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Expansion of brucellosis detection in the country of Georgia by screening household members of cases and neighboring community members



Brucellosis is considered as endemic zoonotic disease in the country of Georgia. However, the burden of the disease on a household level is not known. Therefore, this study sought to determine the benefits of active surveillance coupled to serological screening for the early detection of brucellosis among close contacts of brucellosis cases.


We used an active surveillance approach to estimate the rate of seropositivity among household family members and neighboring community members of brucellosis index cases. All participants were screened using the serum tube agglutination test (SAT). Blood cultures were performed, obtained isolates were identified by a bacteriological algorithm, and confirmed as Brucella spp. using real-time PCR. Further confirmation of Brucella species was done using the AMOS PCR assay.


A total of 141 participants enrolled. Of these, 27 were brucellosis index cases, 86 were household family members, and 28 were neighboring community members. The serological evidence of brucellosis in the household member group was 7% and the rate at the household level was 21%. No screened community members were Brucella seropositive. Majority of brucellosis cases were caused by B. melitensis; only one index case was linked to B. abortus.


We found evidence of brucellosis infection among household family members of brucellosis index cases. B. melitensis was the most common species obtained. Findings of this active surveillance study highlight the importance of screening household family members of brucellosis cases and of the use of culture methods to identify Brucella species in the country of Georgia.

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Brucellosis is a febrile, debilitating worldwide zoonotic illness caused by Gram-negative coccobacilli of the genus Brucella [1]. Human brucellosis is usually linked to ingestion of unpasteurized dairy products of infected ruminant livestock or direct contact with infected animal parts, with inoculation through skin and mucous membranes and more rarely through the inhalation of aerosolized particles [2]. In Georgia, a country in the Caucasus region brucellosis is endemic, but there are still many unanswered epidemiological and clinical questions regarding disease [3,4]. For instance, the burden of the disease among close contacts of brucellosis cases is not known. Epidemiologically, knowledge of contact patterns is critical to design effective control measures for endemic diseases because it allows identification of specific groups in a population for public health planning [5].

Georgia currently uses a passive surveillance approach for brucellosis. This type of surveillance is subject to multiple limitations including underreporting [6]. Several studies conducted in brucellosis-endemic areas have shown the importance and benefits of active surveillance by screening household family members of brucellosis cases [7,8]. In addition, the implementation of an active surveillance program can significantly enhance early disease detection to provide better disease incidence estimates and reduce disease complications. From a population perspective, active surveillance studies have reported high rates of infection among household contacts of brucellosis cases in endemic countries such as Saudi Arabia (19%), Iran (20%), Peru (8%), and recently in Azerbaijan (10%) [9-12].

The aim of this active surveillance study was to determine the burden of brucellosis infection among household family members and neighboring community members of patients with brucellosis in the country of Georgia.


Study population

Between May 2009 and July 2011, individuals 18 years of age or older with confirmed brucellosis at the Medical Parasitology and Tropical Medicine Research Institute (MPTMRI) in Tbilisi were invited to participate as brucellosis index cases for this study. A confirmed brucellosis case was defined as having a compatible clinical symptomatology with an epidemiological link plus a positive laboratory result. A compatible symptomatology was defined as a fever (>38°C) for at least five days and at least two of the following signs or symptoms: sweats, rigors, malaise, fatigue, anorexia, weight loss, arthralgia, myalgias, arthritis, neuritis, neuro-psychiatric symptoms, epididymo-orchitis or changes in liver function tests. An epidemiological link suggestive of brucellosis included assistance with animal birth, involvement in animal husbandry, contact with sick animals, consumption of unpasteurized milk or dairy products, or consumption of undercooked meat. A positive laboratory finding was defined as a titer ≥ 1:200 by the serum tube agglutination test (SAT) [13] and/or isolation of Brucella spp. from blood culture [14]. SAT was performed using serial (x2) dilutions of serum samples and Brucella abortus Antigen (BD), following manufacturer’s instructions. Brucella Positive Control (BD) and Febrile Negative Controls (BD) were utilized to assess the test performance. Written informed consent was obtained from brucellosis cases to participate in the study as an index case and to approach their household family members for brucellosis testing. Then they were administered a standardized questionnaire to collect socio-demographic and epidemiological data, as well as exposure history and clinical information associated with brucellosis.


