The syndemic relationship between tuberculosis (TB) and human immunodeficiency virus (HIV) infection has contributed to high morbidity and mortality worldwide [1] . The World Health Organization (WHO) Africa region is the hardest hit where about 74% of the estimated 1.2 million TB patients co-infected with HIV occurred in 2014 [2] . For many years, efforts to tackle TB and HIV have been largely independent of each other, despite their overlapping epidemiology. The risk of progression from latent to active TB is increased by infection with HIV [3] . Likewise, TB is the most important opportunistic disease that increases progression to acquired immune deficiency syndrome (AIDS) and the number one killer in HIV-positive individuals [4] [5] . Thus effective TB control can contribute to better HIV/AIDS control by reducing the TB burden in people with HIV as well as providing an entry point to HIV prevention and care for people with TB [6] . The HIV prevalence in the general population in Ghana was 1.47% in 2014 which is an indication of a downward trend over a fifteen-year period from 2.3% in 2000 [7] . Studies in Africa and Asia have reported high HIV prevalence in TB patients than are observed in the general population [8] . Routine programme data from TB/HIV sites showed that in 2005, 40 percent of TB patients who were tested for HIV were HIV-positive and in 2006 these went down to 33 percent [9] [10] . Ghana is a high burden TB/HIV country [11] , however very few studies have reported on the prevalence of TB/HIV co-infection in Ghana [12] [13] [14] . These previous studies were single hospital-based in the two big cities in Ghana―Accra and Kumasi. There was the need to conduct a nationwide study to establish the national prevalence of this dual infection. This study was therefore conducted to determine the prevalence of HIV in TB patients in Ghana.

Sixty seven health facilities from the northern and southern sectors of Ghana were involved in the study (Table 1). A total of 517 paired positive sputum samples were received from 517 patients. Out of this, a total of 503 TB patients [335 (66.6%) males and 168 (33.4%) females] had at least one culture positive sample (Table 1). Most patients, 136 (27.0%) were within the age group 25 - 34 years (p < 0.001). There were more new cases 468/503 (93.0%) than old cases 35/503 (7.0%) (p < 0.001). Majority (73.6%), 370 out of 503 were employed in the informal sector (p < 0.001). The difference in HIV seroprevalence rates between males, 36/335 (10.75%) and females, 38/168 (22.6%) was statistically significant (p < 0.05). The seroprevalence of HIV in newly diagnosed TB patients and those already on treatment, was 69/468 (14.7%) and 5/35 (14.3%) respectively (p > 0.05) (Table 2). Out of the 503 dried blood spots tested for HIV, 74 (14.7%) were seropositive. This comprises 71 (14.1%) HIV-1 and 3 (0.6%) HIV-1 & 2. None of the samples were positive for HIV-2 infection alone (Table 3). All the 503 isolates were Mycobacterium tuberculosis complex (MTBC) based on phenotypic identification. The LPA run for all 74 isolates from TB/HIV co-infected patients showed that 70 (94.6%) were Mycobacterium tuberculosis while the remaining 4 (6%) were Mycobacterium africanum (Table 4). Monoresistance to isoniazid and rifampicin were 4 (5.4%) and 1 (1%) respectively. However, resistance to both drugs (multi-drug resistant-MDR) was not observed. Sixty nine (93%) isolates were susceptible to both drugs (Figure 1).

^aPulmonary TB patients in the selected diagnostic centres who have never been treated for TB or have been treated for a period less than one month. ^bAll patients who have been previously treated for TB for a period more than one month. ^cJobs performed outside the formal structures that govern taxes, workplace regulations and social protection schemes. ^dJobs performed within formal structures that govern taxes, workplace regulations and social protection schemes. ^eNot engaged in any gainful occupation. ^fSomeone who attends an educational institution and not engaged in any gainful occupation.

^aFirst Response―a rapid discriminatory assay for HIV-1 and HIV-2 antibodies. ^bInno-Lia―a line immunoblot assay used to confirm the presence of HIV antibodies in reactive HIV samples from initial rapid screening.

