Volume 17, Number 9—September 2011
Dispatch
Bartonella quintana Infections in Captive Monkeys, China
Abstract
Bartonella quintana has been considered to be specifically adapted to humans. Our isolation of the organism from 2 of 36 captive rhesus macaques in China and finding antibodies against B. quintana in 12 of 33 indicates that the reservoir hosts of B. quintana may include primates other than humans.
Bartonella spp. are bacterial hemoparasites with a wide variety of mammalian hosts as reservoirs. Several members of the genus are pathogens of medical and veterinary significance. Most human infections are zoonoses; however, 2 Bartonella spp., B. bacilliformis and B. quintana, are considered to be specifically adapted to humans (1). Although, like other members of the genus, both species generally cause chronic intraerythrocytic bacteremia of little clinical consequence to their reservoir hosts, both are also associated with illness and death (1).
B. quintana infections most frequently cause recurrent fever and pretibial pain (trench fever), endocarditis, and bacillary angiomatosis (2). B. quintana is transmitted by the human body louse (Pediculus humanis humanis), which thrives in the absence of basic sanitation and hygiene; hence, infections are most frequently associated with persons who are homeless or affected by social or civil unrest (3), although they are increasingly encountered in rural communities in developing regions of the world (4,5).
Some reports suggest that humans are not the only reservoir hosts of B. quintana. In 2005, B. quintana was recovered from the blood of a cynomolgus monkey (Macaca fascicularis) imported into the United States from Southeast Asia (6). In addition, infections resulting in chronic bacteremia have been experimentally established in rhesus macaque monkeys (Macaca mulatta) inoculated with B. quintana isolates from infected humans (7,8).
In 2009, blood samples were collected from 36 apparently healthy rhesus macaque monkeys housed in a biologic research institute in Beijing, People’s Republic of China. Breeding, delivery, and raising the young monkeys took place in an outdoor arena that housed a large group of animals; the monkeys were later moved indoors into isolation. Samples were stored at −80°C, thawed, and then plated (400 µL of each) onto 5% (vol/vol) sheep blood–enriched Columbia agar and incubated at 37°C in 5% CO2 for as long as 45 days. After 15 days of incubation, 2 plates yielded putative Bartonella spp. colonies. One plate, inoculated with blood from a 3-year-old female monkey (S13), yielded 13 colonies; the other, inoculated with blood from a 2-year-old male monkey (M22), yielded 2 colonies. Microscopic examination of Gram-stained smears of these colonies revealed small, pleomorphic, gram-negative bacteria; their identity was confirmed by using molecular methods.
DNA extracts were prepared from colonies by using a QIAamp tissue kit (QIAGEN, Hilden, Germany) and incorporated into Bartonella genus–specific PCRs selective for fragments of the 16S rRNA–encoding gene, the 16S–23S rDNA intergenic spacer region (ISR), gltA, ribC, and ftsZ (9–12). Extraction controls (water only) were concurrently prepared with DNA extracts and incorporated into each PCR along with a reagent-only (no DNA) negative control and a reaction-positive control (B. henselae DNA). In all assays, DNA extracts and positive controls yielded amplification products, whereas extraction and reagent-only controls did not.
The nucleotide base sequences of all amplification products were determined. Analysis of sequence data indicated that the 2 isolates possessed indistinguishable gltA, 16S rDNA, and ISR sequences but that their ribC and ftsZ sequences differed from each other by 1 bp mutation. Comparison of these data with those available for validated Bartonella spp. indicated that the sequences of isolates S13 and M22 were most similar to those of B. quintana (ribC 97%, gltA 98%, ISR 98%, ftsZ 99%, and 16S rDNA 100% similarity). These similarity values are higher than those previously proposed as thresholds for delineation of Bartonella spp (13), suggesting that the isolates S13 and M22 were strains of B. quintana.
Figure
Figure. Phylogenetic dendrogram of Bartonella spp., inferred from alignment of concatenated sequence data (4,007 bp) by using a maximum-likelihood algorithm, within the MEGA4 suite (www.megasoftware.net). The strength of proposed branching orders...
We inferred the phylogenetic positions of the 2 isolates within the genus from alignment of concatenated sequence data (all 5 loci). In this inference, isolates S13 and M22 grouped together and formed a well-supported tight cluster with B. quintana and no other Bartonella spp. (Figure). The phylogenetic distances between B. quintana, isolate S13, and isolate M22 were much shorter than those between, for example, Bartonella vinsonii subsp., supporting the classification of isolates S13 and M22 as strains of B. quintana.
Subsequently, by using a commercial indirect immunofluorescence antibody test kit (Euroimmun, Lubeck, Germany), we found antibodies against B. quintana in 33 monkey serum samples. Serum from 12 monkeys yielded a high titer (>320). Serum was available from only 1 of the culture-positive animals, M22, and this sample had a positive titer of 320. Overall, we found B. quintana seroprevalence to be significantly lower in sexually mature monkeys (χ2 = 6.034, p = 0.014), but we found no significant correlation between seroprevalence and age or gender. We obtained the B. quintana isolates ≈6 weeks after blood collection and immediately attempted to resample the 2 infected monkeys. We were able to obtain blood from monkey M22 only; this sample did not yield further isolates. However, the animal remained seropositive, with an anti–B. quintana titer of 320.
What is particularly intriguing about the recovery of B. quintana from the blood of 2 apparently healthy rhesus macaques is that the monkeys were not members of a natural wild population; rather, they had been bred in captivity in suburban Beijing and held in enclosures apart from other animals. This recovery suggests that B. quintana was being maintained in the colony or that monkeys acquired infection from the only other animals they had contact with: humans. High B. quintana seroprevalence in the colony, higher for immature than older animals, suggests that other monkeys had also been exposed to the bacterium, although the true meaning of these findings is unclear, particularly because the specificity of the immunoassay in monkeys in unknown.
Examination of the monkeys from which blood was collected failed to reveal any ectoparasites, and officials at the animal facility reported never seeing ectoparasites on the monkeys. Thus, we are no closer to identifying which species of arthropod, if any, serves as a vector for the monkey-associated B. quintana infection.
Although isolates S13 and M22 should best be considered strains of B. quintana, they are, nonetheless, apparent outliers within the currently recognized diversity of the species. Previous work surveying genetic diversity among 16 human-associated B. quintana isolates of diverse provenance (14) encountered no gltA sequence dissimilarity and only 0.2% ftsZ sequence dissimilarity, whereas isolates S13 and M22 displayed >1% dissimilarity with the B. quintana type strain at both loci. This level of sequence dissimilarity is similar to that reported between the B. quintana type strain and the isolate from a cynomolgus monkey (6). Unfortunately, because those data were not deposited in GenBank, we were unable to directly compare our sequence data with those previously reported for this B. quintana strain. Such comparisons might indicate the existence of nonhuman primate–adapted genotypes within the species.
Ms Huang is a postgraduate student in the Chinese Center for Disease Control and Prevention. Her research focuses on Bartonella spp. infections in human and animals.
Acknowledgments
We thank Fengxia Meng, Liang Lu, Haixia Wu, and Jimin Sun for discussing the results and Dongsheng Ren and Huailei Ma for helping with sampling.
This work was supported by Major National Science and Technology Projects of China grant 2008ZA10004-010 and National Natural Science Foundation of China grant 30371246.
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Cite This Article1These authors contributed equally to this article.
Table of Contents – Volume 17, Number 9—September 2011
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Qiyong Liu, State Key Laboratory for Infectious Diseases Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, PO Box 5, Changping, Beijing 102206, People’s Republic of China
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