For this study, a field team composed of an epidemiologist and a phlebotomist visited the brucellosis index case household to enroll the household family members and neighboring community members. A household family member was defined as an adult or a child (≥5 years old), who consumed at least five meals per week in the same house as the brucellosis index case and/or was living in the same household for at least two months prior to enrollment. For each brucellosis index case, a neighboring community household was systematically selected (three houses away, either to the right or left of the index house). A neighboring community member was defined as an individual five years old or older. For both groups, household and community, all individuals meeting selection criteria were invited to voluntarily participate. Volunteers were enrolled after obtaining written consent. A blood sample was drawn at enrollment, and then again after 2-4 weeks at a follow-up visit. The same questionnaire, used among brucellosis index cases was applied to enrolled household and community members to collect epidemiological data associated with brucellosis. A microbiological testing algorithm and real-time polymerase chain reaction (PCR)-based methods (Target 1, Idaho Technology Inc.) were used to identify Brucella blood culture isolates, while the conventional AMOS PCR assay was used to confirm the Brucella species [14,15].

Several articles have reported the successful use of PCR for the detection of Brucella-specific DNA in blood and serum samples using various platforms [16-20]. This approach provides a rapid tool to confirm the presence of Brucella. In attempt to identify a reliable and reproducible approach for detecting Brucella-specific DNA directly from clinical samples several real-time PCR assays (targeting Brucella T1 [Idaho Technology Inc.], B4/B5, IS711) were tested using various DNA isolation methods and amplification conditions. Although preliminary experiments using spiked samples provided promising results, no reproducible and definite amplification was obtained when using blood or serum samples from acute phase of culture-positive subjects (publication in preparation). Thus, only culture and SAT results were reported.

Ethical approvals

This study protocol was reviewed and approved by institutional review boards at the U.S. Army Medical Research Institute of Infectious Disease, Ft. Detrick, MD (HP-08-25), Walter Reed Army Institute of Research, Silver Spring, MD (WRAIR #1866), and at the National Center for Disease Control and Public Health, Tbilisi, Georgia.


During the study period, a total of 141 participants were enrolled. Of these, 27 were brucellosis index cases, 86 were household family members of index cases, and 28 were neighboring community members. Ninety-three percent (n = 25) of brucellosis index cases were positive for Brucella-specific antibody by SAT (6 cases, 1:200; 3 cases, 1:320; 9 cases, 1:400; 5 cases, 1:640; 1 case, 1:800, and 1 case, 1:1280). Of these, 11 isolates identified by the bacteriological algorithm were confirmed as Brucella spp. by real-time PCR. Furthermore, the AMOS PCR assay confirmed that 10 isolates belonged to B. melitensis and one sample to B. abortus (Figure 1). Additionally, two brucellosis index cases were serologically negative by SAT at enrollment but B. melitensis was isolated, and thus these were subsequently included in the group of index cases.

Figure 1

Amplification of DNAs of Brucella spp isolates by AMOS PCR. From left to right: 100 bp ladder (Sigma Aldrich); Isolate X026, B. melitensis, B. melitensis Positive control, Isolate X033, B. abortus, B. abortus Positive control, Negative control (no DNA), 100 bp ladder.

