaviruses are important pathogens in many species of birds and mammals, including man. They are usually associated with either respiratory or enteric disease. Mouse hepatitis virus (MHV), family Coronaviridae, genus Coronavirus, is a common, highly contagious virus of laboratory mice. The MHV group contains numerous, closely related and highly mutable viruses with either respiratory or enteric tropism [3] . MHV is important both as a natural pathogen of laboratory mice and as a model of coronaviral infection, particularly enteritis in the neonate. As with other enterotropic coronaviruses, outbreaks of enterotropic MHV in naive mouse populations cause enteritis with high mortality among neonates. Older pups and adult mice show minimal or no apparent disease [4, 10] . Observations in enzootically infected mouse populations give reason to suspect that maternally-derived passive immunity is very significant in protecting newborn mice against apparent disease [5, 13, 15] . The passive transfer of immunoglobulins from dam to young in mice differs from that of most other mammals. IgG is absorbed in utero by means of specific receptors in the yolk sac wall, and is selectively absorbed postnatally for up to 134 F.R. Homberger 16 days via IgG receptors in the intestine [6] . Pilot studies with MHV-Y, an enterotropic strain of MHV [t] , have shown that pups born to immune dams and transferred to naive dams at 1 week of age, then challenged with MHV-Y, all developed enteritis. In contrast pups born to naive dams and fosternursed by immune dams were protected against disease. This finding suggested that ingestion of immune milk is essential for passive immunity to enterotropic coronavirus infection and that locally active, intraluminal antibody such as IgA, might play an important role in protecting pups from enteritis. The purpose of the present study was to evaluate the route of transfer and the role of the different immunoglobulins in passive immunity against enterotropic MHV and to determine which viral proteins are recognized by these immunoglobulins. MHV-Y was isolated in NCTC-1469 cells during a natural outbreak of enteritis in infant mice [1] , passaged in infant CD 1 mice and used in the form of a clarified intestinal homogenate. MHV-S was obtained from the American Type Culture Collection, Bethesda, MD and passaged twice in NCTC-1469 cells. NCTC-L929 cell-adapted MHV-3 was obtained from the Institut f/ir Labortierkunde, Universitfit Ziirich, Switzerland and passaged in NCTC-L 929 cells. Outbread CD 1 (Crl-CD 1 Br) albino mice were obtained from Charles River Breeding Laboratories, Portage, MI in filtered containers. All mice were kept in autoclaved microisolator cages (Lab Products, Maywood, NJ) containing pine shavings. Cages were changed aseptically in a laminar flow hood as previously described [2] . All animals were seronegative to MHV. Dams were orally inoculated with a single dose of MHV-Y containing 103 median neonatal enteritis doses of virus or with sterile tissue culture fluid (controls) and bred 10 days later. Pilot studies have shown that oral inoculation results in higher MHV antibody titers than parenteral inoculation and mimics more closely immunity in naturally infected animals. The 10 day interval between immunization and breeding ensured that the dams were not shedding virus when the pups were born (approximately 30 days after inoculation). Adult mice were killed with carbon dioxide gas and neonates by decapitation. Serial blood samples were taken with capillary tubes by periorbital puncture, under methoxyflurane (Metofane, Pitman-Moore Inc., Washington Crossing, N J) anesthesia. Terminal blood samples were obtained from pups by decapitation and from dams by cardiac puncture. Whey was collected by removing the stomach curds from pups, suspending them in phosphate buffered saline (50% w/v) and centrifuging the homogenate at 12,000 × g for 60min. The supernate was stored at -20 °C. Serology Sera and whey were tested for MHV-specific IgG by an enzyme immunoassay (EIA) using MHV-S-infected formalin-fixed NCTC-1469 cells as antigen [ 18] . MHV-S is the prototype strain to which MHV-Y, which grows poorly in cell culture, is most closely related Eli. MHV-specific IgA was best detected with an emzyme-linked immunosorbent assay (ELISA) using purified MHV-3 as antigen. MHV-3 grown in NCTC-L 929 cells was pelleted at 95,000 x g for 2h. The resulting pellet was resuspended in STE buffer (100raM NaC1, Passive immunity to enterotropic MHV 135 10 mM Tris, 1 mM EDTA), layered on a continuous sucrose gradient (50%/30% w/v) and centrifuged for 2 h at 95,000 x g. The visible band was collected, stored at -70 °C and diluted in bicarbonate buffer (pH 9.6) for coating wells of 96-well microtiter plates (Dynatech Laboratories, Alexandria, VA). A peroxidase-labeled goat-anti-mouse IgA conjugate and ABTS substrate (both Kirkegaard and Perry Laboratories, Gaithersburg, MD) were used in the ELISA [12] . Sera of sentinel mice and of dams of replacement litters were screened for MHV antibody by indirect immunofluorescence assay [17] . Attempts to detect MHVspecific IgM used all of the assays described above. Immunoblots were performed on nitrocellulose paper using MHV-S as antigen. MHV-S was propagated in NCTC-1469 cells, and clarified culture fluid was treated overnight at 4 °C with polyethylene glycol-6000 (8 g/100 ml) in the presence of NaC1 (2.2 g/100 ml). The resulting precipitate was centrifuged at 6,000 x g for 60 min. The pellet was resuspended in STE buffer, and layered on a discontinuous gradient (70%/20% sucrose in STE buffer) and centrifuged at 95,000 x g for 90 rain. The visible band was collected and stored in aliquots at -70°C. Purified MHV-S was boiled for 3 rain in sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE) sample buffer and