- Open Access
The oral and conjunctival microbiotas in cats with and without feline immunodeficiency virus infection
Veterinary Research volume 46, Article number: 21 (2015)
The oral and conjunctival microbiotas likely play important roles in protection from opportunistic infections, while also being the source of potential pathogens. Yet, there has been limited investigation in cats, and the impact of comorbidities such as feline immunodeficiency virus (FIV) infection has not been reported. Oral and conjunctival swabs were collected from cats with FIV infection and FIV-uninfected controls, and subjected to 16S rRNA gene (V4) PCR and next generation sequencing. 9,249 OTUs were identified from conjunctival swabs, yet the most common 20 (0.22%) OTUs accounted for 76% of sequences. The two most abundant OTUs both belonged to Staphylococcus, and accounted for 37% of sequences. Cats with FIV infection had significantly lower relative abundances of Verrucomicrobia, Fibrobacteres, Spirochaetes, Bacteroidetes and Tenericutes, and a higher relative abundance of Deinococcus-Thermus. There were significant differences in both community membership (P = 0.006) and community structure (P = 0.02) between FIV-infected and FIV-uninfected cats. FIV-infected cats had significantly higher relative abundances of Fusobacteria and Actinobacteria in the oral cavity, and significantly higher relative abundances of several bacterial classes including Fusobacteria (0.022 vs 0.007, P = 0.006), Actinobacteria (0.017 vs 0.003, P = 0.003), Sphingobacteria (0.00015 vs 0.00003, P = 0.0013) and Flavobacteria (0.0073 vs 0.0034, P = 0.030). The feline conjunctival and oral microbiotas are complex polymicrobial communities but dominated by a limited number of genera. There is an apparent impact of FIV infection on various components of the microbiota, and assessment of the clinical relevance of these alterations in required.
The body harbours vast microbial communities (microbiotas) at different body sites . The microbiota interacts closely with the immune system and alterations in the immune status of the host can result in changes in the microbiota, as has been shown with the fecal, anal and oral microbiotas of humans with human immunodeficiency virus (HIV) infection [2-5]. Feline immunodeficiency virus (FIV), another lentivirus, is disseminated in the cat population worldwide [6-10]. As with HIV in humans, FIV infection can result in progressive immune dysfunction, with a corresponding increase in a variety of infectious disease risks. A variety of ocular and oral manifestations of HIV infection can occur in humans, including both infectious and non-infectious causes , and it is possible that alterations in the local microbiota play a role in the pathophysiology of some of these diseases. Further, the oral microbiota in humans has been shown to have an influence on various infectious diseases, including both oral (e.g. gingivitis, stomatitis, periodontitis) and extra-oral (e.g. infective endocarditis) disease, and alterations of the oral microbiota have been identified in individuals with HIV infection [2,12-14].
Understanding of the normal ocular and oral microbiotas, and changes that occur in response to FIV infection, is important for understanding the impact of FIV infection and the pathophysiology of FIV-associated opportunistic infections. The objectives of this study were to describe the conjunctival and oral bacterial microbiotas and to evaluate the impact of FIV infection.
Materials and methods
Thirty-three cats were enrolled from a broader 5-year longitudinal controlled study investigating the clinical effects of FIV in naturally acquired infection. FIV infection status at the time of enrollment was determined by FIV antibody detectiona and later confirmed using polymerase chain reaction (PCR) for FIV RNAb or virus isolationc. Of the enrolled cats, 19 were FIV-infected and 14 were FIV-uninfected. The cats enrolled in this study represent a convenience sample based on the timing of examination and sample collection for the larger study. FIV-infected cats were sourced from either a feline sanctuary (n = 15) or were privately owned (n = 4). FIV-uninfected cats were sourced from either the same feline sanctuary (n = 2) or were privately owned (n = 12). FIV-infected and uninfected cats were housed indoors and comingled within the sanctuary. Two of the privately owned cats, one FIV-infected and one FIV-uninfected, were allowed outdoors. None of the privately owned FIV-uninfected cats in this study were housed with FIV-infected cats. At the time of examination, all cats were re-tested for FIV antibodies.