The median age of brucellosis index cases was 35 years (range: 19-63), 93% were males, 93% lived in rural areas, 67% had high school education, 41% were farmers, 41% were from Kakheti, and 35% from Kvemo-Kartil regions (eastern Georgia). The most common signs and symptoms after fever for brucellosis index cases were sweats (100%), fatigue (96%), joint pain (93%), malaise (93%), rigors (88%), and to lesser extent back pain (35%), and muscle pain (30%). All brucellosis index cases reported having consumed either of fresh cheese, yogurt, milk, sour cream or sheep cheese in the past four months. They also reported having consumed unpasteurized dairy products (88%) or not boiled milk (15%), using home-made dairy products (67%), and slaughtering at home (59%). Most brucellosis index cases had livestock in their households (81%, sheep, cattle or goats), 63% had direct contact with sick animals, and 43% with aborted livestock in the past four months. Regarding self-protection against brucellosis, 26% had knowledge about disease, 36% washed their hands after handling animals, and none wore gloves when handling animals (Table 1).

Table 1 Characteristics of brucellosis index cases, household family members, and neighboring community members

In the household family member group, the median age was 27 years. Forty three percent of this group was male, 41% had high school education, and 35% were housewives. Over 73% made their dairy products at home, 69% consumed unpasteurized dairy products, and 37% did not boil milk before consumption. They also reported having livestock in the household (87%) and direct contact with sick (34%) or aborted livestock (11%) in the past four months. Moreover, one-third of them had knowledge about the disease, 68% washed hands after handling animals, and only 7% reported wearing gloves when handling animals.

At enrollment, four household members had serological titers ≥1:320 for Brucella. Additionally, two household family members without any clinical manifestations were serologically negative by SAT but positive by blood culture (Table 2). The brucellosis rate among household family members was 7.0% (6/86; 95% confidence interval = 2.9-13.9%), and the brucellosis rate at the household level was 21% (6 out of 27 households had at least one member with brucellosis). Four of the six household family members found to be positive by SAT or by blood culture returned for a follow-up visit, and were symptomatic. The other two cases refused to continue participation thus no follow-up information is available. No epidemiologic risk factor was associated with brucellosis infection in the household family member group.

Table 2 Demographic characteristics, risk factors, and serum agglutination test and culture isolated of six brucellosis cases found among household family members of brucellosis index cases

In the neighboring community group, the median age was 46 years, 39% were males, 43% had high school education, 54% were housewives; and all lived in rural areas. Over 29% did not boil milk before consumption, 69% consumed unpasteurized dairy products, 61% made dairy products at their homes, and 43% did home slaughtering. Sixty-one percent had livestock in the household, 13% had direct contact with sick livestock, and none reported having contact with aborted livestock in the past four months. Most neighboring community members washed their hands after handling animals (89%), but few (8%) reported wearing gloves when handling animals. Additionally, 36% reported having knowledge of brucellosis. No community member was found to be Brucella seropositive by SAT or by blood culture.


In this study, an active surveillance approach was used to obtain evidence of Brucella infection among household family members of brucellosis index cases. The brucellosis rate among household family members was similar to that reported in Peru, Turkey, and recently in the neighboring country of Azerbaijan [7,11,12]. Our findings were consistent with other previous studies addressing the benefits and importance of screening household members of brucellosis index cases in endemic areas [7-12]. Such screening efforts may help reduce the burden of brucellosis and its medical complications, as well as improve treatment outcomes in the country of Georgia.

An interesting finding from this study was the detection of two culture-confirmed brucellosis cases among household family members without any clinical manifestation and serologically negative by SAT. This suggests that SAT, the most widely used method for the laboratory diagnosis of human brucellosis, is not sensitive enough to detect antibodies to Brucella species in subjects with early bacteremia. It is possible that during the active stage of the disease, antinuclear antibodies be a reason for false negative results by SAT [21]. It is also noteworthy that SAT is currently the main laboratory tool supporting confirmation of clinical diagnosis of human brucellosis in Georgia.

