Adenoviruses in fecal samples from asymptomatic rhesus macaques, United States.
Adenoviruses, which can cause infectious diarrhea or respiratory infections in humans, were isolated from monkeys soon after their initial characterization by Rowe et al. (I). Hull et al. (2,3) identified adenoviruses as one of several classes of viruses found as outgrowths from primary cultures of monkey kidney cells that were being cultivated for propagation of poliovirus. Adenoviruses were also found in rectal swab and fecal samples taken from monkeys in captivity (4,5).
The classification of monkey adenoviruses was initially done in a manner analogous to that used for human isolates, i.e., on the basis of differences in their ability to agglutinate erythrocytes from different species. Rapoza classified monkey adenoviruses into 4 hemagglutination subgroups on the basis of their differential agglutination properties with respect to their ability to agglutinate rat, rhesus, and guinea pig erythrocytes (6). Most viruses tested at the time were found to belong to groups 2 and 3; groups 1 and 4 contained only 1 member each. The current classification of macaque adenoviruses by the International Committee on Taxonomy of Viruses has 1 defined species, simian adenovirus A (SAdV-A), to which SAdV-3 has been assigned. SAdV-1 and SAdV-7, while not considered human viruses, are now classified as human adenovirus G (HAdV-G) because of their similarity to a virus (HAdV52) isolated from a human patient with gastroenteritis (7).
Recently, transmission of a monkey adenovirus from captive titi monkeys to a researcher was reported at the California National Primate Research Center (Davis, CA, USA); the researcher may, in turn, have transmitted it to a family member (8). Further, HAdV-52 (7) isolated from a patient with gastroenteritis has been found to be very dissimilar to all previously isolated human adenoviruses but closely related to monkey adenoviruses SAdV-1 and SAdV-7. This similarity raises the possibility that this patient was, in fact, infected with a monkey adenovirus.
We have previously found that adenovirus DNA is readily detected in fecal samples from monkeys who have no symptoms of any clinical adenoviral disease (9). Given the close physical proximity and intermingling of human and monkey populations in several locales in Asia, Africa, and Latin America, better characterization of monkey adenoviruses is of public health importance. To clarify the nature of adenoviruses shed in the feces of asymptomatic monkeys, we attempted to culture adenoviruses from fecal samples from rhesus macaques (Macaca mulatto) housed in 5 primate facilities in the United States.
Materials and Methods
Isolation of Novel Adenoviruses from Rhesus Macaques
Approximately 350 rhesus macaque fecal samples were processed: 150 from Covance (Vienna, VA, USA), 100 from the New England Primate Research Center (Southborough, MA, USA), and 98 from the Tulane National Primate Research Center (Covington, LA, USA). Additional samples were obtained from rhesus macaques housed at the Oregon National Primate Research Center (Beaverton, OR, USA) and the primate facility of the Gene Therapy Program at the University of Pennsylvania (Philadelphia, PA, USA).
Samples were suspended in Hanks' Balanced Salt Solution (Life Technologies, Grand Island, NY, USA), particulates were removed by centrifugation, and the supernatants were sterile filtered through 0.2-[micro]m syringe filters. We injected 100 [micro]L of each filtered sample into BS-C-1 and LLC-MK2 cells grown in culture medium containing 1% Penn-Strep (Mediatech, Herndon, VA, USA) and 50 [micro]g/mL gentamicin. After [approximately equal to] 1-2 weeks, if cytopathic effects typical of adenovirus infection were seen, the presence of adenoviruses in the cultures was confirmed by PCR amplification of an internal 1.9 kb of the hexon, including the region encompassing the hypervariable regions, which is predominantly responsible for conferring serotype specificity. The primer pair used for PCR was 5'-CAGGATGCTTCGGAGTACCTGAG-3' and 5'-TTGGCNGGD ATDGGGT AVAGC ATGTT-3'. The sequence obtained from this region was used to make an initial determination of adenoviral species and novelty of the serotype. Adenovirus isolates were propagated to high titer and purified on cesium chloride gradients by using standard procedures. Viral DNA obtained from purified virus preparations was completely sequenced (QIAGEN, Hilden, Germany).