Physical examination was performed at the time of sampling. Oral and conjunctival swab samples were collected with a sterile Dacron swab from the oral cavity or conjunctival surface, respectively. Oral health and gingival score were determined by visual inspection at the time of examination. The presence of gingivitis, stomatitis, gum recession, tooth root or furcation exposure, purulent material at the gumline, loose teeth or masses was considered evidence of dental disease. The gingival score was determined using the following scale: 0 – normal gingiva with sharp, non-inflamed edges; 1 – marginal gingivitis, minimal inflammation at free margin, no bleeding when pressure applied to the gingiva; 2 – moderate gingivitis, wider of inflammation at gingival margin, bleeding when pressure applied to gingiva; 3 – marked gingivitis, severe inflammation, bleeding can be present or absent when pressure applied to gingiva . As cats were conscious during examinations, probing depths were not assessed and intraoral radiography was not performed.
The study was approved by the Purdue University Animal Care and Use Committee (protocol 1201000568).
DNA extraction was performed using a commercial kitd. The V4 region of the bacterial 16S rRNA gene was then amplified using the primers S-D-Bact-0564-a-S-15 (5′-AYTGGGYDTAAAGNG-3′) and S-D-Bact-0785-b-A-18 (5′-TACNVGGGTATCTAATCC-3′) . Sequencing was performed using an Illumina MiSeqe and 2×250 chemistry.
Mothur v1.33.3  was used to assemble paired end reads and perform downstream analysis. After assembly, sequence files were depleted of sequences that were not consistent with the target amplicon size (240 bp), contained any ambiguous base calls or long runs (>8 bp) of holopolymers, or did not align with the correct 16S rRNA gene region. After alignment with the Silva 16S rRNA reference database , chimeras were detected using UCHIME  and removed. Taxonomy was then assigned using the RDP taxonomy database  and any non-bacterial sequences that remained were removed. Sequences were then binned into operational taxon units (OTUs) at a 3% dissimilarity level.
Wilcoxon signed rank tests were used to compare relative abundances of different phylogenetic groups. Subsampling was performed to normalize sequence number for subsequent analyses  through random selection of a number of sequences that was chosen to optimize both sequence numbers and the number of samples that could be included. Good’s coverage, diversity (inverse Simpson’s index), evenness (Shannon’s evenness index) and richness (Catchall)  were calculated and compared between groups using Wilcoxon signed rank test. Dendrograms were developed based on the Yue and Clayton measure of dissimilarity (a measure of community structure, which considers shared OTUs and their relative abundances) and traditional Jaccard index (a measure of community membership, which just considers the number of shared OTUs, not their abundance) and UniFrac  and analysis of molecular variance (AMOVA) were applied to compare microbial communities. Analysis of molecular variance was also used to compare communities. Principal coordinate analysis (PCoA) and indicator analysis  were also performed. A P value of ≤ 0.05 was considered significant for all analyses.
Cats ranged in age from 5 to 12 years of age (median 7 years). There was no difference in median age of the two groups (FIV-uninfected mean 7.2y, median 8y, range 5-10y; FIV-infected mean 7.3y, median 7y, range 5-12y) (P = 0.90). Four (31%) of the FIV-uninfected cats were neutered males and 9 (69%) were spayed females, while 12 (63%) cats in the FIV-infected group were neutered males and seven (37%) were spayed females (P = 0.15). Four (21%) of the FIV-infected cats were subjectively considered clinically healthy on a general physical examination, while the others had varying degrees of oral, dental, respiratory, skin or ocular disease. Six (46%) of FIV-uninfected cats were clinically normal, with the remaining cats having varying degrees of oral and skin disease. There was no difference in health status between groups (P = 0.24).
A total of 747 559 sequences from 32 cats (19 FIV infected, 13 FIV uninfected) passed all screening tests, with sequence numbers ranging from 956 to 53 810 per sample (mean 23 361, median 21 267). A total of 9249 OTUs was identified, yet the most common 20 (0.22%) OTUs accounted for 76% of sequences. The two most abundant OTUs both belonged to Staphylococcus, and accounted for 37% of sequences.