electrophoretically separated on a 12.5% acrylamide gel at 12mA for 13 h. The proteins from the gel were then electrobtotted onto nitrocellulose paper at 100 V for 6 h [20] . The nitrocellulose paper was stained with Ponceau-S, cut into strips along the visible lanes and saturated in blocking buffer (10% fetal calf serum) overnight. Nitrocellulose strips were twice washed for 10 min in TRIS-buffered saline, covered with test serum or whey at different dilutions and incubated for 3 h at 20 °C. After two more wash cycles, phosphatase-labeled goat anti-mouse IgG, IgA, or IgM conjugate was added and incubated for another 2 h at 20 °C followed by two 10 rain washes. The strips were then stained with BCIP/NBT (5-bromo-4-chloro-3-indolylphosphate/Nitroblue tetrazolium) phosphatase substrate system (Kirkegaard and Perry Laboratories) and air dried. The isotype and titer of MHV immtmoglobulins transferred in utero and in milk, as well as the duration of secretion during lactation were first examined. Immune and naive adult females were bred and allowed to whelp. Serum was collected from half of each litter immediately after birth before suckling to assess intrauterine transfer of passive immunity. The rest of the litter was sacrificed 24 h later to collect serum and whey, then replaced by a litter from a naive dam to maintain the nursing stimulus. On days 5, 10, and 20 post partum, the pups were removed for 2 h and replaced by naive pups which had previously fasted for 4 h. After feeding, serum and whey were collected from these pups. Sera and whey were tested for MHV-specific IgA, IgG, and IgM by EIA or ELISA. MHV-specific IgA and IgG but not IgM could be found in the milk of immunized dams throughout the 20 days of lactation (Table 1) . During this period, IgA titers remained relatively constant, whereas IgG titers peaked at 5 to 10 days and declined by 20 days post partum. Sera of pups sacrificed immediately after birth (day 0) contained MHV-specific IgG, indicating in utero transfer of antibody (Table 2) . Virus-specific IgM could not be detected at any time. In 7 of the 14 replacement litters used to collect whey on days 5, 10, and 20, IgG antibody could be found in the serum (data not shown). This showed that IgG can appear in the serum of naive pups after only 2 h of suckling on an immune dam. Toward the end of lactation, suckling activity declined and pups started to eat solid food. To find out how this change affected passive immunity, adult females were MHV-Y-or sham-inoculated and bred 10 days later. At 1, 2, 3, and 4 weeks of age, two pups from each litter were sacrificed and serum and stomach contents were collected and tested. MHV-IgG, but not IgA or IgM, could be found in the serum of pups suckling immune dams. MHV serum IgG titers peaked at 14 days (Table2), when they reached levels higher than the ones found in their dams' sera collected immediately post partum. Serum IgG titers dropped markedly after weaning at 21 days (Table 2) . MHV-specific IgM could not be detected in sera from either pups or dams. Stomach contents of pups suckling immune dams yielded constant IgG titers and gradually declining IgA titers up to the age of 14 days, but neither isotype of MHV antibody was detected at or beyond 21 days (Table 3 ). This coincided with the macroscopically obvious change of the stomach contents from milk curd to solid food mass. In a final experiment, the titer and duration of passively acquired MHV IgG in serum were evaluated in first, second, and third litter pups weaned from immune vs. naive dams to determine the duration of detectable passive antibody and if the concentration of passively transferred antibody declined with sequential litters. Pups from three consecutive litters born to immune and naive dams were exsanguated at 2, 4, 6, 8, and 10 weeks of age and sera were tested for MHV-specific IgG. Naive males used for breeding also served as sentinels to verify that dams were not re-exposed to MHV, thereby causing booster infections. Passively acquired MHV antibodies persisted in the sera of pups born and nursed by immunized females for 4 to 10 weeks. The MHV serum IgG titers of two week old pups correlated closely with those of their corresponding dam, but dropped substantially during the next two weeks (Table 4 ). Antibodies persisted for 4 weeks in pups born to dams with low MHV IgG serum titers and then declined to undetectable levels. In other animals, serum antibodies could be found through 10 weeks. The duration of passive immunity did not decrease with the second and third litter of individual dams. To ensure that the persisting titers were not due to an inadvertant MHV infection, all sera were tested for IgA, which could be found in the immunized dams later than five months after inoculation but not in any of the offspring (data not shown). Selected whey and serum samples were also examined by Western blot to determine the viral protein specificity of the immunoglobulin isotypes. Serum of mice experimentally infected with other prototype strains of MHV crossreacted with MHV-S. MHV-JHM IgG reacted with all three structural proteins of MHV-S, including glycoprotein S (Fig. 1, lane 1) . MHV-Y serum IgG reacted with the nucleoprotein N and glycoprotein S (Fig. 1, lane 2) . Passively acquired MHV-Y serum IgG in pups (Fig. 1, lane 3) , as well as whey IgG and IgA (Fig. 1, lanes 4 and 6) also reacted with N and S. Reactivity to the M protein of MHV- 12800 1600 1600 800 100 2 6400 4525 800 100 --3 800 4525 100 ---4 3200 4525 800 400 I41 200 5 3200 4525 1131 282 50 50 6-10 ...... 3rdfitter 1 12800 800 25600 800 400 282 200 2 6400 ND e 6400 200 70 --3 100 200 400 50 ---4 3200 1600 4525 200 70 50 -5 6400 3200 4525 800 -100 -6-10 ....... "Reciprocal MHV IgG titer b Reciprocal geometric mean of MHV IgG titer, 2 replicates c Uninfected controls d