Adenoviruses and Cell Culture from ATCC
We obtained 3 adenoviruses from the American Type Culture Collection (ATCC). SAdV-6 (catalog number VR353, originally deposited as SV-39) had been isolated from Macaca spp. monkeys (6,10). SAdV-18 (catalog number VR-943) (4,11) and SAdV-20 (catalog number VR-541, originally deposited as simian adenovirus V340) had been isolated from vervet monkeys (Cercopithecus aethiops) (12). BS-C-1 (C. aethiops monkey kidney cells, ATCC catalog number CCL-26) or LLC-MK2 (M. mulatto monkey kidney cells, ATCC catalog CCL-7) were purchased from ATCC and maintained in culture as recommended.
Propagation and purification were performed for 23 isolates as shown in Table 1; 9 of the isolates were completely sequenced. In addition, we propagated, purified, and sequenced the 3 monkey adenoviruses (SAdV-6, SAdV-18, and SAdV-20) from ATCC. All analyses were conducted at the www.phylogeny.fr sequence analysis server. Nucleotide sequence alignments for each open reading frame (ORE) (after excising introns if necessary) were completed by using ClustalW version 2.0.3, and the alignments were refined by using Gblocks version 0.91b. The alignments were used to construct phylogenetic trees using PhyML version 3.0 aLRT, under the HKY85 model. The resulting trees were rendered by using Treedyn 198.3. Protein sequence alignments and phylogenetic trees were constructed by using the Vector NTI (Life Technologies) and CLC Bio (CLC Bio, Aarhus, Denmark) software packages.
All the macaque adenoviruses that we sequenced were similar to previously sequenced primate adenoviruses with respect to the identity and order of identifiable ORFs organized into defined early and late transcription regions (13). The notable differences observed were in structures of the E3 region genes and of the fiber genes.
Phylogenetic analyses of the nucleotide sequences that encode genes of several of the adenoviral proteins showed the sequences were generally concordant with one another. As examples, the phylogenetic trees for the sequences encoding El a, DNA polymerase, hexon, and E4 34K are shown in Figure 1. The sequences have been compared with each other and with previously sequenced macaque adenoviruses SAdV-1, SAdV-3, SAdV-7, SAdV48, SAdV-49, SAdV-50, titi monkey adenovirus, and cynomolgus adenovirus 1 (8,9,14-17). The human isolate HAdV-52 (7), which is known to be closely related to SAdV-1 and SAdV-7, was also included in the analyses. Macaque adenoviruses form a distinct clade when compared with human or ape adenoviruses (9). However, HADV-F (HAdV-40 and HAdV-41) and HAdV-A (HAdV-12) are also included in the analyses because these species are the most closely related to macaque adenoviruses (14,15).
The phylogenetic trees (Figure 1) show that SAdV-6, obtained from ATCC and sequenced, is similar to SAdV48, which we had previously isolated from stool samples of an apparently healthy macaque (9), and to SAdV-3 (14). These adenoviruses have been grouped together with SAdV-3 as SAdV-A. The 9 adenoviruses that we isolated from rhesus stools are closely related to one another and to 2 other macaque adenoviruses that we had previously isolated and sequenced, SAdV-49 and SAdV-50 (9); these isolates have been grouped as SAdV-B. The adenovirus isolated from a cynomolgus macaque for which a partial sequence (including the hexon) was reported (16) also belongs to this group. The adenovirus of unknown origin that recently caused an outbreak of pneumonia and hepatitis in a colony of new world titi monkeys and sickened an animal handler (5) is distant from these adenoviruses. SAdV-18, which had been deposited with ATCC as an isolate from a vervet monkey in the 1960s (77), was found to be most closely related to HAdV-F members HAdV-40 and HAdV-41 in the protein phylogenies and also for most of the length of its genome (data not shown). HAdV-F is the only human adenovirus species that harbors 2 fiber genes, a feature common in macaque adenoviruses, including FlAdV-G members; however, SAdV-18 differs from HAdV-F members in possessing a single fiber gene.