Alpha and beta diversity were analysed using a subsampled population of 3422 sequences per sample. This resulted in the exclusion of samples from three cats (two FIV-uninfected, one FIV-infected) that repeatedly yielded low sequence numbers. Alpha diversity data are presented in Table 1. Cats with FIV infection had significantly lower relative abundances of Verrucomicrobia, Fibrobacteres, Spirochaetes, Bacteroidetes and Tenericutes, and a higher relative abundance of Deinococcus-Thermus (Table 2). Predominant families and genera among the FIV-infected and FIV-uninfected cats are presented in Table 3. Significant differences in the relative abundance of genera accounting for at least 0.1% of sequences are presented in Table 4.
Dendrograms based on the Yue and Clayton (community structure) and Jaccard (community membership) indices are displayed in Figures 1 and 2. There were significant differences in both community membership (P = 0.006) and community structure (P = 0.02) between FIV-infected and FIV-uninfected cats. Significant differences were also noted by AMOVA for both the Yue & Clayton (P = 0.005) and Jaccard (P < 0.001) index data. Separation of the two groups, with greater variability in membership in the FIV-infected group, was also seen with PCoA (Figure 3).
Forty significant indicator OTUs were identified (Table 5). Eleven of 22 (50%) indicator OTUs for FIV-infected cats were Proteobacteria, compared to zero of the 18 FIV-uninfected indicators (P < 0.01).
One OTU, Pseudomonas, was found in all FIV-infected cats at a relative abundance of at least 1%. Staphylococcus was found in 15/19 (79%) FIV-infected cats, while Escherichia/Shigella was found in 14/19 (74%) at that minimum relative abundance. In contrast, no OTUs were found at a relative abundance of at least 1% in any of the FIV-uninfected samples. Pseudomonas was found in 8/13 (62%) FIV-uninfected samples and was the only OTU found in at least 50% of samples at a relative abundance of 1% of greater.
There were 1 430 615 sequences from 33 samples (19 FIV-infected and 14 FIV-uninfected cats) that entered the final analysis, with sequence numbers ranging from 5587 to 94 647 per sample (mean 43 352, median 38 922, SD 24 725).
Eighteen different phyla were identified (Table 6). FIV-infected cats had significantly higher relative abundances of Fusobacteria and Actinobacteria. Similarly, FIV-infected cats had significantly higher relative abundances of several bacterial classes including Fusobacteria (0.022 vs 0.007, P = 0.006), Actinobacteria (0.017 vs 0.003, P = 0.003), Sphingobacteria (0.00015 vs 0.00003, P = 0.0013) and Flavobacteria (0.0073 vs 0.0034, P = 0.030). The eight most common classes are presented in Figure 4. The predominant genera in each group are listed in Table 7, with genera that were significantly different between the two groups in Table 8.
A subsample of 5587 sequences per sample was used for subsequent analysis. There were no differences in coverage (P = 0.64), diversity (P = 0.44), evenness (P = 0.64) or richness (P = 0.61) between FIV-infected and FIV-uninfected cats.
There were significant differences in microbial community structure (Yue and Clayton index, P = 0.030) but not community membership (Jaccard index, P = 0.18) by UniFrac. In contrast, there was also a significant difference between groups by AMOVA applied to a phylip-formatted distance matrix based on the Jaccard index (P = 0.005) but not the Yue and Clayton index (P = 0.078).
No OTUs were present in all cats in either the FIV-infected or FIV-uninfected groups at a minimum relative abundance of 1%. One OTU, classified as Pseudomonas, was present at that minimum relative abundance in 15/20 FIV-infected cats. Two OTUs, an unclassified Aerococcaceae and Pasteurella, were present at that abundance in 9/14 FIV-uninfected cats. Twenty indicator OTUs were identified, 16 for FIV-infected cats and four for FIV-uninfected cats (Table 9). Indicator OTUs for FIV-uninfected cats were predominantly (75%) Proteobacteria while Firmicutes were the most common indicators in FIV-uninfected cats (9/16, 56%).