We believe that the introduction of additional screening and confirmatory laboratory testing - for instance, culture combined with reliable and reproducible PCR methods -can strengthen the Brucella detection capacity in the country of Georgia. In addition to detecting the Brucella organisms by culture and PCR, results from these methods can be also used to evaluate drug regimens for treatment of brucellosis [22].

The failure of PCR to detect Brucella-specific DNA directly in clinical samples (blood and serum) is supported with recent suggestions in the literature and held within the brucellosis research community that the sensitivity and the specificity of most PCR-based methods are not well established. The real value for use of PCR diagnostics with clinical samples, and hence for diagnosis, has not yet been properly validated [23]. Considerable laboratory work is still required to verify, validate, and establish standard positive and negative controls, internal and inhibition controls, quality assurance and contamination control before PCR could be considered for a routine test for brucellosis diagnosis.

In our study, the overall brucellosis male-to-female ratio was about 8:1. This high gender disparity may be due to occupational exposure differences, since males usually work on the farms and in the care and management of farm animals [24]. Thus, brucellosis is more likely to occur in males than in females in Georgia. This fact was observed in this study, where 93% of brucellosis index cases were males, and 4 out of 6 cases identified in the household family member group were males (Table 2). A similar finding was reported in a previous brucellosis study conducted in Azerbaijan [12]. We have also found that the majority of the brucellosis index cases seeking medical care at MPTMRI were residents of rural areas, mainly from the Georgian regions of Kvemo-Kartli (southeastern) and Kakheti (eastern). Sheep husbandry and shepherding are common activities among rural farmers from eastern Georgia [3,4].

B. melitensis is responsible for the most severe brucellosis infection in humans and is more common in Latin America, the Mediterranean area, Central Asia, and in the Caucasus region [25]. The main reservoirs for B. melitensis are sheep and goats. Human infection with this species is commonly acquired through ingestion of contaminated dairy products or by direct contact with infected animals or animal discharges [26]. In this study, almost all of the brucellosis cases were caused by B. melitensis. Our epidemiological data suggest that occupational exposure to animals is probably the most common cause of human transmission for this Brucella species among male brucellosis index cases and male household family members. In addition, B. melitensis appears to be the predominant species associated with human brucellosis in eastern Georgia.

Interestingly, the data on exposure to modes of Brucella transmission was similar among neighboring community members and household family members (Table 1), while no brucellosis cases were found among community members in the study. We hypothesize that the absence of brucellosis in the community group might be associated with the practice of some preventive measures to control human and animal brucellosis [27]. Neighboring community members compared to their counterparts reported higher percentages for hand washing after handling animals, animal vaccination against brucellosis, and boiling milk before consumption. To our knowledge, there is insufficient evidence on the effectiveness of preventive measures against brucellosis in Georgia. Therefore, further studies are needed to determine whether common preventive measures along with other barriers methods not addressed in this study can help minimize or probably eliminate the risk of human brucellosis transmission.

This study had some limitations. First, the small number of female brucellosis cases limited the statistical power to detect risk factors in this group of participants. It is believed that in the Caucasus region, consumption of unpasteurized dairy products constitutes an important mechanism of brucellosis transmission, mainly among women and children; however, the burden of this probable source of Brucella infection and its public health implication are still not determined. Second, no risk factor was associated with exposure to Brucella among household family members of brucellosis index cases. This lack of association may be attributed to the small number of cases found in this group. Third, the number of community members was relatively small due to non-participation, and thus, the burden of disease in this group may be biased. Finally, most brucellosis cases at MPTMRI were from eastern Georgia, thus our results may not represent the true situation of brucellosis in other regions of the country such as west Georgia. Despite these limitations, it is noteworthy that this study was the first attempt to use an active surveillance approach to evaluate the importance of screening household family members and neighboring community members for brucellosis in the country.


In summary, using an active surveillance approach for brucellosis we found evidence of Brucella infection among household family members of brucellosis index cases, and the high ratio of male-to-female cases suggests the disease is largely occupational. Moreover, almost all brucellosis cases from eastern Georgia were caused by B. melitensis. An active surveillance approach enhances disease detection and provides additional epidemiological data that can be used to behavior change interventions in order to reduce the incidence of human brucellosis in Georgia.