All sequences have been deposited in GenBank. The accession numbers are as follows: simian adenovirus strain A1139, JN880448; strain A1163, JN880449; strain A1173, JN880450; strain A1258, JN880451; strain A1285, JN880452; strain A1296, JN880453; strain A1312, JN880454; strain A1327, JN880455; strain A1335, JN880456; SAdV-6, JQ776547; SAdV-18, FJ025931; and SAdV-20, HQ605912. The accession numbers for other adenovirus sequences used in the analyses are as follows: SAdV-1, NC_006879; SAdV-3, NC_006144; SAdV-7, DQ792570; SAdV-48, HQ241818; SAdV-49, HQ241819; SAdV-50, HQ241820; SAdV-titi, HQ913600; HAdV-2, NC_001405; HAdV-3, NC_011203; HAdV-4, NC_003266; HAdV-12, NC 001460; HAdV-17, HQ910407; HAdV18, GU191019; HAdV-40, NC 001454; HAdV-41, DQ315364; and HAdV-52, DQ923122.
Analysis of the E3 Regions
The gene content and disposition (as discerned by the presence of ORFs) of the E3 regions of the 9 adenoviruses isolated from macaques are shown in Table 2. The 12.5K protein of unknown function, as well as the anti-apoptotic RID-[alpha] and RID-[beta], and the 14.7K proteins (18), are present in all the newly isolated viruses. They all also harbor homologs of the CR1 proteins that contain conserved domains of unknown function designated CR1 and CR2 (19). However we found that in 6 of the newly sequenced adenoviruses, the 2 CR1 proteins (CR1-[alpha] and CR1-[beta]) were fused into a single ORF (Figure 2). An example of the fusion is illustrated in Figure 3, in which the fused CR1 protein (designated CR1-[alpha][beta]) of the adenovirus isolate A1139 E3 region has been aligned with the CR1-[alpha] and CR1-[beta] proteins of the E3 region of A1312. The E3 CR1 proteins possess a single putative transmembrane domain near their C-termini and are likely to have arisen by gene duplication (20,21). The putative transmembrane domain of the CR1-[alpha] protein appears to have fused to the hydrophobic (putative) secretion signal of the CR1-[beta] protein. This fused version indicates that the CR1-[alpha] and CR1-[beta] proteins are likely disposed on opposite sides of the membrane. One possible model for A1163 CR1-[alpha][beta] fused protein (based on a prediction by TMPRED, a software program that makes a prediction of membrane-spanning regions and their orientations; www.ch.EMBnet.org) indicates that the N-terminal hydrophobic domain (residues 3-21) is oriented outside to inside (luminal to cytoplasmic), followed by the CR1-[alpha] segment on the cytoplasmic side of the membrane. This model predicts the central transmembrane domain (residues 151-170) to be oriented inside to outside with the CR1-[beta] segment on the luminal side. The C-terminal transmembrane domain (residues 430-455) would thus be oriented outside to inside, followed by a highly basic stop transfer segment. Separately encoded CR1-[alpha] and -[beta] proteins likely follow this topology as well.
Of the newly sequenced adenoviruses, SAdV-18 exhibited the shortest E3 region. The SAdV-18 genome encodes only one E3 protein, the homologue of the E3 12.5K protein, for which a function has not yet been determined. In this respect, SAdV-18 is similar to SAdV-7 which also has a severely truncated E3 region that encodes only the E3 12.5 K protein (17).
Analysis of the Fiber Genes
The fiber knob domain mediates the initial virus-cell interaction by binding to a cellular receptor. A phylogenetic tree generated on the basis of an alignment of the fiber knob domains of macaque and human adenoviruses is shown in Figure 4. It is evident that the knob domains of the long fiber (fiber 2) of the human adenoviruses belonging to HAdV-F are more similar to those of SAdV-18 than to any other human adenovirus. The SAdV-18 fiber sequence is very similar to the HAdV-F long fiber throughout its length, and the sequence similarity between the knob domains of HAdV-40 and those of SAdV-18 is >90% (Figure 5. HAdV-F species (HAdV-40, HAdV-41, and serologically related isolates) are known to be enteric adenoviruses that frequently cause diarrhea in infants. The HAdV-F long fiber knob can bind the cellular receptor CAR (22), and the SAdV-18 fiber knob would probably be able to do so as well. Notably, the shaft domain of SAdV-18 is 391 residues long (the longest such domain of any primate adenovirus sequenced) and harbors as many as 25 iterations of the [beta]-spiral repeat motif (Figure 5). However, unlike HAdV-F, SAdV-18 contains a single fiber gene.