Four FIV infected cats had a gingival disease score of 0, nine had a score of 1, three had a score of 2 and three had a score of 3. There were no differences in community structure (P = 0.60) (Figure 5) or community membership (P = 0.99) in FIV infected cats with and without severe gingival disease (score ≥ 2). There were also no differences between the relative abundances of any phyla or classes. Similarly, there were no differences in community structure (P = 0.581) and membership (P = 0.31) in FIV-infected cats with dental disease versus those without dental disease.
The feline conjunctiva harbours a large number of diverse phyla, albeit at a lower richness and diversity than has been described in the feline oral cavity or intestinal tract [25-27], or identified in the oral microbiota here. Yet, while the richness and diversity were lower than reported for other mucosal surfaces, the conjunctival microbiota contained an estimate of over 1000 species per sample, a count that far exceeds culture-dependent studies [28-31].
Firmicutes dominated in FIV-uninfected cats. This broad phylum, consisting of a wide range of Gram-positive bacteria, is commonly found at most body sites, albeit with different members of the phylum predominating. For example, Clostridia are dominant Firmicutes in the intestinal tract [25,26,32], while here, Bacilli were most common. This was because of the high relative abundance of Staphylococcaceae. Staphylococci are widespread commensals of mucosal surfaces and are opportunistic pathogens that can be associated with a wide range of infections, including conjunctivitis and ulcerative keratitis [29,33,34]. Their presence in the conjunctival microbiota is not surprising based on the nature of this genus and results of previous culture-dependent studies [29,31].
Proteobacteria were also common, and at a greater relative abundance (30-37%) than in many other body sites. This phylum of Gram-negative bacteria contains a variety of potential opportunistic pathogens, including Pseudomonas and Acinetobacter, two genera that were common in clinically healthy cats.
Significant differences between FIV-infected and FIV-uninfected cats in the relative abundances of numerous phyla (and corresponding lower taxonomic levels) were identified, yet these were among lower abundance phyla, the relevance of which is unclear. The difference in relative abundance of staphylococci was striking, with a 3-fold higher abundance in the FIV-infected group. It is unusual for one genus to comprise such a large (42%) percentage of the microbiota in any body site, and the clinical relevance of this increased relative abundance in FIV-infected cats deserves further study, given the known role of staphylococci in ocular and extra-ocular disease.
Beyond comparisons of relative abundances, there are various ecological tools that can be applied to compare communities. Here, differences in both community membership and the overall microbial community structure were noted, providing more evidence of an altered microbiota community in FIV-infected cats. Another approach is indicator analysis. This is an ecological tool that identifies OTUs that “define” a community . As opposed to assessment of only relative abundance, indicator analysis evaluates both relative abundance and presence or absence in a community, to identify OTUs that are strong indicators or defining characteristics of that population by their presence. Numerous indicator OTUs were identified. Interestingly, half the indicators for FIV-infected cats were Proteobacteria, compared to none for FIV-uninfected cats. While Proteobacteria were not significantly different overall between FIV-infected and FIV-uninfected cats, the predominance of genera from this phylum as indicators in FIV-infected cats suggests that some members of this genus can be specifically altered in response to FIV infection.
Results of this study indicate differences in the microbiota based on FIV status, although results were sometimes conflicting. There were overall differences in microbial community membership and structure in some tests (e.g. UniFrac vs AMOVA) but not others. Assessing the relevance of conflicting results is difficult. The relatively small sample size could have played a role by limiting statistical power, particularly when P values approached significance. Differences in the study populations beyond FIV status must also be considered. While both groups were recruited from a combination of homes and a sanctuary, the differences in distribution of those sources amongst groups could also introduce some bias.
Evaluation of specific taxonomic identifications that were different between groups can be enlightening. Two phyla, Fusobacteria and Actinobacteria, were over-represented in FIV-infected cats. The significantly higher relative abundance of Fusobacteria could be relevant given the role of members of this phylum have in oral disease in other species . Increased Fusobacterium spp has also been identified in the anal and rectal microbiotas of people with HIV [4,5]. Of additional concern is recent evidence that F. nucleatum can increase re-activation of HIV in vitro, indicating a possibility that increased growth of this organism could be a risk modifier for viral replication and disease progression . This has not been reported with FIV and there was no difference in the abundance of Fusobacterium between groups (data not presented), but the notion that an altered microbiota could influence viral activation and disease progression, independent of bacterial infection, should be further investigated in cats. Actinobacteria were also over-represented in the FIV-infected group. In humans, Actinobacteria are a component of plaque  and are more abundant in chronic (versus acute) tooth root infections , but the clinical significance in cats is currently unclear.