  1. 1.

    Pappas G, Papadimitriou P, Akritidis N, Christou L, Tsianos EV. The new global map of human brucellosis. Lancet Infect Dis. 2006;6:91–9.

  2. 2.

    Seleem MN, Boyle SM, Sriranganathan N. Brucellosis: a re-emerging zoonosis. Vet Microbiol. 2010;140:392–8.

  3. 3.

    Akhvlediani T, Clark DV, Chubabria G, Zenaishvili O, Hepburn MJ. The changing pattern of human brucellosis: clinical manifestations, epidemiology, and treatment outcomes over three decades in Georgia. BMC Infect Dis. 2010;10:346.

  4. 4.

    Havas KA, Ramishvili M, Navdarashvili A, Hill AE, Tsanava S, Imnadze P, et al. Risk factors associated with human brucellosis in the country of Georgia: a case-control study. Epidemiol Infect. 2013;141:45–53.

  5. 5.

    Bansal S, Read J, Pourbohloul B, Meyers LA. The dynamic nature of contact networks in infectious disease epidemiology. J Biol Dyn. 2010;4:478–89.

  6. 6.

    Brookmeyer R, Yasui Y. Statistical analysis of passive surveillance disease registry data. Biometrics. 1995;51:831–42.

  7. 7.

    Tabak F, Hakko E, Mete B, Ozaras R, Mert A, Ozturk R. Is family screening necessary in brucellosis? Infection. 2008;36:575–7.

  8. 8.

    Almuneef MA, Memish ZA, Balkhy HH, Alotaibi B, Algoda S, Abbas M, et al. Importance of screening household members of acute brucellosis cases in endemic areas. Epidemiol Infect. 2004;132:533–4.

  9. 9.

    Alsubaie S, Almuneef M, Alshaalan M, Balkhy H, Albanyan E, Alola S, et al. Acute brucellosis in Saudi families: relationship between brucella serology and clinical symptoms. Int J Infect Dis. 2005;9:218–24.

  10. 10.

    Sharifi-Mood B, Metanat M, Alavi-Naini R. Screening of the family members of patients with acute brucellosis in Southeast Iran. Indian J Med Microbiol. 2007;25:176–7.

  11. 11.

    Mendoza-Núñez M, Mulder M, Franco MP, Maas KS, Castañeda ML, Bonifacio N, et al. Brucellosis in household members of Brucella patients residing in a large urban setting in Peru. Am J Trop Med Hyg. 2008;78:595–8.

  12. 12.

    Ismayilova R, Mody R, Abdullayev R, Amirova K, Jabbarova L, Ustun N, et al. Screening of household family members of brucellosis cases and neighboring community members in Azerbaijan. Am J Trop Med Hyg. 2013;88:929–31.

  13. 13.

    Ulu-Kilic A, Metan G, Alp E. Clinical presentations and diagnosis of brucellosis. Recent Pat Antiinfect Drug Discov. 2013;8:34–41.

  14. 14.

    Ruiz J, Lorente I, Perez J, Simarro E, Martinez-Campos L. Diagnosis of brucellosis by using blood cultures. J Clin Microbiol. 1997;35:2417–8.

  15. 15.

    Bricker BJ, Halling SM. Differentiation of Brucella abortus bv. 1, 2, and 4, Brucella melitensis, Brucella ovis, and Brucella suis bv. 1 by PCR. J Clin Microbiol. 1994;32:2660–6.

  16. 16.

    Zerva L, Bourantas K, Mitka S, Kansouzidou A, Legakis NI. Serum is the prefered clinical specimen for diagnosis of human brucellosis by PCR. J Clin Microbiol. 2001;39:1661–4.

  17. 17.