All of the SAdV-B adenoviruses we isolated from macaque fecal samples harbored 2 fiber genes. As discussed above, the only adenoviruses readily isolated from humans that harbor 2 fiber genes belong to HAdV-F (23-25). The 2 fibers of HAdV-F isolates differ in the lengths of the shaft domain: the first fiber ORF harbors a short shaft (187 residues comprising 12 iterations of the [approximately equal to] 16 amino-acid repeat motif, pfam 00608) and the second fiber gene possesses a longer shaft (330-346 residues, comprised of 21 or 22 iterations of the 16 amino-acid repeat motif) (23,25,26). Both fiber proteins are incorporated into mature virions, with each penton base having either a short or a long fiber protein embedded in them (23). Similar to members of HAdV-F, HAdV-G members (macaque adenoviruses SAdV-1 and SAdV-7 and the closely related HAdV-52) also harbor 2 fiber genes. As with HAdV-F, the first fiber gene (fiber 1) encodes the shorter shaft with 9 (SAdV-7) or 10 (SAdV-1 and HAdV-52) motif repeats, and the second fiber gene (fiber 2) encodes the longer fiber shaft, similar in length to that of HAdV-41, which harbors 22 motif repeats. The long fiber of HAdV-F members can bind CAR; a cellular receptor capable of binding the short fiber knob domain has not been identified.
One difference between the newly sequenced adenoviruses we isolated from stool samples (SAdV-B) and previously sequenced adenoviruses with 2 fiber genes (HAdV-40, HAdV-41, SAdV-1, SAdV-7, and HAdV-52) is that first fiber gene (fiber 1) encodes a shaft domain that is longer than the shaft domain of the second fiber gene (fiber 2). The shaft of fiber 1 of the SAdV-B isolates is [approximately equal to] 330 residues long (21 motif repeats, except for SAdV-49 and SAdV-50 which have 1 fewer motif repeat). Except for the length, however, the sequence of the fiber 1 shaft of the SAdV-B isolates is much more similar to the HAdV-F fiber 1 (short) shaft (49.7% sequence identity, 65.6% consensus match; see alignment in Figure 5) than it is to the fiber 1 (short) shaft of SAdV-1 or SAdV-7 (30.8% sequence identity, 47.7% consensus match). The sequence similarity is striking enough to suggest that the HAdV-F short fiber arose by deletions within the shaft domain of a SAdV-B fiber 1-like phylogenetic precursor. In contrast to HAdV-F and HAdV-G members, the second fiber gene of the SAdV-B macaque adenoviruses encodes a shaft domain that is shorter than that of the first fiber, [approximately equal to] 205 residues in length and harboring 14 motif repeats.
For adenoviruses that contain an integrin-binding RGD motif in the penton base proteins, an initial virus-cell interaction mediated by the fiber knob with its receptor (CAR for HAdV-A, C, E and F; CD46 for HAdV-B, and possibly sialic acid for HAdV-D), the penton base-integrin interaction has been shown to be the first step in adenovirus internalization (27). Because HAdV-F members do not contain an integrin that binds the RGD motif in their penton base protein, an as-yet-unidentified cellular-binding partner for the short fiber knob domain has been postulated to mediate virus internalization (27) in a manner analogous to the penton base-RGD interaction. However, all members of SAdV-A and SAdV-B contain the RGD motif in the penton base protein, which suggests that the short fiber (fiber 1 in HAdV-F and HAdV-G, fiber 2 in SAdV-B) may provide a function that is not necessarily analogous to that provided by the penton base-RGD motif. Moreover, because the knob domain of the SAdV-B fiber 1 gene is "elevated" above the knob on fiber 2, it may play a more critical role in the initial virus-receptor interaction than formerly suspected.
We have previously reported the isolation and sequencing of 3 macaque adenoviruses (SAdV-48, SAdV-49 and SAdV-50) from macaque fecal samples (9). Even adenoviral DNA could be detected in most samples by using a sensitive, nested PCR technique, outgrowth of adenoviruses in culture in the monkey cell lines LLC-MK2 or BS-C-1 only ranged from 1% to 16% from various primate colonies. Most of these adenoviruses can be classified into a single subgroup (SAdV-B), although SAdV-A isolates (hexon sequences similar to those of SAdV-48 and SAdV-3) were also identified (Table 1). It is unclear whether these represent a common commensal of the macaque gastrointestinal tract or whether the presence of these adenoviruses in the fecal samples is an artifact of captive status, where virus spread between animals may be more common than in the wild.