Phylum differences were reflected in class level differences. Additionally, Sphingobacteria and Flavobacteria, both members of the phylum Bacteroidetes, were also more common in the FIV-infected group. Both are environmental organisms that can be found on body surfaces [39,40]. One could speculate that decreased local immune response could facilitate the survival of environmental organisms to which an individual is regularly exposed, but there is currently no supporting evidence for this. The statistically significant over-representation of various genera in FIV positive cats and the indicator species that were identified might also suggest that the oral cavity of this group is more amenable to colonization with organisms that are uncommon in healthy individuals, since these tended to be rare members of the community in FIV-uninfected cats.
The difference in staphylococci was interesting given the rather high relative abundance in the FIV-infected group (3.7%, compared to 0.3% in the FIV-uninfected group) and the range of infections that staphylococci can cause. Genus-level identification has limits because of the differences in virulence between different staphylococcal species. Speciation was not attempted because of the very limited species resolution of 16S rRNA gene sequencing for this genus. Yet, the overgrowth of this genus that consists of various important opportunistic pathogens raises concerns for infection risk in these cats.
In addition to Staphylococcus, other indicator OTUs for the FIV-infected group are of potential health concern, such as Porphyromonas (various species implicated in oral disease) [41,42], Streptococcus (different potential opportunistic pathogens, including oral pathogens) , Parvimonas (implicated in oral infections) [44,45] and Gemella (component of dental plaque that has been associated with opportunistic infections) [46,47].
The role of FIV infection in feline oral diseases such as gingivitis and stomatitis in cats is unclear, with some studies reporting an association between FIV infection and the prevalence or severity of oral infections , while others showing no association . It has been suggested that the immune response to chronic antigenic stimulation or dysregulation of the immune response could be associated with increased disease risk  and both of those scenarios could involve the microbiota, as the microbiota is the primary antigenic exposure in the oral cavity and is known to closely interact with the immune system at other body sites [50,51]. Overgrowth of opportunistic pathogens residing in the oral cavity because of advanced immunocompromise is another potential cause.
There was no apparent impact of dental or gingival disease; however, this may be because of the small sample sizes of these subpopulations and the likely multifactorial nature of those diseases. Further, oral swabs provide an overview of the oral cavity but each swab is a composite swab of multiple different ecological niches that are present in the mouth. Therefore, changes in one specific location (e.g. plaque) might not be detected. The likelihood that FIV infection would predispose to oral infections also presumably relates in large part to the degree of immunosuppression. Most of the FIV-infected cats had clinical abnormalities, but the degree of immunocompromise was presumably variable and was not specifically studied. Study of cats with “feline AIDS” might provide more insight into changes associated with advanced immunocompromise.
The feline oral and conjunctival bacterial microbiotas are diverse microbial communities consisting of hundreds or thousands of different species, but with relatively few genera predominating. Feline immunodeficiency virus infection appears to have an impact on these microbiotas. The reasons for the apparent impact of FIV infection on these external microbial communities and the clinical relevance of altered microbiotas require further study.
aFIV/FeLV SNAP combo test, IDEXX Laboratories, Westbrook, ME, USA.
bIDEXX FIV realPCR test, IDEXX Laboratories, West Sacramento, CA, USA.
cUniversity of Glasgow Retrovirus Research Laboratory, Glasgow, UK.
dE.Z.N.A. Stool DNA Kit, Omega Bio-Tek Inc., Doraville, Georgia, USA.
eIllumina, San Diego, USA.