    Navarro E, Escribano J, Fernández J, Solera J. Comparison of three different PCR methods for detection of Brucella spp in human blood samples. FEMS Immunol Med Microbiol. 2002;11; 34(2):147–51.

  18. 18.

    Queipo-Ortuño MI, Colmenero JD, Reguera JM, García-Ordoñez MA, Pachón ME, Gonzalez M, et al. Rapid diagnosis of human brucellosis by SYBR Green I-based real-time PCR assay and melting curve analysis in serum samples. Clin Microbiol Infect. 2005;11(9):713–8.

  19. 19.

    Navarro E, Segura JC, Castaño MJ, Solera J. Use of real-time quantitative polymerase chain reaction to monitor the evolution of Brucella melitensis DNA load during therapy and post-therapy follow-up in patients with brucellosis. Clin Infect Dis. 2006;42(9):1266–73.

  20. 20.

    Castaño MJ, Solera J. Chronic brucellosis and persistence of Brucella melitensis DNA. J Clin Microbiol. 2009;47(7):2084–9.

  21. 21.

    Yumuk Z, Caglayan C, Yavuz CI, Ocak Z, Hamzaoglu O. The pattern of autoantibodies related to false negative results of serological tests in the diagnosis of human brucellosis. Afr J Microbiol Res. 2013;7:1109–13.

  22. 22.

    Elfaki MG, Al-Hokail AA, Nakeeb SM, Al-Rabiah FA. Evaluation of culture, tube agglutination, and PCR methods for the diagnosis of brucellosis in humans. Med Sci Monit. 2005;11:MT69–74.

  23. 23.

    Yu WL, Nielsen K. Review of detection of Brucella spp. by polymerase chain reaction. Croat Med J. 2010;51(4):306–13.

  24. 24.

    Galińska EM, Zagórski J. Brucellosis in humans–etiology, diagnostics, clinical forms. Ann Agric Environ Med. 2013;20:233–8.

  25. 25.

    Garin-Bastuji B, Blasco JM, Grayon M, Verger JM. Brucella melitensis infection in sheep: present and future. Vet Res. 1998;29:255–74.

  26. 26.

    Atluri VL, Xavier MN, de Jong MF, den Hartigh AB, Tsolis RM. Interactions of the human pathogenic Brucella species with their hosts. Annu Rev Microbiol. 2011;65:523–41.

  27. 27.

    Franco MP, Mulder M, Gilman RH, Smits HL. Human brucellosis. Lancet Infect Dis. 2007;7:775–86.

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This study was made possible by the hard work and dedication of multiple host-country investigators. The authors thank all the volunteers for participating in this study and study personnel for their assistance in enrollment and follow-up visits, as well as Sebastian-Santiago for technical assistance. This study was funded by the Defense Threat Reduction Agency (DTRA) through the Cooperative Biological Engagement Program (CBEP-CBR-GG17).


The views expressed herein are those of the authors and do not reflect the official policy or position of the Department of the Army, Department of Defense, or the US Government, or any other organization listed. Some authors are employees of the US government. This work was prepared as part of their official duties and, as such, there is no copyright to be transferred.

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Correspondence to Nino Trapaidze.

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The authors declare that they have no competing interests.

Authors’ contributions

NT, RM, RR, PE, and MN designed the study. NT, LS, NG, SC, ET, MB, NC, KS, ST, and RM conducted the study. LS, CB, and NT conducted the statistical analysis and wrote the draft of the manuscript. TA, RR, RM, MH, PE, and MN revised the manuscript. All authors read and approved the final manuscript.

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Sanodze, L., Bautista, C.T., Garuchava, N. et al. Expansion of brucellosis detection in the country of Georgia by screening household members of cases and neighboring community members. BMC Public Health 15, 459 (2015).

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  • Brucellosis
  • Epidemiology
  • Zoonotic
  • Surveillance
  • Country of Georgia