TB/HIV co-infection is of great public health concern worldwide. This study sought to provide baseline data to inform health policies and actions to address this deadly disease duo in Ghana. Testing for HIV antibodies in TB patients as used in this study seemed an appropriate strategy to determine the burden of TB/HIV. While screening HIV-positive individuals for TB infection may be another option, HIV patients already burdened with stigmatisation may be unwilling to undertake a TB test as well. This assertion corroborates a report [15] showing that TB patients are more likely to accept HIV testing than HIV patients testing for TB. HIV prevalence in TB patients can be used as an indicator of the degree of spread of HIV in the general population. This information is also important for the provision of comprehensive HIV/AIDS care and support. HIV infection rates of up to 48% have been reported among newly diagnosed TB cases in Ghana [20] , but the burden of TB among HIV-infected individuals in Ghana is barely acknowledged. Consistent with the global trend, more males (66.6%) than females (33.4%) were diagnosed with TB in this study [1] . The reasons for gender disparity with regards to TB infection is not well understood though it is believed that some cultural and biological factors may play a role [21] . Majority 70/74 (94.6%) of the TB/HIV co-infected patients were infected with M. tuberculosis which is very similar to what other studies have reported in Ghana [22] [23] . On the contrary, the number of M. africanum (5.4%) isolates was relatively low. Almost 93% of isolates obtained from TB patients were susceptible to both isoniazid and rifampicin. This result may be due to the fact that majority of the patients were new cases and as such had not taken any anti-TB drug before. The overall TB/HIV co-infection prevalence was 14.7% which was consistent with the 14.8% reported earlier in Ghana [9] . However, it was relatively lower than previous rates of 23.2%, 16.8 % and 46.2% respectively reported in Ghana [12] [13] [14] as well as the average rate for Africa (32%) [24] . These previous studies from Ghana were conducted in a very limited number of sites and the study population may not exactly reflect the general population. In Ghana infection with HIV-1 is most common, accounting for over 90% with very few cases of mixed infection of both HIV-1 and HIV-2 reported [25] . Hence it was not surprising to find similar results in this present study. There is an indication that there has been a steady change in the prevalence of TB/HIV co-infection over the last decade. This change in co-infection prevalence might be the result of improvements in public awareness, better treatment regimens and a general decline in HIV prevalence in Ghana [7] . Conversely, TB prevalence in Ghana is reported to be about three times higher than the estimates from WHO prior to the conduct of a TB prevalence survey in 2013 [2] . This suggests that many people are at an increased risk of HIV infection which necessitates a continuous collaborative plan for TB and HIV control activities to ensure comprehensive care for TB/HIV patients.

Some possible limitations in this study were that while TB patients will benefit from this study by knowing their HIV status and thus access treatment and care for both diseases, the same cannot be said for HIV patients who may be harbouring TB since the study focused on TB infected persons and not HIV infected persons. That notwithstanding, the results have been useful in strengthening the implementation of the joint TB/HIV strategy in Ghana. It has also been a vital biological marker of the HIV/AIDS epidemic in Ghana and indicating the impact on TB infection. Funds for the molecular testing part of the study became available in 2017 hence the delay in the publication of the findings.

The prevalence of TB/HIV co-infection was 14.7%, and co-infection was more common in the sexually active age group of 25 - 34 years. Majority of these TB/HIV co-infected patients were infected with M. tuberculosis which were susceptible to both isoniazid and rifampicin. HIV-1 was the most common HIV strain infecting these patients. Further research is needed to monitor the trend and level of interaction between TB and HIV in Ghana.

We are thankful to the laboratory technologists of all the laboratories visited for sample collection and transportation. We also acknowledge the Global Fund against HIV/AIDS, TB & Malaria and the Ghana Health Service for their financial support. The molecular analysis and publication was funded by DELTAS Africa Initiative [Afrique One―ASPIRE/DEL-15-008]. Afrique One―ASPIRE is funded by a consortium of donors including the African Academy of Sciences (AAS), Alliance for Accelerating Excellence in Science in Africa (AESA), the New Partnership for Africa’s Development Planning and Coordinating (NEPAD) Agency, the Wellcome Trust [107753/A/15/Z] and the UK government.

Authors declared that they have no competing interests.

KKA and WKA came out with the study design and supervised the laboratory work. KKA contributed to the writing and editing of the manuscript. RO, CB and NN conducted the conventional TB laboratory work. JK and KB performed the HIV testing. SOA performed the molecular laboratory work, contributed to the manuscript writing and data analysis. GIM assisted with the proposal writing and data analysis. AH edited the study protocols. NAA and FAB contributed to the study implementation by providing reagents and equipment. All authors read and approved the final manuscript before submission.

Addo, K.K., Ampofo, W.K., Owusu, R., Bonsu, C., Nartey, N., Mensah, G.I., Addo, S.O., Bonney, K., Kumi, J., Hesse, A., Addo, N.A. and Bonsu, F.A. (2018) First Nationwide Survey of the Prevalence of TB/HIV Co-Infection in Ghana. Journal of Tuberculosis Research, 6, 135-147. https://doi.org/10.4236/jtr.2018.62013

AFB: Acid fast bacilli

AIDS: acquired immune deficiency syndrome

A-LYS: Alcalic lysis

Anti-TB: Anti-tuberculosis

CPC: Cetylpyridinium Chloride

DOTS: Directly Observed Treatment Short course

DST: Drug susceptibility testing

HIV: Human Immunodeficiency Virus

LJ: Lowenstein-Jensen

LPA: Line probe assay

MDR: Multi-drug resistance

MTBC: Mycobacterium tuberculosis complex

NMIMR: Noguchi Memorial Institute for Medical Research

TB: Tuberculosis

PBS: Phosphate buffer saline

PCR: Polymerase chain reaction

PNB: Para-Nitrobenzoic acid

WHO: World Health Organization

ZN: Ziehl-Neelsen