Avila M, Ojcius DM, Yilmaz O (2009) The oral microbiota: living with a permanent guest. DNA Cell Biol 28:405–411
Brito LCN, Sobrinho APR, Teles RP, Socransky SS, Haffajee AD, Vieira LQ, Teles FR (2012) Microbiologic profile of endodontic infections from HIV- and HIV+ patients using multiple-displacement amplification and checkerboard DNA-DNA hybridization. Oral Dis 18:558–567
Lozupone CA, Li M, Campbell TB, Flores SC, Linderman D, Gebert MJ, Knight R, Fontenot AP, Palmer BE (2013) Alterations in the gut microbiota associated with HIV-1 infection. Cell Host Microbe 14:329–339
McHardy IH, Li X, Tong M, Ruegger P, Jacobs J, Borneman J, Anton P, Braun J (2013) HIV Infection is associated with compositional and functional shifts in the rectal mucosal microbiota. Microbiome 1:26
Yu G, Fadrosh D, Ma B, Ravel J, Goedert JJ (2014) Anal microbiota profiles in HIV-positive and HIV-negative MSM. AIDS 28:753–760
Chhetri BK, Berke O, Pearl DL, Bienzle D (2013) Comparison of the geographical distribution of feline immunodeficiency virus and feline leukemia virus infections in the United States of America (2000–2011). BMC Vet Res 9:2
Hosie MJ, Robertson C, Jarrett O (1989) Prevalence of feline leukaemia virus and antibodies to feline immunodeficiency virus in cats in the United Kingdom. Vet Rec 125:293–297
Ishida T, Washizu T, Toriyabe K, Motoyoshi S, Tomoda I, Pedersen NC (1989) Feline immunodeficiency virus infection in cats of Japan. J Am Vet Med Assoc 194:221–225
Nakamura Y, Nakamura Y, Ura A, Hirata M, Sakuma M, Sakata Y, Nishigaki K, Tsujimoto H, Setoguchi A, Endo Y (2010) An updated nation-wide epidemiological survey of feline immunodeficiency virus (FIV) infection in Japan. J Vet Med Sci 72:1051–1056
Tenorio AP, Franti CE, Madewell BR, Pedersen NC (1991) Chronic oral infections of cats and their relationship to persistent oral carriage of feline calici-, immunodeficiency, or leukemia viruses. Vet Immunol Immunopathol 29:1–14
Bekele S, Gelaw Y, Tessema F (2013) Ocular manifestation of HIV/AIDS and correlation with CD4+ cells count among adult HIV/AIDS patients in Jimma town, Ethiopia: a cross sectional study. BMC Ophthalmol 13:20
Hegde MC, Kumar A, Bhat G, Sreedharan S (2014) Oral microflora: a comparative study in HIV and normal patients. Indian J Otolaryngol Head Neck Surg 66(Suppl 1):126–132
Gonçalves LS, Gonçalves BML, Fontes TV (2013) Periodontal disease in HIV-infected adults in the HAART era: clinical, immunological, and microbiological aspects. Archi Oral Biol 58:1385–1396
Pereira VT, Pavan P, Souza RC, Souto R, Vettore MV, Torres SR, Colombo AP, de Uzeda M, Sansone C, Gonçalves LS (2014) The association between detectable plasmatic HIV viral load and different subgingival microorganisms in HIV-infected Brazilian adults: a multilevel analysis. J Periodontol 85:697–705
Lobprise HB (2012) Oral examination and charting. In: Lobprise HB (ed) Five minute veterinart consult clinical companion: small animal dentistry, 2nd edition. Blackwell Publishing Ltd, Ames, IA
Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, Fierer N, Peña AG, Goodrich JK, Gordon JI, Huttley GA, Kelley ST, Knights D, Koenig JE, Ley RE, Lozupone CA, McDonald D, Muegge BD, Pirrung M, Reeder J, Sevinsky JR, Turnbaugh PJ, Walters WA, Widmann J, Yatsunenko T, Zaneveld J, Knight R (2010) QIIME allows analysis of high-throughput community sequencing data. Nat Methods 7:335–336
Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ, Sahl JW, Stres B, Thallinger GG, Van Horn DJ, Weber CF (2009) Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 75:7537–7541
Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, Peplies J, Glöckner FO (2013) The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res 41:D590–596
Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R (2011) UCHIME improves sensitivity and speed of chimera detection. Bioinformatics 27:2194–2200
Gihring TM, Green SJ, Schadt CW (2012) Massively parallel rRNA gene sequencing exacerbates the potential for biased community diversity comparisons due to variable library sizes. Environ Microbiol 14:285–290
Bunge J, Woodard L, Böhning D, Foster JA, Connolly S, Allen HK (2012) Estimating population diversity with CatchAll. Bioinformatics 28:1045–1047
Lozupone C, Hamady M, Knight R (2006) UniFrac–an online tool for comparing microbial community diversity in a phylogenetic context. BMC Bioinformatics 7:371
Dufrêne M, Legendre P (1997) Species assemblages and indicator species: the need for a flexible asymmetrical approach. Ecol Monogr 67:345–366
Barry KA, Middelbos IS, Vester Boler BM, Dowd SE, Suchodolski JS, Henrissat B, Coutinho PM, White BA, Fahey GC Jr, Swanson KS (2012) Effects of dietary fiber on the feline gastrointestinal metagenome. J Proteome Res 11:5924–5933
Minamoto Y, Hooda S, Swanson KS, Suchodolski JS (2012) Feline gastrointestinal microbiota. Anim Health Res Rev 13:64–77
Sturgeon A, Pinder SL, Costa MC, Weese JS (2014) Characterization of the oral microbiota of healthy cats using next-generation sequencing. Vet J 201:223–229
Prado MR, Rocha MFG, Brito EHS, Girão MD, Monteiro AJ, Teixeira MFS, Sidrim JJ (2005) Survey of bacterial microorganisms in the conjunctival sac of clinically normal dogs and dogs with ulcerative keratitis in Fortaleza, Ceará, Brazil. Vet Ophthalmol 8:33–37
Shewen PE, Povey RC, Wilson MR (1980) A survey of the conjunctival flora of clinically normal cats and cats with conjunctivitis. Can Vet J 21:231–233
Hartmann AD, Hawley J, Werckenthin C, Lappin MR, Hartmann K (2010) Detection of bacterial and viral organisms from the conjunctiva of cats with conjunctivitis and upper respiratory tract disease. J Feline Med Surg 12:775–782
Espínola MB, Lilenbaum W (1996) Prevalence of bacteria in the conjunctival sac and on the eyelid margin of clinically normal cats. J Small Anim Pract 37:364–366
Tun HM, Brar MS, Khin N, Jun L, Hui RK, Dowd SE, Leung FC (2012) Gene-centric metagenomics analysis of feline intestinal microbiome using 454 junior pyrosequencing. J Microbiol Methods 88:368–376
Medhus A, Slettemeås JS, Marstein L, Larssen KW, Sunde M (2013) Methicillin-resistant Staphylococcus aureus with the novel mecC gene variant isolated from a cat suffering from chronic conjunctivitis. J Antimicrob Chemother 68:968–969
Lin C-T, Petersen-Jones SM (2008) Antibiotic susceptibility of bacteria isolated from cats with ulcerative keratitis in Taiwan. J Small Anim Pract 49:80–83
Liu P, Liu Y, Wang J, Guo Y, Zhang Y, Xiao S (2014) Detection of fusobacterium nucleatum and fadA adhesin gene in patients with orthodontic gingivitis and non-orthodontic periodontal inflammation. PLoS One 9:e85280
González OA, Li M, Ebersole JL, Huang CB (2010) HIV-1 reactivation induced by the periodontal pathogens Fusobacterium nucleatum and Porphyromonas gingivalis involves Toll-like receptor 2 [corrected] and 9 activation in monocytes/macrophages. Clin Vaccine Immunol 17:1417–1427
Xu H, Hao W, Zhou Q, Wang W, Xia Z, Liu C, Chen X, Qin M, Chen F (2014) Plaque bacterial microbiome diversity in children younger than 30 months with or without caries prior to eruption of second primary molars. PLoS One 9:e89269
Santos AL, Siqueira JF, Rôças IN, Jesus EC, Rosado AS, Tiedje JM (2011) Comparing the bacterial diversity of acute and chronic dental root canal infections. PLoS One 6:e28088