The species HAdV-B, HAdV-C, and HAdV-E, which cause acute upper respiratory tract disease in humans, also may set up chronic persistent infections in both humans and apes (9,28). In contrast, HAdV-F strains, which frequently cause infectious diarrhea in locales with poor sanitation, are only rarely detected in healthy persons (29). On the other hand, we have found that monkey adenoviruses belonging to SAdV-A and SAdV-B, as well as SAdV-18 (isolated from primary monkey kidney cells ), that bear a strong genetic resemblance to HAdV-F do cause chronic infections in otherwise healthy monkeys. HAdV-F may have evolved as a human intestinal pathogen after a recent cross-species transmission event and is thus less well adapted to human hosts than are HAdV-B, HAdV-C, or HAdV-E.
Macaque adenoviruses are usually not thought to infect humans, but the properties of macaque adenoviruses that constitute the species barrier are not known. Recently documented instances of human infections with macaque adenoviruses (7,8) show that these barriers can sometimes be broken. A more careful investigation of the etiology of infectious diarrhea in areas where monkeys and humans live in proximity (e.g., by PCR of fecal samples followed by sequencing of isolates) could be used to ascertain whether monkey adenoviruses do cause human infections more commonly than is currently surmised.
We thank the PennVector personnel for their help in propagating and purifying adenoviruses.
This work was sponsored by grants from the Bill and Melinda Gates Foundation.
Dr Roy was a senior research investigator at the University of Pennsylvania at the time of this study. His research interests include the characterization of nonhuman primate adenoviruses and viral adaptation to novel host environments.
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Soumitra Roy,  Arbansjit Sandhu, Angelica Medina, David S. Clawson, and James M. Wilson
 Current affiliation: Crucell Holland, Leiden, the Netherlands.
Author affiliation: University of Pennsylvania, Philadelphia, Pennsylvania, USA
Address for correspondence: James M. Wilson, Department of Pathology and Laboratory Medicine, Division of Transfusion Medicine, University of Pennsylvania, TRL, Suite 2000, 125 S 31st St, Philadelphia, PA 19104, USA; email: email@example.com
Table 1. Characterization of adenovirus isolates from rhesus fecal samples obtained from primate facilities in the United States * Isolate Source Particle titer ([dagger]) A1123 ONPRC 4.0 x [10.sup.11] A1128 Covance 6.0 x [10.sup.11] A1129 Covance 6.1 x [10.sup.11] A1139# Covance 4.7 x [10.sup.12] A1161 Covance 2.0 x [10.sup.12] A1163# Covance 5.4 x [10.sup.12] A1166 Covance 2.8 x [10.sup.12] A1169 Covance 1.1 x [10.sup.11] A1173# Covance 5.2 x [10.sup.12] A1179 Covance 4.6 x [10.sup.12] A1258# GTP 1.8 x [10.sup.12] A1261 GTP 8.7 x [10.sup.11] A1285# GTP 2.7 x [10.sup.12] A1296# Covance 5.4 x [10.sup.12] A1297 Covance 3.7 x [10.sup.11] A1312# Covance 6.1 x [10.sup.12] A1313 TNPRC 6.5 x [10.sup.11] A1327# TNPRC 2.4 x [10.sup.12] A1328 NEPRC 6.7 x [10.sup.11] A1329 TNPRC 3.7 x [10.sup.12] A1335# NEPRC 6.0 x [10.sup.12] A1339 TNPRC 3.1 x [10.sup.12] A1340 Covance 5.1 x [10.sup.12] Isolate Total yield Sequence analysis A1123 9.6 x [10.sup.11] Hexon similar to SAdV-3 A1128 1.3 x [10.sup.12] Hexon similar to SAdV-3 A1129 3.8 x [10.sup.13] Hexon (A1128) A1139# 1.8 x [10.sup.12] Full genome A1161 4.3 x [10.sup.13] Hexon similar to SAdV-48 A1163# 5.4 