Lazarevic V, Whiteson K, Hernandez D, François P, Schrenzel J (2010) Study of inter- and intra-individual variations in the salivary microbiota. BMC Genomics 11:523
Hutter G, Schlagenhauf U, Valenza G, Horn M, Burgemeister S, Claus H, Vogel U (2003) Molecular analysis of bacteria in periodontitis: evaluation of clone libraries, novel phylotypes and putative pathogens. Microbiology 149:67–75
Booij-Vrieling HE, van der Reijden WA, Houwers DJ, de Wit WEAJ, Bosch-Tijhof CJ, Penning LC, van Winkelhoff AJ, Hazewinkel HA (2010) Comparison of periodontal pathogens between cats and their owners. Vet Microbiol 144:147–152
Pérez-Salcedo L, Herrera D, Esteban-Saltiveri D, León R, Jeusette I, Torre C, O'Connor A, González I, González I (2013) Isolation and identification of Porphyromonas spp. and other putative pathogens from cats with periodontal disease. J Vet Dent 30:208–213
Han YW, Wang X (2013) Mobile microbiome: oral bacteria in extra-oral infections and inflammation. J Dental Res 92:485–491
Topcuoglu N, Bozdoğan E, Kulekci G (2013) Presence of oral bacterial species in primary endodontic infections of primary teeth. J Clin Pediatr Dent 38:155–160
Uemura H, Hayakawa K, Shimada K, Tojo M, Nagamatsu M, Miyoshi-Akiyama T, Tamura S, Mesaki K, Yamamoto K, Yanagawa Y, Sugihara J, Kutsuna S, Takeshita N, Shoda N, Hagiwara A, Kirikae T, Ohmagari N (2014) Parvimonas micra as a causative organism of spondylodiscitis: a report of two cases and a literature review. Int J Infect Dis 23:53–55
Diaz PI, Chalmers NI, Rickard AH, Kong C, Milburn CL, Palmer RJ, Kolenbrander PE (2006) Molecular characterization of subject-specific oral microflora during initial colonization of enamel. Appl Environ Microbiol 72:2837–2848
Lo WB, Patel M, Solanki GA, Walsh AR (2013) Cerebrospinal fluid shunt infection due to Gemella haemolysans. J Neurosurg Pediatr 11:205–209
Belgard S, Truyen U, Thibault J-C, Sauter-Louis C, Hartmann K (2010) Relevance of feline calicivirus, feline immunodeficiency virus, feline leukemia virus, feline herpesvirus and Bartonella henselae in cats with chronic gingivostomatitis. Berl Munch Tierarztl Wochenschr 123:369–376
Sellon RK, Hartmann K (2012) Feline immunodeficiency virus infection. In: Greene CE (ed) Infectious diseases of the dog and cat, 4th edition. Saunders Elsevier, St. Louis, Missouri, pp 138–149
Wu S, Jiang Z-Y, Sun Y-F, Yu B, Chen J, Dai C-Q, Wu XL, Tang XL, Chen XY (2013) Microbiota regulates the TLR7 signaling pathway against respiratory tract influenza A virus infection. Curr Microbiol 67:414–422
McDermott AJ, Huffnagle GB (2013) The microbiome and regulation of mucosal immunity. Immunology 142:24–31
Maddie’s Fund. [http://www.maddiesfund.org].
This study was supported, in part, by a grant from the Maddie’s Fund. The Purdue Maddie’s Shelter Medicine Program is underwritten by a grant from Maddie’s Fund, The Pet Rescue Foundation [http://www.maddiesfund.org], helping to fund the creation of a no-kill nation. Sequencing was performed at the University of Guelph’s Advanced Analysis Centre.
The authors declare that they have no competing interests.
JSW and AL designed the study, based on an ongoing study designed by AL and JN. JN performed sample collection and animal data collection. MJ performed laboratory analyses. JSW performed data analysis. JSW drafted the manuscript, and all authors contributed to its revision. All authors read and approved the final manuscript.
About this article
Cite this article
Weese, S.J., Nichols, J., Jalali, M. et al. The oral and conjunctival microbiotas in cats with and without feline immunodeficiency virus infection. Vet Res 46, 21 (2015) doi:10.1186/s13567-014-0140-5
- Human Immunodeficiency Virus
- Infective Endocarditis
- Feline Immunodeficiency Virus
- High Relative Abundance