x [10.sup.12] Full genome A1166 1.3 x [10.sup.11] Hexon (A1161) A1169 2.5 x [10.sup.13] Hexon(A1161) A1173# 2.3 x [10.sup.12] Full genome A1179 1.0 x [10.sup.13] Hexon (A1128) A1258# 2.6 x [10.sup.12] Full genome A1261 9.0 x [10.sup.12] Hexon (A1285) A1285# 2.0 x [10.sup.13] Full genome A1296# 7.3 x [10.sup.11] Full genome A1297 7.0 x [10.sup.11] Hexon(A1163) A1312# 8.4 x [10.sup.11] Full genome A1313 1.4 x [10.sup.13] Hexon similar to A1312 A1327# 1.0 x [10.sup.12] Full genome A1328 2.7 x [10.sup.12] Hexon similar to SAdV-49 A1329 9.2 x [10.sup.12] Hexon (A1312) A1335# 2.8 x [10.sup.13] Full genome A1339 5.7 x [10.sup.12] Hexon (A1163) A1340 3.1 x [10.sup.13] Hexon (A1335) * The total yield and the particle titer obtained from a 50-plate (150-mm) preparation are shown. In each case, the hexon region was PCR amplified and sequenced. Boldface indicates the 9 isolates that were completely sequenced. For the other isolates, the hexon sequences that are identical or very closely related (<5% nucleotide sequence dissimilarity) are indicated in parentheses. SAdV, simian adenovirus. ([dagger]) ONPRC, Oregon National Primate Research Center (Beaverton, OR, USA); Covance, Covance, (Vienna, VA, USA); GTP, primate facility of the Gene Therapy Program at the University of Pennsylvania (Philadelphia, PA, USA); TNPRC, Tulane National Primate Research Center (Covington, LA, USA); NEPRC, New England Primate Research Center (Southborough, MA, USA). Note: Boldface indicates the 9 isolates that were completely sequenced indicated with #. Table 2. E3 region proteins of the 11 macaque adenoviruses belonging to SAdV-B isolates from macaque fecal samples compared with the E3 reaions of other macanue adenoviruses * Adenovirus type 12.5K SAdV-A SAdV-3 Present SAdV-6 Present SAdV-48 Present SAdV-B A1173 Present A1285 Present A1312 Present A1139 Present A1163 Present A1258 Present A1296 Present A1327 Present A1335 Present SAdV-49 Present SAdV-50 Present HAdV-G SAdV-1 Present HAdV-52 Present SAdV-7 Present Not yet classified SAdV-18 Present SAdV-20 Present Adenovirus type CR1- CR1- [alpha] [beta] SAdV-A SAdV-3 Present Present SAdV-6 Present Present SAdV-48 Present Present SAdV-B A1173 Present Present A1285 Present Present A1312 Present Present A1139 Fused ([dagger]) A1163 Fused ([dagger]) A1258 Fused ([dagger]) A1296 Fused ([dagger]) A1327 Fused ([dagger]) A1335 Fused ([dagger]) SAdV-49 Fused ([dagger]) SAdV-50 Fused ([dagger]) HAdV-G SAdV-1 Present Present HAdV-52 Present Present SAdV-7 Not present Not present Not yet classified SAdV-18 Not present Not present SAdV-20 Present Present RID-[alpha], Adenovirus type RID-[beta], and 14.7K SAdV-A SAdV-3 Present SAdV-6 Present SAdV-48 Present SAdV-B A1173 Present A1285 Present A1312 Present A1139 Present A1163 Present A1258 Present A1296 Present A1327 Present A1335 Present SAdV-49 Present SAdV-50 Present HAdV-G SAdV-1 Present HAdV-52 Present SAdV-7 Not present Not yet classified SAdV-18 Not present SAdV-20 Present * SAdv, simian adenovirus; HAdv, human adenovirus. ([dagger]) Some members of SAdV-B were found to have a novel configuration in which 2 CR1 proteins were fused into a single open reading frame (see Figures 2, 3).
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|Author:||Roy, Soumitra; Sandhu, Arbansjit; Medina, Angelica; Clawson, David S.; Wilson, James M.|
|Publication:||Emerging Infectious Diseases|
|Date:||Jul 1, 2012|
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